Notes
Article history
The research reported in this issue of the journal was funded by the HTA programme as project number 15/174/24. The contractual start date was in January 2018. The draft report began editorial review in April 2020 and was accepted for publication in July 2020. The authors have been wholly responsible for all data collection, analysis and interpretation, and for writing up their work. The HTA editors and publisher have tried to ensure the accuracy of the authors’ report and would like to thank the reviewers for their constructive comments on the draft document. However, they do not accept liability for damages or losses arising from material published in this report.
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© Queen’s Printer and Controller of HMSO 2021. This work was produced by Fordham et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK.
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Chapter 1 Background
Cognitive–behavioural therapy (CBT) is an amalgam of interventions that emerged from cognitive and behavioural psychological models. It aims to improve patients’ quality of life by changing their maladaptive cognitions that maintain problematic symptoms. The basic principles of CBT are presented in Figure 1.
Cognitive–behavioural therapy can be delivered in different formats. High-intensity CBT has been defined as formal CBT with a trained health professional, predominantly delivered face to face, in an individual or group format. 1 Low-intensity CBT focuses on self-help and can be delivered by health professionals with brief CBT training (non-psychologists) and via several platforms (internet, telephone, paper based or face to face). 1 The distinction can become less clear in some forms of CBT in which high-intensity therapy is combined with low-intensity self-help methods.
A previous overview of CBT reviews,2 conducted in 2012, identified 296 reviews. However, only 11 of these synthesised randomised controlled trial (RCT) evidence; therefore, the conclusions are subject to increased bias. 2 Since this overview,2 there have been many more trials and reviews. There has also been more guidance for conducting and reporting high-quality trials and reviews. 3–6 The existing CBT trial and review evidence base is large, yet the majority of expenditure on psychological treatment research remains focused on CBT effectiveness. 7 Some researchers have argued that CBT is in a ‘virtuous circle: money pours into research, evidence accumulates, more financial support is given to . . . [CBT] . . . and other forms of psychotherapy are excluded’8 (Peter Fonagy, University College London) (Copyright © The Economist Newspaper Limited 2014. Reproduced with permission). In providing a comprehensive cross-sectional map of the best-quality available evidence, we can provide an indication of where CBT has an evidence base to support its effectiveness and where future research resources would be best directed.
Cognitive–behavioural therapy interventions share an underlying process, common therapeutic style and employ similar techniques (e.g. guided discovery), yet the condition-, population- and context-specific protocols can look very different from one another. Because of the commonality of CBT interventions across conditions, it is plausible that CBT can produce a general effect across conditions. However, to date, to our knowledge, there is no overarching estimate regarding the consistency of CBT’s effect across different condition categories. We propose to generate such an effect by performing panoramic meta-analyses (PMAs) on the effect estimates generated in each condition.
The concept and methodology of systematically reviewing systematic reviews is established, and includes quality and reporting guidelines. 9,10 However, the existing reviews of systematic reviews are typically undertaken to compare multiple interventions in one condition. 11,12 For this overview, we are interested in examining one intervention (CBT) across multiple conditions. In this overview, the classification of a ‘condition’ was based on the World Health Organization’s (WHO’s) International Classification of Diseases, Eleventh Revision (ICD-11). 13 The WHO must consider cultural, religious and political differences that can influence condition categorisation. In using this internationally recognised tool, we developed research findings that are meaningful to a global audience. In looking across conditions, we examined the effect of CBT across all populations, with CBT compared with all types of comparator. Our primary outcome is health-related quality of life (HRQoL), and we include three secondary outcomes (depression, anxiety and pain) that would contribute to an individual’s quality-of-life rating.
We employ PMA, which is an emerging methodology to synthesise systematic reviews across conditions. 14,15 When methodological assumptions are met, it allows pooling of effect sizes across conditions. This produces an average effect across conditions, which, because of enlarged sample sizes, is estimated with more precision than within-condition pooled estimates.
Chapter 2 Aim and objectives
Aim
The overarching aim of the overview was to map the existing CBT systematic review evidence base and to examine if CBT produced an across-condition, general effect on HRQoL.
Objectives
To answer these research aims, the following steps were undertaken.
Step 1: data mapping
We identified all available systematic reviews of CBT and mapped these according to:
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conditions (ICD-11 category, severity)
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populations (age, sex, ethnicity, countries where the trials were conducted)
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context (delivery format, care setting, intervention timing)
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quality of the reviews.
The mapping exercise identified where there is/is not a high- or low-quality systematic review or meta-analysis of RCTs examining the effectiveness of CBT.
Step 2: panoramic meta-analysis
Reviews from step 1 that had sufficient quantitative data were entered into a PMA for the primary outcome of HRQoL and for the secondary outcomes of depression, anxiety and pain. Sensitivity analyses based on quality were performed.
If across-condition heterogeneity was not considerable, an across-condition general effect was generated for each outcome. Subgroup analyses based on age, CBT intensity, duration of follow-up and type of comparators were undertaken. We checked every within-condition and subgroup analysis to examine if there was evidence of inconsistency with the overall effect estimate.
In Chapter 6, we explore the extent to which the existing evidence base could be used to guide treatment, commissioning and research investment decisions. The aim of the patient and public input into the overview was to ensure that the overview produced work that remained rooted in the overall aim: to improve health for patients receiving CBT.
Chapter 3 Review methods
The methods for the mapping stage of the overview are presented first, followed by the methods for the PMA. The protocol was registered with PROSPERO, the international prospective register of systematic reviews (number CRD42017078690), and published open access. 16
Mapping
Inclusion and exclusion criteria for the mapping
Types of reviews
We included all reviews that reported RCTs if they met four of the five methodological criteria outlined by the Centre for Reviews and Dissemination (CRD) at the University of York, as part of the Database of Abstracts of Reviews of Effects (DARE). 17 DARE was consulted for its guidance in the application of the criteria:
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Were inclusion/exclusion criteria reported?
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Was the search adequate? (Databases stated, more than one database searched or one database plus checking references, hand-searching, contact with researchers, citation searching, internet searching.)
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Were the included studies synthesised?
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Was the quality of the included studies assessed?
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Are sufficient details about the individual studies presented? (Details on the population/setting, intervention and a result for each included study.)
We included reviews of RCTs comparing CBT with an active or non-active comparator. Reviews containing randomised and non-randomised studies were included only if RCT data were summarised separately. We excluded reviews based on any other study designs (e.g. quasi-randomised, non-randomised).
Type of health condition
The ICD-11 classifies mental and physical diseases, disorders, injuries and other related health problems in a comprehensive and hierarchical fashion, and is used as a standard for both clinical and research purposes. 13 The term condition will be used throughout this report to represent diseases, disorders and injuries. Participants with any conditions recognised by the ICD-11 or its nominal categorisation, and of any severity, were included. Non-health-related problems, such as procrastination, were excluded.
For physical conditions, we categorised reviews under the primary ICD-11 codes. For mental conditions, we used the secondary level of ICD-11 codes listed underneath the primary code of 06 mental, behavioural or neurodevelopmental disorders. A review was categorised according to its primary aims. For example, if a review examined the effectiveness of CBT to improve quality of life for people living with diabetes, then 05: Endocrine diseases was the condition category. However, if a review examined the effectiveness of CBT for improving depression in people living with diabetes, then the review was classified as 6A60-80 mood disorders, with comorbid 05 endocrine diseases. Box 1 shows all of the primary and secondary codes that could be considered in grouping reviews together.
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01 Certain infectious or parasitic diseases.
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02 Neoplasms.
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03 Diseases of the blood.
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04 Diseases of the immune system.
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05 Endocrine, nutritional or metabolic diseases.
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07 Sleep–wake disorders.
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08 Diseases of the nervous system.
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09 Diseases of the visual system.
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10 Diseases of the ear or mastoid process.
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11 Diseases of the circulatory system.
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12 Diseases of the respiratory system.
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13 Diseases of the digestive system.
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14 Diseases of the skin.
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15 Diseases of the musculoskeletal system.
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16 Diseases of the genitourinary system.
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17 Conditions related to sexual health.
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18 Pregnancy, childbirth or the puerperium.
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19 Certain conditions originating in the perinatal period.
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20 Developmental abnormalities.
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21 Symptoms and signs not elsewhere classified.
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6A00-06: neurodevelopmental disorders.
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6A20-25: schizophrenia or other primary psychotic disorders.
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6A40-41: catatonia.
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6A60-80: mood disorders.
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6B00-06: anxiety or fear-related disorders.
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6B20-25: obsessive–compulsive disorders.
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6B40-45: disorders specifically associated with stress.
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6B60-66: dissociative disorders.
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6B80-85: feeding or eating disorders.
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6C00-01: elimination disorders.
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6C20-21: disorders of bodily distress.
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6C40-51: disorders due to substance use or addictive behaviours.
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6C70-73: impulse control disorders.
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6C90-91: disruptive behaviour or dissocial disorder.
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6D10-11: personality disorders and related traits.
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6D30-36: paraphilic disorders.
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6D50-51: factitious disorders.
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6D70-72: neurocognitive disorders.
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6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
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6E40: psychological or behavioural factors not elsewhere classified.
Types of participants
We included participants of any age [children/adolescents (aged < 18 years), adults (aged 18–65 years) and older adults (aged > 65 years)], either sex and any ethnicity.
Types of health-care setting
We included reviews of RCTs that were conducted in any setting [e.g. primary care, secondary care, school/university, institutional (residential care)] and in any country.
Types of delivery timing
We included reviews of RCTs in which CBT was delivered preventatively, as a standard responsive care or as a relapse prevention.
Types of interventions
We included only reviews that evaluated CBT. Interventions were accepted as CBT when authors explicitly stated so in the title, abstract or keywords, or when the review defined the intervention as including at least one cognitive and one behavioural element.
If a trial intervention combined CBT with another therapy and the other therapy was used as a comparator condition (e.g. CBT plus pharmacotherapy compared with pharmacotherapy), then we included these trials. If a trial combined CBT with another therapy and this was compared with another type of comparator [e.g. CBT plus pharmacotherapy compared with wait-list control (WLC)], then we excluded these reviews because we could not extract the isolated effects of CBT.
All modes of CBT delivery were included and categorised into high or low intensity, based on the definitions by Roth and Pilling. 1 High-intensity CBT was defined as face-to-face, individual or group therapy, delivered by a trained CBT therapist. Low-intensity was CBT delivered via media (internet, written, telephone), or was when face-to-face, individual or group CBT was administered by a non-CBT therapist (paraprofessional or layperson). If the review did not report the intensity of the intervention, it was assumed to be high-intensity CBT. We excluded all non-CBTs: cognitive therapy, behavioural therapy, third-wave CBT (e.g. acceptance and commitment therapy, mindfulness therapy), motivational interviewing, stress inoculation therapy, problem-solving therapy and stress management therapy.
Types of comparators
We included reviews that compared CBT with one of the following: (1) a non-CBT-based active comparator (e.g. other psychological therapy, pharmacotherapy), (2) a non-active comparator [e.g. placebo, WLC, treatment as usual (TAU), standard care, no treatment] or (3) a CBT-based active comparator of different intensity [e.g. face-to-face CBT (high intensity) compared with internet-based CBT (low intensity)]. We excluded reviews that compared variations of high-intensity (e.g. group CBT compared with individual CBT) or low-intensity CBT (internet CBT compared with bibliotherapy CBT).
Types of outcomes
We included reviews if they reported data on at least one of the following outcomes: HRQoL, anxiety, depression or a condition-specific outcome (e.g. pain).
Length of follow-up
We included reviews with post-treatment, short-term (< 12 months) or long-term (≥ 12 months) follow-up data. If both short- and long-term follow-up data were reported, the synthesis of only the longest follow-up time point was included.
Search methods for identification of systematic reviews
We followed the principles of the Cochrane Handbook for Systematic Reviews of Interventions3 and recommendations for conducting overviews of systematic reviews9 to identify systematic reviews for the overview.
Information sources
The DARE (up to March 2015), Cochrane Database of Systematic Reviews, MEDLINE (via Ovid), EMBASE (via Ovid), PsycINFO (via Ovid), Cumulative Index to Nursing and Allied Health Literature (CINAHL) (via EBSCOhost), Child Development & Adolescent Studies (via EBSCOhost) and OpenGrey databases were searched on 25–27 April 2018 to identify relevant systematic reviews published between 1992 and 2018. An updated search was run on all the above databases on 30 January 2019, covering the period from April 2018 to 30 January 2019, excluding DARE, which is no longer updated. Owing to the volume of material being processed and the time constraints associated with this process, the reference lists of included reviews were not hand-searched for additional reviews. We did not contact authors for additional information to confirm inclusion/exclusion.
Search strategy
Comprehensive search strategies for each of the eight databases were designed by a senior research information specialist (SK). Each search strategy was developed iteratively, and a sensitivity check was performed in each database for the ability of each strategy to retrieve 36 key known papers (where indexed) that had been identified a priori (see Appendix 1). The included search terms were identified from these reviews and their associated database indexing terms, and with input from the expert consultation group (ECG). The search strategies utilised a combination of free text and controlled vocabulary search terms covering variations of ‘CBT’ searched in the title, abstract or keyword fields, and were combined with validated study-type filters for ‘systematic review’. The Scottish Intercollegiate Guidelines Network systematic review search filters available on the InterTASC (Technology Appraisal Support Collaboration) Information Specialists’ Sub-Group website18 was used to search the MEDLINE, EMBASE and CINAHL databases. The McMaster University Health Information Research Unit systematic review filter19 was modified and used in the PsycINFO search. The full search strategies for all the databases can be found in Appendix 2.
Restrictions
The scoping work identified that the earliest published review of CBT is from 1992. 20 Therefore, we restricted our search to reviews published since 1992. The search was not restricted in terms of language, although we subsequently excluded non-English-language reviews (see Protocol revisions).
Data management
The database search results were exported into Endnote [Clarivate Analytics (formerly Thomson Reuters), Philadelphia, PA, USA] for deduplication and then exported into Covidence (Melbourne, VIC, Australia), a Cochrane technology platform designed and recommended for systematic review management,3 and a final deduplication check was performed. The full texts of reviews shortlisted for full-text analysis were also uploaded to and screened in Covidence. Data extraction was performed using Microsoft Excel® (Microsoft Corporation, Redmond, WA, USA).
Study selection
Two review authors (TS and BF) independently screened the titles and abstracts of all the references identified by the search strategy. The full texts of the selected reviews were obtained via online resources or through Bodleian Libraries. Reviews were screened for eligibility by two review authors (KE and TS), using the criteria stipulated in Inclusion and exclusion criteria for the mapping; disagreements were resolved by consensus or deliberation with a third reviewer (BF).
Data extraction
A bespoke data extraction form was developed. This form was piloted by two reviewers (BF and TS) using the sensitivity check papers recommended by the ECG (see Appendix 1).
We extracted the following information:
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review identification details – author, date of publication, aim, number of included RCTs and number of participants, risk-of-bias tool used
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participant details – primary condition (that which the intervention is primarily aiming to treat) and comorbid conditions, severity, age category (children and adolescents aged < 18 years, adults aged 18–65 years and older adults aged > 65 years), sex, ethnicity
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setting – from where participants were recruited, treatment timing (e.g. preventative, early, standard, relapse prevention) and countries where the individual RCTs were conducted
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intervention details – CBT intensity, and, if available, number, duration and frequency of sessions and intervention content description
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comparator details – description of comparator interventions (active: CBT or non-CBT interventions; non-active: WLC, TAU, no treatment)
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outcomes: what outcome was measured, follow-up period (short or long), the number of RCTs and number of participants summarised for this outcome, and whether or not a meta-analysis was conducted.
No numerical data were extracted at this stage. If a review had looked for one of our relevant outcomes but did not find any CBT RCTs, this was recorded. When available, we extracted information on patients’ perspectives of CBT, for example patient satisfaction ratings, levels of adherence, dropout rates and any reported adverse events. When available, we extracted information on patient satisfaction, acceptability, adverse events and economic evaluations. An example data extraction form can be found in Appendix 3.
Quality assessment of reviews
The methodological quality of all the included systematic reviews was independently assessed by two review authors (KE, TS or BC) using the A MeaSurement Tool to Assess systematic Reviews (AMSTAR)-2 checklist. 4 This checklist assesses the quality of the review design, analysis and reporting, but does not account for the risk of bias of the included RCTs. Because of the overview design (i.e. the review was conducted at the review level), it was outside the scope of this study to return to the RCT level to perform risk-of-bias assessments. Discrepancies between reviewers were adjudicated by another reviewer (BF). We used the online checklist21 (see Appendix 4) to complete the 16 items scored either as ‘yes’, ‘no’ or ‘partial yes.’ This automatically generated a review rating of ‘critically low’, ‘low’, ‘moderate’ or ‘high’ quality. We stratified the reviews based on their AMSTAR-2 score into higher-quality reviews (those rated ‘high’ or ‘moderate’ on the AMSTAR-2 checklist) and lower-quality reviews (those rated as ‘low’ or ‘critically low’) (Beverly Shea, University of Ottawa, 25 March 2019, personal communication).
We calculated the agreement on the overall quality rating between the two main reviewers (KE and TS) using weighted kappa (κw) (interpreted as < 0.20, poor; 0.21–0.40, fair; 0.41–0.60, moderate; 0.61–0.80, good; and 0.81–1.00, very good). 22
Independent, double data extraction was undertaken by two reviewers (KE, TS or BC). All data extraction forms and quality checklists were then cross-checked by a third reviewer (BF). All information from the data extraction sheets was entered into a review database, and graphic representation of quality was provided.
Visualisations mapping
The evidence from all the included systematic reviews was synthesised using the following types of charts, tables and maps.
Bubble chart
The evidence was grouped under the corresponding ICD-11 primary or secondary code. The volume of evidence, in terms of number of reviews, RCTs and participants, was then imported from Microsoft Excel into TIBCO Spotfire® (TIBCO, Software Inc., Palo Alto, CA, USA) software23 to produce a bubble chart. The axes of the bubble charts were very large, ranging from 0 to 45,000 participants. To help readability of the charts, we stratified reviews into those with < 1000 participants and those with ≥ 1000 participants.
Summary tables
The detailed description of each included review was represented in summary tables.
Gap maps
The condition and population and context characteristics extracted from the included reviews were populated in an Excel spreadsheet to identify any gaps in the evidence base, and were summarised.
Panoramic meta-analysis
Inclusion and exclusion criteria
From the reviews identified in the mapping stage, we selected the higher-quality reviews (rated ‘high’ or ‘moderate’ on AMSTAR-2) that contained quantitative data (either a single RCT or a meta-analytic effect estimate generated from pooling across multiple RCTs). We extracted these data for HRQoL, depression, anxiety and pain (the most commonly reported condition-specific outcome).
Reviews often contained multiple meta-analyses conducted on data from the same participants for a single outcome (e.g. CBT vs. active comparators, CBT vs. non-active comparators, symptom response, recovery, relapse, remission). To avoid double-counting studies, one meta-analysis per outcome per condition had to be chosen from each review. We used a predefined, step-by-step, hierarchy system in line with the review objectives. We included the meta-analysis (or single RCT) (1) with the longest follow-up time; (2) with the largest number of included RCTs; (3) that used measurement tools with the highest psychometric properties; (4) with the largest number of participants; (5) for which an active comparator was prioritised over non-active comparators; (6) for which continuous outcomes were prioritised over dichotomous outcomes; (7) for which, within dichotomous outcomes, the odds ratio (OR) was prioritised over the risk ratio (RR); (8) for which a random-effects meta-analysis was prioritised over fixed effects; and (9) for which self-report measures were prioritised over clinician-rated measures.
We then grouped the reviews that included quantitative data on each outcome (HRQoL, depression, anxiety and pain). Some of the reviews shared the same RCTs. To avoid double-counting evidence, we had to select one review to include in the PMA. We used a predefined selection process. 15 If two or more reviews shared the same RCT(s), we included the review (1) with the longest follow-up time, (2) with the highest AMSTAR-2 rating, (3) that was the most recently published, (4) with the largest number of RCTs or (5) with the largest number of participants.
Data extraction
We extracted the following data: number of participants in total and per group, number of participants who achieved the desired outcome in the case of dichotomous outcomes, effect sizes, confidence intervals (CIs), direction of effect, heterogeneity measures and type of meta-analysis. An example data extraction form can be found in Appendix 5.
Data management
Data from the data extraction sheets were entered into a master database (Excel) and exported into Stata® versions 13.1 and 16.0 (StataCorp LP, College Station, TX, USA). The PMAs were conducted by four reviewers (BC, HL, KE and TS).
Data analyses
Heterogeneity tests
We conducted a PMA per outcome measure. Review data were entered into an ICD-11 condition subgroup analysis and we tested the within-condition statistical heterogeneity across the reviews. In parallel, we tested the heterogeneity across the ICD-11 condition subgroup categories.
Assumptions for pooling across conditions
We developed three a priori conditions that must be met for us to pool the effect estimates across ICD-11 conditions categories:
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Intervention homogeneity: the ECG and investigators (see Expert consultation group including patient and public involvement) agreed that, although investigators often use condition-, population- and context-specific protocols, the principles of CBT (see Figure 1) are the same across all conditions. This allows us to make a judgement of intervention homogeneity and, provided the other criteria are met, to pool estimates across conditions.
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Design homogeneity: it is possible that meta-analytic estimates of effects would be moderated by differences between the review’s underlying design and methodologies. The review estimates would also be influenced by the quality of the included RCTs. However, a RCT-level quality assessment was beyond the scope of this overview. Therefore, we used the proxy of assuming that the highest-quality reviews would be more likely to be unbiased in their methods and would probably report from the best-available evidence. We minimised review design (but not RCT design) variation by including only reviews that adhered to the CRD review criteria and were graded as being of high or moderate quality on the AMSTAR-2 tool (higher-quality reviews); hence, we could claim design homogeneity. We ran a sensitivity analysis (which included higher- and lower-quality review data) to ascertain if the variation in review quality affected the homogeneity of effect estimates across conditions.
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Statistical homogeneity: statistical heterogeneity was assessed using the I2 statistic; this is expressed as a percentage. A higher percentage is indicative of greater heterogeneity. I2 reflects the variation in effect estimates between reviews that is attributable to heterogeneity. 24 There is no guidance regarding acceptable heterogeneity for PMAs. We used the guidance for meta-analysis heterogeneity,25 which suggests that I2 of < 75% is acceptable for pooling across the categories.
Panoramic meta-analysis method
The PMA was undertaken using a two-step frequentist approach random-effects model using the ‘metan’ command in Stata (versions 13.1 and 16). The two-step analysis consists of performing a conventional meta-analysis of a series of meta-analyses. The first step is undertaken by the original reviewers in obtaining a pooled treatment effect based on their included trials. Many of these will have been estimated via a random-effects meta-analysis, but some will have been analysed using a fixed-effects approach. Nonetheless, we assume that within-review variability has been appropriately allowed for. In the second step, the pooled estimates (with CIs) from each of the systematic reviews are combined into an overall (over all reviews) pooled estimate. At this point, we use a random-effects approach using the DerSimonian–Laird26 approach. We obtained a pooled estimate from within condition and also across conditions, if the across-condition heterogeneity was < 75%. In the few cases where data required for the meta-analysis, such as standard deviations or CIs, were missing, we referred to the individual RCT paper to extract this information.
Primary analysis
The primary analysis was conducted on continuous, end-point data extracted from higher-quality reviews (AMSTAR-2 rating of ‘moderate’ or ‘high’ quality) if there were more than two systematic review per comparison. The primary outcome was HRQoL and the secondary outcomes were depression, anxiety and pain.
We analysed the standardised mean differences (SMDs). When reviews reported values as mean differences, we converted the pooled estimate into a SMD using the standard deviation reported. 27 We reported the 95% CIs and the prediction intervals. These offer a prediction of the distribution of SMDs from future reviews, perhaps in other conditions that have not been included in our overview.
Secondary analysis
Some reviews reported change scores only; we pooled these separately because of concerns that these may be biased as a result of regression to the mean. 28 We performed separate PMAs for RRs and ORs.
We grouped reviews that directly compared high- with low-intensity CBT, irrespective of the condition, and analysed this group separately.
Transforming the standardised mean difference into a mean difference
To make meaningful interpretations, the overall pooled estimate (i.e. the SMD) for each outcome was transformed into a mean difference. The SMD was multiplied by the standard deviation of the most commonly used outcome measure (e.g. Beck Depression Inventory for depression) for each outcome. 29 To find a suitable standard deviation for the measurement tool, we identified a higher-quality review, which included a low risk-of-bias RCT that had used the most common outcome measure. From that trial, we extracted the standard deviation of the outcome measure at baseline.
Publication bias
When ≥ 10 reviews were included in the meta-analysis, publication bias and small-study effects were tested for using Egger’s regression intercept30 and a visual assessment of funnel plot asymmetry. We used a conservative value of p < 0.1 at CIs of 95% to reflect asymmetry.
Subgroup analysis
Subgroup analyses were agreed a priori and were performed if four or more reviews were included in the meta-analysis across all conditions for each of the outcomes on the following: (1) CBT intensity (high/low intensity), (2) age (children and adolescents, adults, older adults), (3) duration of follow-up (short: < 12 months, long: > 12 months) and (4) comparator group (active, non-active). The subgroups were separated using the ‘by()’ command in Stata.
We ran interaction tests between the subgroups using an exploratory meta-regression. The meta-regression used the method of moments estimate of between-study variance and the ‘metareg’ command in Stata.
If we identified any reviews that directly compared high-intensity CBT with low-intensity CBT, we grouped these reviews together by outcomes (HRQoL, depression, anxiety and pain). If their estimates were homogeneous, then we pooled across the reviews as an example of direct comparison.
Sensitivity analysis
To test whether or not the quality of the reviews moderated the effect estimate and or heterogeneity, we ran a sensitivity analysis in which we included data from all reviews, irrespective of their AMSTAR-2 quality, for each outcome PMA. Then we compared the heterogeneity and pooled effect estimates between the sensitivity analyses and the primary analyses (which included only data from higher-quality reviews, i.e. those of ‘high’ and ‘moderate’ AMSTAR-2 quality).
We also conducted a sensitivity analysis in the HRQoL PMA for the two subscales of the Short Form questionnaire-12 items (SF-12)/Short Form questionnaire-36 items (SF-36) instruments. These instruments include a physical composite score and a mental composite score, but the tool does not pool them together. We prioritised the physical component scale (as recommended by the ECG; see Expert consultation group including patient and public involvement), then we re-ran the analyses using the mental component scale to determine if this changed the results.
Consistency of effect
We employed an ontological argument, which suggests that a lack of inconsistency across evidence suggests consistency of effect. 31 We examined the effect estimates from each condition subgroup (pooled effect across all reviews conducted within one condition), subgroup analyses (e.g. active/non-active comparator groups), sensitivity analyses (including the additional condition subgroup analyses) and secondary analyses (e.g. pooled effects across dichotomous outcomes). If any analyses produced a statistically significant effect in favour of the group (comparator or CBT) that was contrary to the overall pooled effect estimate, then the evidence for the general effect was inconsistent across the included conditions. If we did not identify any contrary evidence across any of the conditions or subgroups, then we declared that the overall effect was consistent across all included conditions.
Expert consultation group including patient and public involvement
We worked with a CBT ECG consisting of clinical academics (n = 6), research academics (n = 8) and patient representatives (n = 4). We met with this group directly on three occasions (January 2018, February 2019 and September 2019) and communicated via telephone/e-mail throughout the overview process. For each meeting, the group was sent a workbook of the work to date and a set of questions for the members to comment on. These were collected at the end of each meeting to ensure that all members’ contributions were collated and recognised. The group was not involved in any of the data extraction or quality assessment of the reviews. The ECG provided advice on methods and interpretation, but the final decisions were taken by the study investigators.
Expert consultation group meeting 1: January 2018
In the first meeting, we achieved consensus on the search strategy (terms and databases), the inclusion/exclusion criteria (population, intervention, comparison, outcomes, review design), data extraction form (data to extract) and analysis plan (avoid double-counting of RCTs, subgroup analyses).
Expert consultation group meeting 2: February 2019
The results of the data screening and extraction and the plan for the data synthesis were presented at this meeting. The ECG agreed the following actions:
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Protocol amendment to include both pooled and single trial data in the PMAs
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Protocol amendment to include behavioural outcomes as condition-specific outcomes.
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The ECG did not reach consensus on how the generalisation framework should be used (see Chapter 6). Beth Fordham, Jeremy Howick and Karla Hemming were to continue work on how this could be conceptualised for sharing with the ECG at the next meeting.
Expert consultation group meeting 3: September 2019
The preliminary results were presented at the third meeting. The ECG were in agreement for the mapping and PMA processes. We agreed to prioritise higher-quality reviews over any-quality reviews. However, again, we did not reach agreement on the generalisation framework. The ECG agreed that there was intervention homogeneity, but could not agree that CBT always effects change through the same mechanisms. It agreed that CBT is implemented via the core principles (see Figure 1), but it felt that it was important to recognise that the mechanisms for change would be different for patients living with different conditions. The ECG suggested that a review of all the mechanistic evidence for CBT’s effectiveness was required in order to assume that there is a common mechanism of action.
The patient and public involvement (PPI) representatives guided our visual representation of the data and reflected that the real-life mechanisms of CBT will ‘feel’ very different for each individual receiving the treatment.
Protocol revisions
We intended to translate non-English-language reviews. However, the resource and time allocations were unprepared for the number and complexity of reviews that were found. On discussion with the National Institute for Health Research (NIHR) Health Technology Assessment (HTA) programme board, we made a change to the protocol and excluded non-English-language reviews at the full-text screening stage.
In the protocol, we selected three general outcomes (HRQoL, depression and anxiety) and suggested collecting condition-specific outcomes, such as psychosis and physical/physiological outcomes. Subsequently, we chose to present the three general outcomes plus the most commonly reported other outcome, which was pain.
We had not envisaged the problem of a review reporting the mental and the physical component subscales of the SF-12 HRQoL tool separately. After consulting the ECG, we selected the physical subscale to be included in the primary analysis, and conducted a sensitivity analysis using the mental subscale data to examine if that affected the PMA estimates and heterogeneity.
Other specific changes included to:
-
include both single RCT data and pooled meta-analysis data in a PMA
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include behavioural outcomes as condition-specific outcomes
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prioritise higher-quality reviews over any-quality reviews.
All the above changes were approved by the NIHR HTA programme board.
In response to comments from reviewers of the draft HTA monograph, we have included prediction intervals to our primary panoramic meta-analyses.
Chapter 4 Results: mapping
Process of study selection
The initial search of eight databases in April 2018 retrieved 12,339 references, and the updated search in January 2019 retrieved 916 references. In total, 7738 titles and abstracts were screened after deduplication, from which 2948 reviews were selected for full-text analysis. On full-text analysis, 494 systematic reviews32–523 were selected for final inclusion. Data extraction for the mapping was done for all these reviews, the synthesis of which is presented in this chapter. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram describing each of these stages is presented in Figure 2.
Excluded studies
We excluded 2454 reviews at the full-text screening stage. Nearly half of these exclusions (1108/2454, 45%) were because the review did not provide a synthesis of CBT trials. Ten per cent (237/2454) of reviews were excluded because they were not available in English. References for the excluded reviews along with their reasons for exclusion are presented in Appendix 6.
Description of the included systematic reviews
We included 494 systematic reviews, which reported 2052 RCTs involving 221,128 participants. 32–523 The included reviews were synthesised in three main formats: summary tables, bubble charts and gap maps.
Summary tables
The summary tables provide comprehensive details of all the 494 included reviews, split into the ICD-11 codes (see Appendix 7, Tables 5–33).
Bubble charts
The 494 systematic reviews identified by the search examine the effectiveness of CBT on HRQoL, depression, anxiety or a condition-specific outcome in conditions represented in 14 out of 20 primary (physical) and 13 out of 20 secondary (mental) ICD-11 codes. This equates to 68% of all ICD-11 categories (27/40). ‘Mood disorders [6A60-80]’ were the most researched condition (92 reviews, 272 RCTs, 42,676 participants). The primary and secondary ICD-11 categories that are represented in the included reviews are listed in the unshaded rows presented in Box 2; those that are not represented (i.e. evidence gaps) are listed in the shaded rows in Box 2. The volume of reviews, trials and participants are represented in two bubble maps in Figure 3: (1) conditions that include < 1000 participants and (2) conditions that include > 1000 participants.
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01 Certain infectious or parasitic diseases.
-
02 Neoplasms.
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03 Diseases of the blood.
-
04 Diseases of the immune system.
-
05 Endocrine, nutritional or metabolic diseases.
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07 Sleep–wake disorders.
-
08 Diseases of the nervous system.
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09 Diseases of the visual system.
-
10 Diseases of the ear or mastoid process.
-
11 Diseases of the circulatory system.
-
12 Diseases of the respiratory system.
-
13 Diseases of the digestive system.
-
14 Diseases of the skin.
-
15 Diseases of the musculoskeletal system.
-
16 Diseases of the genitourinary system.
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17 Conditions related to sexual health.
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18 Pregnancy, childbirth or the puerperium.
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19 Certain conditions originating in the perinatal period.
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20 Developmental abnormalities.
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21 Symptoms and signs NOS (MG30 pain, MG22 fatigue, MG43.6 excessive weight gain).
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6A00-06: neurodevelopmental disorders.
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6A20-25: schizophrenia or other primary psychotic disorders.
-
6A40-41: catatonia.
-
6A60-80: mood disorders.
-
6B00-06: anxiety or fear-related disorders.
-
6B20-25: obsessive–compulsive disorders.
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6B40-45: disorders specifically associated with stress.
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6B60-66: dissociative disorders.
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6B80-85: feeding or eating disorders.
-
6C00-01: elimination disorders.
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6C20-21: disorders of bodily distress.
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6C40-51: disorders due to substance use or addictive behaviours.
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6C70-73: impulse control disorders.
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6C90-91: disruptive behaviour or dissocial disorder.
-
6D10-11: personality disorders and related traits.
-
6D30-36: paraphilic disorders.
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6D50-51: factitious disorders.
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6D70-72: neurocognitive disorders.
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6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
-
6E40: psychological or behavioural factors NOS (MB23.0 aggressive behaviour).
NOS, not otherwise specified.
Shading indicates the ICD-11 categories that are not represented in the included reviews (i.e. evidence gaps).
Gap maps
We produced a gap map that details the context and population characteristics of all the reviews conducted within each ICD-11 category (see Appendix 8, Tables 34–37). We have summarised the information in the following section.
Context characteristics of the included reviews
In Table 1, we present the number of reviews that included trials conducted in different contexts. One review could include some trials conducted in one context and also include trials conducted in another context. Therefore, that one review could represent two or more context characteristics. Consequently, the percentages presented across the rows will not always add up to 100% (n = 494 reviews). The shaded cells represent how many reviews did not report on this characteristic.
Reviews | Reviews, n (%) | |||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Who: severity | What: intensity | When: delivered | Where: participants recruited | Follow-up | ||||||||||||||||||
Subclinical | Clinical | Chronic | Severe | NR | High | Low | NR | Preventative | Standard | Relapse prevention | NR | Community | GP primary | Outpatients | Inpatients | School/university | Institution | NR | Short term | Long term | NR | |
Reviews included in mapping: N = 494 (2052 RCTs; 221,128 participants) | 16 (3) | 216 (44) | 19 (4) | 10 (2) | 247 (50) | 397 (80) | 139 (28) | 8 (2) | 29 (6) | 463 (94) | 7 (1) | 0 (0) | 92 (19) | 41 (8) | 114 (23) | 35 (7) | 36 (7) | 4 (1) | 283 (57) | 402 (81) | 130 (26) | 7 (1) |
Context characteristics well reported
Nearly all the included reviews (486/494, 98%) reported whether or not they examined high- or low-intensity CBT. The majority were conducted on high-intensity CBT, but low-intensity CBT trials were included in 28% (139/494) of reviews across 14 out of 40 (35%) ICD-11 categories. Nearly all reviews (487/494, 99%) reported when follow-up data were collected. One-third of reviews (130/494, 26%) included a long-term (> 12 months) follow-up time point.
Context characteristics poorly reported
Only half of the reviews (247/494, 50%) reported on the severity of participants’ symptoms. Of these, the majority described participants as having a clinical diagnosis (216/494, 44%), with no further description on the severity of the symptoms (i.e. chronic or severe). Only 3% (16/494) of reviews examined participants with subclinical symptoms.
Over half of the included reviews (283/494, 57%) did not report from which care setting they had recruited their samples. Of the reviews that did report this, the majority recruited their samples from outpatient settings (114/494, 23%).
Context characteristics rarely examined
All the included reviews reported when the intervention was delivered (494/494, 100%); only 7% (36/494) examined the use of CBT in a preventative context.
Population characteristics of the included reviews
In Table 2, we present the number of reviews that included trials with samples representing different characteristics. One review could include some trials conducted with one type of population (e.g. children and adolescents) and other trials conducted with another population (e.g. adults), or one trial that included children, adolescents and adults. Therefore, that one review could represent two (or more) sample characteristics. Consequently, the percentages presented across the rows will not always add up to 100% (n = 494 reviews). The shaded cells represent how many reviews did not report on this characteristic.
Reviews | Reviews, n (%) | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Age (years) | Sex | Ethnicity | Continent where the included RCTs were conducted | ||||||||||||||
< 18 | 18–65 | > 65 | NR | < 50% female sample | > 50% female sample | Mixed | NR | < 25% non-white sample | 25–75% non-white sample | > 75% non-white sample | Mixed | NR | Europe, North America, Australasia | Asia | Africa, South America | NR | |
Reviews included in mapping: N = 494 (2052 RCTs; 221,128 participants) | 108 (22) | 378 (77) | 30 (6) | 19 (4) | 44 (9) | 167 (34) | 65 (13) | 218 (44) | 10 (2) | 6 (1) | 9 (2) | 11 (2) | 458 (93) | 231 (47) | 37 (8) | 8 (2) | 218 (44) |
Population characteristics well reported
Most reviews reported the age of their samples (475/494, 96%); of these, only 6% (30/494 reviews, 81 RCTs and 6629 participants) were conducted with an older adult population.
Population characteristics poorly reported
Most reviews (458/494, 93%) did not report the ethnicity of the samples of their included trials. Of the 36 reviews that did report the ethnicity of their samples, we found an equal number of reviews that reported more white than non-white participants (10/494, 2%) and that reported more non-white than white participants (10/494, 2%).
Nearly half of the reviews (218/494, 44%) did not report on the sex of their trial samples or the country where their included trials were conducted. When reported, a higher number of reviews had a greater representation of female participants (167/494, 34%) in their trial samples, and most reviews included trials conducted in Europe, North America and Australasia (231/494, 47%).
The AMSTAR-2 review quality rating
Every review (n = 494) was assessed twice (by KE and TS) using the AMSTAR-2 checklist. The agreement between reviewers (KE and TS) in assessing the quality of reviews using the AMSTAR-2 checklist was good (327/494, 66%) (κw = 0.63, 95% CI 0.62 to 0.65). Figure 4 presents the proportion of reviews conducted over the preceding 20 years, classified into the four AMSTAR-2 quality categories.
Over the previous 20 years, the quality of systematic reviews has improved; however, in the latest time epoch (2015–19), we still identified that 36% of the included reviews were of critically low quality and only 29% of reviews were classified as being of moderate or high quality.
Table 3 represents the item summaries from the AMSTAR-2 checklist. Of the ‘critical’ items on the checklist, 68% (336/494) of the reviews failed to register the protocol before commencement of the review (item 2), 76% (373/494) failed to provide the list of excluded studies along with the reasons for exclusion of each (item 7) and 50% (248/494) of reviews did not report an adequate search strategy.
AMSTAR-2 items | Response, n (%) | ||
---|---|---|---|
Yes | Partial yes or 0 | No | |
Components of PICO in research questions and inclusion criteria (item 1) | 266 (54) | – | 228 (46) |
Protocol registered before commencement of the review (item 2)a | 153 (31) | 5 (1) | 336 (68) |
Justification for selection of study design for inclusion (item 3) | 80 (16) | – | 414 (84) |
Adequacy of the literature search (item 4)a | 67 (14) | 179 (36) | 248 (50) |
Study selection performed in duplicate (item 5) | 325 (66) | – | 169 (34) |
Data extraction performed in duplicate (item 6) | 322 (65) | – | 172 (35) |
Justification for excluding individual studies (item 7)a | 108 (22) | 13 (3) | 373 (76) |
Included studies reported in adequate detail (item 8) | 106 (21) | 350 (71) | 38 (8) |
Risk of bias from individual studies being included in the review (item 9)a | 291 (59) | 27 (5) | 176 (36) |
Reporting funding sources of included studies (item 10) | 48 (10) | – | 446 (90) |
Appropriateness of meta-analytical methods (item 11)a | 292 (59) | 195 (39) | 7 (1) |
Assessment of potential impact of risk of bias on results of the review (item 12) | 196 (40) | 186 (38) | 112 (23) |
Consideration of risk of bias when interpreting the results of the review (item 13)a | 277 (56) | – | 217 (44) |
Explanation/discussion of heterogeneity observed (item 14) | 299 (61) | – | 195 (39) |
Assessment of presence and likely impact of publication bias (item 15)a | 209 (42) | 70 (14) | 215 (44) |
Reporting conflicts of interest and funding (item 16) | 376 (76) | – | 118 (24) |
Patient perspective and safety data
Of the 494 reviews, 118 (24%) reviews reported data on dropout rates, adherence and satisfaction analyses. Twenty reviews32,53,56,68,78,103,133,153,165,198,219,234,244,251,266,367,376,402,464,469 searched for safety data, of which nine reviews included reports of adverse events occurring in the CBT groups. We have summarised all the patient perspective and safety data under the relevant conditions in Box 3.
Adelman et al. 34 reported that children, adolescents and adults with anxiety disorders are more likely to drop out of CBT than out of WLC groups (OR 1.76, 95% CI 1.27 to 2.44). Participants were more likely to drop out of internet-based CBT than out of face-to-face CBT (OR 1.36, 95% CI 0.79 to 2.33).
Three reviews of anxiety disorders in children and adolescents reported no difference in the risk of participants dropping out between CBT and WLC groups (OR 0.94, 95% CI 0.58 to 1.51),509 TAU groups (OR 1.01, 95% CI 0.31 to 3.3)227 or placebo-pill control groups (RR 0.53, 95% CI 0.30 to 0.95). 487
A review reported that more RCTs of CBT with adult participants than those with older adults report attrition levels below the 15% attrition threshold (67% vs. 40%). 252
Mood disordersThe dropout rates of adults and older adults from CBT groups ranged from 7% to 40%217,420 and were not significantly different between CBT and comparator groups (active or non-active). 59,145,280,501
Anxiety and/or moodDropout rates for CBT ranged from 6% to 50% across children/adolescent and adult populations. 101,459 A review45 found no difference in dropout rates between high- and low-intensity (internet-based CBT) interventions (OR 0.79, 95% CI 0.57 to 1.09).
Obsessive–compulsive disorders (hypochondriasis)A review of adults with hypochondriasis reported no difference between CBT and TAU/pharmacotherapy/placebo comparator in the likelihood for participants to drop out of their trial arm (OR 1.14, 95% CI 0.56 to 2.32). 450
Obsessive–compulsive disorders (body dysmorphic disorder)No difference was detected in the number of children/adolescents and adults who dropped out between CBT and WLC groups (RR 1.00, 95% CI 0.96 to 1.05), and the effects of CBT on depression outcomes were not altered if dropouts were treated as non-responders. 195
Eating disordersA review of adults with bulimia nervosa/binge-eating disorder reported no difference in dropout rates between CBT and active or non-active comparator groups [F(2,55) = 1.66; p = 0.20]. 179 This remained true in adults with binge-eating disorder when CBT was an adjunct to pharmacotherapy [i.e. fluoxetine alone (22%) or fluoxetine plus CBT (23%)]. 378
Stress disordersTwo reviews reported dropout rates of between zero and 30%355,422 from CBT in adult populations with post-traumatic stress disorder, and that these rates did not differ significantly between the CBT and other active comparator groups. 96
Bodily distress disordersThere were no significant differences in dropout rates between CBT and progressive muscle relaxation groups in adults with medically unexplained symptoms (SMD 0.98, 95% CI 0.83 to 1.15; n = 90). 469
AddictionOne review reported, without statistics, that fewer adults with psychostimulant abuse disorder dropped out of CBT groups than out of the TAU groups. 312
NeoplasmsTwo reviews report very similar dropout rates from CBT interventions: 15% and 22%. 65,238
Nervous system disorders (post-viral fatigue)Castell et al. 93 reported that 17% of adults with post-viral fatigue syndrome dropped out of the CBT groups. Participants were more likely to drop out of CBT than out of a no-treatment control (RR 1.71, 95% CI 1.29 to 2.27), but not when compared with other active comparators170 (RR 0.97, 95% CI 0.28 to 1.25), including exercise interventions266 (RR 0.59, 95% CI 0.28 to 1.25).
Conditions with symptoms of painThree reviews reported that a range of 0–22% of patients dropped out of CBT interventions for pain patients in both adult and children/adolescent populations. 32,285,375
Disorders of the ear (tinnitus)One review examined adults’ and older adults’ satisfaction with internet-based CBT and found that more participants dropped out of internet-based CBT than out of an online education programme. 213
Adherence MoodAcross the trials of adults with depression, the adherence rates ranged greatly, from 10% to 100%. 165,459 A review of CBT for depression in children and adolescents reported that only 50% completed the full CBT programme. 106 Adherence rates were reported to significantly predict treatment response (β = 0.90; p < 0.001). 240
Anxiety and moodAdherence (defined as between 75% and 100% adherence) rates from RCTs of children/adolescents (86%), adults and older adults (24–90%) across anxiety and depression ranged from 24% to 90%. 327,356,466
Eating disordersIn children and adolescents with bulimia nervosa or EDNOS, the adherence rates were similar between CBT and other psychotherapies (family therapy). 243 However, one review of bulimia nervosa in children, adolescents and adults estimated that 16% (95% CI 13% to 19%) of participants did not complete the CBT intervention. 438
Adherence rates were similar between high-intensity and low-intensity (i.e. internet-based) CBT. 353 However, the acceptability ratings were higher for high-intensity CBT than for internet-based CBT. 367
Conditions with symptoms of painOne review of predominantly male (92%) veterans with comorbid pain, depression and substance abuse reported completion rates of only 38% for CBT interventions. 58
InsomniaA review of internet-based CBT for insomnia reported that 78% of adult participants (range 67–100%) completed their treatment. 97 The review also reported that 71% of participants found internet-based CBT ‘mostly’ or ‘very’ effective.
Satisfaction MoodOne review49 suggests that older adults prefer psychological therapies, such as CBT, over pharmacotherapy because the side effects of pharmacotherapy become more problematic with increased comorbidity in older age. 49
There was no difference between children’s and adolescents’ reported levels of acceptability for CBT, compared with WLC or TAU comparator groups. 510
Anxiety and moodTwo reviews46,324 reported that 62–100% of adults were satisfied with internet-based CBT. One review324 found that participants reported more enjoyment when they were communicating with a therapist in face-to-face CBT.
Eating disordersThe acceptability ratings were higher for high-intensity CBT than for internet-based CBT. 367
Stress disordersOne review reported, in great depth, the acceptability of CBT for children and adolescents with post-traumatic stress disorder. 291 It is recognised to be acceptable for children and their caregivers, but there are concerns regarding the trauma exposure component. This is considered central to the effectiveness of CBT, but some evidence suggests that this element is linked to patient dropout rates. CBT is delivered most commonly in a clinic, but this review suggests that home delivery could be more acceptable. It also suggests that CBT delivered in a group setting is more acceptable than individual CBT in ethnically diverse, urban children in the USA. 291
PsychosisCognitive–behavioural therapy was reported to be less acceptable than TAU for schizophrenia patients in one review,66 whereas another review116 found no difference in acceptability. Therapists reported that it was harder to engage younger schizophrenic patients with the CBT intervention. 51
Disorders of the ear (tinnitus)Participants reported that the intervention was not engaging enough, and authors suggested that it might be too much of a commitment for those with low distress levels. 213
Adverse eventsOne or two patients per CBT group reported that their symptoms worsened because of participation in CBT in adults with post-viral fatigue syndrome,56,103,266 bodily distress (medically unexplained symptoms)469 and mixed mental conditions (mood disorder, anxiety and obsessive–compulsive disorders). 53 Adverse events were reported in reviews of other conditions, such as people with substance misuse conditions during withdrawal, schizophrenic patients and eating disorder patients, but there was no evidence to suggest that this was due to participating in CBT. 133,198,219,234
EDNOS, eating disorder not otherwise specified.
Overall, there does not seem to be a great difference in dropout rates between CBT and active or non-active comparator groups. However, it appears that more participants drop out of low-intensity internet-based CBT than out of face-to-face CBT, and patients reported greater satisfaction with the therapeutic relationship in face-to-face CBT. Older adults appeared to drop out more than younger adults, but they also reported preferring psychological therapies, such as CBT, over pharmacological therapies. There may be certain groups who do not find CBT acceptable; for example, one review of mainly male veterans reported very low completion rates. 58 Participants with common mental and physical conditions seemed generally satisfied with CBT, but schizophrenic patients seemed more likely to find CBT an unacceptable treatment option. In relation to adverse events, there is a lack of reporting on safety data from CBT reviews. However, the evidence we found does not suggest that participating in CBT could cause harm to participants.
Chapter 5 Results: panoramic meta-analysis
The map of the CBT review evidence base included 494 reviews. Of these, 171 reviews included data suitable for inclusion in the PMAs. The majority of the reviews reported in the mapping exercise, but excluded from the PMA, were not suitable because we could not extract the CBT RCT-specific data in isolation for any of the four outcomes (n = 279). This could be for any one of the following reasons:
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The review may not have performed a meta-analysis or reported any quantitative data from single RCTs.
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The review may have looked for RCTs reporting on the outcome but not identified any evidence.
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We may have been unable to extract CBT RCT data in isolation, for example a review that presented a subgroup analysis of 10 CBT trials, but one of these trials was not a RCT. We could not isolate the purely CBT RCT evidence; therefore, the data were not included in the PMA. To have included these RCTs, we would have needed to return to the original RCT and perform a new meta-analysis including only the RCT data.
Of the 126 reviews eligible for the end-point PMA, 7132,37,39,46,50,59,63,68,89,102,117,126,134,143,149,165,167–169,175,188,193,197–199,205,206,211,219–221,227,231,234–236,246,249,251,259,261,267,275,286,291,299,315,317,340,343,347,357,369,371,373,397,401,405,409,432,445,446,448,450,454,464,469,480,484,507,518 were higher-quality reviews (i.e. ‘moderate’ or ‘high’ on AMSTAR-2); the primary analyses for each outcome were conducted using these 71 higher-quality reviews. The PRISMA flow diagram describing review selection for the PMAs from the mapping stage is presented in Figure 5.
For reviews reporting data as change scores or dichotomous outcomes (RR, OR), separate PMAs for each outcome were undertaken; these are presented in Appendices 9–12.
Health-related quality of life
We identified 24 higher-quality systematic reviews32,39,63,165,188,193,219,220,231,235,236,275,286,299,317,343,347,371,409,445,446,464,469,518 that met the eligibility criteria to be included in the HRQoL PMA. One review343 included two meta-analyses for different disorders; hence, the number of comparisons is 25. These reviews included 49 RCTs, 4304 participants and represent 12 out of 40 ICD-11 categories (30%), as presented in Box 4. The white rows represent those ICD-11 codes that are represented in the primary analysis, the purple rows represent those conditions that are represented in the sensitivity analyses (see Sensitivity analysis) and the orange rows represent those ICD-11 codes that are not represented.
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01 Certain infectious or parasitic diseases.
-
02 Neoplasms (in lower-quality reviews only).
-
03 Diseases of the blood.
-
04 Diseases of the immune system.
-
05 Endocrine, nutritional or metabolic diseases.
-
07 Sleep–wake disorders.
-
08 Diseases of the nervous system.
-
09 Diseases of the visual system.
-
10 Diseases of the ear or mastoid process.
-
11 Diseases of the circulatory system.
-
12 Diseases of the respiratory system.
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13 Diseases of the digestive system (in lower-quality reviews only).
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14 Diseases of the skin.
-
15 Diseases of the musculoskeletal system.
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16 Diseases of the genitourinary system.
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17 Conditions related to sexual health.
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18 Pregnancy, childbirth or the puerperium.
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19 Certain conditions originating in the perinatal period.
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20 Developmental abnormalities.
-
21 Symptoms and signs NOS (MG30 pain, MG22 fatigue).
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6A00-06: neurodevelopmental disorders.
-
6A20-25: schizophrenia or other primary psychotic disorders.
-
6A40-41: catatonia.
-
6A60-80: mood disorders.
-
6B00-06: anxiety or fear-related disorders.
-
6B20-25: obsessive–compulsive disorders.
-
6B40-45: disorders specifically associated with stress.
-
6B60-66: dissociative disorders.
-
6B80-85: feeding or eating disorders.
-
6C00-01: elimination disorders.
-
6C20-21: disorders of bodily distress.
-
6C40-51: disorders due to substance use or addictive behaviours.
-
6C70-73: impulse control disorders.
-
6C90-91: disruptive behaviour or dissocial disorder.
-
6D10-11: personality disorders and related traits.
-
6D30-36: paraphilic disorders.
-
6D50-51: factitious disorders.
-
6D70-72: neurocognitive disorders.
-
6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
-
6E40: psychological or behavioural factors NOS (MB23.0 aggressive behaviour).
NOS, not otherwise specified.
White rows represent ICD-11 codes represented in the primary analysis, purple shaded rows represent ICD-11 codes represented in the sensitivity analyses and orange shaded rows represent ICD-11 codes that are not represented in the HRQoL PMA.
The most commonly used measure of HRQoL was the Short Form questionnaire-36 items (SF-36) (n = 6). Other measurements included the Quality of Life Inventory (n = 5), the EuroQol-5 Dimensions (n = 2), the WHO Quality of Life-BREF (n = 1), the Global Assessment of Functioning (n = 1) and the Modular System for Quality of Life-54 (n = 1). The remaining reviews used population-specific (e.g. KIDSCREEN-27; KINDL-R; Comprehensive Quality of Life Scale, Intellectual Disability) or condition-specific [e.g. Fibromyalgia Impact Questionnaire, ADHD (attention deficit hyperactivity disorder) Impact Module-Adult™, Quality of Life in Alzheimer’s Disease, Diabetes Quality of Life for Youths] quality-of-life measurements.
Some reviews included trials with mixed characteristics, for example one review could include trials with adults and with older adults; in such a case, we would record that there was one review with adult data and one with older adult data. Consequently, the counts do not always add to 24 reviews. The mapping results demonstrate that the majority of these meta-analyses were focused on adults (n = 21), with only three reviews of children/adolescents and one review of older people. A higher number of reviews (12/24) had samples that included more female than male participants than reviews with samples of more male than female participants (6/24). Only three reviews reported the ethnicity of their samples: two reviews had samples with < 25% non-white participants and one included a sample with > 75% non-white participants.
The majority of reviews reported on the management of clinical conditions (16/24), through high-intensity CBT (17/24), delivered in outpatient settings (16/24), and with short-term follow-up (19/24). Seven reviews shared these three contexts but were conducted across different conditions. The majority of the included RCTs were from Europe, North America and Australasia (21/24).
The number of reviews containing only one trial was 6 out of 25; for some conditions, the numbers in each trial were very small (Figure 6). Comparators were active (8/24), mixed (3/24) and non-active (13/24).
Primary analysis
Within-condition heterogeneity (I2) varied between 0% and 56%, and across-condition heterogeneity was 32%; hence, the criteria for PMA were met. The pooled across-condition SMD between control groups and CBT intervention groups gave a modest effect in favour of CBT on outcomes of HRQoL (SMD 0.23, 95% CI 0.14 to 0.33) (see Figure 6). Variation in effects was observed across conditions; for example, in aggression, the estimate mean effect was almost zero, although it was estimated with considerable uncertainty (SMD –0.02, 95% CI –0.28 to 0.32), whereas, in anxiety disorders, the estimated effect was positive and was estimated with much greater certainty (SMD 0.42, 95% CI 0.20 to 0.64). This heterogeneity is reflected in the resulting prediction intervals, which, indicated for the overall effect (within any given condition), were between –0.03 and 0.50, indicating, at worst (and with little support in the prediction interval), a small negative effect of CBT for some conditions and, at best, a large positive effect for other conditions.
No publication bias was detected using funnel plots (Figure 7) and Egger’s test showed that there were no small-study effects (p = 0.18).
Mean difference in health-related quality of life
We identified a standard deviation (10.93 points) of the SF-36 physical composite score from a trial,525 deemed to have a low risk of bias, in a higher-quality review. 464 The SMD translated to an estimated mean difference on the SF-36 of 3 points (95% CI 2 to 4 points).
Subgroup analysis
The only interaction test that was statistically significant was between reviews of CBT compared with active comparators and reviews of CBT compared with non-active comparators. All other subgroup interaction tests were not statistically significant and are, therefore, consistent with the general effect of CBT on HRQoL outcomes.
Cognitive–behavioural therapy intensity
Overall, high- and low-intensity CBT reviews were distributed evenly across the different conditions and characteristics. High- and low-intensity CBT reviews both included populations diagnosed with 6B00-06 anxiety or fear-related disorders, 6A60-80 mood disorders, 6A00-06 neurodevelopmental disorders, 6B20-25 obsessive–compulsive disorders, 21 pain and 6B40-45 disorders specifically associated with stress. They included patients with chronic symptoms (6A60-80 mood disorders and 21 pain). The reviews included children, adolescents and adults, of both sexes, from all care settings in Europe, North America, Australasia and Asia. Reviews of both intensities included long-term follow-up data. Reviews of high-intensity, but not low-intensity, CBT included (1) populations diagnosed with 6C20-21 disorders of bodily distress, 08 diseases of the nervous system or 6A20-25 schizophrenia or other primary psychotic disorders; (2) older adults; and (3) CBT delivered in a preventative context. Reviews of low-intensity, but not high-intensity, CBT were conducted in populations diagnosed with 6C40-4H addiction and MB23 aggressive behaviour.
There was little difference between effect estimates in reviews of high-intensity and low-intensity CBT, although heterogeneity was substantially higher for low-intensity CBT (SMD 0.23, 95% CI 0.03 to 0.42; I2 = 68%) than for high-intensity CBT (SMD 0.21, 95% CI 0.11 to 0.32; I2 = 0%) (Figure 8). The interaction test between high- and low-intensity CBT reviews was not statistically significant (p = 0.99).
We identified three reviews318,343,521 (four RCTs, 243 participants; two reviews of lower quality and one review of higher quality) that directly compared high- with low-intensity CBT interventions on HRQoL outcomes in 6B00-06 anxiety or fear-related disorders and 6A60-80 mood disorders. One review provided separate data for both 6B01 panic and 6B04 social anxiety disorder populations, and so the PMA included four meta-analyses. In this subset of direct comparisons, there was no difference between high- and low-intensity CBT (SMD 0.15, 95% CI –0.10 to 0.40; I2 = 0%) (Figure 9).
The direct evidence (see Figure 9) comparing high- with low-intensity CBT in 6B00-06: Anxiety and 6A60-80: Mood disorders supports our indirect evidence (see Figure 8) from subgroup analyses of high and low intensity. In summary, we have found no direct or indirect evidence that high- or low-intensity CBT produced different effect sizes.
Type of comparators
The choice of comparator had a significant effect on the treatment estimates. Comparison to an active intervention was associated with a very small effect (SMD 0.09, 95% CI –0.01 to 0.19; I2 = 0%) (Figure 10). The active comparators tested in these reviews were education, exercise, pharmacotherapy, physiotherapy, psychotherapy/counselling and relaxation. Comparison with a non-active control was associated with a larger effect estimate (SMD 0.31, 95% CI 0.18 to 0.45; I2 = 40%). The interaction test was statistically significant (p = 0.04).
Duration of follow-up
Effect estimates were higher in reviews reporting short-term follow-up (SMD 0.29, 95% CI 0.17 to 0.42; I2 = 30%) than in reviews reporting long-term follow-up (SMD 0.11, 95% CI 0.02 to 0.20; I2 = 0%) (Figure 11). However, the interaction test did not find a statistically significant difference between the groups (p = 0.06).
Age
Effect estimates were similar in reviews of children and adolescents (SMD 0.20, 95% CI –0.15 to 0.56; I2 = 0%) and adults (SMD 0.23, 95% CI 0.14 to 0.33; I2 = 39%) (Figure 12). However, the sample sizes were much smaller in the reviews of children and adolescents, and the consequent CIs crossed zero. The interaction test did not find a statistically significant difference between the children/adolescents and adult groups (p = 0.06). The effect size for older adults was larger (SMD 0.39, 95% CI –0.24 to 1.02), but was generated from one review, with one trial and only 39 participants, and, again, the 95% CIs crossed zero (see Figure 12).
Sensitivity analysis
The sensitivity analysis was conducted with an additional 10 reviews that had been rated as low or critically low on the AMSTAR-2. Therefore, the sensitivity analysis was conducted with 34 reviews (76 RCTs, 7466 participants). 32,39,63,82,165,188,193,219,220,231,235,236,270,275,276,279,286,299,317,329,343,347,356,371,409,413,445,446,464,467,469,513,518,521 Inclusion of lower-quality reviews increased the estimate of effect (SMD 0.28, 95% CI 0.17 to 0.38) and raised the levels of heterogeneity (I2 = 71%) (see Appendix 9, Figure 15). This analysis included reviews from more physical conditions: 13: Digestive system, 02: Neoplasms, 08: Headaches and epilepsy and 21: Symptoms such as tinnitus and fatigue (see Box 4). All of the additional within-condition group estimates were consistent with the general effect, that is, an absence of inconsistent effects.
We re-ran the PMA replacing the physical component scores with the mental component scores from the SF-12/SF-36 in the two reviews that presented both the physical and the mental component scores. 220,464 The replacement did not change the overall effect or heterogeneity rating for the HRQoL outcome (SMD 0.24, 95% CI 0.14 to 0.33; I2 = 38%) (see Appendix 9, Figure 16).
Health-related quality-of-life change scores and risk ratio data
Four reviews (four RCTs, 185 participants), two of higher and two of lower quality, presented HRQoL data as change scores. 158,246,406,523 These included reviews of 6B00-06 anxiety and 6A60-80 mood disorders, 13 digestive system, 21 pain and 12 respiratory system disorders. The overall pooling reported acceptable heterogeneity and a moderate effect in favour of CBT (SMD 0.58, 95% CI 0.15 to 1.00; I2 = 66%) (see Appendix 9, Figure 17).
One lower-quality review (two RCTs, 145 participants) presented HRQoL data as a RR. 170 This review identified a large effect (SMD 1.57, 95% CI 0.78 to 2.37; I2, not applicable) in favour of CBT (see Appendix 9, Figure 18).
Discussion
From the highest-quality reviews, we found that CBT produced consistent, positive effects on HRQoL across 10 different conditions. Effect estimates suggest a modest, long-term improvement, compared with no intervention. These effects became very small when CBT is compared with other active treatments, including education, exercise, pharmacotherapy, physiotherapy, psychotherapy/counselling and relaxation. We did not find a difference between the effect sizes of reviews conducted with low-intensity CBT or high-intensity CBT.
The effect estimates were generated by synthesising data from samples of children, adolescents and adults, of both sexes, mainly living in countries in Europe, North America and Australasia. There is a lack of higher-quality evidence of CBT’s effectiveness for older adults.
We do not know if CBT will be effective when delivered preventatively or when delivered to patients with severe or subclinical symptoms. We do not know if CBT is equally effective across different ethnic groups nor do we know its effect for people living in countries in Africa, Asia or South America.
Depression
We identified 48 higher-quality systematic reviews37,39,46,50,59,63,117,126,143,167–169,175,197–199,205,206,220,221,231,234,235,246,249,261,267,275,286,299,340,357,369,371,373,401,405,409,432,445,446,448,450,454,469,480,484,507 that met the eligibility criteria to be included in the primary depression PMA. One review included six meta-analyses for different disorders; hence, the number of comparisons is 53. These included 130 RCTs and 14,073 participants, and represent 16 out of 40 possible ICD-11 categories (40%). Box 5 includes the ICD-11 codes represented in the primary PMA (white cells) and those codes not represented (shaded cells).
-
01 Certain infectious or parasitic diseases.
-
02 Neoplasms.
-
03 Diseases of the blood.
-
04 Diseases of the immune system.
-
05 Endocrine, nutritional or metabolic diseases.
-
07 Sleep–wake disorders.
-
08 Diseases of the nervous system.
-
09 Diseases of the visual system.
-
10 Diseases of the ear or mastoid process.
-
11 Diseases of the circulatory system.
-
12 Diseases of the respiratory system.
-
13 Diseases of the digestive system.
-
14 Diseases of the skin.
-
15 Diseases of the musculoskeletal system.
-
16 Diseases of the genitourinary system.
-
17 Conditions related to sexual health.
-
18 Pregnancy, childbirth or the puerperium.
-
19 Certain conditions originating in the perinatal period.
-
20 Developmental abnormalities.
-
21 Symptoms and signs NOS (MG30 pain, MG22 fatigue).
-
6A00-06: neurodevelopmental disorders.
-
6A20-25: schizophrenia or other primary psychotic disorders.
-
6A40-41: catatonia.
-
6A60-80: mood disorders.
-
6B00-06: anxiety or fear-related disorders.
-
6B20-25: obsessive–compulsive disorders.
-
6B40-45: disorders specifically associated with stress.
-
6B60-66: dissociative disorders.
-
6B80-85: feeding or eating disorders.
-
6C00-01: elimination disorders.
-
6C20-21: disorders of bodily distress.
-
6C40-51: disorders due to substance use or addictive behaviours.
-
6C70-73: impulse control disorders.
-
6C90-91: disruptive behaviour or dissocial disorder.
-
6D10-11: personality disorders and related traits.
-
6D30-36: paraphilic disorders.
-
6D50-51: factitious disorders.
-
6D70-72: neurocognitive disorders.
-
6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
-
6E40: psychological or behavioural factors NOS (MB23.0 aggressive behaviour, QE01 caregiver stress).
NOS, not otherwise specified.
White rows represent ICD-11 codes represented in the primary analysis; purple shaded rows represent ICD-11 codes that are not represented in the depression PMA.
The most commonly used measure of depression was the Beck Depression Inventory (n = 22). Other measurements included the Hamilton Depression Rating Scale (n = 7), the Hospital Anxiety and Depression Scale (n = 4), the Patient Health Questionnaire-9 items (n = 2), the Montgomery–Åsberg Depression Rating Scale (n = 2), the Center for Epidemiologic Studies Depression Scale (n = 2), the Profile of Mood States (n = 1), the Depression Anxiety Stress Scale (n = 1) and the Hopkins Symptoms Checklist (n = 1). The remaining reviews used population-specific depression measures [Glasgow Depression Scale for People with a Learning Disability (n = 1), Children’s Depression Inventory-revised (n = 3)].
The majority of these meta-analyses were focused on adults (37/48), with seven reviews focusing on adolescents/children and one review focusing on older people. More reviews had samples that included more female than male participants (23/48) than samples with more male than female participants (9/48). Only seven reviews reported the ethnicity of their samples. Of these, four reviews had samples with < 25% non-white participants and one included a sample with > 75% non-white participants.
The majority of reviews reported on the management of clinical conditions (26/48), on interventions of high intensity (26/48), delivered in outpatient settings (27/48), and with short-term follow-up (39/48). The majority of included RCTs in the reviews were from Europe, North America and Australasia (33/48). Many of the reviews contained only one trial (54%, 26/48), and, for some conditions, such as personality disorders, the numbers in those trials were very small (see Appendix 10, Figure 19).
Primary analysis
Within-condition heterogeneity (I2) varied between 0% (6D10-11: Personality disorders) and 86.3% (6A60-80: Mood disorders), and across-condition heterogeneity was 81%. The across-condition heterogeneity was too high for us to pool across the ICD-11 category groups (see Appendix 10, Figure 19). Ten of the within-condition groups reported effects in favour of CBT with some certainty. However, aggression, eating disorders, mixed mental conditions, nervous system disorders and stress-related disorders report within-condition effects of close to zero.
The heterogeneity was too high to pool across ICD-11 categories in any of the subgroup or sensitivity analyses. There was no evidence of publication bias or of small-study effects (Egger’s test p = 0.87) (see Appendix 10, Figure 20).
Discussion
Depression was the most commonly reported outcome in the review evidence base. The variation between the effect estimates generated for the within-condition subgroups was too wide-ranging to pool across the ICD-11 condition groups. No further subgroup or sensitivity analyses were conducted to compare with the primary analysis.
Anxiety
We identified 34 higher-quality systematic reviews37,39,89,134,143,168,175,205,227,234–236,246,249,251,259,275,286,291,315,340,343,347,371,373,397,409,432,445,446,450,464,469,480 that met the eligibility criteria. Two reviews included meta-analyses for different disorders; hence, the number of comparisons is 36. These included 59 RCTs and 4673 participants, and represent 13 out of 40 possible ICD-11 categories (33%). Box 6 includes the ICD-11 codes represented in the primary PMA (white rows), those conditions represented in the sensitivity analysis only, namely lower-quality reviews (purple rows) and those codes not represented (orange rows).
-
01 Certain infectious or parasitic diseases.
-
02 Neoplasms.
-
03 Diseases of the blood.
-
04 Diseases of the immune system.
-
05 Endocrine, nutritional or metabolic diseases.
-
07 Sleep–wake disorders.
-
08 Diseases of the nervous system.
-
09 Diseases of the visual system.
-
10 Diseases of the ear or mastoid process.
-
11 Diseases of the circulatory system.
-
12 Diseases of the respiratory system.
-
13 Diseases of the digestive system.
-
14 Diseases of the skin.
-
15 Diseases of the musculoskeletal system.
-
16 Diseases of the genitourinary system.
-
17 Conditions related to sexual health.
-
18 Pregnancy, childbirth or the puerperium.
-
19 Certain conditions originating in the perinatal period.
-
20 Developmental abnormalities.
-
21 Symptoms and signs NOS (MG30 pain, MG22 fatigue).
-
6A00-06: neurodevelopmental disorders.
-
6A20-25: schizophrenia or other primary psychotic disorders.
-
6A40-41: catatonia.
-
6A60-80: mood disorders.
-
6B00-06: anxiety or fear-related disorders.
-
6B20-25: obsessive–compulsive disorders.
-
6B40-45: disorders specifically associated with stress.
-
6B60-66: dissociative disorders.
-
6B80-85: feeding or eating disorders.
-
6C00-01: elimination disorders.
-
6C20-21: disorders of bodily distress.
-
6C40-51: disorders due to substance use or addictive behaviours.
-
6C70-73: impulse control disorders.
-
6C90-91: disruptive behaviour or dissocial disorder.
-
6D10-11: personality disorders and related traits.
-
6D30-36: paraphilic disorders.
-
6D50-51: factitious disorders.
-
6D70-72: neurocognitive disorders.
-
6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
-
6E40: psychological or behavioural factors NOS (MB23.0 aggressive behaviour).
NOS, not otherwise specified.
White rows represent ICD-11 codes represented in the primary analysis, purple rows represent ICD-11 codes represented in the sensitivity analyses and orange rows represent ICD-11 codes that are not represented in the anxiety PMA.
The most commonly used measure of anxiety was the Beck Anxiety Inventory (BAI) (n = 9). Other measurements included the Hospital Anxiety and Depression Scale (n = 6), the State–Trait Anxiety Inventory (n = 6), the Hamilton Anxiety Rating Scale (n = 1), the Hopkins Symptom Checklist (n = 1) and the Profile of Mood States (n = 1). The remaining reviews used population-specific [Glasgow Anxiety Scale for People with an Intellectual Disability, Revised Children’s Manifest Anxiety Scale (n = 4)] or condition-specific [Generalised Anxiety Disorder-7 (n = 3), Dental Anxiety Scale, Cardiac Anxiety Questionnaire] measurements.
The majority of these meta-analyses focused on adults (23/34), with seven reviews of adolescents/children and two reviews of older people. More reviews had samples that included more female than male participants (14/34) than samples with more male than female participants (9/34). Only five reviews reported the ethnicity of their samples. Of these, four reviews had samples with > 75% white participants and none included a sample with < 25% white participants.
The majority of reviews reported on the management of clinical conditions (20/34), on interventions of high intensity (29/34), delivered in outpatient settings (22/34), and with a short-term follow-up (27/34). The majority of included RCTs were from Europe, North America and Australasia (22/34). Out of 34 reviews, 24 contained only one trial, and, in some cases, the numbers in each trial were very low (Figure 13 presents the data).
These analyses also included reviews with trials conducted in less common contexts and populations, for example patients with subclinical mood (6A60-80) conditions (n = 1), and CBT delivered in preventative contexts to mood disorder (6A60-80), psychosis (6A20-25) (n = 2) and inpatient psychosis patients (n = 2), and to older adults living with stress disorders (6B40-45), obsessive disorders (6B20-25), anxiety (6B00-06) and mood (6A60-80) disorders (n = 2). None of these specific reviews produced effect estimates that were inconsistent with the primary anxiety PMA.
Primary analysis
Within-condition heterogeneity varied between 0% (MG30 pain) and 75% (6B40-45 stress-related disorders) and across-condition heterogeneity was 62%. The pooled across-condition SMD gave a modest effect in favour of CBT on outcomes of anxiety (SMD 0.30, 95% CI 0.18 to 0.43) (see Figure 13). The prediction intervals for the overall effect were –0.28 to 0.88. No inconsistent effects were identified across the conditions.
Once again, variation in effects was observed across conditions. This heterogeneity is reflected in the resulting prediction interval, which, indicated for the overall effect (within any given condition), was between –0.28 to 0.88, indicating a possible small negative effect of CBT for some conditions and, at best, a large positive effect for other conditions.
There was no evidence of publication bias or of small-study effects (Egger’s test p = 0.70) (see Appendix 11, Figure 21).
Mean difference in anxiety
We transformed the across-condition SMD into a mean difference of the most commonly reported anxiety outcome, the BAI. 526 We identified a standard deviation (13.46 points) of the BAI from a low risk-of-bias trial525 in a higher-quality review. 464 The SMD translated to an estimated mean difference on the BAI of 4 points (95% CI 2 to 6 points).
Subgroup analysis
None of the interaction tests between the subgroups was significant and the evidence is consistent with the primary anxiety PMA.
Cognitive–behavioural therapy intensity
Reviews of low- and high-intensity CBT examined similar populations and conditions. The ICD-11 categories that were represented by high-intensity CBT only, and not low-intensity CBT, were 6A20-25 schizophrenia or other primary psychotic disorders, 6D10-11 personality disorders and related traits, 6A00-06 neurodevelopmental disorders and 12 diseases of the respiratory system. The populations who were sampled in reviews of high-intensity CBT but not in reviews of low-intensity CBT were older adults (06B40-45 disorders specifically associated with stress, 6B20-25 obsessive–compulsive disorders, 6B00-06 anxiety or fear-related disorders and 6A60-80 mood disorders) and subclinical populations (6A60-80 mood disorders). High-intensity, but not low-intensity, CBT reviews included trials delivered in preventative contexts (6A20-25 schizophrenia or other primary psychotic disorders and 6A60-80 mood disorders) and to inpatient samples (6A20-25 schizophrenia or other primary psychotic disorders).
The heterogeneity was too high to pool across the low-intensity CBT reviews (I2 = 78%). The low-intensity CBT reviews included trials examining CBT delivered via paraprofessionals (n = 3) or via the internet (n = 4). The heterogeneity was much lower in high-intensity CBT reviews (SMD 0.28, 95% CI 0.15 to 0.42; I2 = 54%). The interaction test between high- and low-intensity CBT reviews was not statistically significant (p = 0.62) (see Appendix 11, Figure 22).
We identified five reviews87,306,343,360,521 (11 RCTs, 503 participants) that directly compared high- with low-intensity CBT interventions on anxiety outcomes in 6B00-06: Anxiety, 6A60-80: Mood and pain [including tinnitus 21 Symptoms and signs not otherwise specified (MG30 pain)] conditions. In this subset of direct comparisons, there was no difference between high- and low-intensity CBT (SMD 0.03, 95% CI –0.14 to 0.21; I2 = 20%) (see Appendix 11, Figure 23). This direct evidence comparing high- with low-intensity CBT in anxiety and mood and pain conditions supports our indirect evidence (see Appendix 11, Figure 22) from the high- and low-intensity CBT subgroup analyses. We have found no direct or indirect evidence that high- or low-intensity CBT produce different effect sizes.
Type of comparators
The effect was larger and significant when CBT was compared with non-active comparators (SMD 0.37, 95% CI 0.19 to 0.55; I2 = 64%) and smaller and non-significant when compared with active comparators (SMD 0.19, 95% CI 0.00 to 0.37; I2 = 49%) (see Appendix 11, Figure 24). However, the interaction test between the two groups was not significant (p = 0.24).
Duration of follow-up
Effect estimates were higher in reviews reporting long-term follow-up (SMD 0.38, 95% CI 0.15 to 0.60; I2 = 66%) than in those reporting short-term follow-up (SMD 0.27, 95% CI 0.12 to 0.43; I2 = 59%) (see Appendix 11, Figure 25). However, the interaction test did not find a statistically significant difference between the groups (p = 0.48).
Age
Effect estimates were similar in reviews of children and adolescents (SMD 0.37, 95% CI 0.12 to 0.62; I2 = 67.1%) and adults (SMD 0.32, 95% CI 0.15 to 0.48; I2 = 63.6%). The estimates in the two reviews of older adults were much lower and the 95% CIs crossed zero (SMD 0.06, 95% CI –0.30 to 0.43; I2 = 0%) (see Appendix 11, Figure 26). The interaction test did not find a statistically significant difference between the three groups (p = 0.69).
Sensitivity analyses
We identified 56 reviews (117 RCTs, 11,409 participants)34,37,39,89,134,143,168,171,175,205,215,216,227,234–236,241,246,249,251,259,266,275,277,286,291,294,306,315,329,340,343,347,356,371,373,377,379,397,398,409,410,413,425,429,432,445,446,450,463,464,466,469,480,497,513 of any quality with data suitable for inclusion in the sensitivity anxiety PMA. Five reviews had separate valid data representing different conditions; therefore, the total number of comparisons in the all-quality anxiety PMA is 64. Inclusion of lower-quality reviews increased the heterogeneity across conditions (I2 = 76%) beyond our threshold for pooling across the conditions (see Appendix 11, Figure 27). All of the ICD-11 category within-condition effects were consistent with the primary analysis for anxiety outcomes.
Anxiety change scores/dichotomous outcomes
Four lower-quality reviews (four RCTs, 255 participants) reported anxiety outcome data as change scores. 56,105,336,457 These included reviews of 6B00-06 anxiety, 6A60-80 mood disorders and 08 diseases of the nervous system. The heterogeneity was too high (I2 = 88.1%) to pool across the reviews (see Appendix 11, Figure 28). One lower-quality review433 reported an OR (one RCT, 112 participants) and found a large effect in favour of CBT (SMD 1.01, 95% CI 0.96 to 1.06; I2, not applicable) (see Appendix 11, Figure 29). One lower-quality review332 (one RCT, 27 participants) reported a risk difference and presented a moderate effect in favour of CBT (SMD 0.36, 95% CI 0.01 to 0.71; I2, not applicable) (see Appendix 11, Figure 29). There were no data that were inconsistent with the primary analysis for anxiety outcomes from any of the change score or dichotomous data.
Discussion
The primary PMA reported that CBT produces a small, but meaningful, long-term improvement in anxiety symptoms. Results from the primary, subgroup, sensitivity subgroups, change scores and dichotomous data PMAs are all consistent with the primary PMA. Some individual reviews were conducted in less frequently researched contexts (e.g. trials conducted in Africa), under-represented populations (e.g. older adults) and less frequently researched delivery formats (e.g. preventative CBT). Every review generated effect estimates that were consistent with the overall general effect.
Cognitive–behavioural therapy was effective when it was delivered via high-intensity methods, but there was too much variation to conclude whether or not CBT was effective when it was delivered via low-intensity methods. However, there were no statistically significant differences between any of the subgroup tests.
The effect estimates were generated by synthesising data from samples of children, adolescents and adults, of both sexes, mainly living in countries in Europe, North America and Australasia. There is a lack of higher-quality evidence of CBT’s effectiveness for older adults.
We do not know if CBT will be effective when delivered preventatively or when delivered to patients with severe or subclinical symptoms. We do not know if CBT is effective across different ethnic groups nor do we know its effect for people living in countries in Africa, Asia or South America.
Pain
We identified 10 higher-quality systematic reviews32,68,102,134,149,188,211,251,317,446 that met the eligibility criteria. These included 22 RCTs (2581 participants) and represent 5 out of 40 possible ICD-11 categories (13%). Box 7 presents the ICD-11 codes represented in the primary PMA (white rows), those codes represented in the sensitivity analysis (i.e. lower-quality reviews) (purple rows) and those codes not represented (orange rows).
-
01 Certain infectious or parasitic diseases.
-
02 Neoplasms.
-
03 Diseases of the blood.
-
04 Diseases of the immune system.
-
05 Endocrine, nutritional or metabolic diseases.
-
07 Sleep–wake disorders.
-
08 Diseases of the nervous system (only lower-quality reviews).
-
09 Diseases of the visual system.
-
10 Diseases of the ear or mastoid process.
-
11 Diseases of the circulatory system.
-
12 Diseases of the respiratory system.
-
13 Diseases of the digestive system [DA01.11 oral mucositis (related to cancer treatments)].
-
14 Diseases of the skin.
-
15 Diseases of the musculoskeletal system (FA00–05 osteoarthritis).
-
16 Diseases of the genitourinary system.
-
17 Conditions related to sexual health.
-
18 Pregnancy, childbirth or the puerperium.
-
19 Certain conditions originating in the perinatal period.
-
20 Developmental abnormalities.
-
21 Symptoms and signs NOS (MG30 pain).
-
6A00-06: neurodevelopmental disorders.
-
6A20-25: schizophrenia or other primary psychotic disorders.
-
6A40-41: catatonia.
-
6A60-80: mood disorders.
-
6B00-06: anxiety or fear-related disorders.
-
6B20-25: obsessive–compulsive disorders.
-
6B40-45: disorders specifically associated with stress.
-
6B60-66: dissociative disorders.
-
6B80-85: feeding or eating disorders.
-
6C00-01: elimination disorders.
-
6C20-21: disorders of bodily distress.
-
6C40-51: disorders due to substance use or addictive behaviours.
-
6C70-73: impulse control disorders.
-
6C90-91: disruptive behaviour or dissocial disorder.
-
6D10-11: personality disorders and related traits.
-
6D30-36: paraphilic disorders.
-
6D50-51: factitious disorders.
-
6D70-72: neurocognitive disorders.
-
6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
-
6E40: psychological or behavioural factors NOS.
White rows represent ICD-11 codes represented in the primary analysis, purple shaded rows represent ICD-11 codes represented in the sensitivity analyses and orange shaded rows represent ICD-11 codes that are not represented in the pain PMA.
The most commonly used measure of pain was the 100-mm visual analogue scale (VAS) (n = 6). Other measurements included the numerical rating scale of pain intensity (n = 3), the Wong–Baker Faces Pain Rating Scale (n = 2), the modified von Korff scale (n = 1), the Chronic Pain Grade questionnaire (n = 1) and the McGill Pain Questionnaire (n = 1).
The majority of these meta-analyses were focused on adults (6/10),102,134,149,188,211,317 three reviews focused on adolescents/children32,68,446 and one review did not report the age of the samples. 251 All of the reviews included samples that were equally balanced between male and female participants. Only one review63 reported the ethnicity of its samples (> 75% white participants).
Two reviews specified examining CBT in patients with chronic symptoms of pain, anxiety and mood conditions. Half of the reviews examined high-intensity and half of the reviews examined low-intensity CBT. One review examined using CBT to prevent pain developing post orthodontic treatments, but all the others were using CBT in response to diagnosed problems. Two reviews observed the use of CBT for inpatients with pain conditions, whereas the remaining reviews examined CBT in outpatient/community settings. Three reviews included long-term follow-ups (abdominal pain, back pain, anxiety and mood disorders). Four reviews included only one trial, and five reviews included < 100 participants (Figure 14).
Primary analysis
The across-condition heterogeneity was 64% and the pooled across-condition SMD gave a modest effect in favour of CBT on outcomes of pain (SMD 0.23, 95% CI 0.05 to 0.41) (see Figure 14). The prediction intervals for the overall effect were –0.28 to 0.74.
There was no evidence of publication bias, nor of small-study effects (Eggers test p = 0.19) (see Appendix 12, Figure 30).
Mean difference in pain
We transformed the across-condition SMD into a mean difference of the most commonly reported pain outcome, the 100-mm VAS. We identified a standard deviation (27 mm) of the VAS from a trial527 with a low risk of bias in a higher-quality review. 32 The SMD translated to an estimated mean difference on the VAS of 6 mm (95% CI 1 to 11 mm).
Subgroup analysis
There were no statistically significant interaction effects between any subgroups; therefore, the evidence is consistent with the primary analysis.
Cognitive–behavioural intensity
High- and low-intensity CBT was examined in both children/adolescent and adult populations. The only review149 of preventative CBT delivered low-intensity treatment. There were no other differences in the populations or contexts tested with high- and low-intensity CBT.
The heterogeneity was too high to pool separately across the low-intensity CBT reviews (I2 = 84%). The low-intensity CBT reviews included trials examining CBT delivered by paraprofessionals (n = 4), through self-help tools (n = 6). The heterogeneity was much lower in high-intensity CBT reviews (SMD 0.19, 95% CI 0.01 to 0.37; I2 = 18%) (see Appendix 12, Figure 31). The interaction test between high- and low-intensity reviews was not statistically significant (p = 0.87).
No reviews directly compared the effectiveness of low-intensity compared with high-intensity CBT on pain outcomes. Therefore, no direct evidence is available to compare with our indirect evidence.
Type of comparators
The effect was larger when CBT was compared with non-active comparators (SMD 0.59, 95% CI 0.07 to 1.11; I2 = 69%) and was very small when compared with active comparators (SMD 0.14, 95% CI –0.11 to 0.38; I2 = 73%) (see Appendix 12, Figure 32). However, the difference between the two groups was not statistically significant when tested with the interaction test (p = 0.86).
Duration of follow-up
Effect estimates were higher in reviews reporting short-term follow-up (0.32, 95% CI 0.04 to 0.59; I2 = 70.5%) than in reviews reporting long-term follow-up (0.19, 95% CI 0.08 to 0.31; I2 = 0%) (see Appendix 12, Figure 33). However, the interaction test did not find a statistically significant difference between the groups (p = 0.62).
Age
The effect estimates extracted from reviews conducted in children and adolescent populations were too varied (I2 = 87%) to justify pooling across them. Conversely, there was 0% heterogeneity between the reviews in adult populations and the pooled effect was modest (SMD 0.21, 95% CI 0.12 to 0.31; I2 = 0%) (see Appendix 12, Figure 34). The interaction test between (1) children and adolescents and (2) adults did not find a significant difference between these groups (p = 0.68).
Sensitivity analysis
We identified 16 reviews (19 comparisons, 39 RCTs, 4592 participants)32,68,102,134,149,188,211,222,251,266,306,317,348,413,446,473 of any quality with data suitable for inclusion in the sensitivity pain PMA. This introduced 08: Nervous system disorders into the analysis. In the sensitivity analysis, all of the ICD-11 within-condition groups were consistent with the primary analysis for pain outcomes. Inclusion of lower-quality reviews marginally reduced the estimate of effect and heterogeneity (SMD 0.21, 95% CI 0.11 to 0.31; I2 = 51%), compared with the primary PMA (see Appendix 12, Figure 35).
Pain change scores/dichotomous data
The reviews that reported dichotomous data were consistent with the primary analysis. One lower-quality review, Palermo et al. ,354 presented pain outcome data as ORs. This review demonstrated a non-significant effect for CBT (SMD 7.99, 95% CI –2.72 to 18.70) (see Appendix 12, Figure 36). One lower-quality review, Bernardy et al. ,64 reported pain outcome data as risk differences and showed a non-significant effect for CBT (SMD 0.08, 95% CI –0.03 to 0.19) (see Appendix 12, Figure 36).
Discussion
From a smaller data set of the highest-quality reviews, we found that CBT produced consistent improvements in pain outcomes across six different conditions. Effect estimates suggest a modest long-term improvement in comparison with any other comparator intervention. We did not find a difference in the effect sizes between reviews conducted with low-intensity CBT and those conducted with high-intensity CBT.
The effect estimates were generated by synthesising data from samples of children, adolescents and adults, of both sexes, mainly living in countries in Europe, North America and Australasia. To our knowledge, there is no higher-quality evidence of CBT’s effectiveness for older adults.
The included reviews presented evidence to suggest that CBT can improve pain outcomes when CBT is delivered preventatively to patients with chronic or subclinical symptoms, but there is no evidence regarding severe symptoms. We do not know if CBT is equally effective across different ethnic groups, nor do we know its effect for people living in countries in Africa, Asia or South America.
Chapter 6 Generalisation
One of the aims of the project was to consider the extent to which the existing evidence base could be used to guide treatment, commissioning and research investment decisions.
This necessitated a layer of questions:
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In the existing evidence base of systematic reviews, is there evidence of a general effect of CBT across different conditions (categorised by the ICD-11)?
Yes. Our PMA analyses (see Chapter 5) concluded that CBT does produce a general effect across conditions. We were able to meet the criteria of statistical, intervention and design homogeneity for our primary outcome of HRQoL, and two out of three secondary outcomes (anxiety and pain). We can feel confident in generalising the effect across these condition categories.
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Can we assume that this effect is robust across all the specific conditions represented in each ICD-11 code?
In our methodology, we classified physical conditions at the primary ICD-11 code level and mental conditions at the secondary level. In each category, there are many subconditions. For some ICD-11 categories, such as musculoskeletal diseases (15), we have reviews representing three (arthropathies, spine conditions and osteopathies) of the five subcategories, whereas for others, such as respiratory disorders (12), we have reviews representing only one subcategory [lower respiratory tract diseases: asthma and chronic obstructive pulmonary disease (COPD)] out of six. We suggest that, as we found no evidence of inconsistent evidence, the effect of CBT will remain consistent across all conditions subsumed beneath each ICD-11 category. The consistency of effect mirrors and reassures the CBT field’s move towards transdiagnostic approaches. For example, literature suggests that a transdiagnostic manual is equally effective as condition-specific manuals for treating patients with all types of eating disorders (anorexia, bulimia, binge-eating and eating disorders not otherwise specified). 528 The benefit of using a transdiagnostic approach is that it is suitable for people with multiple conditions. Our PPI representatives suggested that this was a very important point, particularly because, with an ageing population, more and more people will live with multiple comorbidities.
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Can we assume that this general effect is robust across conditions (ICD-11) that are represented by lower-quality reviews only?
Yes. We performed sensitivity analyses and found that the inclusion of lower-quality reviews increased the heterogeneity of review effect estimates, but did not alter the SMD. We can feel confident in generalising the effect across higher- and lower-quality systematic review evidence.
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Can we assume that our general effect is robust across the populations and contexts?
Yes. We found no evidence of inconsistency in effect. We mapped the population and context details of the included reviews. We found no reviews, condition analyses or subgroup analyses that reported a statistically significant effect in favour of the comparator over CBT. Table 4 details the population, context and conditions of the reviews included in the primary HRQoL analyses. We identified each review from those populations or contexts that were under-represented and presented the individual review effect estimate. None of the individual or pooled meta-analyses produced an estimate that was inconsistent with the general effect of CBT on HRQoL.
Generalisation parameter | Details from the included reviews |
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Condition | |
Severity of symptoms | Most reviews examined the effect of CBT in patients who received a clinical diagnosis. Three reviews examined the effectiveness of CBT specifically for patients with chronic symptoms and found consistent effects: |
Population | |
Age | Reviews were conducted with children and adolescents (3/24) living with anxiety and/or mood445,446 and pain32 conditions and older adults with mood disorders (1/24)347 and adults (20/24) in nine different conditions (including anxiety, mood and pain conditions). The age subgroup analysis (see Chapter 5) did not identify a difference between children/adolescents and adults. The older adult review produced a consistent, but uncertain, effect (0.39, 95% CI –0.24 to 1.02)347 |
Sex | The majority of the reviews were conducted with samples that were equally represented by male and female participants (21/24 reviews). One review of patients with neck pain had a female participant sample of > 75% and reported a consistent but uncertain effect (0.28, 95% CI –0.11 to 0.68).63 Two reviews reported samples with > 75% male participants. The review conducted in anxiety reported an uncertain but consistent effect (0.21, 95% CI –0.04 to 0.47).464 The effect was the same for the review conducted in bodily distress (0.36, 95% CI –0.11 to 0.82)469 |
Ethnicity | Very few reviews reported the ethnicity of their samples. Of the five reviews that did, four included > 75% white participants. These all produced consistent evidence:
|
Context | |
Country | Five reviews included trials that were conducted in Asia. These were conducted in:All other trials included in the reviews were conducted in Europe, North America and Australasia |
Health-care setting | Only five reviews recruited participants from inpatient settings. These were conducted in:All other review samples were recruited from community, primary and outpatient settings |
Health-care timing | One review implemented CBT as a preventative intervention for patients with schizophrenia (0.09, 95% CI –0.21 to 0.39).219 The other reviews examined CBT delivered as a standard treatment |
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Can we infer that this treatment effect might be observed across conditions that are not included in the current systematic review evidence base?
Our systematic approach meant that we classified reviews by the primary condition that the CBT was aiming to treat. For example, if a review examined the use of CBT to reduce symptoms of depression [i.e. a mood disorder (6A60-80)] in patients with COPD (12: respiratory disorder), then the review was classified as a review of the effectiveness of CBT for 6A60-80: Mood disorders with comorbid 12: Respiratory disorder (COPD). However, if CBT improves HRQoL in patients with mood disorders and comorbid COPD, then CBT is also improving quality of life for COPD patients. As quality of reviews did not affect the general effect, we generated a list of conditions for which CBT is effective from those reviews included in the sensitivity analyses. The following comorbid conditions are represented in the HRQoL, anxiety and pain outcome sensitivity analyses, but not represented in the primary list of conditions: intellectual disabilities (6A00-4), brain injury (6D70-2), dementia (6D70-2), migraines (08), epilepsy (08), circulatory diseases (11), COPD (12), irritable bowel syndrome (13), arthritis (15), tinnitus (21) and fatigue (21). Therefore, we conclude that CBT’s effect is consistent across 22 out of 40 ICD-11 codes (55%), as presented in Box 8.
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01 Certain infectious or parasitic diseases (1C60-62: HIV).
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02 Neoplasms.
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03 Diseases of the blood.
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04 Diseases of the immune system.
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05 Endocrine, nutritional or metabolic diseases.
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07 Sleep–wake disorders.
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08 Diseases of the nervous system.
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09 Diseases of the visual system.
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10 Diseases of the ear or mastoid process.
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11 Diseases of the circulatory system.
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12 Diseases of the respiratory system.
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13 Diseases of the digestive system.
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14 Diseases of the skin.
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15 Diseases of the musculoskeletal system.
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16 Diseases of the genitourinary system (GA33 pregnancy loss).
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17 Conditions related to sexual health.
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18 Pregnancy, childbirth or the puerperium.
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19 Certain conditions originating in the perinatal period.
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20 Developmental abnormalities.
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21 Symptoms and signs NOS (MG30 pain, MG22 fatigue, MC41 tinnitus).
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6A00-06: neurodevelopmental disorders (6A02 autism, 6A00 intellectual disability and 6A05 ADHD).
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6A20-25: schizophrenia or other primary psychotic disorders.
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6A40-41: catatonia.
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6A60-80: mood disorders.
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6B00-06: anxiety or fear-related disorders.
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6B20-25: obsessive–compulsive disorders.
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6B40-45: disorders specifically associated with stress.
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6B60-66: dissociative disorders.
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6B80-85: feeding or eating disorders.
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6C00-01: elimination disorders.
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6C20-21: disorders of bodily distress.
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6C40-51: disorders due to substance use or addictive behaviours.
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6C70-73: impulse control disorders.
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6C90-91: disruptive behaviour or dissocial disorder.
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6D10-11: personality disorders and related traits.
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6D30-36: paraphilic disorders.
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6D50-51: factitious disorders.
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6D70-72: neurocognitive disorders (6D80-86: dementia).
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6E20-21: mental or behavioural disorders associated with pregnancy, childbirth or the puerperium.
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6E40: psychological or behavioural factors NOS (MB23.0 aggressive behaviour).
HIV, human immunodeficiency virus; NOS, not otherwise specified.
Purple shaded rows indicate the ICD-11 categories that are not represented in any of the PMAs.
To generalise beyond the conditions and comorbidities represented in this overview is a challenging area for CBT, in which there are a diverse range of strongly held perspectives. We specified a priori that we would use a model of generalisation529,530 to guide our thinking, which necessitated that the evidence met three assumptions:
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Statistical homogeneity in the systematic reviews being used to generate the estimate of effect. This was fulfilled.
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Clinical homogeneity populations and contexts represented in the overview represent the contexts to which the generalisation is being made.
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Shared mechanisms of action, which is the assumption that CBT effects change by changing the same or similar mediating variables across all conditions.
This would mean that, to assume an effect of CBT on HRQoL in a condition that has no systematic review evidence, there should be evidence of a general effect on HRQoL among similar patients, contexts and settings (i.e. there is no reason to believe that the treatment should work differently or be harmful). For the final assumption of shared mechanisms to be met, the highest level of evidence we would seek is that that from multiple mediation analyses.
As described, the ECG met on several occasions. We collectively agreed on the criteria for statistical homogeneity and the importance of consistency of effects, and that these were met in the PMA. For clinical homogeneity, we agreed the data extraction variables and framework, and were able to demonstrate where there is adequate evidence on context and where there is not adequate evidence (see Table 4). We demonstrated consistent effects for children, adolescents and adults, of both sexes, with clinical diagnoses, living in Europe, North America and Australasia, being treated in community, primary and secondary care settings with CBT being delivered in response to a diagnosis. However, there was less certainty for older adults, with subclinical, chronic or severe symptoms, living in Asia, Africa or South America, being treated in an inpatient setting or receiving CBT preventatively.
We did not search specifically for systematic reviews of mediation studies. At a basic level, the ECG and investigators were able to agree that the principles of CBT are the same regardless of the condition, namely that we intervene to modify thoughts and feelings, to influence behaviours and, ultimately, to improve health outcomes. The challenge is that the range of thoughts, feelings and behaviours is quite wide, and the ECG and investigators were unable to agree that CBT works through the same therapeutic mechanisms for every condition for which it has been used. The ECG recommended that future research should target identifying what the mechanisms of CBT are for each population. If these mechanisms could improve symptoms in other populations, then the evidence for effectiveness could be meaningfully generalised across the conditions. This will be a judgement call and there are likely to be situations in which details on mechanisms are available and similar to those included in reviews, and that the context and characteristics align to provide confidence in broader generalisation. The ECG suggested that a systematic review of mediation studies of CBT would be helpful in this respect, but this was outside the scope of this study.
Chapter 7 Discussion
Principal findings and their meaning
Cognitive–behavioural therapy has been evaluated (with systematic reviews) in most conditions (68%, 27/40 of ICD-11 categories). These reviews have summarised the RCT evidence of whether or not CBT improved outcomes in these conditions. The review estimates were similar enough between the different conditions for us to generate a general (as opposed to a condition-specific) effect estimate. We found that CBT produced a modest general benefit to HRQoL, anxiety and pain outcomes. The evidence was consistent across all 22 out of 40 (55%) conditions (and comorbidities), populations and contexts that have been tested.
The estimates for depression outcomes between conditions were too different; therefore, we could not produce a pooled general effect estimate. Although there were many more reviews in the depression PMA, the reviews used fewer different outcome measurements than in HRQoL, anxiety and pain PMAs. Therefore, it is unlikely that the high heterogeneity is due to the variation in the outcome measurements used. CBT has been shown to be very effective for people with clinical depression. 531,532 Our overview does not suggest that CBT is not effective for symptoms of depression, only that there was a great variation in how effective it was for changing depression symptoms across different conditions.
Cognitive–behavioural therapy was effective whether it was delivered in high- or low-intensity formats. This is not to imply that CBT can be delivered in high- or low-intensity formats interchangeably. The findings simply state that when low-intensity CBT has been tested in RCTs and synthesised into reviews, we found that it improved HRQoL, anxiety and pain outcomes. This adds strength to the argument that the mechanisms by which CBT is effective remain effective when delivered via high- or low-intensity formats.
Cognitive–behavioural therapy was effective in the short and long term. However, there was a paucity of reporting on the longer-term follow-ups (i.e. > 5 years post intervention); therefore, we have not captured the importance of relapse. We highlighted in the mapping exercise that there is a paucity of systematic review evidence regarding relapse prevention; this is an essential consideration to take into account when interpreting these findings.
When we pooled reviews that compared CBT with active interventions (e.g. pharmacotherapy, psychotherapy, exercise, education or relaxation), the effect estimates became very small. We found a significant interaction in the HRQoL analyses between those reviews that compared CBT with an active comparator and those that compared CBT with an inactive comparator. This could suggest that CBT and these other active interventions share mechanisms that improve HRQoL for patients.
We assume that CBT will help children, adolescents and adults, but we are uncertain as to how much it will help older adults, as there is less available evidence for this age population. We feel confident that CBT will be equally effective for male and female participants. The evidence base over-represents people who live in Europe, North America and Australasia, and poorly reports the ethnicity of the samples in the reviews. Consequently, we do not know if the effects will translate across people of different ethnicities in Europe, North America or Australasia or, to people who live in Asia, Africa or South America.
Strengths
When an individual systematic review pools evidence across many trials, the sample sizes can remain small. Small sample sizes mean that the effect estimate is less certain. One of the major strengths of this overview is that, by pooling data from many reviews across conditions, we become more certain of the effect estimates. Our HRQoL and anxiety outcome estimates include > 4000 participants, which guidance suggests indicates a certain effect. 533
To maintain the lowest risk of bias and the greatest design homogeneity, we conducted our primary analyses with the highest-quality (rated ‘moderate’ or ‘high’ on the AMSTAR-2 checklist) reviews. The most common criticism of all the reviews was that we, as readers, could not access a review protocol to check if the authors had performed what they had intended to perform and had not simply ‘cherry-picked’ results to present in the review publication. Another common problem was reviews not reporting the reasons why they excluded trials from their review. Without this information, we cannot check if there was any bias towards including some, but not other, trials. Our sensitivity analyses suggest that the higher-quality reviews report consistent findings (less heterogeneity), compared with poorer-quality reviews, but the quality of the reviews did not alter the effect estimates.
As the inclusion of the lower-quality reviews did not alter the effect estimates, we concluded that the general effect is consistent across conditions represented by higher- and lower-quality reviews. We also suggested that the effect could be generalised to comorbid conditions represented by these reviews. Consequently, the general effect can be generalised to over half (55%) of all conditions represented in the ICD-11.
Weaknesses
The main methodological weakness was due to our restriction in remaining at the review level, as opposed to including RCT-level extraction and analysis. The mapping exercise identified 494 reviews. Of these, 279 were not included in the PMA because we could not extract the purely CBT RCT evidence. For example, a review that synthesised 10 CBT RCTs with three non-RCTs would be excluded from the PMA unless the review had presented any of the purely RCT evidence in isolation (even if it was one single RCT, which we could include). Similarly, if a review included 30 CBT RCTs combined with six mindfulness-based cognitive therapy RCTs, then this would have been excluded unless the review also presented a separate CBT subgroup analysis. The only way we would have been able to include these RCTs would have been to return to the original RCTs, extract the data and perform a meta-analysis of those data for entry into the PMA. This was a conflicting decision. The evidence base was so large that we did not have the resources to perform RCT-level extraction or analysis, but this was at the expense of many RCTs being excluded from the PMAs.
Another consequence of remaining at the review level was the limitation of the quality assessments. A review of high quality may include RCTs judged to have a high risk of bias. Without performing additional RCT-level assessment and a separate analysis of RCTs with low risks of bias, we could not restrict the data to the best-quality RCT-level data.
This overview does not examine the health economics of the CBT evidence base, which is an essential element of commissioning and is the context of evidence-based medicine. We could not perform this analysis because it was beyond the scope of this current overview.
Our method for classifying reviews was to represent each review in one ICD-11 code. We classified the review by the primary condition the CBT was being used to treat. For example, a review of CBT for depression in COPD patients was classified as a review of CBT for depression with comorbid COPD. This meant that we could not reflect the multimorbidity represented in these reviews. A total of 158 out of 494 reviews included a comorbid condition such as alcohol abuse or dementia. Our methodology means that we have under-represented the number of different conditions for which CBT has been used to improve HRQoL and reduce symptoms of depression, anxiety and pain.
We have mapped the systematic review data across each condition and by the following groups: ‘who’ (populations with different clinical severity), ‘what’ (the CBT intensity format) and ‘when’ (delivered at what time, i.e. preventatively, in response to clinical diagnosis or as a relapse prevention). We were restricted to reporting and analysing the review-level data. Reviews often combined RCTs conducted across multiple subgroups. We did not perform RCT-level exploration of the subgroups, which limits the accuracy of our findings.
Our indirect (intensity subgroup analyses) and direct (high- compared with low-intensity CBT reviews) evidence suggested no difference in effectiveness between using high-intensity and using low-intensity CBT. However, although reviews of high-intensity CBT produced broadly similar estimates of CBT’s effectiveness, the estimates from low-intensity reviews varied widely. The large variation in the low-intensity CBT estimates may be due to our definition of low-intensity CBT. 1 We combined face-to-face delivery of CBT by paraprofessionals with self-help delivery of CBT (e.g. internet CBT). Future subgroup analyses could test if these two methods of delivery moderate the effectiveness of CBT.
When a review did not report how CBT was delivered in the included trials (i.e. high- or low-intensity CBT), we assumed that it was delivered face to face by a specialist (high intensity). We made this assumption because high-intensity CBT was the original and most common delivery method. When we developed our data extraction methods, we checked the trials in reviews that did not specify the CBT intensity. We found that these trials had tested high-intensity CBT. However, we did not check the included trials for every review included in our overview; therefore, this assumption may have led to us over-representing high-intensity CBT.
We made another assumption, whereby, if a review did not specify the time when the follow-up data were collected, we presumed that it was short term (< 12 months post intervention). We made this assumption because the majority of trials employed short-term follow-ups. However, as before, this assumption may be incorrect for some reviews.
Although most reviews estimated their effects with a random-effects meta-analysis, a few used a fixed-effects approach. We made an assumption that the within-review variability had been appropriately allowed for. If this assumption was incorrect, then our results might underestimate the amount of variation within conditions.
To make a meaningful interpretation of our effect estimates, we transformed them into mean differences using the standard deviation of the target outcome measure. If the value of this standard deviation is not a good approximate to the true standard deviation for this outcome, we might be underestimating or overestimating the effect size for each outcome considered.
We used techniques, such as using workbooks to record personal reflections, in the ECG meetings to ensure that each member could contribute equally. However, the debates often became polarised between academic discussions. Nevertheless, talking to PPI representatives more informally and during breaks generated rich feedback that helped the research group. On reflection, we should have included a formal forum at the end of each ECG meeting in which every member could summarise the day’s discussion and ask specific questions.
Implications
We have high-quality systematic review evidence, which demonstrates that, in comparison to no intervention, CBT improves HRQoL, anxiety and pain outcomes by a modest amount. This includes CBT that is delivered through low- and high-intensity formats. The benefit has been consistent in every condition, population and context in which it has been tested and synthesised into a systematic review. There are some conditions and contexts in which we are less certain about generalising the estimates from the PMA. These include conditions for which there is no similar condition already included in the review (e.g. vision impairments), or if CBT is being applied in contexts that we believe will vary substantially because of, among other things, cultural issues and health beliefs.
We have used a framework of broader generalisation that has considered pathophysiological rationale alongside the traditional quality indicators used in evidence-based medicine. 534,535 The early proponents of evidence-based medicine were more subtle in their approach, and demanded that values, circumstances, expertise and even pathophysiologic rationale be considered, especially when generalising evidence from clinical trials. 536,537 The most prominent evidence-based medicine rule of evidence is the GRADE system, which does not allow any role for pathophysiologic rationale at all, even though it does allow for recommendations to populations outside the trial (generalising). 5 We suggested that using the results of the PMA alongside knowledge of mechanistic actions of CBT in particular situations may enable the generalisation of this effective treatment (CBT) to a greater range of physical and mental conditions (and hence patients).
Chapter 8 Conclusion
Cognitive–behavioural therapy can help patients cope with the challenges of living with mental and physical conditions. We have found that it consistently improves quality of life and reduces anxiety and pain symptoms for people living with many different conditions across the 19 ICD-11 categories for which we have systematic review evidence. CBT has been tested in many different populations and contexts, and all these reviews report effects that are consistent with our general effects. High- and low-intensity CBT appear to be equally effective. The biggest area of uncertainty is around whether sociological constructs, such as ethnicity, religion, culture, country or language, could moderate the effectiveness of CBT or whether it will be equally effective across these constructs. We suggest that CBT will be effective for the conditions represented in the ICD-11 codes we have represented in the overview. However, we are unclear if the general effect can be applied to conditions that are not represented at all in the overview.
Chapter 9 Recommendations
Future research
The overview suggests a general benefit of CBT in physical and mental conditions. However, we also identified some unanswered questions. These are not presented in an order of priority:
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We do not know what the mediating variables for CBT’s effectiveness are, nor do we know whether or not these are different across conditions. We recommend a review or an overview of CBT mechanisms across conditions.
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We do not know the longer-term effects of CBT. Reviews of CBT trials that monitor their participants over ≥ 5 years, and that account for the relapse in patients, are needed to see if the effects remain across all conditions.
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We found that CBT produced a modest benefit in HRQoL, anxiety and pain outcomes. Clinical research should focus on identifying how these effects from CBT can be magnified. For example –
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Examining if the delivery of CBT can be modified to increase adherence and reduce dropouts (e.g. examining if the location of therapy delivery influences attendance rates).
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Prioritising assessments of treatment fidelity and quality to check whether or not the therapists delivering CBT are adhering to the same core CBT principles. 1 A novel method to check the content of face-to-face CBT consultations is to use artificial intelligence to monitor if a therapist has used a core CBT technique.
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We were not confident to recommend that CBT would work equally for older adults because of an absence of evidence. We are aware of new reviews and existing trials that suggest that CBT will be equally effective for older adults (aged > 65 years). 538 For example, a large, recent review found that the effects for psychotherapy (including CBT) on depression outcomes were equal between adults (aged 24–55 years), older adults (aged 55–75 years) and the oldest adults (aged > 75 years old). 538
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We were unsure, owing to a lack of reporting on ethnicity of trial samples, whether or not CBT would be equally effective across ethnic groups. Another review of psychotherapy (including CBT) on depression outcomes between racial/ethnic groups concluded that race/ethnicity did not moderate the effectiveness of psychotherapy. However, authors highlight the problems of defining an ethnic group and encourage future research to include country of residence, language, religion and race in a definition of ethnicity. 539
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Owing to an absence of evidence of trials conducted in Africa, Asia and South America, we were unsure if the general effects of CBT would apply to people living in those countries. The overview excluded reviews not published in English. Future research could prioritise reviews of CBT that include trials conducted in Africa, Asia or South America to see if the effects are the same as they have been in Europe, North America and Australasia.
Acknowledgements
Cognitive Behavioural Therapy – Overview Expert Consultation Group (CBT-O ECG)
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Bethan Copsey, Medical Statistician, School of Medicine, University of Leeds.
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Roshan das Nair, Professor of Clinical Psychology, School of Medicine, University of Nottingham.
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Katherine Edwards, Research Assistant, Reviews and Implementation Group, University of Liverpool.
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Douglas Findlay, Patient and Public Representative, who was an ECG member and reviewed the report.
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Beth Fordham, Senior Psychology Fellow, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford.
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Daniel Freeman, Professor of Clinical Psychology, Department of Psychiatry, University of Oxford, who was a member of the ECG and reviewed the report.
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Zara Hansen, CBT therapist specialising in pain conditions, NDORMS, University of Oxford.
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Karla Hemming, Professor of Biostatistics, Institute of Applied Health Research Professor of Biostatistics, University of Birmingham.
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Robert Howard, Professor of Psychiatry, Institute of Mental Health, University College London.
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Jeremy Howick, Senior Fellow, Department of Philosophy, University of Oxford.
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Sarah E Lamb, Mireille Gillings Professor of Health Innovation, College of Medicine and Health, University of Exeter.
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Hopin Lee, Research Fellow, NDORMS, University of Oxford.
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Richard Lilford, Professor and Director of National Institute for Health Research Applied Research Centre West Midlands, University of Birmingham, who was a member of the ECG.
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Michael Lyle, Patient and Public Representative, who was a member of the ECG.
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Paul Salkovskis, Professor of Clinical Psychology and Director for the Doctorate in Clinical Psychology, University of Oxford, who was a member of the ECG and reviewed the report.
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Michael Sharpe, Professor of Psychological Medicine, Department of Psychiatry, University of Oxford.
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Paul Stallard, Professor of Child and Family Mental Health, Department for Health, University of Bath.
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Thavapriya Sugavanam, Research Fellow, NDORMS, University of Oxford.
Personal communications
Personal communication with Georgina MacKenzie, PROSPERO Project Manager/Research Project Support Officer, 2018 regarding operationalising the CRD guidelines.
Personal communication with Beverly Shea, developer of the AMSTAR-2 checklist, 2019, regarding the re-classification of the four AMSTAR-2 quality ratings into higher (‘high’ and ‘moderate’ AMSTAR-2 ratings) and lower quality (‘low’ and ‘critically low’ AMSTAR-2 ratings) reviews.
Contributions of authors
Dr Beth Fordham (https://orcid.org/0000-0001-5996-3563) (Senior Health Psychology Fellow) was the principal investigator and the grant holder.
Dr Thavapriya Sugavanam (https://orcid.org/0000-0002-3033-2028) (Post-doctoral Research Assistant) contributed to the protocol development, database selection, search term selection, reference management, title/abstract screening, full-text screening, data extraction, quality assessment, data analysis, interpretation and report writing.
Ms Katherine Edwards (https://orcid.org/0000-0002-1092-0092) (Research Associate) contributed to the full-text retrieval, reference management, title/abstract screening, full-text screening, data extraction, quality assessment, data analysis, interpretation and report writing.
Professor Karla Hemming (https://orcid.org/0000-0002-2226-6550) (Professor of Biostatistics) has expertise in PMA. She made a large contribution to the design, procedure, analysis, interpretation and report writing.
Dr Jeremy Howick (https://orcid.org/0000-0003-0280-7206) (Senior Fellow) has expertise in Epistemology Philosophy of Medicine. He developed the generalisation methodology and contributed to the report writing.
Dr Bethan Copsey (https://orcid.org/0000-0001-9783-6549) (Post-doctoral Research Fellow) designed and ran the PMA and contributed to the data extraction and interpretation.
Dr Hopin Lee (https://orcid.org/0000-0001-5692-0314) (Post-doctoral Research Fellow) contributed to the data analysis, interpretation and writing.
Ms Milla Kaidesoja (https://orcid.org/0000-0003-0372-8251) (HiLIFE Research Trainee) contributed to the data extraction, generalisation and interpretation.
Ms Shona Kirtley (https://orcid.org/0000-0002-7801-5777) (Senior Information Specialist) led the database search and keyword selection aspects of the overview and commented on the methods section of the final report.
Assistant Professor Sally Hopewell (https://orcid.org/0000-0002-6881-6984) (Associate Professor of Trials and Reviews) has methodology expertise and contributed to the design, procedure and interpretation.
Professor Roshan das Nair (https://orcid.org/0000-0001-8143-7893) (Professor of Clinical Psychology) contributed to the methodological design, interpretation and report writing. Professor das Nair has a special interest in cultural and minority representation.
Professor Robert Howard (https://orcid.org/0000-0002-3071-2338) (Professor of Psychiatry) was a member of the ECG and contributed to the report writing and dissemination.
Professor Paul Stallard (https://orcid.org/0000-0001-8046-0784) (Professor of Child and Family Mental Health) was a member of the ECG and contributed to the report writing and dissemination.
Ms Julia Hamer-Hunt (Patient and Public Representative) was an ECG member, reviewed the report and contributed to the plain English summary of the report.
Professor Zafra Cooper (https://orcid.org/0000-0001-7963-656X) (Professor of Psychiatry) was a member of the ECG, reviewed the report and contributed to the report writing.
Professor Sarah E Lamb (https://orcid.org/0000-0003-4349-7195) (Professor of Rehabilitation) was mentor to Dr Beth Fordham throughout the entire project. She contributed to every stage of this project from the design to the interpretation and writing.
Publication
Fordham B, Sugavanam T, Edwards K, Stallard P, Howard R, das Nair R, et al. The evidence for cognitive behavioural therapy in any condition, population or context: a meta-review of systematic reviews and panoramic meta-analysis. Psychol Med 2021;51:21–9.
Data-sharing statement
Requests for access to data should be addressed to the corresponding author.
Disclaimers
This report presents independent research funded by the National Institute for Health Research (NIHR). The views and opinions expressed by authors in this publication are those of the authors and do not necessarily reflect those of the NHS, the NIHR, NETSCC, the HTA programme or the Department of Health and Social Care. If there are verbatim quotations included in this publication the views and opinions expressed by the interviewees are those of the interviewees and do not necessarily reflect those of the authors, those of the NHS, the NIHR, NETSCC, the HTA programme or the Department of Health and Social Care.
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Appendix 1 Sensitivity check papers
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Cuijpers P, van Straten A, Andersson G. Internet-administered cognitive behavior therapy for health problems: a systematic review. J Behav Med 2008;31:169–77.
de Arellano MA, Lyman DR, Jobe-Shields L, George P, Dougherty RH, Daniels AS, et al. Trauma-focused cognitive–behavioral therapy for children and adolescents: assessing the evidence. Psychiatr Serv 2014;65:591–602.
Dutra L, Stathopoulou G, Basden SL, Leyro TM, Powers MB, Otto MW. A meta-analytic review of psychosocial interventions for substance use disorders. Am J Psychiatry 2008;165:179–87.
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Hesser H, Weise C, Westin VZ, Andersson G. A systematic review and meta-analysis of randomized controlled trials of cognitive–behavioural therapy for tinnitus distress. Clin Psychol Rev 2011;31:545–53.
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O'Toole MS, Zachariae R, Renna ME, Mennin DS, Applebaum A. Cognitive behavioral therapies for informal caregivers of patients with cancer and cancer survivors: a systematic review and meta-analysis. Psycho-Oncology 2017;26:428–37.
Pallesen S, Mitsem M, Kvale G, Johnsen BH, Molde H. Outcome of psychological treatments of pathological gambling: a review and meta-analysis. Addiction 2005;100:1412–22.
Pearson FS, Lipton DS, Cleland CM, Yee DS. The effects of behavioral/cognitive-behavioral programs on recidivism. Crime Delinq 2002;48:476–96.
Peng XD, Huang CQ, Chen LJ, Lu ZC. Cognitive behavioural therapy and reminiscence techniques for the treatment of depression in the elderly: a systematic review. J Int Med Res 2009;37:975–82.
Pineros-Leano M, Liechty JM, Piedra LM. Latino immigrants, depressive symptoms, and cognitive behavioral therapy: a systematic review. J Affect Disord 2017;208:567–76.
Powers MB, Vedel E, Emmelkamp PM. Behavioral couples therapy (BCT) for alcohol and drug use disorders: a meta-analysis. Clin Psychol Rev 2008;28:952–62.
Rector NA, Beck AT. Cognitive behavioral therapy for schizophrenia: an empirical review. J Nerv Ment Dis 2001;189:278–87.
Richmond H, Hall AM, Copsey B, Hansen Z, Williamson E, Hoxey-Thomas N, et al. The effectiveness of cognitive behavioural treatment for non-specific low back pain: a systematic review and meta-analysis. PLOS One 2015;10:e0134192.
Santacruz I, Orgiles M, Rosa AI, Sanchez-Meca J, Mendez X, Olivares J. [Generalized anxiety, separation anxiety and school phobia: the predominance of cognitive–behavioural therapy.] Psicologia Conductual 2002;10:503–21.
Shinohara K, Honyashiki M, Imai H, Hunot V, Caldwell DM, Davies P, et al. Behavioural therapies versus other psychological therapies for depression. Cochrane Database Syst Rev 2013;10:CD008696.
Smith SM, Sonego S, Ketcheson L, Larson JL. A review of the effectiveness of psychological interventions used for anxiety and depression in chronic obstructive pulmonary disease. BMJ Open Respir Res 2014;1:e000042.
Sockol LE, Epperson CN, Barber JP. A meta-analysis of treatments for perinatal depression. Clin Psychol Rev 2011;31:839–49.
Soo S, Moayyedi P, Deeks J, Delaney B, Lewis M, Forman D. Psychological interventions for non-ulcer dyspepsia. Cochrane Database Syst Rev 2004;1:CD002301.
Taylor S, Asmundson GJG, Coons MJ. Current directions in the treatment of hypochondriasis. J Cogn Psychother 2005;19:285–304.
Thompson-Brenner HJ. Implications for the Treatment of Bulimia Nervosa: A Meta-analysis of Efficacy Trials and a Naturalistic Study of Treatment in the Community. PhD thesis. Ann Arbor, MI: University of Michigan; 2002.
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van Straten A, Geraedts A, Verdonck-de Leeuw I, Andersson G, Cuijpers P. Psychological treatment of depressive symptoms in patients with medical disorders: a meta-analysis. J Psychosom Res 2010;69:23–32.
Appendix 2 Detailed search strategies for review
MEDLINE
Database and platform
Ovid MEDLINE® Epub Ahead of Print, In-Process & Other Non-Indexed Citations, Ovid MEDLINE® Daily and Ovid MEDLINE®, 1946 to present.
Search filter
Scottish Intercollegiate Guidelines Network systematic review search filter for MEDLINE (via Ovid) [www.sign.ac.uk/search-filters.html (accessed February 2019)].
Date search was conducted
Original: 25 April 2018 (for publication years 1992 to present) (2967 references).
Updated: 30 January 2019 (for publication years 2018–19) (359 references).
Search strategy
-
(cognitive adj2 behavio?r adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab,kw.
-
(cognitive adj2 behavio?ral adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab,kw.
-
CBT.ti,ab,kw.
-
Cognitive Therapy/
-
or/1-4
-
Meta-Analysis as Topic/
-
meta analy$.tw.
-
metaanaly$.tw.
-
Meta-Analysis/
-
(systematic adj (review$1 or overview$1)).tw.
-
exp Review Literature as Topic/
-
or/6-11
-
cochrane.ab.
-
embase.ab.
-
(psychlit or psyclit).ab.
-
(psychinfo or psycinfo).ab.
-
(cinahl or cinhal).ab.
-
science citation index.ab.
-
bids.ab.
-
cancerlit.ab.
-
or/13-20
-
reference list$.ab.
-
bibliograph$.ab.
-
hand-search$.ab.
-
relevant journals.ab.
-
manual search$.ab.
-
or/22-26
-
selection criteria.ab.
-
data extraction.ab.
-
28 or 29
-
Review/
-
30 and 31
-
Comment/
-
Letter/
-
Editorial/
-
animal/
-
human/
-
36 and 37
-
36 not 38
-
or/33-35,39
-
12 or 21 or 27 or 32
-
41 not 40
-
5 and 42
-
limit 43 to yr = ‘1992-2018’.
EMBASE
Database and platform
Embase, 1974–2018, week 17 (via Ovid).
Search filter
The SIGN systematic review filter for EMBASE (via Ovid) [www.sign.ac.uk/search-filters.html (accessed February 2019)].
Date search was conducted
Original: 25 April 2018 (for publication years 1992 to present) (4862 references).
Update: 30 January 2019 (for publication years 2018–19) (192 references).
Search strategy
-
(cognitive adj2 behavio?r adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab,kw.
-
(cognitive adj2 behavio?ral adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab,kw.
-
CBT.ti,ab,kw.
-
Cognitive Therapy/
-
exp Cognitive Behavioral Therapy/
-
or/1-5
-
exp Meta Analysis/
-
((meta adj analy$) or metaanalys$).tw.
-
(systematic adj (review$1 or overview$1)).tw.
-
or/7-9
-
cancerlit.ab.
-
cochrane.ab.
-
embase.ab.
-
(psychlit or psyclit).ab.
-
(psychinfo or psycinfo).ab.
-
(cinahl or cinhal).ab.
-
science citation index.ab.
-
bids.ab.
-
or/11-18
-
reference list$.ab.
-
bibliograph$.ab.
-
hand-search$.ab.
-
relevant journals.ab.
-
manual search$.ab.
-
or/20-24
-
selection criteria.ab.
-
data extraction.ab.
-
26 or 27
-
review.pt.
-
28 and 29
-
Letter.pt.
-
Editorial.pt.
-
animal/
-
human/
-
33 and 34
-
33 not 35
-
or/31-32,36
-
10 or 19 or 25 or 30
-
38 not 37
-
6 and 39
-
limit 40 to yr = ‘1992-2018’.
Cumulative Index to Nursing and Allied Health Literature
Database and platform
CINAHL (via EBSCOhost).
Search filter
The SIGN systematic review filter for CINAHL (via EBSCOhost) [www.sign.ac.uk/search-filters.html (accessed February 2019)].
Date search was conducted
Original: 25 April 2018 (for publication years 1992 to present) (1062 references).
Update: 30 January 2019 (for publication years 2018–19) (174 references).
Search strategy
-
(TI (cognitive N2 behaviour N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behaviour N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI (cognitive N2 behavior N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behavior N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI (cognitive N2 behavioural N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behavioural N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI cognitive N2 behavioral N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB cognitive N2 behavioral N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI ‘CBT’) OR (AB ‘CBT’)
-
(MH ‘Cognitive Therapy’) OR (SU ‘Cognitive Therapy’)
-
S1 OR S2 OR S3 OR S4 OR S5 OR S6
-
(MH Meta Analysis)
-
(TX ‘meta analys*’)
-
(TX ‘metaanaly*’)
-
(MH ‘Literature Review+’)
-
(TX systematic N1 (review or overview))
-
S8 OR S9 OR S10 OR S11 OR S12
-
(PT ‘Commentary’)
-
(PT ‘Letter’)
-
(PT ‘Editorial’)
-
(MH Animals)
-
S14 OR S15 OR S16 OR S17
-
S13 NOT S18
-
S7 AND S19
-
PY 1992-2018
-
S20 AND S21
PsycINFO
Database and platform:
PsycINFO, 1967 to April week 2 2018 (via Ovid).
Search filter
McMaster Hedges Maximises Specificity Systematic Review filter for PsycINFO (via Ovid) (modified) [https://hiru.mcmaster.ca/hiru/HIRU_Hedges_PsycINFO_Strategies.aspx#Reviews (accessed February 2019)].
Date search was conducted
Original: 27 April 2018 (for publication years 1992 to present) (2190 references).
Update: 30 January 2019 (for publication years 2018–19) (150 references).
Search strategy
-
(cognitive adj2 behavio?r adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab.
-
(cognitive adj2 behavio?ral adj3 (therap$ or theor$ or intervention$ or train$ or treatment$ or psychotherap$ or programme$ or program$ or method$ or approach$)).ti,ab.
-
CBT.ti,ab.
-
Cognitive Behavior Therapy/
-
or/1-4
-
meta-analy$.tw.
-
systematic review.md.
-
meta analysis.md.
-
search:.tw.
-
or/6-9
-
5 and 10
-
limit 11 to yr = ‘1992-2018’
Notes
The McMaster Hedges Maximises Specificity Systematic Review filter for PsycINFO was modified in the following way:
-
Changed ‘meta-analysis.tw.’ to ‘meta-analy$.tw.’
-
Added ‘systematic review.md.’ and ‘meta analysis.md.’
This was to account for known missing papers with ‘meta-analyses’ or ‘meta-analytic’ in the abstract and for papers that do not use ‘search’ (e.g. where ‘retrieval’ or ‘databases surveyed’ is used). If the papers are systematic reviews or reviews, they should be assigned the methodology heading (‘.md.’).
Cochrane Database of Systematic Reviews
Database and platform
Cochrane Database of Systematic Reviews [via The Cochrane Library: http://cochranelibrary-wiley.com/cochranelibrary/search/ (accessed May 2020)].
Date search was conducted
Original: 26 April 2018 (for publication years 1992 to present) (176 references).
Update: 30 January 2019 (for publication years 2018–19) (20 references).
Search strategy
-
(cognitive next/2 behaviour* next/3 therap*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 theor*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 intervention*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 train*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 treatment*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 psychotherap*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 programme*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 program*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 method*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behaviour* next/3 approach*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 therap*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 theor*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 intervention*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 train*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 treatment*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 psychotherap*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 programme*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 program*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 method*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
(cognitive next/2 behavior* next/3 approach*):ti,ab,kw in Cochrane Reviews (Reviews only)
-
‘CBT’:ti,ab,kw in Cochrane Reviews (Reviews only)
-
[mh ‘Cognitive Therapy’] in Cochrane Reviews (Reviews only)
-
#1 or #2 or #3 or #4 or #5 or #6 or #7 or #8 or #9 or #10 or #11 or #12 or #13 or #14 or #15 or #16 or #17 or #18 or #19 or #20 or #21 or #22
-
#23 Publication Year from 1992 to 2018
Database of Abstracts of Reviews of Effects
Database and platform
Database of Abstracts of Reviews of Effect [via The Cochrane Library: https://cochranelibrary-wiley.com/cochranelibrary/search/ (accessed May 2020)].
Date search was conducted
Original: 26 April 2018 (for publication years 1992 to present) (610 references).
Update: no updated search on DARE as no longer updated.
Search strategy
-
cognitive next/2 behaviour* next/3 therap*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 theor*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 intervention*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 train*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 treatment*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 psychotherap*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 programme*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 program*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 method*:ti,ab,kw in Other Reviews
-
cognitive next/2 behaviour* next/3 approach*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 therap*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 theor*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 intervention*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 train*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 treatment*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 psychotherap*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 programme*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 program*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 method*:ti,ab,kw in Other Reviews
-
cognitive next/2 behavior* next/3 approach*:ti,ab,kw in Other Reviews
-
‘CBT’:ti,ab,kw in Other Reviews
-
[mh ‘Cognitive Therapy’] in Other Reviews
-
#1 or #2 or #3 or #4 or #5 or #6 or #7 or #8 or #9 or #10 or #11 or #12 or #13 or #14 or #15 or #16 or #17 or #18 or #19 or #20 or #21 or #22
-
#23 Publication Year from 1992 to 2018.
Child Development and Adolescent Studies
Database and platform
Child Development and Adolescent Studies (via EBSCOhost).
Date search was conducted
Original: 25 April 2018 (for publication years 1992 to present) (177 references).
Update: 30 January 2019 (for publication years 2018–19) (21 references).
Search strategy
-
(TI (cognitive N2 behaviour N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behaviour N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AS (cognitive N2 behaviour N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI (cognitive N2 behavior N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behavior N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AS (cognitive N2 behavior N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI (cognitive N2 behavioural N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB (cognitive N2 behavioural N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AS (cognitive N2 behavioural N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI cognitive N2 behavioral N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AB cognitive N2 behavioral N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*)) OR (AS cognitive N2 behavioral N3 (therap* or theor* or intervention* or train* or treatment* or psychotherap* or programme* or program* or method* or approach*))
-
(TI ‘CBT’) OR (AB ‘CBT’) OR (DE ‘CBT’)
-
(DE ‘Cognitive Therapy’) OR (SU ‘Cognitive Therapy’)
-
(DE ‘Cognitive-behavioral therapy’) OR (DE ‘Cognitive behavioral therapy’) OR (DE ‘Cognitive-behavioural therapy’) OR (DE ‘Cognitive behavioural therapy’) OR (DE ‘Cognitive-behavior therapy’) OR (DE ‘Cognitive behavior therapy’) OR (DE ‘Cognitive-behaviour therapy’) OR (DE ‘Cognitive behaviour therapy’)
-
(DE ‘BEHAVIOR therapy’) OR (SU ‘BEHAVIOR therapy’) OR (DE ‘BEHAVIOUR therapy’) OR (SU ‘BEHAVIOUR therapy’) OR (DE ‘BEHAVIORAL therapy’) OR (SU ‘BEHAVIORAL therapy’) OR (DE ‘BEHAVIOURAL therapy’) OR (SU ‘BEHAVIOURAL therapy’)
-
S1 OR S2 OR S3 OR S4 OR S5 OR S6 OR S7 OR S8
-
(DE ‘SYSTEMATIC reviews (Medical research)’) OR (DE ‘systematic review’) OR (SU ‘SYSTEMATIC reviews (Medical research)’) OR (DE ‘review’)
-
(DE ‘META-analysis’) OR (SU ‘META-analysis’)
-
(DE ‘Literature Review’)
-
(TX ‘metaanaly*’)
-
(TX ‘meta analy*’)
-
(TX systematic N3 (review or overview))
-
S10 OR S11 OR S12 OR S13 OR S14 OR S15
-
S9 AND S16
-
DT 1992-2018
-
S17 AND S18.
OpenGrey
Database and platform
OpenGrey [via www.opengrey.eu/ (accessed February 2019)].
Date search was conducted
Original: 26 April 2018 (295 references).
Update: 30 January 2019 (0 references).
Search strategy
-
‘cognitive behavioral’ OR ‘cognitive behavioural’ OR ‘cognitive behavior’ OR ‘cognitive behaviour’ OR ‘CBT’.
Appendix 3 Data extraction form for mapping
Data extraction | Notes |
---|---|
Review ID (surname, year) | |
Reviewer completing form | |
Date completed | |
Reference citation (first author, title, journal, volume, issue) | |
Published in last 5 years (Y/N) | |
Aim of the review | |
Design of included studies [RCT n = [participants n = ]] | |
Any risk-of-bias tool employed (Y/N) [Detail] | RoB not just quality assessment tool. Report the actual tool used in ‘details’ |
Primary health problem | Report ICD-11 for every health problem reported |
Secondary health problem | |
Severity (mild, moderate, severe, NR) | Select one or many or ‘unclear’ |
Age categories [number of RCTs] | Select one or many of children, adolescents, adults, older adults or ‘not reported’ or ‘unclear’ |
Other characteristics reported: (1) gender, (2) ethnicity, (3) other specific/unique information | Report top-level information on (1) gender (2) ethnicity and (3) if available other information (but do not need to search) |
Where recruited [number of RCTs] | Report as the review has reported: clinic, university, internet, etc |
When delivered [number of RCTs] | Drop-down list [(1) preventative (2) preventative for relapse (3) early intervention (4) standard treatment (5) mixed (6) not reported (7) other (standard treatment is the norm, the others are if review specifies a target)] |
Countries included [number of RCTs] | |
CBT high/low/combined: description of CBT |
|
CBT overall: number of sessions, duration and frequency | As much as is available in the review. Can synthesise ourselves but only at this top level |
CBT content description 1 [number of RCTs/total RCTs] | Report high-intensity intervention first then low intensity |
CBT description 2 [number of RCTs/total] | Complete for every type of CBT category the review includes |
CBT description 3 [number of RCTs/total] | |
CBT description 4 [number of RCTs/total] | |
CBT description 5 [number of RCTs/total] | |
Control description 1 [number of RCTs] | If review synthesises all non-active/active together, then extract as such; if reported as separate control groups, then we can extract as such and then later we will combine |
Control description 2 [number of RCTs] | |
Control description 3 [number of RCTs] | |
Control description 4 [number of RCTs] | |
Control description 5 [number of RCTs] | |
Other details | Only most pertinent information if required |
HRQoL category | Choose (1) category, (2) category but no data available, (3) not measured. If HRQoL emerges at individual RCT level, then we extract (but only for HRQoL) |
How measured [name(s) of instruments/method] | Specific name of outcome |
When measured [pegged time point?] | Short (majority < 12 months), long (majority ≥ 12 months) or ‘unclear’ [if the review reports where the follow-up time points are pegged to, i.e. post randomisation, post intervention, then report] |
Number of RCTs [number of participants] | Number of RCTs [number of participants] |
Meta-analysis [Y/N] | If no meta-analysis, please report the direction of results (i.e. in favour or not in favour of CBT) |
Depression category | Choose (1) category, (2) category but no data available, (3) not measured |
How measured [name(s) of instruments/method] | Specific name of outcome |
When measured [pegged time point?] | Short (majority < 12 months), long (majority ≥ 12 months) or ‘unclear’ [if the review reports where the follow-up time points are pegged to, i.e. post randomisation, post intervention, then report] |
Number of RCTs [number of participants] | Number of RCTs [number of participants] |
Meta-analysis [Y/N] | If no meta-analysis, please report the direction of results (i.e. in favour or not in favour of CBT) |
Anxiety category | Choose (1) category (2) category but no data available (3) not measured |
How measured [name(s) of instruments/method] | Specific name of outcome |
When measured [pegged time point?] | Short (majority < 12 months), long (majority ≥ 12 months) or ‘unclear’ [if the review reports where the follow-up time points are pegged to, i.e. post randomisation, post intervention, then report] |
Number of RCTs [number of participants] | Number of RCTs [number of participants] |
Meta-analysis [Y/N] | If no meta-analysis, please report the direction of results (i.e. in favour or not in favour of CBT) |
Physical/physiological category | Choose (1) category, (2) category but no data available, (3) not measured |
How measured [name(s) of instruments/method] | Specific name of outcome |
When measured [pegged time point?] | Short (majority < 12 months), long (majority ≥ 12 months) or ‘unclear’ [if the review reports where the follow-up time points are pegged to, i.e. post randomisation, post intervention, then report] |
Number of RCTs [number of participants] | Number of RCTs [number of participants] |
Meta-analysis [Y/N] | If no meta-analysis, please report the direction of results (i.e. in favour or not in favour of CBT) |
Psychosis category | Choose (1) category, (2) category but no data available, (3) not measured |
How measured [name(s) of instruments/method] | Specific name of outcome |
When measured [pegged time point?] | Short (majority < 12 months), long (majority ≥ 12 months) or ‘unclear’ [if the review reports where the follow-up time points are pegged to, i.e. post randomisation, post intervention, then report] |
Number of RCTs [number of participants] | Number of RCTs [number of participants] |
Meta-analysis [Y/N] | If no meta-analysis, please report the direction of results (i.e. in favour or not in favour of CBT) |
All other outcomes reported in review | List format e.g. (1) PANSS psychosis |
Overall | See AMSTAR-2 PDF21 |
Mechanism data | Extraction of entire section ‘How the intervention might work’ (for Cochrane reviews), or similar (other reviews), and/or direct data: namely changes to beliefs such as self-efficacy or hypotheses for mechanisms such as presented in the discussions |
Acceptability | |
Satisfaction | |
Adverse effects | |
Economic analyses |
Appendix 4 The AMSTAR-2 checklist
Reproduced from Shea et al. 4 with permission. Copyright © 2017, BMJ Publishing Group Ltd. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/.
Appendix 5 Data extraction form for the panoramic meta-analysis
Meta-analysis details | |
---|---|
HRQoL | |
GRADE or equivalent | |
Intervention vs. control group | |
Age group | |
When measured | |
Name of outcome instrument | Specific name of instrument on which meta-analysis was conducted |
Number of RCTs | |
Continuous SMD or MD [S/MD post or S/MD of change] (± favours intervention or not) | |
Number of participants | |
S/MD (effect size) and type [95% CI] | Hedges or Cohen (± favours intervention or not) |
I 2 | |
Fixed or random effects | |
Reference | |
Depression | |
GRADE or equivalent | |
Intervention vs. control group | |
Age group | |
Name of outcome instrument | |
When measured | |
Number of RCTs | |
Binary OR or RR (± favours intervention or not) | |
Number of participants | |
Number of events | |
OR/RR [95% CI] | |
I 2 | |
Fixed or random effects | |
Continuous SMD or MD [S/MD post or S/MD of change] (± favours intervention or not) | |
Number of participants | |
S/MD (effect size) and type [95% CI] | |
I 2 | |
Fixed or random effects | |
Reference | |
Anxiety | |
GRADE or equivalent | |
Intervention vs. control group | |
Age group | |
Name of outcome instrument | |
When measured | |
Number of RCTs | |
Binary OR or RR (± favours intervention or not) | |
Number of participants | |
Number of events | |
OR/RR [95% CI] | |
I 2 | |
Fixed or random effects | |
Continuous SMD or MD [S/MD post or S/MD of change] (± favours intervention or not) | |
Number of participants | |
S/MD (effect size) and type [95% CI] | |
I 2 | |
Fixed or random effects | |
Reference | |
Physical/physiological | |
GRADE or equivalent | |
Intervention vs. control group | |
Age group | |
When measured | |
Name of outcome instrument | |
Number of RCTs | |
Binary OR or RR (± favours intervention or not) | |
Number of participants | |
Number of events | |
OR/RR [95% CI] | |
I 2 | |
Fixed or random effects | |
Continuous SMD or MD [S/MD post or S/MD of change] (± favours intervention or not) | |
Number of participants | |
S/MD (effect size) and type [95% CI] | |
I 2 | |
Fixed or random effects | |
Reference | |
Psychosis | |
GRADE or equivalent | |
Intervention vs. control group | |
Age group | |
Name of outcome instrument | |
When measured | |
Number of RCTs | |
Binary OR or RR (± favours intervention or not) | |
Number of participants | |
Number of events | |
OR/RR [95% CI] | |
I 2 | |
Fixed or random effects | |
Continuous SMD or MD (± favours intervention or not) | |
Number of participants | |
S/MD (effect size) and type [95% CI] | |
I 2 | |
Fixed or random effects | |
Reference |
Appendix 6 References to studies excluded at the full-text screening stage, with reasons for exclusion
Studies excluded because no English full text or translation available (n = 237)
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Ahmadnia E, Haseli A, Karamat A. [Therapeutic interventions conducted on improving women’s sexual satisfaction and function during reproductive ages in Iran: a systematic review.] J Mazandaran Univ Med Sci 2017;27:146–62.
Ahonen S, Kivela SL. [Effects of cognitive and behavioral treatments on primary insomnia in old age.] Duodecim 2010;126:794–802.
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Algar MJM, Garcia PB. [Approach to anxiety in patients diagnosed with cancer.] Psicooncologia 2016;13:227–48.
Almeida Lima Junior N, Lopes Paes DG, Belchior Pontes GC, Gomes Sancho A, da Silva Rosa JL, Dias Faria ÁC. Possíveis impactos do transtorno de ansiedade social no processo de envelhecimento. Fisioterap Bras 2018;19:577–81.
Almeida AM, Lotufo Neto F. [Cognitive–behavioral therapy in prevention of depression relapses and recurrences: a review.] Rev Bras Psiquiatr 2003;25:239–44.
Ambresin G, De Roten Y, Despland JN. [Psychotherapy of depression in primary care.] Schweiz Arch Neurol Psychiatr 2016;167:147–54.
Andanson J, Pourre F, Maffre T, Raynaud JP. [Social skills training groups for children and adolescents with Asperger syndrome: a review.] Arch Pediatr 2011;18:589–96.
Arteriole N. [Cognitive–Behavioral Therapy in Bipolar Disorder.] PhD thesis. Caen: Université de Caen Normandie & Université de Caen UFR de médecine; 2013.
Auclair V, Harvey PO, Lepage M. [Cognitive behavioral therapy and the treatment of ADHD in adults.] Sante Ment Que 2016;41:291–311.
Bacaltchuk J, Hay P. [Treatment of bulimia nervosa: a synthesis of evidence.] Rev Bras Psiquiatr 1999;21:184–7.
Banti S, Borri C, Montagnani MS, Cargioli C, Belli S, Cotugno B, et al. [Premenstrual disphoric disorder: an update.] J Psychopathol 2012;18:261–72.
Barreto EMDP, Elkis H. [Evidences from the efficacy of the cognitive behavior therapy on schizophrenia.] Rev Psiquiatr Clin 2007;34:204–7.
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Bellino S, Zizza M, Di Lorenzo R, Paradiso E, Falakfarsa R, Fulcheri M, et al. [Combined therapy of major depressive disorder: a critical review.] Italian J Psychopathol 2002;8:401–16.
Bellver Perez A, Moreno P. [Psychosocial risks and psychological intervention in the transplanted bone marrow patients.] Psicooncologia 2009;6:65–81.
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Bomba J. [Research on psychotherapy effectiveness in treatment of mental and behavioural disorders in children and adolescents.] Psychoterapia 2010:37–47.
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Boschi M, Santandrea S, Vanti C. [Efficacy of cognitive behavioural therapy in non-specific neck pain: a systematic review.] Sci Riabil 2010;12:5–15.
Bottlender M, Kohler J, Soyka M. [The effectiveness of psychosocial treatment approaches for alcohol dependence – a review.] Fortschr Neurol Psychiatr 2006;74:19–31.
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Bruun Wyller V, Bjorneklett A, Brubakk O, Festvag L, Follestad I, Malt U, et al. [Diagnosis and Treatment of Chronic Fatigue Syndrome/Myalgic Encephalopathy (CFS/ME).] Report from Knowledge Centre No. 9. Oslo: National Knowledge Centre for Health Services at the Norwegian Institute of Public Health (NIPH); 2006.
Calzolari L, Fioravanti G. [A comparison between acceptance and commitment therapy and cognitive behavioural therapy: a review of literature.] Psicoter Cogn Comportamental 2016;22:103–17.
Caselli G, Manfredi C, Ruggiero GM, Sassaroli S. [Cognitive behavioural therapy for anxiety disorders: a review of efficacy studies.] Psicoter Cogn Comportamental 2016;22:81–101.
Castelein S, Knegtering H, Van Meijel B, Van Der Gaag M. [Dutch guideline on Schizophrenia 2012: basic care within the areas of psychosocial interventions and nursing care.] Tijdschr Psychiatr 2013;55:707–14.
Cavadas LF, Ribeiro L. [Management of adult secondary insomnia in primary health care.] Acta Med Port 2011;24:135–44.
Copanitsanou P, Sourtzi P. [The effect of educational interventions for the reduction of nursing staff’s occupational stress: systematic review.] Nosileftiki 2016;55:250–62.
Cuijpers P, Dekker J. [Psychological treatment of depression; a systematic review of meta-analyses.] Nederlands Tijdschr Geneesk 2005;149:1892–7.
Daga G, Quaranta M, Notaro G, Urani C, Amianto F, Fassino S. [Family therapy and eating disorders in young female patients: state of the art.] Ital J Psychopathol 2011;17:40–7.
Dahm KT, Landmark B, Kirkehei I, Reinar LM. [The Effects of School Health Services for Children and Young People’s Health and Growing Up Conditions.] Report from Knowledge Centre No. 17. Oslo: National Knowledge Centre for Health Services at the Norwegian Institute of Public Health (NIPH); 2010.
Dahm KT, Smedslund G, Havelsrud K, Hafstad E, Reinar LM. [Psychological Interventions for Children and Youth with Serious Somatic Illness in Primary Care.] Report from Knowledge Centre No.10. Oslo: National Knowledge Centre for Health Services at the Norwegian Institute of Public Health (NIPH); 2014.
de Almeida AM, Lotufo Neto F. [Cognitive–behavioral therapy in prevention of depression relapses and recurrences: a review.] Rev Bras Psiquiatr 2003;25:239–44.
de Carvalho MR, Nardi AE, Range B. [Comparison between cognitive, behavioral and cognitive–behavioral approaches in the treatment of panic disorder.] Rev Psiquiatr Clin 2008;35:66–73.
de Cerqueira ACR, Nardi AE. [Depression and multiple sclerosis: on overview.] Rev Bras Neurol 2011;47:11–6.
de Haan E, Huyser C, Boer F. [Obsessive–compulsive disorder in children and adolescents.] Tijdschr Psychiatr 2005;47:229–38.
de Haan L, Bakker JM. [Effectivity of individual psychotherapy in schizophrenia. A review of recent studies.] Tijdschr Psychiatr 2000;42:751–8.
Deffieux X, Billecocq S, Demoulin G, Rivain AL, Trichot C, Thubert T. [Pelvic floor rehabilitation for female urinary incontinence: mechanisms of action.] Progr Urol 2013;23:491–501.
Ding Y. [A review of the psychological characteristics and intervention of patients with malignant tumor before and atter treatment.] J Clin Rehabil Tissue Eng Res 2007;11:7951–4.
Dingemans AE, Bruna MJ, Van Furth EF. [Binge eating disorder. A review.] Tijdschr Psychiatr 2001;43:321–31.
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dos Reis E, Camargo Novelli MMP, Fernandes Guerra RL. Intervenções realizadas com grupos de cuidadores de idosos com síndrome demencial: revisão sistemática. Cad Bras Terap Ocup 2018;26:646–57.
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Ducasse D, Denis H. [Pathological nighttime fears in children: clinical specificities and effective therapeutics.] Encephale 2015;41:323–31.
Duchesne M, Appolinario JC, Range BP, Freitas S, Papelbaum M, Coutinho W. [Evidence of cognitive–behavioral therapy in the treatment of obese patients with binge eating disorder.] Rev Psiquiatr Rio Grande Sul 2007;29:80–92.
박 수 인, 김 연 지, 오 의. 만성적인 신체질환을 가진 환자의 우울 감소를 위한 전화기반 인지행동치료의 효과: 메타분석. J Kor Acad Psychiatr Ment Health Nurs 2018;27:227–39.
김지현, 오복자. 수면장애가 있는 중장년 환자에게 적용한 비약물적 중재의 효과: 메타분석. Kor Adult Nurs 2016;28:13–29.
Elisha D, Karny N, Styr BB. [Psychotherapy – outcome studies and guidelines for evidence-based care policy in Israel.] Harefuah 2011;150:269–74, 302.
Espanol Armengol N, Mijan De La Torre A. [Eating disorders in obesity.] Rev Esp Obes 2006;4:317–27.
Fagiolo D, Berardelli I. [Use of cognitive–behavioural techniques in the treatment of headaches: a systematic review of the last 10-years’ literature.] Med Psicosomat 2007;52:117–24.
Faller H, Herschbach P. [Psychooncological interventions – how successful are they?] Nervenheilkunde 2011;30:133–7.
Fan RM, Yang L. [Progress in clinical treatment of insomnia.] Chin J Clin Rehabil 2006;10:149–51.
Fernandes PA, de Carvalho MR. [Neurobiological changes after cognitive–behavioral therapy of obsessive–compulsive disorder.] Psicologia: Teoria e Pesquisa 2016;32:1–9.
Fischer-Terworth C, Probst P, Glanzmann PG, Knorr CC. [Psychological interventions in dementia: an evaluative review.] Z Psychiatr Psycholog Psychotherap 2009;57:195–206.
Flores-Valdez IH, Leon-Santos MP, Vera-Hernandez E, del Rocio Hernandez Pozo M. [Psychological interventions on stress management and reduction for hypertensive patients: a review of their effectiveness.] Psychologia: Avances de la Disciplina 2013;7:25–44.
Fodor KE, Bitter I. [Psychological interventions following trauma to prevent posttraumatic stress disorder: a systematic review of the literature.] Orvosi Hetilap 2015;156:1321–4.
Foldes-Busque G, Marchand A, Landry P. [Early detection and treatment of panic disorder with or without agoraphobia.] Can Fam Physician 2007;53:1686–93.
Fond G, Franc N. [Treating specific childhood phobia in a single session? A systematic review of the literature.] Encephale 2013;39:109–14.
Fritsche G, Kroner-Herwig B, Kropp P, Niederberger U, Haag G. [Psychological therapy of migraine: systematic review.] Schmerz 2013;27:263–74.
Fu L, Wu MB, Hu Y. [Influence of cognitive behavioural therapy on depression, medication adherence and quality of life in people living with HIV/AIDS (PLHIV): a systematic review.] Chin J Evid Based Med 2014;14:734–42.
Gärtner-Tschacher N. [The effectiveness of combined active physiotherapy and cognitive, behavioural or cognitive–behavioural therapy approaches in patients with musculoskeletal pain.] Manuelle Therapie 2005;9:11–34.
Gai X-S, Lan G-R, Liu X-P. [A meta-analytic review on treatment effects of attention deficit/hyperactivity disorder children in China.] Acta Psychol Sin 2009;40:1190–6.
Gajdos P, Rigo A. [Irritable bowel syndrome: comorbid psychiatric disorders and psychological treatment options.] Orvosi Hetilap 2018;159:2115–21.
Galindo-Vazquez O, Perez-Barrientos H, Alvarado-Aguilar S, Rojas-Castillo E, Alvarez-Avitia MA, Aguilar-Ponce JL. [Cognitive behavioral therapy effects in cancer patients: a review.] Gaceta Mexicana de Oncologia 2013;12:108–15.
Garcia-Perez L, Valdivia-Salas S. [Acceptance and commitment therapy for social anxiety disorder: a systematic review.] Behav Psychol 2018;26:37–92.
Garcia-Torres F, Alos FJ, Perez-Duenas C. [Posttraumatic stress disorder in cancer survivors: a review of the psychological treatments available.] Psicooncologia 2015;12:293–301.
Garcia-Vera MP, Moreno N, Sanz J, Gutierrez S, Gesteira C, Zapardiel A, et al. [Efficacy and clinical utility (effectiveness) of treatments for adult victims of terrorist attacks: a systematic review.] Behavioral Psychology/Psicologia Conductual: Revista Internacional Clinica y de la Salud 2015;23:215–44.
Garcia-Vera MP, Sanz J. [Analysis of the situation of treatments for smoking cessation based on cognitive–behavioral therapy and nicotine patches.] Psicooncologia 2006;3:269–89.
Gellato C. [Eye Movement Desensitization and Reprocessing and Cognitive–Behavioral Therapy in the Treatment of Adult’s Post Traumatic Syndrome Disorder.] PhD thesis. Marseille: Université d’Aix-Marseille II; 2009.
Gomes JB, Matte BC, Vivan A, Viana A, Bortoncello CF, Salum GA, et al. [Cognitive behavioral therapy with family intervention for children and adolescents with obsessive compulsive disorder: a systematic review.] Rev Psiquiatr Rio Grande Sul 2011;33:121–7.
Gomez Puente JM, Martinez-Marcos M. [Overweight and obesity: effectiveness of interventions in adults.] Enfermeria Clin 2018;28:65–74.
Gonzalez Larrabe I, Torre Mollinedo F, Telletxea Benguria S, Arizaga Maguregi A. [Update in the multidisciplinary treatment of fibromyalgia.] Dolor 2008;23:194–206.
Groschwitz RC, Plener PL. [Psychotherapeutic interventions for non-suicidal self-injury.] Nervenheilkunde 2013;32:30–6.
Gunthner A, Batra A. [Prevention of burnout by stress management.] Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz 2012;55:183–9.
Guzman GAR, Lemus CAD, Garcia RR, Agraz FP. [Cognitive behavioral therapy for binge eating disorder: a review.] Psiquiatria 2005;21.
Haidl TK, Rosen M, Ruhrmann S, Klosterkotter J. [Social anxiety in individuals with clinical high-risk state for psychosis.] Fortschritte der Neurologie-Psychiatrie 2018;87:284–97.
Hauser W, Bernardy K. [Psychotherapeutic procedures for fibromyalgia syndrome.] Z Rheumatol 2015;74:584–90.
Hautzinger M, Meyer TD. [Psychotherapy for bipolar disorder: a systematic review of controlled studies.] Nervenarzt 2007;78:1248–60.
Hautzinger M, Wetzel H, Scheurich A, Mainz Univ, Saarland Univ, Rostock Univ, et al. [Serotonin 1A-agonist and Cognitive Behavior Therapy in Relapse Prevention of Alcoholics. Evaluation of Efficacy of Different Treatment Modalities and their Combination.] 2001.
Hautzinger M. [Behavioural therapy with affective and neurological disorders in the elderly.] Verhaltenstherapie & Verhaltensmedizin 2002;23:195–212.
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Herr L, Mingebach T, Becker K, Christiansen H, Kamp-Becker I. [A systematic review of the effectiveness of parent-based interventions for children aged two to twelve years.] Kindheit Entwicklung: Z Klin Kinderpsychol 2015;24:6–19.
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Huang F-F, Li Z-J, Han H-Y, Xiong H-F, Ma Y. [Cognitive behavioral therapy combined with pharmacotherapy for obsessive compulsive disorder: a meta-analysis.] Chin Ment Health J 2013;27:643–9.
한수연, 황지혜, 김초희, 장혜영, 방경숙. 소아암 환자의 형제자매 중재에 관한 연구논문의 체계적 문헌고찰. Child Health Nurs Res 2017;23:394–404.
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López RNA, Girona FG. [Cognitive–behavioral therapy in the treatment of generalized anxiety.] Metas de Enfermería 2011;14:70–3.
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Larsson B. [Cognitive outcome of childhood depression using cognitive behavior therapy.] Lakartidningen 2002;99:1810–2, 5–9.
Larun L, Dalsbo TK, Hafstad E, Reinar LM. [Effects of Interventions for Prevention of Sick Leave and Disability for Health Personnel]. Report from Knowledge Centre No. 2. Oslo: Knowledge Centre for Health Services at the Norwegian Institute of Public Health (NIPH); 2014.
Lefio LA, Villarroel SR, Rebolledo C, Zamorano P, Rivas K. [Effective interventions in the problematic use of alcohol and other drugs.] Pan Am J Public Health 2013;34:257–66.
Leibetseder M, Laireiter AR, Vierhauser M, Hittenberger B. [Efficacy and effectiveness of psychological and psycho-pharmacological treatments in pathological gambling – a meta-analysis.] Sucht 2011;57:275–85.
Leichsenring F, Leibing E. [How effective are psychoanalytic-oriented therapy and behavioral therapy by personality disorders?] Forum der Psychoanalyse 2003;19:378–85.
Leite CEP, Vicentini HC, dos Santos Neves J, Torres AR. [Emetophobia: a critical review about an understudied disorder.] J Bras Psiquiatr 2011;60:123–30.
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Li JY, Ge LJ. [Epidemiologic characteristics and therapy of social anxiety.] J Clin Rehabil Tissue Eng Res 2007;11:10644–7.
Li J, Liu L, Li MQ, Zhang WW, Si Y. [Evidence-based evaluation of therapeutic measures for sleep disorders.] Chin J Contemp Neurol Neurosurg 2013;13:398–404.
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Lin W-C. [Cognitive behavioral treatment for insomnia on cancer patients: a systematic review.] Chin J Psychol;52:173–88.
Lincoln TM, Suttner C, Nestoriuc Y. [Effects of cognitive interventions for schizophrenia: a meta-analysis.] Psychologische Rundschau 2008;59:217–32.
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Liu Y-C, Lan Y-L, Liu C-J, Chou Y-J. [The 10-year meta-analysis of cognitive–behavioral group therapy for depressive symptoms.] Chin J Psychol 2008;50:383–402.
Loeber S, Dinter C, Mann K. [Psychotherapeutic treatment for addiction and comorbid depression.] Sucht 2011;57:373–81.
Lopes LO, Cachioni M. [Psychoeducational intervention for caregivers of elderly with dementia: a systematic review.] J Bras Psiquiatr 2012;61:252–61.
Mao Z-H, Zhao X-D. [Comprehensive analysis of articles on counseling and psychotherapy researches (2000–2009) in Chinese Mental Health Journal.] Chin Ment Health J 2011;25:254–8.
Marquez S, de la Vega R. [Exercise addiction: an emergent behavioral disorder.] Nutricion Hospitalaria 2015;31:2384–91.
Martin A, Gaab J. [Chronic fatigue syndrome. Evidenced-based psychotherapy for chronic medically unexplained fatigue.] Psychotherapeut 2011;56:231–8.
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Studies excluded because of broad definition of cognitive–behavioural therapy (n = 119)
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Hesser H, Weise C, Westin VZ, Andersson G. A systematic review and meta-analysis of randomized controlled trials of cognitive-behavioral therapy for tinnitus distress. Clin Psychol Rev 2011;31:545–53. https://doi.org/10.1016/j.cpr.2010.12.006
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De Groot V, Beckerman H. Rehabilitation to treat MS-related fatigue: the TREFAMS research programme. Mult Scler 2016;22(Suppl. 3):40–1.
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Dickinson C, Whittingham K, Sheffield J, Wotherspoon J, Boyd R. Efficacy of interventions to improve psychological adjustment for parents who have an infant diagnosed with neurodevelopmental disability: a systematic review. Devel Med Child Neurol 2018;60(Suppl. 1):20.
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Falsaperla R, Saporito MAN, Di Stefano V, Pavone P. A31 Pandas: tip of the iceberg. Riv Ital Pediatr 2017;43(Suppl. 2):15.
Fangtham M, Nash JL, Hyon S, Bannuru RR, Wang C. Non-pharmacological treatment on fatigue, depression, disease activity, and quality of life of systemic lupus erythematosus: a systematic review [abstract]. Arthr Rheumatol 2017;69(Suppl. 10).
Farris M, Devoe D, Addington J. Attrition rates in treatment trials: a systematic review and meta-analysis of clinical high-risk for psychosis interventions. Early Interv Psychiatry 2018;12(Suppl. 1):182.
Ferreira PH, Ho KK, Pinheiro MB, Aquino Silva D, Miller C, Grunstein R, et al. Sleep interventions for osteoarthritis and spinal pain: a systematic review of randomized control trials. Osteoarthr Cartil 2018;26(Suppl. 1):S243.
Fishpool K, Jones B, Hewlett S, Ndosi M. 277 Online interventions for addressing psychological distress in people with rheumatoid arthritis and other long-term conditions: a systematic review. Rheumatology 2018;57(Suppl. 3).
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Gaudin D, Krafcik B, Mansour T, Alnemari AA. P160 – considerations in spinal fusion surgery for chronic lumbar pain: psychosocial factors, rating scales, and perioperative patient education: a review of the literature. Glob Spine J 2017;7:268S–9S.
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Goyal D, Parikh T, Fitzgerald J, Pruett J. 5.50 Assessment and treatment of irritability in children and adolescents: a review of literature for evidence-based recommendations. J Am Acad Child Adolesc Psychiatry 2018;57:S242–3.
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van der Gaag M, Ising H. Latest developments of psychological psychosis prevention strategies in the Netherlands. Early Interv Psychiatry 2018;12(Suppl. 1):76.
van der Gaag M, Smit F, Bechdolf A, French P, Linszen DH, Yung A, et al. Preventing a first episode of psychosis: a meta-analysis. Schizophr Res 2014;153(Suppl. 1):S42.
van der Gaag M, Smit F, Bechdolf A, French P, Linszen DH, Yung AR, et al. Preventing a first episode of psychosis: meta-analysis of randomized controlled prevention trials. Schizophr Bull 2013;39(Suppl. 1):S356.
van der Gaag M, Velthorst E, Smit F, Meyer C, Koeter M, Fett AK, et al. The battle for ameliorating negative symptoms has a restart. Early Interv Psychiatry 2014;8(Suppl. 1):23.
van der Gaag M, Velthorst E, Smit F, Meyer C, Koeter M, Fett AK, et al. Psychotherapy in people with negative symptoms. Eur Arch Psychiatry Clin Neurosci 2015;265(Suppl.):S40.
van Straten A, Van Der Zweerde T, Morin C, Lancee J. Cognitive and behavioural therapies in the treatment of insomnia: a systematic metaanalysis of all the literature. J Sleep Res 2018;27(Suppl. 1):167.
Vandepitte S, Van Den Noortgate N, Putman K, Verhaeghe S, Faes K, Annemans L. Effectiveness of supporting informal caregivers of people with dementia: a systematic review. Value Health 2015;18(7):A407–8.
Vasa RA. 8.5 Assessment and management of anxiety in youth with ASD. J Am Acad Child Adolesc Psychiatry 2018;57:S134–5.
Verberne D, Spauwen P, Van Heugten C. Neuropsychological interventions for treating neuropsychiatric consequences of acquired brain injury: a systematic review. Brain Injury 2017;31(6–7):797.
Vitinius F, Bassou S, Albus C. Psychotherapeutic and psychiatric interventions after bonemarrow/stemcell transplantation – a systematic review. J Psychosom Res 2011;70:621–2.
Vitinius F, Imlau C, Albus C. Psychosocial strain and therapeutic approaches of hereditary neurological diseases: a systematic review. J Psychosom Res 2013;74:560.
Vitinius F, Piontek K, Albus C. Psychosocial interventions to improve quality of life, depression and anxiety in lung transplant patients – a systematic review of randomized controlled trials. J Psychosom Res 2011;70:620.
Vollm B, Gibbon S, Khalifa N, Duggan C, Stoffers J, Huband N, et al. S08-01-Cochrane reviews of pharmacological and psychological interventions for antisocial personality disorder (ASPD). Eur Psychiatry 2010;25(Suppl. 1):90.
Walling AD. Which treatments are effective for reducing adolescent alcohol abuse? Am Fam Physician 2010;82:532–4.
Wang C, Bayes S. Effectiveness of acupuncture as an add-on treatment for women with postnatal depression: a systematic review. Women Birth 2018;31(Suppl. 1):S27.
Wang Z. Errors in Meta-analysis of trial comparing effectiveness and safety of cognitive behavioral therapy with pharmacotherapy for childhood anxiety disorders. JAMA Pediatr 2018;172:983–4. https://doi.org/10.1001/jamapediatrics.2018.2951
Wearden AJ, Russell C, Emsley R, Fairclough G, Kyle SD. Sleep and fatigue in chronic fatigue syndrome. Psychosom Med 2016;78:A24.
Webb M. A review of web-based applications used to support self-management of non-specific chronic low back pain. Br J Pain 2017;11(Suppl. 2):51–2.
Wendebourg MJ, Heesen C, Finlayson M, Meyer B, Pottgen J, Kopke S. Patient education for people with multiple sclerosis associated fatigue: a systematic review. Mult Scler 2016;22(Suppl. 3):700.
Whale R, Bucur M. Systematic review of randomised interventions for preonset phase psychosis. Early Interv Psychiatry 2010;4(Suppl. 1):116.
White D, Luther L. Efficacy of cognitive behavior therapy in early psychosis. Schizophr Bull 2017;43(Suppl. 1):S209.
Wiener J, Mehta S, Iruthayarajah J, Janssen S, Teasell R. The effectiveness of cognitive behavioural therapy for the management of post-stroke depressive symptoms. Arch Phys Med Rehabil 2017;98:e137.
Williams A, Eccleston C, Morley S. 1012 Systematic review and meta-analysis of psychological treatments for persistent pain in adults, excluding headache. Eur J Pain 2009;13(Suppl. 1):S284.
Williams A, Morley S. Systematic review and meta-analysis of psychological treatments for persistent pain in adults, excluding headache. J Pain 2009;10:S62.
Yoshinaga N, Nosaki A, Unozawa K, Hayashi Y, Shimizu E. A systematic review of cognitive behavioral therapy in nursing field in Japan. Asia Pac Psychiatry 2015;7(Suppl. 1):26.
Zafar Usmani A, Ni Cheng J, Smith BJ, Carson KV. A meta-analysis (Cochrane review) of pharmacological and psychological interventions for anxiety and depression in COPD. Respirology 2010;15(Suppl. 1):A19.
Zangi HA. The evidence for patient education in inflammatory arthritis. Ann Rheum Dis 2014;73(Suppl. 2):55–6.
Studies excluded because duplicates/superceded/withdrawn (n = 170)
Abbott RA, Martin AE, Newlove-Delgado TV, Bethel A, Whear RS, Thompson Coon J, Logan S. Recurrent abdominal pain in children: summary evidence from 3 systematic reviews of treatment effectiveness. J Pediatr Gastroenterol Nutr 2018;67:23–33. https://doi.org/10.1097/MPG.0000000000001922
Aggarwal VR, Lovell K, Peters S, Javidi H, Joughin A, Goldthorpe J. Psychosocial interventions for the management of chronic orofacial pain. Cochrane Database Syst Rev 2011;11:CD008456. https://doi.org/10.1002/14651858.CD008456.pub2
Akechi T, Okuyama T, Onishi J, Morita T, Furukawa TA. WITHDRAWN: Psychotherapy for depression among incurable cancer patients. Cochrane Database Syst Rev 2018;11:CD005537. https://doi.org/10.1002/14651858.CD005537.pub3
Alessi C, Vitiello MV. Insomnia (primary) in older people. BMJ Clin Evid 2011;2011:2302.
Andrews G, Cuijpers P, Craske MG, McEvoy P, Titov N. Computer therapy for the anxiety and depressive disorders is effective, acceptable and practical health care: a meta-analysis. PLOS ONE 2010;5:e13196. https://doi.org/10.1371/journal.pone.0013196
Anie KA, Green J. Psychological therapies for sickle cell disease and pain. Cochrane Database Syst Rev 2002;2:CD001916.
Anie KA, Green J. Psychological therapies for sickle cell disease and pain. Cochrane Database Syst Rev 2012;2:CD001916. https://doi.org/10.1002/14651858.CD001916.pub2
Apóstolo J, Bobrowicz-Campos E, Rodrigues M, Castro I, Cardoso D. The effectiveness of non-pharmacological interventions in older adults with depressive disorders: a systematic review. Int J Nurs Stud 2016;58:59–70.
Arroyo K, Lundahl B, Butters R, Vanderloo M, Wood DS. Short-term interventions for survivors of intimate partner violence: a systematic review and meta-analysis. Trauma Violence Abuse 2015;2.
Ashman L, Duggan L. Interventions for learning disabled sex offenders. Cochrane Database Syst Rev 2002;2:CD003682.
Auclair V, Harvey P-O, Lepage M. La thérapie cognitive-comportementale dans le traitement du TDAH chez l’adulte. Sante Mental Quebec 2016;41:291–311.
Bandelow B, Seidler-Brandler U, Becker A, Wedekind D, Rüther E. Meta-analysis of randomized controlled comparisons of psychopharmacological and psychological treatments for anxiety disorders. World J Biol Psychiatry 2007;8:175–87.
Beelmann A, Losel F. El entrenamiento en habilidades sociales en la prevencion temprana de la delincuencia: los efectos en la conducta antisocial y la competencia social. Psicothema 2006;18:603–10.
Belleville G, Cousineau H, Levrier K, St-Pierre-Delorme MÈ. Meta-analytic review of the impact of cognitive–behavior therapy for insomnia on concomitant anxiety. Clin Psychol Rev 2011;31:638–52. https://doi.org/10.1016/j.cpr.2011.02.004
Beltman MW, Oude Voshaar RC, Speckens AE. Cognitive–behavioural therapy for depression in people with a somatic disease: meta-analysis of randomised controlled trials Br J Psychiatry 2010;197:11–9.
Bender JL, Radhakrishnan A, Diorio C, Englesakis M, Jadad AR. Can pain be managed through the internet? A systematic review of randomized controlled trials. Pain 2011;152:1740–50. https://doi.org/10.1016/j.pain.2011.02.012
Bernardy K, Füber N, Köllner V, Häuser W. Efficacy of cognitive–behavioral therapies in fibromyalgia syndrome – a systematic review and metaanalysis of randomized controlled trials. J Rheumatol 2010;37:1991–2005. https://doi.org/10.3899/jrheum.100104
van Beugen S, Ferwerda M, Hoeve D, Rovers MM, Spillekom-van Koulil S, van Middendorp H, Evers AW. Internet-based cognitive behavioral therapy for patients with chronic somatic conditions: a meta-analytic review. J Med Internet Res 2014;16:e88. https://doi.org/10.2196/jmir.2777
Bisson J, Andrew M. Psychological treatment of post-traumatic stress disorder (PTSD). Cochrane Database Syst Rev 2005;2:CD003388. https://doi.org/10.1002/14651858.CD003388.pub2
Bisson J, Andrew M. Psychological treatment of post-traumatic stress disorder (PTSD). Cochrane Database Syst Rev 2007;3:CD003388. https://doi.org/10.1002/14651858.CD003388.pub3
Bisson JI, Ehlers A, Matthews R, Pilling S, Richards D, Turner S. Psychological treatments for chronic post-traumatic stress disorder. Systematic review and meta-analysis. Br J Psychiatry 2007;190:97–104.
Brasure M, MacDonald R, Fuchs E, Olson CM, Carlyle M, Diem S, et al. Management of Insomnia Disorder. Comparative Effectiveness Review No. 159. Report No: 15(16)-EHC027-EF. Rockville, MD: Agency for Healthcare Research and Quality (US); 2015.
Brennan L, Murphy KD, Shaw KA, McKenzie JE. WITHDRAWN: Psychological interventions for overweight or obesity. Cochrane Database Syst Rev 2014;5:CD003818. https://doi.org/10.1002/14651858.CD003818.pub3
Buchanan J, Zakrzewska J. Burning mouth syndrome. BMJ Clin Evid 2008;14:1301.
Buckley LA, Pettit T, Adams CE. Supportive therapy for schizophrenia. Cochrane Database Syst Rev 2007;18:CD004716.
Casacalenda N, Perry JC, Looper K. Remission in major depressive disorder: a comparison of pharmacotherapy, psychotherapy, and control conditions. Am J Psychiatry 2002;159:1354–60. https://doi.org/10.1176/appi.ajp.159.8.1354
Chang CW, Mu PF, Jou ST, Wong TT, Chen YC. The effectiveness of non-pharmacological interventions on fatigue in children and adolescents with cancer: a systematic review. JBI Libr Syst Rev 2012;10:574–614. https://doi.org/10.11124/jbisrir-2012-60
Chi NC, Demiris G, Lewis FM, Walker AJ, Langer SL. Behavioral and educational interventions to support family caregivers in end-of-life care: a systematic review. Am J Hosp Palliat Care 2016;33:894–908.
Cleary M, Hunt G, Matheson S, Siegfried N, Walter G. Psychosocial interventions for people with both severe mental illness and substance misuse. Cochrane Database Syst Rev 2008;1:CD001088. https://doi.org/10.1002/14651858.CD001088.pub2
Cormac I, Jones C, Campbell C. Cognitive behaviour therapy for schizophrenia. Cochrane Database Syst Rev 2002;1:CD000524.
Covin R, Ouimet AJ, Seeds PM, Dozois DJ. A meta-analysis of CBT for pathological worry among clients with GAD. J Anxiety Disord 2008;22:108–16.
Cuijpers P, van Straten A, Andersson G. Internet-administered cognitive behavior therapy for health problems: a systematic review. J Behav Med 2008;31:169–77. https://doi.org/10.1007/s10865-007-9144-1
Cuijpers P, van Straten A, Smit F. Psychological treatment of late-life depression: a meta-analysis of randomized controlled trials. Int J Geriatr Psychiatry 2006;21:1139–49. https://doi.org/10.1002/gps.1620
Cuijpers P, van Straten A, Warmerdam L, Andersson G. Psychotherapy versus the combination of psychotherapy and pharmacotherapy in the treatment of depression: a meta-analysis. Depress Anxiety 2009;26:279–88. https://doi.org/10.1002/da.20519
de Arellano MA, Lyman DR, Jobe-Shields L, George P, Dougherty RH, Daniels AS, et al. Trauma-focused cognitive–behavioral therapy for children and adolescents: assessing the evidence. Psychiatr Serv 2014;65:591–602. https://doi.org/10.1176/appi.ps.201300255
Driessen E, Cuijpers P, Hollon SD, Van HL, Dekker JJ. [The efficacy of psychological treatments for depression: a review of recent research findings.] Tijdschr Psychiatr 2014;56:455–62.
Eccleston C, Williams AC, Morley S. Psychological therapies for the management of chronic pain (excluding headache) in adults. Cochrane Database Syst Rev 2009;2:CD007407. https://doi.org/10.1002/14651858.CD007407.pub2
Edwards AG, Hailey S, Maxwell M. Psychological interventions for women with metastatic breast cancer. Cochrane Database Syst Rev 2004;2:CD004253. https://doi.org/10.1002/14651858.CD004253.pub2
Edwards AG, Hulbert-Williams N, Neal RD. Psychological interventions for women with metastatic breast cancer. Cochrane Database Syst Rev 2008;3:CD004253. https://doi.org/10.1002/14651858.CD004253.pub3
Elderton AJ. Posttraumatic Growth in Survivors of Interpersonal Violence in Adulthood. PhD thesis. Oxford: University of Oxford; 2013.
Ewing DL, Monsen JJ, Thompson EJ, Cartwright-Hatton S, Field A. A meta-analysis of transdiagnostic cognitive behavioural therapy in the treatment of child and young person anxiety disorders. Behav Cogn Psychother 2015;43:562–77. https://doi.org/10.1017/S1352465813001094
Ford AC, Quigley EM, Lacy BE, Lembo AJ, Saito YA, Schiller LR, et al. Effect of antidepressants and psychological therapies, including hypnotherapy, in irritable bowel syndrome: systematic review and meta-analysis. Am J Gastroenterol 2014;109:1350–65. https://doi.org/10.1038/ajg.2014.148
Furlong M, McGilloway S, Bywater T, Hutchings J, Smith SM, Donnelly M. Behavioural and cognitive–behavioural group-based parenting programmes for early-onset conduct problems in children aged 3 to 12 years. Cochrane Database Syst Rev 2012;2:CD008225.
Galsworthy-Francis L. The Development and Exploration of the Experiences of Humiliation Scale (EHS) in an Eating Disordered Population. Leicester: University of Leicester; 2012.
Gandy M, Sharpe L, Perry KN. Cognitive behavior therapy for depression in people with epilepsy: a systematic review. Epilepsia 2013;54:1725–34. https://doi.org/10.1111/epi.12345
Gartlehner G, Gaynes BN, Amick HR, Asher GN, Morgan LC, Coker-Schwimmer E, et al. Comparative benefits and harms of antidepressant, psychological, complementary, and exercise treatments for major depression: an evidence report for a clinical practice guideline from the American College of Physicians. Ann Intern Med 2016;164:331–41. https://doi.org/10.7326/M15-1813
Gómez Puente JM, Martínez-Marcos M. Sobrepeso y obesidad: eficacia de las intervenciones en adultos. Enferm Clin 2018;28:65–74.
Goschwitz R, Plener P. Psychotherapeutic interventions for non-suicidal self-injury. Nervenheilkd Z Interdiszip Fortbild 2013;32:30–6.
Gregory VL. Cognitive–behavioral therapy for comorbid bipolar and substance use disorders: a systematic review of controlled trials. Ment Health Subst Use 2011;4:302–13.
Haniffa M, Lasserson TJ, Smith I. Interventions to improve compliance with continuous positive airway pressure for obstructive sleep apnoea. Cochrane Database Syst Rev 2004;4:CD003531. https://doi.org/10.1002/14651858.CD003531.pub2
Hay PJ, Bacaltchuk J. Psychotherapy for bulimia nervosa and binging. Cochrane Database Syst Rev 2000;2:CD000562.
Hay PJ, Bacaltchuk J. Psychotherapy for bulimia nervosa and binging. Cochrane Database Syst Rev 2001;3:CD000562.
Hay PJ, Bacaltchuk J. Psychotherapy for bulimia nervosa and binging. Cochrane Database Syst Rev 2003;1:CD000562. https://doi.org/10.1002/14651858.CD000562
Hay PJ, Bacaltchuk J. Bulimia nervosa. BMJ Clin Evid 2008;2008:1009.
Hay PJ, Bacaltchuk J, Stefano S. Psychotherapy for bulimia nervosa and binging. Cochrane Database Syst Rev 2004;3:CD000562. https://doi.org/10.1002/14651858.CD000562.pub2
Haynes RB, Ackloo E, Sahota N, McDonald HP, Yao X. Interventions for enhancing medication adherence. Cochrane Database Syst Rev 2008;2:CD000011. https://doi.org/10.1002/14651858.CD000011.pub3
Hazell P. Depression in children and adolescents. BMJ Clin Evid 2011;2011:1008.
Hetrick SE, Cox GR, Merry SN. Treatment-resistant depression in adolescents: is the addition of cognitive behavioral therapy of benefit? Psychol Res Behav Manag 2011;4:97–112.
Hetrick SE, Cox GR, Merry SN. Where to go from here? An exploratory meta-analysis of the most promising approaches to depression prevention programs for children and adolescents. Int J Environ Res Public Health 2015;12:4758–95. https://doi.org/10.3390/ijerph120504758
Hjorthøj C, Fohlmann A, Nordentoft M. Treatment of cannabis use disorders in people with schizophrenia spectrum disorders – a systematic review. Addict Behav 2009;34:520–5. https://doi.org/10.1016/j.addbeh.2009.02.001
Ho BPV, Carter M, Stephenson J. Anger management using a cognitive–behavioural approach for children with special education needs: a literature review and meta-analysis. Int J Disab Dev Educ 2010;57:245–65.
Hofmann SG, Sawyer AT, Korte KJ, Smits JA. Is it beneficial to add pharmacotherapy to cognitive–behavioral therapy when treating anxiety disorders? A meta-analytic review. Int J Cogn Ther 2009;2:160–75.
Hofmann SG, Smits JA. Cognitive–behavioral therapy for adult anxiety disorders: a meta-analysis of randomized placebo-controlled trials. J Clin Psychiatry 2008;69:621–32.
Huang FF, Li ZJ, Han HY, Xiong HF, Ma Y, et al. Cognitive behavioral therapy combined with pharmacotherapy for obsessive compulsive disorder: a meta-analysis. Chin Ment Health J 2013;27:643–9.
Huertas-Ceballos AA, Logan S, Bennett C, Macarthur C. WITHDRAWN: Psychosocial interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood. Cochrane Database Syst Rev 2014;2:CD003014. https://doi.org/10.1002/14651858.CD003014.pub3
Irwin MR, Cole JC, Nicassio PM. Comparative meta-analysis of behavioral interventions for insomnia and their efficacy in middle-aged adults and in older adults 55+ years of age. Health Psychol 2006;25:3–14.
James A, Soler A, Weatherall R. Cognitive behavioural therapy for anxiety disorders in children and adolescents. Cochrane Database Syst Rev 2005;4:CD004690. https://doi.org/10.1002/14651858.CD004690.pub2
James AC, James G, Cowdrey FA, Soler A, Choke A. Cognitive behavioural therapy for anxiety disorders in children and adolescents. Cochrane Database Syst Rev 2013;6:CD004690. https://doi.org/10.1002/14651858.CD004690.pub3
Jones C, Cormac I, Mota J, Campbell C. Cognitive behaviour therapy for schizophrenia. Cochrane Database Syst Rev 2000;2:CD000524.
Jones C, Cormac I, Silveira da Mota Neto JI, Campbell C. Cognitive behaviour therapy for schizophrenia. Cochrane Database Syst Rev 2004;4:CD000524.
Jones C, Hacker D, Meaden A, Cormac I, Irving CB. WITHDRAWN: Cognitive behaviour therapy versus other psychosocial treatments for schizophrenia. Cochrane Database Syst Rev 2011;4:CD000524. https://doi.org/10.1002/14651858.CD000524.pub3
Jones C, Hacker D, Cormac I, Meaden A, Irving CB. Cognitive behaviour therapy versus other psychosocial treatments for schizophrenia. Cochrane Database Syst Rev 2012;4:CD008712. https://doi.org/10.1002/14651858.CD008712.pub2
Kaltenthaler E, Shackley P, Stevens K, Beverley C, Parry G, Chilcott J. A systematic review and economic evaluation of computerised cognitive behaviour therapy for depression and anxiety. Health Technol Assess 2002;6(22). https://doi.org/10.3310/hta6220
Kavanagh J, Oliver S, Lorenc T, Caird J, Tucker H, Harden A, et al. School-based cognitive–behavioural interventions: a systematic review of effects and inequalities. Health Sociol Rev 2009;18:61–78.
Kenworthy T, Adams CE, Bilby C, Brooks-Gordon B, Fenton M. WITHDRAWN: Psychological interventions for those who have sexually offended or are at risk of offending. Cochrane Database Syst Rev 2008;4:CD004858. https://doi.org/10.1002/14651858.CD004858.pub2
Kisely S, Campbell LA, Skerritt P. Psychological interventions for symptomatic management of non-specific chest pain in patients with normal coronary anatomy. Cochrane Database Syst Rev 2005;1:CD004101. https://doi.org/10.1002/14651858.CD004101.pub2
Kisely SR, Campbell LA, Skerritt P, Yelland MJ. Psychological interventions for symptomatic management of non-specific chest pain in patients with normal coronary anatomy. Cochrane Database Syst Rev 2010;1:CD004101. https://doi.org/10.1002/14651858.CD004101.pub3
Kisely SR, Campbell LA, Yelland MJ, Paydar A. Psychological interventions for symptomatic management of non-specific chest pain in patients with normal coronary anatomy. Cochrane Database Syst Rev 2012;6:CD004101. https://doi.org/10.1002/14651858.CD004101.pub4
Klimas J, Field CA, Cullen W, O’Gorman CS, Glynn LG, Keenan E, et al. Psychosocial interventions to reduce alcohol consumption in concurrent problem alcohol and illicit drug users. Cochrane Database Syst Rev 2012;11:CD009269. https://doi.org/10.1002/14651858.CD009269.pub2
Klimas J, Field CA, Cullen W, O’Gorman CS, Glynn LG, Keenan E, et al. Psychosocial interventions to reduce alcohol consumption in concurrent problem alcohol and illicit drug users: Cochrane Review. Syst Rev 2013;2:3. https://doi.org/10.1186/2046-4053-2-3
Köllner V, Häuser W, Klimczyk K, Kühn-Becker H, Settan M, Weigl M, Bernardy K, Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften. [Psychotherapy for patients with fibromyalgia syndrome. Systematic review, meta-analysis and guideline.] Schmerz 2012;26:291–6. https://doi.org/10.1007/s00482-012-1179-8
Kroenke K. Efficacy of treatment for somatoform disorders: a review of randomized controlled trials. Psychosom Med 2007;69:881–8.
Larkin D, Lopez V, Aromataris E. Non-pharmacological interventions for cancer-related fatigue in men treated for prostate cancer: a systematic review. JBI Libr Syst Rev 2012;10:3764–811.
Larun L, Brurberg KG, Odgaard-Jensen J, Price JR. Exercise therapy for chronic fatigue syndrome. Cochrane Database Syst Rev 2015;2:CD003200. https://doi.org/10.1002/14651858.CD003200.pub3
Larun L, Brurberg KG, Odgaard-Jensen J, Price JR. Exercise therapy for chronic fatigue syndrome. Cochrane Database Syst Rev 2016;12:CD003200.
Lewandowski LM, Gebing TA, Anthony JL, O’Brien WH. Meta-analysis of cognitive–behavioral treatment studies for bulimia. Clin Psychol Rev 1997;17:703–18.
Linde K, Sigterman K, Kriston L, Rücker G, Jamil S, Meissner K, Schneider A. Effectiveness of psychological treatments for depressive disorders in primary care: systematic review and meta-analysis. Ann Fam Med 2015;13:56–68. https://doi.org/10.1370/afm.1719
Lip GY, Lane DA, Millane TA, Tayebjee MH. Psychological interventions for depression in adolescent and adult congenital heart disease. Cochrane Database Syst Rev 2003;3:CD004394. https://doi.org/10.1002/14651858.CD004394
Liu HX, Liang QJ, Xiao P, Jiao HX, Gao Y, Ahmetjiang A. The effectiveness of cognitive–behavioural therapy for temporomandibular disorders: a systematic review. J Oral Rehabil 2012;39:55–62. https://doi.org/10.1111/j.1365-2842.2011.02239.x
Lockwood C, Page T, NursCert H, Conroy-Hiller T. Effectiveness of individual therapy and group therapy in the treatment of schizophrenia. JBI Libr Syst Rev 2004;2:1–44.
Macdonald G, Higgins JP, Ramchandani P, Valentine JC, Bronger LP, Klein P, et al. Cognitive–behavioural interventions for children who have been sexually abused. Cochrane Database Syst Rev 2012;5:CD001930. https://doi.org/10.1002/14651858.CD001930.pub3
Macdonald GM, Higgins JP, Ramchandani P. Cognitive–behavioural interventions for children who have been sexually abused. Cochrane Database Syst Rev 2006;4:CD001930. https://doi.org/10.1002/14651858.CD001930.pub2
Macea DD, Gajos K, Daglia Calil YA, Fregni F. The efficacy of Web-based cognitive behavioral interventions for chronic pain: a systematic review and meta-analysis. J Pain 2010;11:917–29. https://doi.org/10.1016/j.jpain.2010.06.005
Malouff JM, Thorsteinsson EB, Rooke SE, Bhullar N, Schutte NS. Efficacy of cognitive behavioral therapy for chronic fatigue syndrome: a meta-analysis. Clin Psychol Rev 2008;28:736–45.
Marshall M, Lockwood A. Early intervention for psychosis. Cochrane Database Syst Rev 2004;2:CD004718.
Marson AG, Maguire M, Ramaratnam S. Epilepsy. BMJ Clin Evid 2009;2009:1201.
Matthews EE, Arnedt JT, McCarthy MS, Cuddihy LJ, Aloia MS. Adherence to cognitive behavioral therapy for insomnia: a systematic review. Sleep Med Rev 2013;17:453–64. https://doi.org/10.1016/j.smrv.2013.01.001
Mayo-Wilson E. Media-delivered Behavioural and Cognitive Behavioural Therapy for Anxiety: A Systematic Review of Effectiveness and an Exploratory Study of Consumer Preferences. PhD thesis. Oxford: Oxford University; 2011.
Mayo-Wilson E, Montgomery P. Media-delivered cognitive behavioural therapy and behavioural therapy (self-help) for anxiety disorders in adults. Cochrane Database Syst Rev 2013;9:CD005330. https://doi.org/10.1002/14651858.CD005330.pub4
McDaid C, Trowman R, Golder S, Hawton K, Sowden A. Interventions for people bereaved through suicide: systematic review. Br J Psychiatry 2008;193:438–43. https://doi.org/10.1192/bjp.bp.107.040824
Meyer T, Hautzinger M. Cognitive behavioral therapy in addition to pharmacotherapy for manic depressive disorders: empirical results. Der Nervenarzt 2002;73:620–8.
Montgomery P, Dennis J. Cognitive behavioural interventions for sleep problems in adults aged 60+. Cochrane Database Syst Rev 2002;2:CD003161.
Montgomery P, Dennis J. A systematic review of non-pharmacological therapies for sleep problems in later life. Sleep Med Rev 2004;8:47–62. https://doi.org/10.1016/S1087-0792(03)00026-1
Morin CM, Hauri PJ, Espie CA, Spielman AJ, Buysse DJ, Bootzin RR. Nonpharmacologic treatment of chronic insomnia. An American Academy of Sleep Medicine review. Sleep 1999;22:1134–56. https://doi.org/10.1093/sleep/22.8.1134
Ng TK, Wong DFK. The efficacy of cognitive behavioral therapy for Chinese people: a meta-analysis. Aust N Z J Psychiatry 2018;52:620–37. https://doi.org/10.1177/0004867417741555
Oakley-Browne MA, Adams P, Mobberley PM. Interventions for pathological gambling. Cochrane Database Syst Rev 2000;2:CD001521.
Oakley-Browne MA, Adams P, Mobberley PM. WITHDRAWN: Interventions for pathological gambling. Cochrane Database Syst Rev 2007;1:CD001521. https://doi.org/10.1002/14651858.CD001521.pub2
Oei TP, Dingle G. The effectiveness of group cognitive behaviour therapy for unipolar depressive disorders. J Affect Disord 2008;107:5–21.
O’Kearney R. Benefits of cognitive–behavioural therapy for children and youth with obsessive–compulsive disorder: re-examination of the evidence. Aust N Z J Psychiatry 2007;41:199–212.
Orgeta V, Qazi A, Spector A, Orrell M. Psychological treatments for depression and anxiety in dementia and mild cognitive impairment: systematic review and meta-analysis. Br J Psychiatry 2015;207:293–8. https://doi.org/10.1192/bjp.bp.114.148130
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Appendix 7 Summary tables of included systematic reviews grouped according to the conditions they targeted as per the ICD-11
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Uwimana and Louw465 2007 | Human immunodeficiency virus | NA | Critically low | 1 (NR) | Adults | NR | Group CBT | NA | Peer support counselling | NA | Short | ✓ | ✓ | ✓ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Berry et al.65 2017 | Neoplasms | NA | Low | 1 (118) | Adults | The Netherlands | Face-to-face CBT (couples therapy) | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ≤ |
Boutin73 2007 | Malignant neoplasms of breast | NA | Critically low | 2 (213) | Adults | NR | Individual CBT | NA | NR | NR | Short–long | ✗ | ✓ | ✗ | ✗ |
Ernst et al.137 2006 | Malignant neoplasms of breast | NA | Critically low | 1 (92) | NR | NR | Therapist-led group CBT + standard oncological care | NA | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Hines et al.209 2011 | Malignant neoplasms | Cognitive dysfunction | Moderate | 1 (40) | Adults | USA | Individual CBT+ telephone booster | NA | NA | WLC | Short | ✓ | ✗ | ✗ | ✗ |
Juvet et al.238 2009 | Malignant neoplasms of breast | NA | Moderate | 1 (114) | Adults | Israel | Group CBT | NA | Relaxation + guided support | TAU | Short | ≤ | ≤ | ≤ | ✓ |
Mirosevicet al.313 2019 | Malignant neoplasms | NA | Critically low | 4 (625) | Adults | NR | Group CBT | NA | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Mustafa et al.322 2013 | Malignant neoplasms of breast | NA | Moderate | 1 (63) | Adults | Australia | Individual CBT | NA | NA | TAU | Short–long | ≤ | ✓ | ✓ | ✓ |
Ye et al.513 2018 | Malignant neoplasms of breast | NA | Low | 10 (1939) | Adults | USA, China, Ireland, France, the Netherlands, Australia | Individual CBT | NA | Behavioural placebo, relaxation, drug | WLC, TAU | Short | ✓ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Amato Nesbit et al.41 2019 | Diabetic peripheral neuropathy | NA | Critically low | 1 (19) | Adults | NR | Individual CBT | NA | NA | Sham | Short | ✗ | ✗ | ✗ | ✓ |
Elliot136 2012 | Diabetes mellitus | Depression | Critically low | 2 (158) | Adults | The Netherlands, USA | Group CBT, individual CBT | NA | Education, blood glucose awareness training | NA | Short–long | ✗ | ✓ | ✗ | ✓ |
Uchendu and Blake463 2017 | Diabetes mellitus | Depression, anxiety | Low | 6 (NR) | Adults | The Netherlands, USA, Sweden | Group CBT, individual CBT | Telephone CBT | NA | TAU, NR | Long | ✓ | ✓ | ✓ | ✓ |
Reviews in this ICD-11 primary classification 06 mental, behavioural or neurodevelopmental problems are presented at the secondary level of classification.
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Goode et al.174 2018 | ADHD | NA | Critically low | 1 (119) | Children, adolescents | NR | NR | NA | NA | TAU | Short | ✗ | ≤ | ≤ | ✓ |
Jensen et al.230 2016 | ADHD | Anxiety, depression | Low | 2 (85) | Adults | NR | Manualised group CBT or individual CBT | NA | NA | TAU | Short | ≤ | ✓ | ✓ | ✓ |
Kemper et al.244 2018 | ADHD | NA | High | 1 (119) | Children, adolescents | NR | NR | NA | NA | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Lopez et al.286 2018 | ADHD | NA | High | 6 (277) | Adults | Sweden, Finland, Spain, Iceland, USA | Individual CBT | Internet-based CBT | Relaxation, education, cognitive training, drug | WLC | Short | ✓ | ✓ | ✓ | ✓ |
Vidal-Estrada et al.481 2012 | ADHD | NA | Critically low | 3 (146) | Adults | NR | Individual CBT + medication | NA | Medication | NA | Short | ✗ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Álvarez-Jiménez et al.40 2011 | Psychosis | NA | Moderate | 1 (309) | Adults | NR | Manualised individual CBT | NA | Supportive counselling therapy | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Anagnostopoulou et al.43 2018 | Psychosis | NA | Critically low | 1 (30) | Adolescents | UK | Individual CBT | NA | Family therapy | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Armando et al.51 2015 | Psychosis | NA | Critically low | 1 (309) | Adolescents, adults | NR | NR | NA | Supportive counselling + TAU | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Bighelli et al.66 2018 | Psychosis | NA | Moderate | 2 (323) | Adults | UK, Norway | Individual CBT | NA | NA | WLC | Short | ′ | ′ | ✗ | ✓ |
Bird et al.67 2010 | Early-onset psychosis | NA | Moderate | 3 (529) | Adults | NR | Group CBT, individual CBT | NA | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Buckley et al.79 2015 | Psychosis | NA | High | 5 (349) | Adults | USA, UK, Italy | Individual CBT | NA | Supportive therapy | NA | Short | ✗ | ✓ | ✗ | ✓ |
Davies et al.116 2018 | Psychosis | NA | Moderate | 6 (712) | Adolescents, adults | Canada, UK, Germany, Australia | Individual CBT (French and Morrison540 protocol) | NA | Drug | Needs-based intervention | Long | ✗ | ✗ | ✗ | ✓ |
de Koning et al.121 2009 | Attenuated psychosis syndrome | NA | Critically low | 1 (128) | Adults | Germany | Comprehensive individual CBT | NA | Supportive counselling | NA | Long | ✗ | ✗ | ✗ | ✓ |
Devoe et al.128 2018 | Attenuated psychosis syndrome | NA | Moderate | 3 (236) | Young adults | Canada, the Netherlands, Australia | Individual CBT + TAU, individual CBT + placebo | NA | Supportive therapy, supportive therapy + placebo drug | TAU + monitoring | Short | ✗ | ✗ | ✗ | ✓ |
Devoe et al.127 2019 | Psychosis | NA | Low | 6 (843) | Young adults | Canada, the Netherlands, UK, Australia, New Zealand | Individual CBT, individual CBT +TAU, individual CBT + placebo, individual CBT + monitoring | NA | Supportive therapy, supportive therapy + placebo | TAU + monitoring | Long | ✗ | ✗ | ✗ | ✓ |
Gaag et al.161 2014 | Psychosis | NA | Moderate | 9 (768) | Adults | UK, the Netherlands, Canada, Germany, Norway | Individually tailored case formulation + culturally adapted CBT | NA | Supportive counselling, social activity treatment | Attention placebo, TAU | Short | ✗ | ✗ | ✗ | ✓ |
Hutton and Taylor219 2014 | Psychosis | NA | Moderate | 3 (324) | Adults | Canada, Australia, the Netherlands | Individual CBT | NA | Supportive therapy | Monitoring | Long | ✓ | ✓ | ✓ | ✓ |
Jacobsen et al.226 2018 | Psychosis | NA | Low | 1 (90) | Adults | UK | NR | NA | NA | TAU | Long | ✗ | ′ | ′ | ✓ |
Jones et al.234 2012 | Psychosis | NA | Moderate | 5 (378) | Adults | NR | Group CBT, individual CBT | NA | Supportive psychotherapy, family intervention, supportive counselling, enhanced supportive therapy, befriending, TAU | TAU | Long | ✓ | ✓ | ✓ | ✓ |
Jones et al.235 2018 | Psychosis | NA | High | 14 (1561) | Adults | Scotland, Germany, UK, the Netherlands, Canada, USA, China | Group CBT, individual CBT | NA | Psychoeducation, family intervention, supportive psychotherapy, health education, group social skills training, supportive counselling, social activities therapy, befriending | NA | Short–long | ✓ | ✓ | ✓ | ✓ |
Jones et al.236 2018 | Psychosis | NA | High | 12 (1827) | Adults | UK, Pakistan, China | Individual CBT | NA | NA | TAU | Long | ✓ | ✓ | ✓ | ✓ |
Kennedy and Xyrichis245 2017 | Psychosis | NA | Low | 2 (105) | Adults | USA, Australia | Group CBT, TORCH541 individual CBT | NA | Supportive therapy, befriending | NA | Short | ✗ | ✗ | ✗ | ✓ |
Kluwe-Schiavon et al.254 2013 | Psychosis | NA | Critically low | 1 (40) | Adults | NR | Individual CBT | NA | Cognitive remediation therapy | TAU | Short | ≤ | ✗ | ✗ | ✓ |
Lawrence et al.269 2006 | Psychosis | NA | Critically low | 1 (88) | Adults | Australia, UK, Germany | Group CBT | NA | Psychoeducation | TAU, NR | Long | ✗ | ✓ | ✓ | ✓ |
Laws et al.270 2018 | Psychosis | NA | Critically low | 9 (626) | Adults | NR | Group CBT, individual CBT | NA | Psychoeducation, befriending, drug | WLC, TAU | Short | ✓ | ✗ | ✗ | ✓ |
Lockwood et al.283 2004 | Psychosis | Social anxiety | Critically low | 4 (825) | Adults | UK, NR | Group CBT, individual CBT | NA | Supportive counselling | WLC, TAU | Short–long | ✓ | ✓ | ✓ | ✓ |
Mehl et al.304 2015 | Delusional disorder | NA | Critically low | 5 (842) | Adults | NR | Individual CBT for psychosis | NA | Supportive therapy, social activity therapy, family intervention | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Naeem et al.323 2016 | Psychosis | NA | Critically low | 7 (1128) | Adults | NR | Individual CBT for psychosis, group CBT for psychosis, culturally adapted individual CBT for psychosis | NA | Supportive counselling, befriending | TAU | Short–long | ′ | ✓ | ′ | ✓ |
Rector and Beck380 2001 | Psychosis | NA | Critically low | 6 (341) | Adults | NR | NR | NA | Problem-solving, supportive therapy, informal support, befriending | TAU | Short | ✗ | ✓ | ✗ | ✓ |
Sarin et al.394 2011 | Psychosis | NA | Moderate | 5 (623) | Adults | NR | Group CBT, individual CBT | NA | Other psychotherapy (family intervention, supportive therapy) | TAU | Short, NR | ✗ | ✓ | ✓ | ′ |
Skelton et al.414 2015 | Delusional disorder | NA | Moderate | 1 (17) | Adults | NR | Individual CBT | NA | NA | Attention placebo | Short | ≤ | ✓ | ✓ | ✓ |
Turner et al.458 2014 | Psychosis | NA | Low | 8 (497) | NR | NR | Group CBT, individual CBT | NA | Supportive counselling | NA | Short | ✗ | ✗ | ✗ | ✓ |
van der Gaag et al.161 2014 | Psychosis | NA | Low | 9 (768) | Adults | UK, Norway, Germany, the Netherlands, Canada | Individual CBT | NA | Supportive counselling, social activity treatment | TAU, attention placebo | Short | ✗ | ✗ | ✗ | ✓ |
Velthorst et al.476 2015 | Psychosis | NA | Critically low | 2 (238) | Adults | USA, Germany | Group CBT, individual CBT | NA | Cognitive remediation | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Wood et al.503 2016 | Psychosis | NA | Low | 1 (29) | Adults | UK | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ✓ |
Zhao et al.518 2015 | Psychosis | NA | High | 1 (41) | Adults | Germany | Group CBT | NA | Group psychological programme | NA | Short | ✓ | ≤ | ≤ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Ackermann and Williams33 2002 | Premenstrual dysphoric disorder | NA | Critically low | 1 (49) | NR | NR | Individual CBT | NA | NA | Placebo | NR | ✗ | ✓ | ✗ | ✗ |
Ahern et al.36 2018 | Depressive disorder | NA | Critically low | 24 (2379) | Adults | Sweden, Australia, USA, Norway, UK, the Netherlands, Spain | NA | Internet-based CBT + therapist, internet-based CBT + administrative support | Individual CBT | WLC, TAU, attention control | Short | ✗ | ✓ | ✗ | ✗ |
Akechi et al.37 2008 | Depressive disorder | Metastatic breast cancer | High | 1 (92) | Adults | NR | Group CBT | NA | NA | TAU | NR | ≤ | ✓ | ✓ | ✗ |
Antoniades et al.48 2014 | Depressive disorder | NA | Low | 1 (63) | Adults | NR | NA | Culturally adapted internet-based CBT | NA | WLC | Short | ✗ | ✓ | ✗ | ✗ |
Apóstolo et al.49 2015 | Depressive disorder | NA | Moderate | 1 (92) | Older adults | UK | Individual CBT + TAU (modified for older people) | NA | Talking control group | TAU | Short | ✓ | ✓ | ✗ | ✗ |
Babowitch and Antshel55 2016 | Depressive disorder | Substance abuse | Critically low | 1 (40) | Adolescents | NR | Individual CBT, family CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Beltman et al.59 2010 | Depressive disorder | Cancer, HIV, MS, RA, vascular disease, COPD, renal failure | Moderate | 6 (725) | Adults | NR | Group CBT, individual CBT | NA | Other psychotherapy | WLC, TAU | Short | ✗ | ✓ | ✗ | ✗ |
Bennett et al.61 2015 | Subthreshold depression | Epilepsy, IBD | Low | 2 (71) | Children, adolescents | Serbia and Montenegro, USA | Individual CBT | NA | NA | TAU (counselling, depression information leaflet) | Short–long | ✓ | ✓ | ✗ | ✓ |
Briani et al.76 2018 | Depressive disorder | Pain (knee osteoarthritis) | Low | 1 (69) | Adults | NR | NA | Internet-based CBT | NA | TAU | Short | ≤ | ✓ | ✗ | ✗ |
Butler et al.82 2018 | Bipolar or related disorder | NA | Low | 4 (405) | Adults | UK, USA, Germany, Canada | Individual CBT, individual CBT for insomnia | NA | Psychoeducation, supportive therapy | TAU | Short–long | ✓ | ✓ | ✗ | ✓ |
Casacalenda et al.92 2002 | Depressive disorder | NA | Critically low | 1 (239) | Adults | NR | Individual CBT | NA | Imipramine (drug), interpersonal therapy | Placebo | Short | ✗ | ✓ | ✗ | ✗ |
Clevenger et al.104 2018 | Depressive disorder | NA | Critically low | 1 (40) | Children, adolescents, adults | NR | Individual CBT + SSRI | NA | SSRI | NA | Long | ✗ | ✓ | ✗ | ✗ |
Compton et al.106 2002 | Depressive disorder | NA | Critically low | 1 (57) | Children, adolescents | NR | Individual CBT | NA | Non-focused supportive intervention | NA | Long | ✗ | ✓ | ✗ | ✗ |
Cuijpers et al.113 2009 | Subthreshold depression | Subthreshold depression | Critically low | 10 (1159) | Adolescent, adults | NR | Group CBT (coping with depression) | Guided self-help CBT (coping with depression) | Internet-based CBT | WLC, TAU | Short | ✗ | ✓ | ✗ | ✗ |
Cuijpers et al.112 2013 | Depressive disorder | NA | Low | 9 (506) | Adults | USA, UK, Romania | Acute phase individual CBT + 3 or 4 booster (Beck542 protocol) | NA | Drug | NA | Short–long | ✗ | ✓ | ✗ | ✗ |
Cuijpers et al.111 2017 | Depressive disorder | Diabetes | Low | 3 (200) | Adults | NR | Individual CBT | NA | Cognitive therapy, behavioural activation | NA | NR | ✗ | ✓ | ✗ | ✗ |
Das et al.114 2019 | Depressive disorder | Heart failure | Critically low | 1 (60) | Adults | USA | NR | NA | Exercise | TAU | Short | ✗ | ✓ | ✗ | ✗ |
de Mello et al.145 2005 | Depressive disorder | NA | Critically low | 3 (204) | Adults | NR | Individual CBT | NA | Interpersonal therapy | NA | Short | ✗ | ✓ | ✗ | ✗ |
Dekker123 2008 | Depressive disorder | Stroke, diabetes (type 2) | Critically low | 2 (174) | NR | NR | Individual tailored CBT | NA | Diabetes education | Attention placebo, no intervention | Short | ✗ | ✓ | ✗ | ✗ |
Demissie et al.124 2018 | Bipolar or related disorder | NA | Low | 2 (91) | Adults | Brazil | Group CBT | NA | NA | TAU | Short–long | ✓ | ✓ | ✓ | ✓ |
Ebrahim et al.132 2012 | Depressive disorder | NA | Low | 8 (1400) | Adults | USA, Canada, Pakistan, Iran, the Netherlands | Mostly individualised face-to-face CBT | Internet-based CBT, CBT (delivered by female health workers) | Drug | No intervention, TAU | NR | ✗ | ✓ | ✗ | ✗ |
Escobar and Gorey138 2018 | Depressive disorder | NA | Low | 5 (485) | Adults | USA | Group CBT, individual CBT | Telephone CBT | NA | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Fernie et al.146 2015 | Depressive disorder | Epilepsy | Low | 1 (59) | Adults | NR | Individual CBT | NA | NA | WLC | NR | ✗ | ✓ | ✗ | ✗ |
Forman-Hoffman et al.153 2016 | Depressive disorder | NA | Low | 1 (123) | Children, adolescents | USA, NR | Individual CBT | NA | Drug, CBT + drug | Placebo | Short | ✓ | ✓ | ✗ | ✗ |
Franco et al.156 2018 | Depressive disorder | Diabetes | Critically low | 2 (345) | Adults | NR | NA | Internet-based CBT | NA | WLC, TAU | Short | ✓ | ′ | ✓ | ✓ |
Gertler et al.165 2015 | Depressive disorder | Brain injury | High | 2 (177) | Adults | USA | Individual CBT | NA | Supportive psychotherapy | WLC | Short | ✓ | ✓ | ✗ | ✗ |
Griffiths et al.180 2010 | Depressive disorder | NA | Low | 5 (2166) | Adults | USA | NA | Internet-based CBT | NA | WLC, attention control, passive control | Short–long | ✗ | ✓ | ≤ | ✗ |
Guidi et al.184 2016 | Depressive disorder | NA | Moderate | 1 (40) | Adults | NR | Individual CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Haibach et al.186 2014 | Depressive disorder | Substance abuse | Critically low | 1 (66) | Adults | USA | Integrated individual CBT | NA | 12-step facilitation | NA | Long | ✗ | ✓ | ✗ | ✓ |
Hall and Skelton190 2012 | Depressive disorder | Caregivers (dementia) | Critically low | 1 (42) | Adults | UK | CBT family intervention for caregivers | NA | NR | NR | Short | ✗ | ✓ | ✗ | ✗ |
Hamers et al.191 2018 | Depressive disorder | Intellectual disabilities | Low | 1 (32) | Adults | NR | Manualised individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Hart et al.196 2012 | Depressive disorder | Cancer (mixed) | Low | 1 (78) | Adults | USA | NA | Group CBT (delivered by social worker) | Crisis consultation and individual therapy | NA | Short | ✗ | ✓ | ✗ | ✗ |
van Hees et al.202 2013 | Depressive disorder | NA | Low | 3 (333) | Adults | NR | Individual CBT | NA | Interpersonal therapy | NA | Short | ✗ | ✓ | ✗ | ✗ |
Hennemann et al.204 2018 | Depressive disorder | NA | Low | 1 (84) | Adults | Sweden | NA | Internet-based CBT | NA | TAU | Long | ✓ | ✓ | ✓ | ✗ |
Hetrick et al.205 2016 | Depressive disorder | NA | Moderate | 4 (1600) | Children, adolescents | Australia, New Zealand, USA | Manualised group CBT | Telephone CBT | NA | No intervention, TAU, attention placebo | Long | ✗ | ✓ | ✓ | ✗ |
Hetrick et al.206 2011 | Depressive disorder | NA | Moderate | 2 (536) | Children, adolescents | UK, NR | Individual CBT + SSRI | NA | SSRI | NA | Short | ✗ | ✓ | ✗ | ✗ |
Hides et al.207 2010 | Depressive disorder | Substance abuse | Critically low | 1 (66) | Adults | NR | NA | Group CBT | Group 12-step facilitation | NA | Short | ✗ | ✓ | ✗ | ✓ |
Hundt et al.217 2014 | Depressive disorder | Substance use disorder | Critically low | 3 (357) | Older adults | NR | Group CBT | Telephone CBT | 12-step facilitation | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Huntley et al.218 2012 | Depressive disorder | NA | Moderate | 3 (113) | Adults | UK | Group CBT + usual care | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Ijaz et al.220 2018 | Treatment resistant depressive disorder | Treatment resistant | Moderate | 1 (242) | Adults | UK | Individual CBT | NA | NA | TAU | Long | ✓ | ✓ | ✗ | ✗ |
Jackson et al.224 2015 | Depressive disorder | Epilepsy | Moderate | 1 (30) | Adolescents | Serbia | Individual CBT | NA | NA | TAU | Short | ✓ | ✓ | ≤ | ✗ |
Jeyanantham et al.231 2017 | Depressive disorder | Heart failure | Moderate | 5 (204) | Adults | USA | Face-to-face individual CBT ± telephone sessions (delivered by a therapist) | Face-to-face individual CBT (delivered by nurse) + telephone sessions | Exercise, CBT + exercise | TAU | Short | ✓ | ✓ | ✗ | ✓ |
Jiang et al.232 2018 | Depressive disorder | Heart failure | Low | 5 (383) | Adults | Philippines, USA | Face-to-face group CBT and individual CBT (delivered by a therapist) ± telephone call | Face-to-face CBT (delivered by nurse) ± telephone call | NR | NR | Short | ✓ | ✓ | ′ | ✓ |
Karyotaki et al.240 2017 | Depressive disorder | NA | Moderate | 13 (3876) | Adults | Switzerland, Australia, the Netherlands, UK, Germany, Spain | NA | Self-guided internet-based CBT | NA | TAU, WLC, attention placebo, no intervention | Short | ✗ | ✓ | ✗ | ✗ |
Kavanagh et al.241 2009 | Depressive disorder | NA | Critically low | 2 (1153) | Adolescents | USA, Australia | Coping with depression | Coping with depression (delivered by teachers) | NA | No intervention | Short | ✗ | ′ | ✓ | ✗ |
Kiosses et al.250 2011 | Depressive disorder | NA | Critically low | 1 (100) | Older adults | NR | NR | NA | Drug | NA | NR | ≤ | ✓ | ≤ | ≤ |
Klein et al.253 2007 | Depressive disorder | NA | Critically low | 1 (88) | Adolescents | NR | Group CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Krishna et al.261 2015 | Depressive disorder | NA | Moderate | 1 (96) | Adults | The Netherlands | Group CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Lane et al.264 2013 | Depressive disorder | Congenital heart disease | Moderate | 0 (0) | Adolescents, adults | NR | NA | NA | NA | NA | NA | ≤ | ≤ | ✗ | ≤ |
Li et al.277 2017 | Depressive disorder | Diabetes | Low | 3 (336) | Adults | NR | Group CBT/individual CBT (diabetes specific and generic) | NA | Diabetes education | TAU, WLC | Short | ′ | ✓ | ✓ | ′ |
Li et al.278 2018 | Depressive disorder | NA | Low | 2 (468) | Adults | UK, Japan | Individual CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Linde et al.280 2015 | Depressive disorder | NA | Moderate | 7 (1273) | Adults | NR | Individual CBT | Telephone CBT, internet-based CBT | Drug, counselling | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Luckett et al.288 2011 | Depressive disorder | Cancer (head and neck) | Moderate | 1 (184) | Adults | USA | NA | Individual CBT (delivered by nurse) | NA | TAU | Short | ≤ | ✓ | ≤ | ✗ |
Ma et al.289 2014 | Depressive disorder | NA | Low | 1 (208) | Children, adolescents | UK | Individual CBT | NA | Fluoxetine (drug) | NA | Short | ✗ | ✓ | ✗ | ✗ |
Markowitz et al.296 2011 | Depressive disorder | Diabetes | Critically low | 1 (51) | Adults | NR | Individual CBT | NA | Education | NA | Short | ✗ | ✓ | ✗ | ✓ |
Mewton and Andrews308 2016 | Depressive disorder | Including suicide ideation | Critically low | 2 (208) | Adults | NR | NR | Internet-based CBT | High-intensity CBT, interperson therapy, drug + clinical management | Placebo + clinical management | Short | ✗ | ✓ | ✗ | ✗ |
Michaelis et al.309 2018 | Depressive disorder | Epilepsy | Critically low | 1 (NR) | Children | NR | Individual CBT | NR | NR | NR | Short | ≤ | ✓ | ≤ | ≤ |
Moore et al.318 2017 | Depressive disorder | NA | Low | 5 (631) | Adults | Taiwan, England, Australia, Hong Kong, Sweden | Group CBT | NA | Guided internet-based CBT | WLC, TAU | Short–long | ✓ | ✓ | ✗ | ✗ |
Napa et al.325 2017 | Depressive disorder | Caregivers (psychosis) | Critically low | 1 (21) | Adults | NR | Family CBT relapse prevention | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Noh334 2018 | Depressive disorder | Homeless youth | Critically low | 1 (27) | Adolescents, young adults | Republic of Korea | Group CBT | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Opoka and Lincoln344 2017 | Depressive disorder | Psychosis | Critically low | 1 (30) | Adults | NR | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ′ | ✓ |
Orgeta et al.347 2014 | Depressive disorder | Dementia | Moderate | 2 (82) | Older adults | UK, USA | Individual CBT | NA | NA | TAU | Short | ✓ | ′ | ✓ | ✓ |
Osugo and Cooper350 2016 | Depressive disorder | Intellectual disabilities | Critically low | 1 (32) | Adults | NR | Individual CBT | NA | NA | TAU | Short | ′ | ′ | ✓ | ✗ |
Oud et al.352 2019 | Subthreshold depression | Subclinical depression or clinical depressive disorder | Low | 4 (976) | Children, adolescents | USA, the Netherlands | Group CBT, individual CBT | Mixed CBT (group CBT/bibliotherapy CBT/online CBT) | NA | Placebo, online monitoring | Short | ✓ | ✓ | ✗ | ✗ |
Pfeiffer et al.365 2011 | Depressive disorder | NA | Low | 7 (488) | Adults | NR | Group CBT | NA | Peer support interventions | NA | Short | ✗ | ✓ | ✗ | ✗ |
Riper et al.383 2013 | Depressive disorder | Alcohol misuse | Low | 1 (164) | Adults | USA | Individual CBT for depression + TAU | NA | NA | TAU + placebo | Short | ✗ | ✓ | ✓ | ✓ |
Robinson et al.386 2011 | Depressive disorder | Including suicide ideation | Low | 1 (90) | Adolescents, young adults | NR | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✓ |
Sharp et al.405 2013 | Depressive disorder | Diabetes | Moderate | 1 (167) | Adults | The Netherlands | NA | Computerised CBT (adapted from coping with depression) | NA | WLC | Short | ≤ | ✓ | ✓ | ✓ |
Shi et al.407 2018 | Depressive disorder | HIV | Low | 4 (319) | NR | USA | Individual CBT | NA | Education on HIV medication adherence | TAU | Short–long | ✗ | ✓ | ✓ | ✓ |
So et al.420 2013 | Depressive disorder | NA | Moderate | 5 (976) | Adults | Sweden, the Netherlands, Germany | NA | Internet-based CBT (unguided, guided) | NA | WLC, TAU | Short | ′ | ✓ | ✗ | ✗ |
Soares-Weiser et al.421 2007 | Bipolar or related disorder | NA | Moderate | 1 (253) | Adults | UK | Individual CBT | NA | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Ssegonja et al.427 2019 | Subthreshold depression | Subsyndromal | Low | 7 (3931) | Children, adolescents | Australia, USA, UK, the Netherlands | Group CBT (‘Friends’, ‘PRP’, ‘the resourceful adolescent’, ‘Friends for life’) | Group CBT (delivered by health-care professionals, teachers and psychologists) | Bibliotherapy, supportive expressive therapy | TAU, WLC, brochure, attention control | Long | ✗ | ✓ | ✗ | ✗ |
Starkstein and Brockman428 2017 | Depressive disorder | Parkinson’s disease | Critically low | 1 (80) | Adults | NR | Individual CBT | NA | NA | Clinical monitoring | Short | ✗ | ✓ | ✗ | ✗ |
Taylor and Montgomery444 2007 | Depressive disorder | NA | Low | 1 (30) | Adolescents | NR | Group CBT | NA | Relaxation | WLC | Short | ✗ | ✓ | ✗ | ✗ |
Thomas et al.448 2006 | Depressive disorder | MS | Moderate | 3 (106) | Adults | NR | Group CBT, individual CBT | Telephone CBT | Drug | TAU, WLC | Short | ≤ | ✓ | ✗ | ✓ |
Townsend et al.454 2010 | Depressive disorder | NA | Moderate | 1 (93) | Children, adolescents | USA | Group adolescent coping with depression | NA | Life skills tutoring | NA | Long | ✗ | ✓ | ≤ | ✗ |
Twomey et al.462 2017 (Deprexis) | Depressive disorder | NA | Moderate | 8 (2402) | Adults | USA, Germany, Switzerland | NA | Computerised CBT (Deprexis) | NA | WLC, TAU | Short | ✗ | ✓ | ′ | ✗ |
Vandepitte et al.472 2016 | Anxiety and depression | Caregivers (dementia) | Low | 2 (292) | Adults | Spain | Group CBT | NA | NA | TAU | Short | ✓ | ✓ | ✗ | ✗ |
Venning et al.477 2009 | Depressive disorder | NA | Critically low | 5 (2195) | Children, adolescents | USA, New Zealand, Australia | Group CBT [‘PEP’, ‘PRP’, ‘Problem-solving for Life’, ‘RAP-kiwi’, ‘the resourceful adolescent’) | NA | NA | TAU, NR | Long | ✗ | ✓ | ✓ | ✗ |
Wang et al.485 2008 | Depressive disorder | Diabetes | Critically low | 1 (42) | Adults | NR | Individual CBT | NA | Diabetes self-management education | NA | Short | ✗ | ✓ | ✗ | ✓ |
Wang et al.488 2017 | Depressive disorder | Diabetes | Low | 2 (368) | Adults | The Netherlands, Germany | NR | NA | Diabetes education | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Wang et al.486 2018 | Depressive disorder | Post stroke | Critically low | 22 (1911) | Adults | UK, China | Individual CBT ± drug | NA | Drug | Placebo, placebo or drug, attention control, TAU | Short | ✗ | ✓ | ′ | ✗ |
Ward489 2007 | Depressive disorder | Racial and ethnic minority women | Critically low | 1 (267) | Adults | USA | NR | NA | Drug | TAU | Short | ✓ | ✓ | ✗ | ✗ |
Wilson et al.501 2008 | Depressive disorder | NA | Moderate | 2 (148) | Older adults | USA | Individual CBT | NA | Focused visual imagery, education, psychodynamic therapy | NA | Short | ✓ | ✓ | ✗ | ✗ |
Woltz et al.502 2012 | Depressive disorder | Heart failure | Critically low | 1 (74) | Adults | USA | Individual CBT | NA | Walking programme | Attention control | Short | ✗ | ✓ | ✗ | ✗ |
Xiao et al.506 2017 | Depressive disorder | Cancer (breast) | Low | 1 (60) | Adults | USA | Individual CBT | NA | NA | No intervention | Short | ✗ | ✓ | ✗ | ✗ |
Xie et al.507 2015 | Depressive disorder | Parkinson’s disease | Moderate | 6 (381) | Adults | UK, USA, China | Individual CBT + drug/monitoring, mixed individual CBT + telephone sessions | Bibliotherapy (self-help) | Drug, telephone support | Monitoring, no intervention | Short | ✗ | ✓ | ✗ | ✓ |
Yang et al.510 2017 | Depressive disorder | NA | Low | 3 (93) | Children | NR | Group CBT | NA | NA | WLC, no intervention, placebo | Short | ✗ | ✓ | ✗ | ✗ |
Ye et al.512 2016 | Bipolar or related disorder | NA | Low | 1 (76) | Adults | USA, Germany | Individual CBT | NA | Education, support therapy | NA | Short | ✗ | ✓ | ✗ | ✓ |
Zhang et al.517 2018 | Depressive disorder | NA | Critically low | 3 (164) | Adults | NR | Individual CBT | Internet-based CBT | NA | Placebo | Long | ✗ | ✓ | ✗ | ✗ |
Zhou et al.520 2014 | Depressive disorder | NA | Low | 1 (334) | Adolescents | NR | Individual CBT + drug | NA | Drug | NA | Short | ✗ | ✓ | ✗ | ✗ |
Zhou et al.519 2016 | Depressive disorder | NA | Low | 3 (1066) | Adults | NR | NA | Internet-based CBT | NA | Attention control, WLC | Short–long | ✓ | ✓ | ✓ | ✗ |
The reviews in Table 11 are labelled using the tertiary-level ICD-11 labels:
-
6B00 Generalised anxiety disorder
-
6B01 Panic disorder
-
6B02 Agoraphobia
-
6B03 Specific phobia
-
6B04 Social anxiety disorder
-
6B05 Separation anxiety disorder
-
6B06 Selective mutism.
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Adelman et al.34 2014 | GAD, SAD, panic, phobia | NA | Low | 34 (2029) | Children, adults | NR | NA | Computerised CBT | High-intensity CBT | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Baardseth et al.54 2013 | Anxiety | NA | Critically low | 2 (123) | Adults | NR | NR | NA | Short-term dynamic psychotherapy, emotion-focused therapy | NR | NA | ✗ | ✗ | ✓ | ✓ |
Bandelow et al.57 2007 | GAD, SAD, panic | NA | Critically low | 13 (NR) | NR | NR | NR | NA | Drug | NA | Short | ✗ | ✗ | ✓ | ✗ |
Caldirola et al.84 2018 | Panic | NA | Critically low | 1 (150) | Adults | The Netherlands | Individual CBT, individual CBT + SSRI | NA | SSRI | NA | Long | ✗ | ✗ | ✓ | ✗ |
Carpenter et al.89 2018 | GAD, panic | NA | Moderate | 1 (43) | Adults | NR | Individual CBT | NA | NA | Placebo (non-directive) | Short | ✗ | ✗ | ✓ | ✗ |
Cartwright-Hatton et al.90 2004 | Anxiety | NA | Critically low | 10 (636) | Children, adolescents | USA, Australia | Group CBT, individual CBT | NA | NA | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Clond105 2016 | Anxiety | NA | Critically low | 1 (42) | Children, adolescents | USA | A brief form of individual CBT based on ‘Coping Cat’ and the C.A.T. Project543 | NA | EFT | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Davis et al.118 2015 | GAD, phobia, separation | NA | Critically low | 1 (51) | Children, adolescents | NR | Group CBT | NA | NA | WLC | Long | ✗ | ′ | ✓ | ✗ |
de Souza Moura et al.122 2015 | Panic | NA | Critically low | 1 (36) | Adults | NR | Individual CBT | NA | Physical exercise | NA | Long | ✗ | ✗ | ✓ | ✗ |
Ewing et al.139 2015 | Anxiety | NA | Moderate | 20 (2099) | Children | NR | Trans-diagnostic individual CBT or group CBT | NA | NA | WLC | NC | ✗ | ✗ | ✓ | ✗ |
Farrer et al.144 2013 | SAD, exam anxiety | NA | Low | 3 (300) | Adults | Australia, Spain, UK | NA | Internet-based CBT | Education | WLC | Short | ✗ | ′ | ✓ | ✗ |
Foa et al.151 2002 | GAD, panic | NA | Critically low | 2 (425) | Adults | NR | Individual CBT | NA | Drug | Placebo | Short | ✗ | ✗ | ✓ | ✗ |
Hall et al.189 2016 | GAD | NA | Moderate | 5 (242) | Older adults | NR | Group CBT, individual CBT | NA | Information only, enhanced usual care, supportive psychotherapy, drug, acceptance and commitment therapy | NA | Short | ✗ | ✗ | ✓ | ✓ |
Hendriks et al.203 2008 | GAD, panic, SAD, agoraphobia | NA | Low | 7 (396) | Older adults | NR | Group CBT, individual CBT | NA | Supportive psychotherapy | WLC, TAU, discussion group | Short | ✗ | ✓ | ✓ | ✗ |
James et al.227 2015 | Anxiety | NA | Moderate | 10 (707) | Children, adolescents | NR | Group CBT, school-based group CBT, clinic-based group CBT, modular CBT, individual CBT, ‘Facing your Fears’ programme, manualised group CBT | NA | Group CBT with parental advice, group support and attention, family-based CBT, family-based education support, social recreation programme, CBT without cognitive restructuring (IAFS) | TAU, WLC | Long | ✗ | ✗ | ✓ | ✗ |
Jayakody et al.228 2014 | Anxiety | NA | Low | 0 (0) | Adults | NR | NA | NA | NA | NA | NA | ≤ | ✗ | ≤ | ✗ |
Kishita and Laidlaw252 2017 | GAD | NA | Critically low | 7 (323) | Older adults | NR | Group CBT, individual CBT | NA | Supportive therapy, telephone calls, discussion groups | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Kreslins et al.259 2015 | Anxiety | Autistic spectrum disorder | Moderate | 7 (283) | Children, adolescents | NR | Group CBT, individual CBT, mixed individual CBT + group CBT | NA | NA | WLC, TAU | Short | ✗ | ✗ | ✓ | ✗ |
Kreuze et al.260 2018 | Mixed anxiety, SAD | NA | Low | 13 (1073) | Children, adolescents | USA, Australia, Germany, UK | Group CBT, individual CBT | Audio CBT, partially guided CBT, computerised CBT | ‘Test-busters’, computer-assisted education support and attention, education support | WLC, TAU, placebo | Short | ✗ | ′ | ′ | ✓ |
Kumar and Malone262 2008 | Panic | Alcohol dependence | Critically low | 2 (122) | Adults | NR | Group CBT, individual CBT | NA | Exposure, alcohol treatment programme, internet self-help | NA | Long | ≤ | ✓ | ✓ | ✓ |
Markowitz et al.295 2014 | Panic | NA | Critically low | 1 (91) | Adults | The Netherlands | Individual CBT | NA | Interpersonal therapy | NA | Short | ✗ | ✗ | ✓ | ✓ |
Michail et al.310 2017 | SAD | Psychosis | Moderate | 1 (16) | Adults | Australia | Group CBT | NA | NA | WLC | Short | ✓ | ✓ | ✓ | ✓ |
Oldham-Cooper and Loades342 2017 | Anxiety | NA | Low | 4 (257) | Children, adolescents | Australia, USA | Manualised individual CBT ‘Coping Cat’ | NA | NA | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Opriş et al.346 2012 | Phobia (flying) | NA | Critically low | 1 (45) | Adults | NR | NR | NA | Behavioural therapy + virtual reality exposure | NA | Short | ✗ | ✗ | ✓ | ✓ |
Østergaard349 2018 | Selective mutism | NA | Critically low | 1 (21) | Children | NR | Individual CBT (integrated behaviour therapy for selective mutism) | NA | NA | WLC | Short–long | ✗ | ✗ | ✓ | ′ |
Pateraki and Morris358 2018 | Anxiety | Asthma | Moderate | 1 (94) | Children, adolescents, adults | UK | Individual CBT | NA | NA | TAU | Short | ✗ | ✗ | ✓ | ✗ |
Perna and Caldirola361 2017 | Panic (treatment resistant) | NA | Critically low | 1 (58) | Adults | NR | Individual CBT | NA | SSRI | NA | Short | ✗ | ✗ | ✓ | ✓ |
Perna et al.362 2011 | Agoraphobia with panic | NA | Critically low | 1 (49) | Older adults | NR | NR | NA | Drugs | WLC | Short | ✗ | ✗ | ✓ | ✓ |
Podina et al.368 2016 | Anxiety | NA | Critically low | 8 (404) | Children, adolescents | NR | NA | Internet-based CBT | High-intensity CBT | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Pompoli et al.370 2016 | Panic with or without agoraphobia | NA | Moderate | 18 (1090) | Adults | NR | Group CBT, individual CBT | NA | NA | WLC | Short | ✗ | ✗ | ✓ | ✓ |
Provencher et al.372 2011 | Anxiety | Bipolar | Critically low | 1 (108) | NR | NR | Individual CBT for PTSD | NA | NA | TAU | Short | ✗ | ≤ | ✓ | ✓ |
Reinholt and Krogh381 2014 | Anxiety | NA | Critically low | 5 (1240) | Adults | NR | Trans-diagnostic group CBT and individual CBT | NA | NA | TAU, WLC | Short | ✗ | ✗ | ✓ | ✗ |
Schade et al.395 2003 | Anxiety | Substance abuse (alcohol) | Critically low | 2 (206) | Adults | NR | Group CBT, individual CBT | NA | Substance abuse treatment | NA | Short | ✗ | ✗ | ✓ | ✓ |
Schwartze et al.398 2017 | Panic | NA | Low | 1 (12) | Adults | NR | Group CBT | NA | Drug | NA | Short | ✗ | ′ | ✓ | ✓ |
Singh and Gorey411 2018 | SAD | NA | Critically low | 1 (26) | Adults | NR | Individual CBT | NA | Mindfulness-based cognitive therapy | NA | Short | ✗ | ✗ | ✓ | ✗ |
Singh and Servern410 2018 | Anxiety | NA | Critically low | 3 (326) | Adults, older adults | Romania, Sweden, Switzerland, Austria, Germany | NA | Internet-based CBT guided group, unguided and guided individual CBT | NA | WLC | Short | ✓ | ✓ | ✓ | ✗ |
Stoll et al.433 2017 | Anxiety | Chronic fatigue syndrome/ myalgic encephalomyelitis | Low | 1 (112) | Children, adolescents | The Netherlands | NA | Internet-based CBT | NA | TAU | Short–long | ✗ | ✗ | ✓ | ✓ |
Stratford et al.434 2015 | Anxiety | Bipolar | Critically low | 2 (149) | Adults | USA, Brazil | Group CBT and individual CBT for borderline personality disorder and PTSD | NA | NA | TAU | Short | ✗ | ✗ | ✓ | ✗ |
Sukhodolsky et al.435 2013 | Anxiety | Autism | Moderate | 5 (224) | Children, adolescents | NR | Group CBT, individual CBT | NA | Social recreation | WLC, TAU | Short | ✗ | ✗ | ✓ | ✗ |
Torous et al.453 2017 | SAD | NA | Critically low | 1 (52) | Adults | NR | NA | CBT app | Interpersonal therapy app | NA | Short | ✗ | ≤ | ✓ | ✗ |
Usmani et al.464 2017 | Anxiety | COPD | High | 1 (238) | Adults | USA | Group CBT | NA | Education | NA | Long | ✓ | ✗ | ✓ | ✓ |
Verberne et al.478 2018 | Anxiety | Acquired brain injury | Low | 1 (12) | Adults | NR | Individual CBT | NA | NA | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Waddell et al.482 2007 | Anxiety | NA | Critically low | 1 (594) | Children, adolescents | Australia | NA | ‘Friends’ child group CBT (delivered by teachers) | NR | NR | Long | ✗ | ✓ | ✓ | ✗ |
Wang et al.487 2017 | Anxiety | NA | Low | 20 (1811) | Children, adolescents | Australia, USA, Spain, Mexico, Ireland | Group CBT, individual CBT, mixed group CBT + individual CBT | NA | Education, non-specific counselling | Placebo, no intervention, TAU, group attention support | Short | ✗ | ✗ | ✓ | ✗ |
Warwick et al.490 2017 | Anxiety | Autistic spectrum disorders | Critically low | 19 (1085) | Children, adolescents | NR | Group CBT, individual CBT | NA | NR | WLC | Short | ✗ | ✗ | ✓ | ✗ |
Wersebe et al.497 2013 | SAD | NA | Low | 8 (403) | Adults | USA, China, Europe, Australia, NR | Group CBT, intensive group CBT | NA | NA | Placebo, WLC, TAU | Short | ✗ | ✗ | ✓ | ✓ |
Wide Boman et al.499 2013 | Phobia (dental) | NA | Low | 1 (41) | Adults | USA | NR | NA | Behavioural therapy | WLC, positive dental experience | Long | ≤ | ✗ | ✓ | ✗ |
Yang et al.509 2018 | SAD | NA | Moderate | 14 (1000) | Children, adolescents | NR | Group CBT, individual CBT | Internet-based CBT | Not used in analysis | WLC, placebo, no intervention | Short | ′ | ′ | ✓ | ✗ |
Zhou et al.521 2018 | GAD, SAD, panic, separation, selective mutism | NA | Low | 78 (5035) | Children, adolescents | USA, Australia, Spain, UK, Iran, Norway, the Netherlands, China, Denmark, Canada, Switzerland, Germany, Sweden, Turkey | Group CBT ± parental involvement, individual CBT ± parental involvement, parent CBT, mixed individual CBT + group CBT | Internet-based CBT, bibliotherapy CBT | Bibliotherapy CBT, group behavioural therapy, individual behavioural therapy + parental involvement | No intervention, WLC, TAU, placebo | Short | ✓ | ✗ | ✓ | ✗ |
Zhu et al.522 2014 | GAD | NA | Moderate | 4 (199) | Adults | NR | Group CBT, individual CBT | NA | Non-directive therapy, minimal contact control, supportive psychotherapy, discussion groups | NA | NR | ✗ | ✗ | ✓ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Dèttore et al.126 2015 | OCD | NA | Moderate | 5 (420) | Children, adolescents, adults | Sweden, UK, USA, Australia, UK and USA mixed | NA | Internet-based CBT, behavioural therapy steps, web-camera family-based CBT | Online non-directive therapy, progressive relaxation, bibliotherapy | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Funderburk et al.159 2018 | Hypochondriasis | NA | Critically low | 2 (104) | Adults | NR | Individual CBT, enhanced individual CBT, individual CBT + physiotherapy | NA | Physiotherapy/exercise | WLC | Short | ✗ | ✗ | ✓ | ✓ |
Grist and Cavanagh181 2013 | OCD | NA | Moderate | 1 (204) | Adults | NR | NA | Computerised CBT | E-mail therapy | NA | Short | ✗ | ′ | ✓ | ✓ |
Harrison et al.195 2016 | Body dysmorphic disorder | NA | Moderate | 5 (225) | Children, adolescents, adults | NR | Individual CBT | Internet-based CBT | Anxiety management, psychoeducation + telephone calls, supportive therapy | WLC | Short | ✗ | ✓ | ✗ | ✗ |
Ipser et al.221 2009 | Body dysmorphic disorder | NA | High | 2 (73) | Adults | NR | Individual CBT | NA | NA | WLC, no intervention | Short | ≤ | ✓ | ✓ | ✓ |
Julien et al.237 2016 | OCD | NA | Critically low | 2 (134) | NR | NR | Individual CBT | NA | Inference-based therapy, exposure and response prevention therapy | NA | Short | ✓ | ′ | ✓ | ✓ |
O’Kearney et al.340 2006 | OCD | NA | Moderate | 6 (351) | Children, adolescents | Australia, USA, Brazil, the Netherlands, UK | Individual CBT, group CBT, family CBT | NA | Medication | Placebo, WLC, NR | Short | ≤ | ✓ | ✓ | ✓ |
Petricone-Westwood et al.364 2018 | Hypochondriasis | Diabetes, cardiac, cancer | Critically low | 3 (NR) | Adults | NR | NR | Internet-based CBT | Motivational enhancement therapy | Online discussion, NR | Short | ✗ | ✗ | ✓ | ✗ |
Schwartze et al.397 2016 | OCD | NA | Moderate | 3 (253) | Adults | NR | Group CBT | NA | Drug | NA | Short–long | ✗ | ✓ | ✓ | ✓ |
Skapinakis et al.412 2016 | OCD | Depression | Moderate | 9 (231) | Adults | NR | Individual CBT | NA | Drug | WLC, placebo | Short | ✗ | ✗ | ✓ | ✓ |
Stock and Andrews431 2004 | OCD | NA | Critically low | 1 (112) | Children, adolescents | NR | Individual CBT | NA | Drug | Placebo | Short | ✗ | ✗ | ✓ | ✓ |
Thomson and Page450 2007 | Hypochondriasis | NA | Moderate | 3 (294) | Adults | UK, the Netherlands, USA | Individual CBT | NA | NA | WLC, TAU, placebo | Short–long | ✗ | ✓ | ✓ | ✓ |
Watson and Rees492 2008 | OCD | Paediatric OCD | Critically low | 4 (189) | Children, adolescents | UK, Australia, USA | Individual CBT, group CBT, mixed individual CBT + group CBT | NA | NA | WLC, placebo | Short | ✗ | ✗ | ✓ | ✓ |
Weston et al.498 2016 | OCD | Autism spectrum disorder | Low | 1 (46) | Adolescents, adults | UK | Individual CBT | NA | Anxiety management | NA | Short | ✗ | ′ | ✓ | ✓ |
Williams et al.500 2006 | Body dysmorphic disorder | NA | Critically low | 1 (19) | Adults | NR | Individual CBT | NA | NA | WLC | Short | ✗ | ✓ | ✗ | ′ |
Wootton504 2016 | OCD | NA | Critically low | 6 (462) | Children, adolescents, adults | Sweden, UK, USA, Norway, Australia, multiple countries | NA | Remote CBT (internet-based CBT, computerised CBT, video conferencing CBT, bibliotherapy CBT, telephone CBT) | Face-to-face CBT, relaxation | WLC, attention control | Short–long | ✗ | ✗ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Arends et al.50 2012 | Adjustment disorder | NA | Moderate | 2 (204) | Adults | Netherlands | Group CBT, individual CBT | NA | NA | TAU, no intervention | Long | ≤ | ✓ | ✗ | ✗ |
Bisson69 2010 | PTSD | Physical injury | Critically low | 3 (358) | Adults | NR | Individual CBT | NA | Person-centred therapy | TAU, no intervention | Short–long | ✗ | ✓ | ✓ | ✓ |
Blainey70 2012 | PTSD | Birth trauma | Critically low | 1 (56) | Adults | NR | Individual CBT | NA | NA | TAU | NR | ✗ | ✗ | ✓ | ✓ |
Brooks et al.77 2018 | PTSD | NA | Critically low | 1 (21) | Adults | USA | Individual CBT (modified for disaster workers) | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✓ |
Cary and McMillen91 2012 | PTSD | NA | Critically low | 3 (333) | Children, adolescents | NR | Trauma-focused individual CBT | NA | NA | WLC, standard community care, non-directive supportive care | Long | ✗ | ✓ | ✓ | ✓ |
Chen et al.96 2018 | PTSD | Sexual abuse | Low | 1 (14) | Children | Syria | Individual CBT | NA | EMDR | NA | Short | ✗ | ≤ | ≤ | ✓ |
Ehring et al.135 2014 | PTSD | NA | Low | 1 (74) | Adults | NR | Trauma-focused individual CBT | NA | Present-centred therapy | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Field and Cottrell147 2011 | PTSD | Sexual abuse | Critically low | 1 (14) | Children | Iran | Individual CBT | NA | EMDR | NA | Short | ✗ | ✗ | ✓ | ✓ |
Forman-Hoffman et al.154 2018 | PTSD | Combat assault | Low | 9 (809) | Adults | NR | Individual CBT ‘Seeking safety’ | NA | Exposure therapy, imaginal exposure, relaxation | WLC,TAU | Short | ′ | ✓ | ✓ | ✗ |
Forneris et al.155 2013 | PTSD | Motor vehicle, industrial, non-sexual assault | Low | 3 (105) | Adults | Australia | Brief individual CBT | NA | Supportive counselling | NA | Short | ✗ | ✓ | ✓ | ✓ |
Furuta et al.160 2018 | PTSD | Traumatic birth | Low | 2 (161) | Adults | Sweden, USA | Trauma-focused individual CBT | Internet-based CBT + TAU | NA | WLC + TAU, attention control + TAU | Short | ✗ | ✗ | ✓ | ✓ |
Gillies et al.169 2016 | PTSD | Exposed to traumatic events | Moderate | 5 (319) | Children, adolescents | USA, Netherlands, Iran | Trauma-focused individual CBT | NA | Play therapy, EMDR | TAU | Short | ≤ | ✓ | ✓ | ✓ |
Guest et al.183 2016 | PTSD | Post vehicle accident | Low | 2 (95) | Adults | China, Germany | Individual CBT | NA | Self-help book CBT | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Ho and Lee212 2012 | PTSD | NA | Critically low | 8 (227) | Adults | NR | Trauma-focused individual CBT | NA | EMDR | NA | Short | ✗ | ✓ | ✓ | ✓ |
Khan et al.247 2018 | PTSD | Traumatic events | Critically low | 1 (23) | Adults | NR | NR | NA | EMDR | NA | Short | ✗ | ✓ | ′ | ′ |
Kim et al.249 2013 | PTSD | NA | Moderate | 1 (55) | NR | USA | Individual CBT | NA | NA | WLC | NR | ✗ | ✓ | ✓ | ✓ |
Kowalik et al.257 2011 | PTSD | Sexual abuse | Critically low | 4 (427) | Children | NR | Individual CBT or parent–child CBT, sexual specific/trauma-focused/adapted for sexually abused pre-school children (CBT-SAP) | NA | Non-directive support therapy, child-centred play therapy | NA | Short | ✗ | ✗ | ✓ | ✓ |
Leigh-Hunt and Perry272 2015 | PTSD | Offenders | Low | 1 (44) | Adults | USA | Group CBT | NA | NA | TAU | Short | ≤ | ≤ | ✓ | ✓ |
Lewis et al.275 2018 | PTSD | NA | High | 6 (437) | Adults | USA, Sweden, Iraq, UK | NA | Internet-based CBT | Other internet-based psychological therapy | WLC, TAU | Short | ✓ | ✓ | ✓ | ✓ |
Mabey and van Servellen290 2014 | PTSD | Severe mental illness (depression, bipolar, schizophrenia) | Critically low | 1 (108) | Adults | USA | Individual CBT | NA | NA | TAU | Short | ≤ | ✓ | ✓ | ✓ |
Macedo et al.292 2018 | PTSD | NA | Moderate | 1 (156) | Adults | NR | Individual CBT | NA | Brief treatment programme (breathing + psychoeducation) | NA | Long | ✗ | ✗ | ✓ | ✗ |
Moreno-Alcázar et al.320 2017 | PTSD | NA | Moderate | 3 (119) | Children, adolescents | NR | Individual CBT | NA | EMDR | NA | Short | ✗ | ✓ | ✓ | ✓ |
Nocon et al.333 2017 | PTSD | War displacement | Critically low | 1 (399) | Children | Sri Lanka | Individual CBT | NA | NA | WLC | Short | ✗ | ✓ | ✓ | ✓ |
O’Donnell et al.338 2018 | Adjustment disorder | NA | Critically low | 1 (54) | Adults | NR | NA | Self-help bibliotherapy | NA | WLC | Short | ✗ | ✓ | ✓ | ✗ |
Palic and Elklit355 2011 | PTSD | Refugees | Critically low | 5 (106) | Adults | Vietnam, Cambodia, mixed southern Asian nationality | Culturally sensitive individual CBT for South East Asians, individual CBT | NA | Psychoactive medication, exposure therapy | WLC | Short | ✓ | ✓ | ✓ | ✓ |
de Medeiros Passarela et al.303 2010 | PTSD | Sexual abuse | Low | 2 (136) | Children, adolescents | USA, Australia | Family/parent CBT | NA | NA | TAU | Short | ✗ | ✗ | ✓ | ✓ |
Patel et al.357 2014 | PTSD | Torture survivors | High | 1 (16) | Adults | Sweden | Individual CBT | NA | Behavioural exposure | NA | Short | ✓ | ✓ | ✓ | ✓ |
Roberts et al.385 2009 | PTSD | NA | Moderate | 3 (248) | Adults | NR | Trauma-focused individual CBT | NA | Supportive counselling | WLC | Long | ✗ | ✗ | ✓ | ✓ |
Roberts et al.384 2016 | PTSD | Substance misuse | Moderate | 1 (353) | Adults | USA | Group CBT or individual CBT: ‘seeking safety’, integrated CBT | NA | Group women’s health education | NA | Short–long | ✗ | ✗ | ✓ | ✓ |
Rodenburg et al.387 2009 | PTSD | NA | Critically low | 2 (52) | Children, adolescents | NR | NR | NR | EMDR | NA | Short | ✗ | ✗ | ✓ | ✓ |
Russell and Davis391 2007 | PTSD | Sexual assault | Critically low | 1 (10) | Adults | NR | NR | NA | NA | WLC | Short | ✗ | ✓ | ✗ | ✓ |
Schwartze et al.399 2017 (PTSD) | PTSD | NA | Moderate | 1 (24) | Adults | NR | Culturally adapted group CBT | NA | Applied muscle relaxation + TAU | NA | Short | ✗ | ′ | ✓ | ✓ |
Sebastian and Nelms402 2017 | PTSD | Sexual violence | Critically low | 1 (50) | NR | Democratic republic of Congo | NR | NA | EFT | NA | Short | ✗ | ≤ | ✓ | ✓ |
Silverman et al.408 2008 | PTSD | Sexual abuse, traumatic event | Critically low | 3 (164) | Children, adolescents | Iran, NR | Trauma-focused group CBT, trauma-focused individual CBT | NA | EMDR | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Sin et al.409 2017 | PTSD | Psychosis | Moderate | 3 (145) | Adults | USA, UK | Trauma-focused individual CBT | NA | Brief psychoeducation | TAU | Short–long | ✓ | ✓ | ✓ | ✓ |
Soo and Tate422 2007 | Acute stress disorder | Traumatic brain injury | Moderate | 1 (24) | Adults | UK | Individual CBT | NA | Supportive counselling | NA | Short | ✗ | ✗ | ✓ | ✗ |
Sullivan and Simonson436 2016 | PTSD | Refugees | Critically low | 1 (31) | Children, adolescents | USA (refugees/immigrants from Burundi, Congo, Kenya, Liberia, Rwanda, Somalia, Tanzania, Myanmar, Nepal, Russia, Bosnia, Afghanistan, Iraq, Turkey and Uzbekistan) | Trauma-focused individual CBT | NA | Child-centred play therapy | NA | Short | ✗ | ✗ | ✓ | ✗ |
Swan et al.439 2017 | PTSD | Psychosis | Critically low | 1 (108) | Adults | USA | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ≤ |
Torchalla and Strehlau452 2018 | PTSD | Workplace trauma | Critically low | 1 (31) | Adults | USA | Trauma-focused individual CBT | NA | NA | No intervention | Short | ✗ | ✗ | ✓ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Brownley et al.78 2016 | BED | NA | Low | 7 (699) | Adults | USA | Therapist-led individual CBT, partially therapist-led individual CBT | Guided or pure self help | Interpersonal therapy | WLC | Short | ✗ | ✓ | ✗ | ✓ |
de Jong et al.120 2018 | Bulimia nervosa, BED, EDNOS | NA | Low | 1 (130) | Adults | UK | NR | NA | Interpersonal therapy | NA | Long | ✗ | ✗ | ✗ | ✓ |
Flament et al.148 2012 | BED and anorexia nervosa | NA | Critically low | 1 (108) | Adults | Italy | Individual CBT | NA | Drug | NA | Long | ✗ | ✗ | ✗ | ✓ |
Flodgren et al.150 2015 | BED | NA | High | 1 (128) | Adults | USA | NA | Video-teleconference CBT | Face-to-face CBT | NA | Short | ✓ | ✓ | ✗ | ✓ |
Ghaderi and Andersson166 1999 | Mixed | NA | Critically low | 5 (334) | NR | NR | NR | NA | Drug, supportive–expressive therapy, interpersonal therapy | WLC | Short | ✗ | ✗ | ✗ | ✓ |
Ghaderi et al.167 2018 | Bulimia nervosa | NA | Moderate | 9 (949) | Adults | USA, Switzerland, the Netherlands | Individual CBT, group CBT, mixed individual CBT + group CBT | Self-help, guided self-help | Interpersonal therapy, behavioural weight loss | WLC, placebo | Short–long | ≤ | ✓ | ✗ | ✓ |
Grenon et al.179 2017 | BED | NA | Moderate | 4 (328) | Adults | USA, Canada | Group CBT | NA | Behavioural therapy, interpersonal therapy, group psychodynamic interpersonal therapy | NA | Short | ✗ | ′ | ✗ | ✓ |
Grenon et al.178 2018 | Bulimia nervosa, BED | NA | Critically low | 1 (42) | Adults | USA | Group CBT | NA | Behavioural therapy | NA | Short | ✗ | ′ | ✗ | ✓ |
Hay and Claudino200 2010 | Mixed | NA | Critically low | 3 (220) | Adults | NR | Individual CBT for bulimia nervosa | NA | Guided self-help CBT | WLC | Short | ≤ | ✓ | ✗ | ✓ |
Hay et al.201 2012 | Bulimia nervosa | NA | Low | 1 (33) | Adults | NR | Individual CBT | NA | Individual nutritional counselling | NA | Long | ✗ | ✗ | ✗ | ✓ |
Hay et al.199 2001 | Anorexia nervosa | NA | Moderate | 4 (141) | Adults | USA, Canada | Individual CBT | NA | Drug | NA | Short | ✗ | ✓ | ✗ | ✓ |
Hay et al.198 2009 | Bulimia nervosa | NA | Moderate | 17 (1367) | Adults | USA, Canada, UK, Australia | Group CBT or individual CBT for bulimia, mixed group CBT + individual CBT | NA | Self-monitoring, CBT/exposure and response prevention, interpersonal therapy, behavioural therapy, short-term focal psychotherapy, psychoeducation, supportive–expressive therapy, hypo behavioural therapy, prescriptive therapy non-directive counselling and ‘focused evocative unfolding’ | WLC, no intervention | Short | ✗ | ✓ | ✗ | ✓ |
Hay et al.197 2015 | Anorexia nervosa | NA | Moderate | 2 (56) | Adults | New Zealand, Germany | Individual CBT | NA | Interpersonal therapy, SSCM, FPDT | Optimised TAU | Long | ✗ | ✓ | ✗ | ✓ |
Hilbert et al.208 2019 | BED | NA | Low | 5 (494) | Adults | NR | Group CBT, individual CBT | NA | Weight loss treatment, drug | NA | Short | ✗ | ′ | ✗ | ✓ |
Keel and Haedt243 2008 | Bulimia nervosa, EDNOS | NA | Critically low | 1 (85) | Adolescents | NR | NA | CBT guided self-care | Family therapy | NA | Long | ✗ | ✗ | ✗ | ✓ |
Loucas et al.287 2014 | Anorexia nervosa, bulimia nervosa, BED, EDNOS | NA | Low | 4 (474) | Adults | NR | NA | Internet-based CBT, CD-ROM CBT | High-intensity face-to-face CBT | WLC, TAU | Short–long | ✗ | ✗ | ✗ | ✓ |
Miniati et al.311 2018 | Anorexia nervosa | NA | Low | 1 (56) | Adults | NR | Individual CBT | NA | Interpersonal therapy | Non-specific supportive clinical management | Short | ✗ | ✗ | ✗ | ✓ |
Norris et al.337 2019 | Mixed | NA | Critically low | 5 (249) | Adults | Australia, UK, USA, Germany | Enhanced individual CBT | NA | NR | NR | Short | ✗ | ✗ | ✗ | ✓ |
Palavras et al.353 2017 | BED | NA | Low | 3 (261) | Adults | USA, Switzerland | Group CBT, individual CBT | Guided self-help | Behavioural weight loss therapy, interpersonal therapy | NA | Long | ✗ | ✗ | ✗ | ✓ |
Peat et al.359 2017 | BED | NA | Critically low | 2 (170) | Adults | NR | Group CBT | NA | Behavioural weight loss therapy | NA | Long | ✗ | ✓ | ✗ | ✓ |
Pittock et al.367 2018 | Bulimia nervosa | NA | Low | 1 (196) | Adults | USA | NA | Internet-based CBT | Face-to-face CBT | NA | Long | ✗ | ✗ | ✗ | ✓ |
Polnay et al.369 2014 | Bulimia nervosa | NA | Moderate | 3 (133) | Adults | USA, Norway | Group CBT (delivered by doctoral qualified psychologists) | NA | NA | WLC | Short | ✗ | ✓ | ✗ | ✓ |
Reas and Grilo378 2008 | BED | NA | Critically low | 1 (108) | Adults | USA | Individual CBT | NA | Fluoxetine | Placebo | Short | ✗ | ✗ | ✗ | ✓ |
Svaldi et al.438 2018 | Bulimia nervosa | NA | Moderate | 4 (295) | Adolescents, adults | NR | Individual CBT | NA | (Active arms not included in analysis) | WLC | Short | ✗ | ✓ | ✗ | ✓ |
Watson et al.491 2016 | Mixed | NA | Low | 1 (76) | Adults | USA | NA | Internet-based CBT | Psychoeducation | NA | Short | ✗ | ✗ | ✗ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Nezu et al.328 2001 | Bodily distress or experience disorder | NA | Critically low | 1 (50) | Adults | NR | Group CBT | NA | NA | WLC | Short | ✗ | ✓ | ✗ | ✓ |
van Dessel et al.469 2014 | Bodily distress or experience disorder | NA | High | 4 (504) | Adults | USA, Spain, Germany, the Netherlands | Group CBT, individual CBT | NA | Progressive muscle relaxation | TAU | Short–long | ✓ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Dugosh et al.130 2016 | Opioid addiction | NA | Critically low | 1 (60) | NR | NR | Individual CBT + methadone maintenance treatment | NA | Methadone maintenance treatment | NA | Long | ✓ | ✗ | ✗ | ✗ |
Eccleston et al.133 2017 | Opioid misuse | Chronic back/neck pain | Moderate | 1 (42) | Adults | NR | Group CBT, individual CBT for the prevention of opioid misuse | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✓ |
Harada et al.193 2018 | Due to use of stimulants | Amphetamine-type stimulants | High | 1 (160) | Adults | Australia | NA | Internet-based CBT | NA | WLC | Short | ✓ | ✗ | ✗ | ✗ |
Minozzi et al.312 2016 | Due to use of hallucinogens | Psychostimulant | High | 0 (0) | Adults | NA | NA | NA | NA | NA | NA | ✗ | ≤ | ✗ | ≤ |
Stevens et al.429 2018 | Internet gaming disorder | NA | Critically low | 3 (148) | Adolescents, NR | China, Republic of Korea, NR | Group CBT, group CBT + medication | NA | Medication only, physical exercise | No intervention | Short | ✗ | ✓ | ✓ | ✗ |
van der Maas et al.468 2019 | Gambling disorder | NA | Critically low | 1 (66) | Adults | Sweden | NA | Internet-based CBT and e-mail and discussion groups | NA | WLC | Long | ✗ | ✓ | ✓ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Davidson and Tran115 2014 | Personality disorder | NA | Critically low | 1 (106) | Adults | NR | Individual CBT for personality disorder | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Gibbon et al.168 2010 | Personality disorder | Cocaine dependence | Moderate | 1 (43) | Adults | UK | Individual CBT | NA | NA | TAU | Short | ≤ | ✓ | ✓ | ✗ |
Matusiewicz et al.298 2010 | Personality disorder | NA | Critically low | 4 (348) | Adults | NR | Individual CBT | NA | Brief dynamic therapy, brief relational therapy | WLC, TAU | Short | ✗ | ✓ | ✓ | ✓ |
Stoffers et al.432 2012 | Personality disorder | NA | Moderate | 1 (106) | Adults | UK | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Sleight415 2016 | Mild neurocognitive disorder | Cancer (breast) | Critically low | 1 (41) | Adults | USA | Individual CBT intervention ‘Memory and Attention Adaption Training’ | NA | NA | WLC | Short | ✓ | ✗ | ✗ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Bledsoe and Grote71 2006 | Depressive disorder | Pregnancy and postpartum depression | Critically low | 3 (172) | Adults | UK, France | Home-based individual CBT | NA | NA | TAU, placebo, NR | Short | ✗ | ✓ | ✗ | ✗ |
Craig and Howard109 2009 | Postnatal depression | NA | Critically low | 5 (502) | Adults | NR | Individual CBT, individual CBT + antidepressants, group CBT | Individual CBT (delivered by early-childhood nurses), group CBT (delivered by health visitors) | Non-directive counselling, psychodynamic therapy, antidepressants | TAU | Short–long | ≤ | ✓ | ✗ | ✗ |
De Crescenzo119 2014 | Postnatal depression | NA | Moderate | 1 (35) | Adults | NR | Individual CBT + paroxetine | NA | Paroxetine only | NA | Short | ✗ | ✓ | ✗ | ✗ |
Dennis125 2004 | Postnatal depression | NA | Critically low | 1 (176) | Adults | Finland | Individual CBT with between-session telephone support | NA | NA | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Huang216 2018 | Postnatal depression | NA | Low | 6 (510) | Adults | Canada, Australia, France, Iran | Individual CBT, group CBT | Internet-based CBT | NA | TAU | Short | ′ | ✓ | ✓ | ✗ |
Lau267 2017 | Postnatal depression | Pregnancy loss, PTSD, depression | Moderate | 6 (530) | Adults | Canada, USA, Australia, Germany, Sweden | NA | Internet-based CBT with therapist support | NA | TAU, WLC | Short | ✗ | ✓ | ✓ | ✗ |
Lavender268 2016 | Antenatal depression | NA | Critically low | 1 (55) | Adults | USA | Modified individual CBT | NA | NR | NR | Short | ✗ | ✓ | ≤ | ✗ |
Leis273 2009 | Postnatal depression | NA | Critically low | 1 (37) | Adults | Australia | NA | CBT (delivered by early-childhood nurses) | Support sessions | NA | Short | ✗ | ✓ | ✗ | ✗ |
LoGiudice284 2018 | Undergoing IVF | NA | Critically low | 1 (31) | Adults | Iran | Group CBT | NA | NR | NR | Short | ≤ | ✓ | ✓ | ✗ |
Maguire294 2018 | Postnatal depression | NA | Critically low | 2 (172) | Adults | Germany, Australia | Group CBT, individual CBT | NA | NA | TAU | Short | ✗ | ✗ | ✓ | ✗ |
McDonagh301 2014 | Postnatal depression | NA | Low | 1 (35) | Adults | Canada | NR | NA | Paroxetine only | NA | Short | ✗ | ✓ | ✗ | ✗ |
Mendelson307 2017 | Perinatal anxiety, depression | NA | Low | 1 (39) | Adults | USA | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ≤ | ✗ |
Nillni331 2018 | Perinatal anxiety, depression | NA | Critically low | 1 (105) | Adults | NR | Individual CBT | NA | NA | TAU + parent mentor programme | Short | ✗ | ✓ | ✓ | ✗ |
Perveen363 2013 | Postnatal depression | NA | Critically low | 5 (607) | Adults | UK, USA, Australia | Individual CBT (delivered by therapists) | CBT (delivered by health visitor or research staff) | NA | TAU | Short | ✗ | ✓ | ✓ | ✗ |
Sangsawang393 2018 | Postnatal depression | NA | Critically low | 1 (47) | Adolescents | USA | NA | CBT adapted for Apache adolescents, ‘Living in Harmony’ programme | Educational support | NA | Short | ✗ | ✓ | ≤ | ≤ |
Scope400 2013 | Postnatal depression | NA | Low | 1 (192) | Adults | Australia | Group CBT | NA | Group + individual counselling | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Stevenson430 2010 | Postnatal depression | NA | Moderate | 1 (192) | Adults | Australia | Group CBT | NA | Group counselling | NA | Short | ✗ | ✓ | ✗ | ✗ |
van Ravesteyn471 2017 | Antenatal depression | NA | Low | 1 (1300) | Adults | NR | Group CBT, individual CBT | NA | Supportive counselling, psychoeducation, health-care visits | TAU, booklet | Short | ✗ | ✓ | ✗ | ✗ |
Webb494 2004 | Perinatal psychosis | Perinatal period | Moderate | 0 (0) | Adults | NR | NA | NA | NA | NA | NA | ✗ | ✗ | ≤ | ✗ |
ICD-11 primary/secondary | Condition description | Study | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition-specific | ||||||||
|
|
Adelufosi35 2017 | Female genital mutilation | Critically low | 0 (0) | Children, adults | NR | NA | NA | NA | NA | NA | ✗ | ≤ | ≤ | ≤ |
|
|
Andersen44 2016 | NA | Moderate | 5 (435) | Adults | Australia, USA | Transdiagnostic individual or group CBT | Transdiagnostic internet-based CBT + e-mail/telephone | NA | WLC | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Andrews46 2018 | NA | Moderate | 53 (8279) | Adults | NR | NA | Internet-based CBT | High-intensity face-to-face CBT, bibliotherapy CBT | WLC ± discussion group, WLC ± attention placebo, TAU, information, self-monitoring | Short–long | ✗ | ✓ | ✓ | ✓ |
|
|
Armento52 2012 | Parkinson’s disease | Critically low | 2 (174) | Older adults | NR | Individual CBT, 1 session of individual CBT + telephone sessions | NA | Supportive therapy | Clinical monitoring | Short | ✓ | ✓ | ✓ | ✓ |
|
|
Arnberg53 2014 | NA | Low | 21 (1855) | Children, adolescents, adults | Australia, Sweden, Switzerland | NA | Internet-based CBT | High-intensity individual CBT, online supportive therapy | WLC, online forum | NR | ✗ | ✓ | ✓ | ✓ |
|
|
Bower74 2003 | NA | Low | 1 (NR) | Adults | NR | NR | NA | Non-directive counselling | NA | Long | ✗ | ✓ | ≤ | ✗ |
|
|
Cape86 2010 | NA | Critically low | 11 (709) | Adults | Australia, UK | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Chibanda99 2015 | HIV | Low | 1 (13) | Adults | China | Group CBT | NA | NA | WLC | Short | ✗ | ✓ | ≤ | ✗ |
|
|
Clarke101 2015 | NA | Low | 1 (1477) | Adolescents | Australia | NA | Internet-based CBT | NA | WLC | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Coventry108 2008 | COPD | Low | 1 (48) | Adults | USA | Individual CBT | NA | Education | NA | NR | ✗ | ✓ | ✓ | ✗ |
|
|
Davies117 2014 | NA | Moderate | 4 (198) | Adults | Australia, Canada, Spain | NA | Internet-based CBT | Other psychotherapy | WLC, no intervention | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Ebert131 2015 | NA | Low | 11 (778) | Children, adolescents | Australia, the Netherlands, New Zealand, Sweden | NA | Internet-based CBT | NA | WLC, placebo | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Farrand143 2015 | Myocardial infarction, multiple sclerosis | Moderate | 2 (235) | Adults | NR | NA | Internet-based CBT | NA | TAU, attention control | Long | ✗ | ✓ | ✓ | ✓ |
|
|
Fulton158 2018 | Breast cancer | Critically low | 1 (13) | Adults | NR | Group CBT | NA | Supportive therapy | NA | Short | ✓ | ′ | ′ | ✗ |
|
|
Garcia-Escalera162 2016 | NA | Low | 14 (1337) | Children, adults | Australia, UK, USA | Transdiagnostic individual or group CBT | Transdiagnostic internet-based CBT | NA | WLC, discussion group | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Giummarra171 2018 | Traumatic injury | Low | 3 (366) | Adults | Australia, the Netherlands | Individual CBT, modular CBT | Internet-based CBT | Supportive counselling | TAU | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Gonçalves173 2015 | NA | Low | 3 (67) | Adults | NR | Individual CBT | NA | NA | WLC | Short | ✗ | ✗ | ✓ | ✓ |
|
|
Gould175 2012 | NA | Moderate | 3 (172) | Older adults | NR | Individual CBT | NA | Drug, supportive therapy | TAU | Long | ✗ | ✓ | ✓ | ✗ |
|
|
Gregory177 2018 | NA | Critically low | 2 (53) | Adults | USA | Individual CBT, group CBT | NA | NR | NR | Short | ✗ | ✗ | ✓ | ✗ |
|
|
Grist182 2018 | NA | Low | 3 (408) | Children, adolescents | The Netherlands, Sweden | NA | Internet-based CBT | High-intensity, face-to-face CBT | WLC | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Hobbs214 2011 | Alcohol dependence | Critically low | 2 (131) | Adults | NR | NR | NA | NR | NR | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Huang215 2018a | NA | Critically low | 2 (79) | Adults | Australia, USA | Group CBT | Internet-based CBT | NA | Placebo, no intervention | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Jennings229 2015 | Learning disability | Critically low | 1 (32) | Adults | UK | Individual CBT | NA | NA | TAU | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Kaltenthaler239 2006 | NA | Low | 1 (274) | Adults | UK, USA | NA | Internet-based CBT | NA | TAU, information | Short | ≤ | ✓ | ✓ | ≤ |
|
|
Kayrouz242 2018 | NA | Moderate | 1 (159) | Adults | Iraq | NA | Internet-based CBT | NA | WLC | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Mac-donald291 2016 | Childhood abuse | Moderate | 6 (658) | Children, adolescents | Australia, Norway, USA | Individual CBT, trauma-focused individual CBT, sexual-abuse individual CBT, child individual CBT | NA | Supportive therapy, child-centred therapy | WLC, TAU | Short | ≤ | ✓ | ✓ | ✓ |
|
|
Mayo-Wilson299 2013 | NA | High | 22 (2001) | Adults | Australia, Canada, the Netherlands, Spain, Sweden, UK, USA | NA | Internet-based CBT, telephone CBT, bibliotherapy CBT, mixed CBT (bibliotherapy + internet-based CBT) | High-intensity CBT | WLC, TAU | Short | ✓ | ✓ | ✓ | ✓ |
|
|
Mehndiratta305 2013 | Epilepsy | Critically low | 1 (37) | Older adults | Australia | Group CBT | NA | NA | TAU | Short | ✗ | ✓ | ≤ | ✓ |
|
|
Montero-Marin315 2018 | NA | Moderate | 4 (495) | Adults | Spain, USA, Norway | Group CBT, individual CBT | NA | Progressive relaxation, applied relaxation | NA | Short–long | ′ | ✓ | ✓ | ✓ |
|
|
Naidu324 2016 | NA | Low | 5 (390) | Adults | Sweden, Australia | NA | Internet-based CBT | High-intensity face-to-face individual or group CBT | NA | Short | ✗ | ≤ | ✓ | ✗ |
|
|
Newby327 2016 | NA | Low | 14 (1606) | Adults, older adults | Sweden, Canada, Australia, UK, Switzerland, Germany, Austria | NA | Transdiagnostic internet-based CBT | Relaxation | WLC, TAU, discussion, forum | Short | ✓ | ✓ | ✓ | ✗ |
|
|
Ng329 2018 | NA | Critically low | 1 (NR) | Adults, older adults | China | Group CBT | NA | NA | WLC, no intervention | Short | ✓ | ≤ | ✓ | ✗ |
|
|
Noble332 2018 | Epilepsy | Critically low | 1 (59) | Adults | Australia | Individual CBT | NA | NA | WLC | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Noone335 2018 | Dementia | Low | 2 (82) | Older adults | UK, USA | Individual CBT | NR | NA | TAU | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Normann336 2018 | NA | Critically low | 2 (122) | Adults | NR | Individual CBT | NA | Metacognitive therapy | NA | Short–long | ✗ | ✓ | ✓ | ✗ |
|
|
Olthuis343 2016 | NA | Moderate | 28 (4998) | Adults | Australia, Austria, Germany, the Netherlands, Sweden, Switzerland | NA | Internet-based CBT | High-intensity face-to-face CBT | WLC, attention control, information, discussion | Short–long | ✓ | ✗ | ✓ | ✓ |
|
|
Opoka344 2018 | Psychosis | Critically low | 1 (150) | Adults | NR | Individual CBT | NA | NA | TAU | Short | ✗ | ✗ | ✗ | ✓ |
|
|
O’Sullivan351 2016 | War-affected children and young people | Critically low | 2 (102) | Children, adolescents | Democratic Republic of the Congo | Group trauma-focused CBT | NA | NA | WLC | ✗ | ′ | ✓ | ✓ | |
|
|
Păsărelu356 2017 | NA | Low | 4 (283) | Adults | Sweden, Australia | NA | Transdiagnostic internet-based CBT | NA | WLC | Long | ✓ | ✓ | ✓ | ✗ |
|
|
Pennant360 2015 | NA | Low | 15 (2615) | Children, adolescents, young adults | NR | NA | Computerised CBT | High-intensity face-to-face CBT, attention bias modification, computer control | WLC, TAU, no intervention | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Purgato373 2018 | NA | Moderate | 1 (313) | Children, adolescents, adults | Thailand, China, Iraq, Democratic Republic of the Congo | Trauma-focused individual CBT | Web-based CBT, group CBT (delivered by school staff and paraprofessionals) | NA | TAU, no intervention, general support, WLC | Short | ✓ | ✓ | ✓ | ✓ |
|
|
Rasing377 2017 | NA | Critically low | 16 (4422) | Adolescents | Australia, USA, the Netherlands, Canada | Group CBT | NA | Activity | Information | Long | ✗ | ✓ | ✓ | ✗ |
|
|
Reavell379 2018 | Cardiovascular disease | Low | 1 (38) | Adults | Australia | Individual CBT | NA | NA | TAU | Long | ′ | ✓ | ✓ | ≤ |
|
|
Rodrigues388 2011 | NA | Critically low | 5 (132) | Adults | NR | Individual CBT | NA | Drug | WLC | Short | ✗ | ✗ | ✓ | ✓ |
|
|
Smith418 2014 | COPD | Low | 4 (378) | Adults | Norway, Australia, USA | Group CBT, individual CBT | NA | COPD education | TAU | Short | ′ | ✓ | ✓ | ✗ |
|
|
Snoek419 2002 | Diabetes | Critically low | 8 (85) | Adults | NR | Group CBT, individual CBT | NA | Non-prescriptive therapy | No intervention | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Spain423 2015 | Autism spectrum disorder | Critically low | 1 (37) | Adults | UK | Individual CBT for OCD | NA | Anxiety management | NA | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Spek424 2007 | NA | Low | 10 (1465) | Adults | NR | NA | Internet-based CBT | NA | WLC, TAU, placebo, self-monitoring, information, online discussion group | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Spies425 2013 | HIV/AIDS | Critically low | 3 (250) | Adults | Hong Kong, USA | Group CBT, individual CBT | NA | Supportive psychotherapy, peer counselling, intervention control | No intervention | NR | ✓ | ✓ | ✓ | ✗ |
|
|
Tay442 2018 | Dementia | Critically low | 1 (50) | Older adults | NR | Individual CBT (for mild to moderate dementia patients) | NA | NA | TAU | Short | ✗ | ✓ | ′ | ✗ |
|
|
Thabrew445 2018 | Long-term physical health problems | High | 8 (770) | Children, adolescents | USA, UK, India, Australia, Serbia, Montenegro | Group CBT, individual CBT, home-based individual CBT, clinic-based group CBT, transdiagnostic CBT | NA | Education, supportive psychotherapy, supportive non-directive therapy, non-directive behavioural counselling | WLC, TAU, information | Short–long | ✓ | ✓ | ✓ | ✓ |
|
|
Thabrew446 2018b | Long-term physical health problems | High | 4 (469) | Children, adolescents | USA, Germany | NA | Internet-based CBT or Web-MAP | Specialised headache treatment, education, applied relaxation | WLC | Short–long | ✓ | ✓ | ✓ | ✓ |
|
|
Troeung457 2013 | Parkinson’s disease | Critically low | 1 (80) | Older adults | USA | Individual CBT | NA | NA | Clinical monitoring | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Twomey461 2015 | NA | Low | 25 (3716) | Adults | NR | Individual CBT, group CBT | Computerised CBT, guided CBT, telephone CBT | NA | WLC, no intervention, TAU | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Twomey459 2017 (MoodGYM) | NA | Critically low | 11 (4570) | Adults | Australia, Ireland, UK, Norway | NA | Internet-based CBT ‘MoodGYM’ | Telephone support or website | TAU, no intervention | Short | ✗ | ✓ | ≤ | ✗ |
|
|
Valimaki466 2017 | NA | Low | 1 (187) | Adolescents | New Zealand | NA | Computerised CBT ‘SPARX’ | NA | TAU | Short | ✗ | ′ | ✓ | ✗ |
|
|
Verdeli479 2006 | NA | Critically low | 3 (118) | Adolescents | NR | Group CBT, individual CBT, school-based CBT | NA | Interpersonal therapy | No intervention, WLC, attention support | Short | ✗ | ✓ | ✓ | ✗ |
|
|
Wang484 2013 | NA | Moderate | 2 (115) | Adults | Hong Kong | Group CBT, individual CBT | NA | Dejian mind–body intervention | WLC | Short | ✗ | ✓ | ≤ | ✗ |
|
|
Watts493 2015 | NA | Critically low | 48 (6926) | Adults | NR | Individual CBT (delivered by therapists, psychologists) | CBT (delivered by nurses, social workers, behavioural health specialists) | NA | TAU | Short | ✗ | ✓ | ✓ | ✗ |
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Yatham511 2018 | NA | Critically low | 2 (615) | Children, adolescents | Palestine | Individual CBT ‘teaching recovery techniques’, individual CBT adapted ‘teaching recovery techniques’ | NA | NA | WLC | Short | ✗ | ′ | ✓ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Bohra 201372 | Insomnia | Pain | Critically low | 1 (51) | Older adults | NR | Group CBT for insomnia | NA | Stress management and wellness | NA | Short | ✗ | ✗ | ✗ | ✓ |
Brasure 201675 | Insomnia | NA | Low | 11 (1182) | Adults | USA, UK, Europe | Group CBT for insomnia, individual CBT for insomnia | Self-help CBT for insomnia, internet-based CBT for insomnia | Sleep hygiene, self-help | Internet sham, placebo (drug), WLC, TAU | Short | ✗ | ✗ | ✗ | ✓ |
Budhrani 201580 | Insomnia | Breast cancer | Critically low | 1 (72) | Adults | NR | Individual CBT | NA | NR | NR | Short | ✗ | ✗ | ✗ | ✓ |
Cheng 201297 | Insomnia | NA | Low | 4 (300) | Adults | USA, Canada, Sweden | NA | Computerised CBT for insomnia | NA | WLC, self-monitoring | Short | ✗ | ✗ | ✗ | ✓ |
Cheung 201898 | Insomnia | NA | Critically low | 1 (139) | Adults | UK | NA | Group CBT (delivered by health visitors) | NA | Sleep monitoring | Long | ✗ | ✗ | ✗ | ✓ |
Gebara 2018163 | Insomnia | Depression | Critically low | 3 (124) | Adults | USA, Sweden | Group CBT, individual CBT | NA | Drug, relaxation | WLC | Short | ✗ | ✓ | ✗ | ✓ |
Johnson 2016233 | Insomnia | Cancer | Critically low | 5 (621) | Adults | NR | Individual CBT for insomnia, group CBT for insomnia | Video-based CBT for insomnia | Behavioural placebo, mindfulness-based cancer recovery | WLC, TAU | Short | ✗ | ✗ | ✗ | ✓ |
Koffel 2015255 | Insomnia | NA | Low | 6 (408) | Adults | NR | Group CBT | NA | Sleep/pain education | WLC, TAU, diary-keeping | Short | ✗ | ✓ | ✗ | ✓ |
Mitchell 2012314 | Insomnia | NA | Critically low | 3 (201) | Adults, older adults | Norway, Canada, China | Group CBT, individual CBT | NA | Drug | NA | Short–long | ✓ | ✓ | ✓ | ✓ |
Montgomery 2003316 | Insomnia | NA | Moderate | 2 (102) | Older adults | USA | Group CBT, individual CBT | NA | NA | WLC, placebo | Short | ≤ | ✗ | ✗ | ✓ |
Morin 1999321 | Insomnia | NA | Critically low | 1 (24) | Adults | NR | Multicomponent group CBT | NA | NA | WLC | Long | ✗ | ✗ | ✗ | ✓ |
Navarro-Bravo 2015326 | Insomnia | NA | Critically low | 5 (456) | Adults | NR | Individual CBT | NA | Stress management and wellness, sleep hygiene education | WLC, TAU | Short | ✗ | ✗ | ✗ | ✓ |
Okajima 2011339 | Insomnia | NA | Critically low | 4 (226) | Adults | NR | Group CBT, individual CBT | NA | Drug | WLC, placebo, TAU | Long | ✗ | ′ | ✗ | ✓ |
Phelps 2017366 | Insomnia | NA | Critically low | 1 (81) | Adults | USA | NR | NA | Sleep hygiene | NA | Short | ✗ | ✗ | ✗ | ✓ |
Seyffert 2016403 | Insomnia | NA | Low | 11 (1886) | Adults | Canada, Hong Kong, UK, Sweden, the Netherlands, Germany, USA | NA | Internet-based CBT | Group CBT, telehealth CBT, internet-based CBT without support, internet control, imagery relief therapy | WLC | Short–long | ✗ | ✓ | ✗ | ✓ |
Smallfield 2018416 | Insomnia | NA | Critically low | 1 (60) | Older adults | NR | NA | Telephone CBT (delivered using workbook) | NA | Information | Short | ✗ | ✗ | ✗ | ✓ |
Taylor 2014443 | Insomnia | Depression, PTSD, alcohol abuse | Critically low | 4 (132) | Adults | NR | Individual CBT | Self-help CBT with telephone support | NA | Placebo, WLC, NR | Short | ✗ | ✓ | ✓ | ✓ |
Trauer 2015455 | Insomnia | NA | Moderate | 5 (240) | Adults | Canada, USA, China, Australia | Group CBT for insomnia, individual CBT for insomnia | NA | Sleep hygiene education | WLC, placebo, tablets | Short–long | ✗ | ✗ | ✗ | ✓ |
Twomey 2013460 | Insomnia | NA | Critically low | 33 (5768) | Adults | Australia, UK, Spain, USA, Switzerland, Canada, Germany | NA | Computerised CBT | High-intensity face-to-face CBT, psychoeducation, computer-guided self-relaxation | WLC, TAU, NR | Short | ✗ | ✓ | ✓ | ✓ |
Werner-Seidler 2018496 | Insomnia | NA | Low | 2 (173) | Adolescents, young adults | The Netherlands, UK | NA | eCBT for insomnia | NA | WLC | Short | ≤ | ✓ | ✓ | ✓ |
Wu 2015505 | Insomnia | Medical/psychiatric conditions | Low | 10 (609) | Adults | NR | Individual CBT for insomnia, individual CBT for insomnia + drug | NA | Sleep hygiene, escitalopram plus quasi desensitisation, mindfulness-based stress reduction, obstructive sleep apnoea surgery, wellness education, audiotape relaxation training | WLC, TAU | Short | ✗ | ′ | ′ | ✓ |
Zachariae 2016516 | Insomnia | NA | Low | 11 (1460) | Adults | NR | NA | Internet-based CBT for insomnia | NR | WLC | Short | ✗ | ✗ | ✗ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Bagnell 200756 | Post-viral fatigue syndrome | NA | Low | 4 (459) | Children, adults | NR | Individual CBT | NA | Relaxation, guided support group | TAU, WLC, no intervention | Long | ✓ | ✓ | ✓ | ✓ |
Carlson 201788 | Psychogenic non-epileptic seizures | NA | Low | 1 (34) | Adults | USA | Individual CBT | NA | NA | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Castell 201193 | Post-viral fatigue syndrome | NA | Critically low | 16 (1457) | Adults | NR | Individual CBT, group CBT | NA | Education/support, relaxation, supportive listening, adaptive pacing, counselling | WLC, placebo, injection, TAU, medical care | Short | ✓ | ′ | ′ | ′ |
Cleare 2015103 | Post-viral fatigue syndrome | NA | Critically low | 9 (1552) | Children, adolescents, adults | NR | Group CBT, individual CBT | Internet-based CBT | Guided support, relaxation, education and support, psychoeducation, specialist medical care | No intervention, TAU | Long | ✓ | ✓ | ✓ | ✓ |
Cross 2015110 | Epilepsy or seizures | NA | Critically low | 2 (60) | Adolescents, adults | NR | Group CBT, individual CBT | NA | Supportive counselling | No intervention, TAU | Short | ✓ | ✓ | ✗ | ✓ |
Gillings 2007170 | Post-viral fatigue syndrome | NA | Low | 4 (NR) | Adults | NR | NR | NA | Relaxation and guided support | No intervention | Short–long | ✓ | ✓ | ✓ | ✓ |
Koychev 2017258 | Parkinson’s disease | NA | Critically low | 1 (45) | Adults | NR | Individual CBT | NA | NA | WLC | Short | ′ | ✓ | ✓ | ✓ |
Larun 2017266 | Post-viral fatigue syndrome | NA | Low | 2 (331) | Adults | UK, USA | Individual CBT | NA | Anaerobic activity therapy, cognitive therapy, relaxation, specialist medical care, adaptive pacing therapy, graded exercise therapy | NA | Long | ′ | ✓ | ✓ | ✓ |
Maguire 2011293 | Epilepsy or seizures | NA | Critically low | 2 (60) | Adolescents, adults | NR | NR | NA | Supportive counselling | TAU, no intervention | Short | ✓ | ✓ | ✗ | ✓ |
Martlew 2014297 | Epilepsy or seizures | NA | Moderate | 1 (66) | Adults | UK | Individual CBT | NA | NA | TAU | Short | ≤ | ✓ | ✓ | ✓ |
Price 2008371 | Post-viral fatigue syndrome | NA | Moderate | 8 (1050) | Adults | UK, USA, the Netherlands, Australia | Group CBT, individual CBT | NA | Education, relaxation, psychodynamic, exercise, cognitive therapy, counselling, guided support group | WLC, TAU, no intervention | Short | ✓ | ✓ | ✓ | ✓ |
Reid 2011103 | Post-viral fatigue syndrome | NA | Critically low | 1 (69) | Children, adolescents | NR | Individual CBT | NA | NA | No intervention | Short | ≤ | ≤ | ≤ | ✓ |
Russell 2017390 | Post-viral fatigue syndrome | NA | Critically low | 1 (640) | Adults | NR | Individual CBT | NA | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Walklet 2016483 | Motor neuron diseases or related disorders | NA | Low | 2 (60) | Adults | NR | Individual CBT | Na | NA | TAU | Short | ✓ | ✗ | ✗ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Fackrell 2017140 | Hyperacusis | NA | Critically low | 1 (60) | Adults | NR | Individual CBT | NA | NA | WLC | Long | ✓ | ✓ | ✓ | ✓ |
Hoare 2011213 | Tinnitus | NA | Low | 8 (410) | Adults, older adults | UK | Therapist-delivered individual CBT | Internet-based CBT | Internet-based education, education, minimal contact education relaxation, tinnitus retraining therapy | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Toivonen 2017451 | Tinnitus | NA | Moderate | 1 (64) | Adults | Sweden | NA | Internet-based CBT | Asynchronous web-based acceptance and commitment therapy | Online discussion forum | Short–long | ✓ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of patients) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Kew 2016246 | Asthma | NA | High | 6 (134) | Adults | UK, India, Belgium, Canada, Italy | Individual CBT | NA | NA | WLC, no intervention TAU, self-management | Short | ✓ | ✓ | ✓ | ✓ |
Yorke 2015514 | Asthma | NA | Low | 1 (40) | Adults | NR | Individual CBT | NA | Self-management intervention | NA | Short | ✓ | ≤ | ′ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Amorim 201842 | Dentofacial parafunctional disorders | NA | Low | 1 (57) | Adults | Germany | NA | CBT (delivered by health-care professional) | Occlusal splint | NA | Short | ✗ | ✓ | ≤ | ✓ |
Clarkson 2010102 | Oral mucositis | Cancer | Low | 2 (68) | Adults | USA | Individual CBT | NA | Hypnosis, relaxation and imagery | Therapist contact, TAU | Short | ≤ | ✗ | ✗ | ✓ |
Cong 2018107 | Irritable bowel syndrome | NA | Critically low | 2 (149) | Adults | UK, Sweden | NA | Internet-based CBT, self-management CBT | NA | WLC, TAU | Short | ✓ | ✓ | ≤ | ✓ |
Ford 2019152 | Irritable bowel syndrome | NA | Critically low | 5 (307) | Adults | USA, New Zealand, Sweden | NA | Internet-based CBT, self-administered/minimal contact CBT | NA | NR | Short | ✗ | ✗ | ✗ | ✓ |
Hanlon 2018192 | Irritable bowel disorder/syndrome | NA | Moderate | 7 (770) | Adolescents, adults | Sweden, UK, USA, Australia | NA | Internet-based CBT | Stress management, drug | TAU, placebo | Short–long | ✓ | ✓ | ✓ | ✓ |
Li 2014279 | Irritable bowel syndrome | NA | Low | 4 (NR) | Adults | Australia, USA, the Netherlands, UK | Individual CBT (delivered by psychologists) | Internet-based CBT (delivered by nurses) | Relaxation, drug | TAU, WLC | Short | ✓ | ′ | ′ | ✓ |
Li 2018276 | Irritable bowel syndrome | NA | Low | 1 (199) | Adults | New Zealand | NA | Internet-based CBT | NA | TAU | Short | ✓ | ✗ | ≤ | ✓ |
Thakur 2018447 | Irritable bowel disorder | NA | Critically low | 1 (32) | Adults | Iran | Group CBT | NA | NA | WLC | Short | ✗ | ✓ | ≤ | ≤ |
Zijdenbos 2009523 | Irritable bowel syndrome | NA | Critically low | 4 (497) | Adults | NR | Group CBT, individual CBT | NA | NA | TAU, placebo, education | Short–long | ✓ | ✗ | ✗ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Chan 201294 | Diseases of the skin | NA | Critically low | 1 (16) | Adults | UK | Group CBT (delivered by psychologist) | NA | NA | TAU | Short | ✓ | ✗ | ✗ | ✗ |
Chida 2007100 | Atopic eczema | NA | Critically low | 1 (55) | Adults | Germany | Individual CBT | NA | Dermatological education | NA | Long | ≤ | ✓ | ✓ | ✓ |
Lert 2010274 | Vitiligo | NA | Low | 1 (16) | Adults | UK | Group CBT | NA | NA | TAU | Short | ✓ | ✗ | ✗ | ✗ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Tao 2017441 | Menopausal hot flushes | Breast Cancer | Critically low | 2 (518) | Adults | UK, the Netherlands | Individual CBT | NA | Physical exercise | TAU, WLC | Short | ✗ | ✗ | ✗ | ✓ |
Tremblay 2008456 | Menopausal hot flushes | NA | Low | 1 (29) | Adults | NR | Group CBT | NA | NA | WLC | Short | ✓ | ✗ | ✗ | ✓ |
van Driel 2018470 | Menopause | Breast cancer | Low | 1 (173) | Adults | NR | Group CBT | NA | NA | WLC | Short | ✗ | ✗ | ✗ | ✓ |
Vélez Toral 2014474 | Menopause | NA | Critically low | 1 (140) | Adults | NR | Individual CBT | NA | Self-help CBT | WLC | Short | ✓ | ✓ | ≤ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Khera 2011248 | Male erectile dysfunction | NA | Critically low | 0 (0) | Adults | NA | NA | NA | NA | NA | NA | ≤ | ✗ | ✗ | ≤ |
Reviews falling under ICD-11 primary code 21 (Table 29) have been subdivided into those with mental conditions and those with physical conditions. The reviews are listed under each of their respective categories.
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Mental conditions | |||||||||||||||
Ali 201539 | Aggression | Intellectual disabilities | High | 1 (179) | Adults | UK | NA | Manualised group CBT anger management therapy (delivered by lay therapist) | NA | WLC, TAU | Short | ✓ | ✓ | ✓ | ✓ |
Smedslund 2007417 | Aggression | NA | Moderate | 0 (0) | Adults | NA | NA | NA | NA | NA | NA | ✗ | ≤ | ≤ | ≤ |
Chen 201895 | Fear of cancer | Cancer | Critically low | 1 (88) | NR | NR | Blended individual CBT + additional electronic consultations | NA | NR | NR | Short | ✓ | ✓ | ✓ | ✗ |
Liu 2018282 | Fear of falling | NA | Moderate | 5 (1103) | Older adults | NR | NA | Group or individual CBT (delivered by nurses) | Tai Chi | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Iyengar 2018223 | Suicidal behaviour | NA | Critically low | 1 (40) | Adolescents | NR | Integrated individual CBT and group CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Lai 2014263 | Suicidal behaviour | NA | Critically low | 2 (351) | Adults | NR | NA | Internet-based CBT | Information website | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Leavey 2017271 | Suicidal behaviour | NA | Low | 3 (551) | Adults | USA, the Netherlands, Australia | NA | Internet-based CBT | Information website | TAU | Short | ✗ | ✓ | ✗ | ✗ |
Scott 2016401 | Stress | Caregiver (dementia) | Moderate | 4 (505) | Adults | NR | NA | Technology-based CBT | NA | WLC | Short | ✓ | ✓ | ✓ | ✗ |
Physical conditions | |||||||||||||||
Abbott 201732 | Chronic pain | NA | High | 5 (369) | Children, adolescents | Germany, USA, Australia, the Netherlands | Individual CBT | CD-ROM CBT | Education, medical dietary advice | WLC | Short–long | ✓ | ✓ | ✓ | ✗ |
Anie 201547 | Chronic pain | Sickle cell disease | Moderate | 1 (53) | Adolescents | USA | Family home-based group CBT | NA | Disease education | NA | Long | ≤ | ≤ | ✗ | ✓ |
Bender 201160 | Chronic pain | NA | Moderate | 4 (299) | Children, adolescents, adults | USA, Germany, Canada | NA | Family internet-based CBT + online support, internet-based CBT + e-mail/telephone support | Internet psychoeducation with support | WLC | Short | ≤ | ✓ | ✓ | ✓ |
Bernardy 201363 | Chronic pain | NA | High | 13 (840) | Children, adolescents, adults | Europe, USA | Group CBT, individual CBT, mixed group CBT + individual CBT | NA | Exercise, FMS education and information | WLC, TAU, attention control | Short | ✓ | ✓ | ✗ | ✓ |
Bernardy 201964 | Chronic pain | NA | Low | 3 (212) | Adults | Spain, USA, Canada | NA | Guided or unguided internet-based CBT | High-intensity CBT | WLC, TAU | Short | ✓ | ✓ | ✗ | ✓ |
Birnie 201868 | Chronic pain | NA | Moderate | 1 (20) | Children, adolescents | Greece | NA | CBT (delivered by non-psychologists) | Hypnosis | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Burgstaller 201481 | Chronic pain | NA | Moderate | 4 (191) | Adults | USA, Norway, UK, the Netherlands | Individual CBT | NA | NA | TAU | Short–long | ✗ | ✓ | ✓ | ′ |
Caemmerer 201283 | Excessive weight gain | Schizophrenia and schizoaffective, bipolar, schizotypal, depression and personality disorders | Critically low | 1 (61) | Adults | NR | Individual CBT | NA | NR | NR | Short | ✗ | ✗ | ✗ | ✓ |
Cantor 201485 | Fatigue | Fatigue | Critically low | 1 (12) | Adults | NR | Individual CBT for social anxiety | NA | NA | WLC | NR | ✗ | ✗ | ✓ | ✓ |
Eccleston 2015134 | Chronic pain | NA | Moderate | 1 (54) | Adults | The Netherlands | Individual CBT | NA | NA | WLC | Short | ✓ | ✗ | ✓ | ✓ |
Farley 2012141 | Excessive weight gain | Smoking | Moderate | 1 (44) | Adults | USA | Weight gain individual CBT | NA | NA | TAU, standard cessation counselling + placebo | Long | ✗ | ✗ | ✗ | ✓ |
Fleming 2016149 | Chronic pain | NA | High | 1 (54) | Adults | China | NA | Self-help listening to 10 minutes of CBT | Brain wave music therapy | No intervention | Short | ≤ | ✗ | ✗ | ✓ |
Frank 2014157 | Chronic pain | NA | Critically low | 1 (701) | Adults | UK | NA | Group CBT + advice (delivered by physiotherapist) | Advice | NA | Long | ✓ | ✗ | ✗ | ✓ |
George 2008164 | Chronic pain | NA | Moderate | 1 (223) | Adults | NR | Individual CBT + physiotherapy | NA | Physiotherapy | WLC | NC | ✗ | ✗ | ✗ | ✓ |
Greenwood 2016176 | Chronic pain | NA | Moderate | 1 (130) | Adults | NR | Individual CBT + supervised exercise (TAU) | NA | NA | Supervised exercise (TAU) | Long | ✓ | ✗ | ✗ | ✓ |
Gupta 2018185 | Chronic pain | NA | Critically low | 1 (61) | Adults | NR | Group CBT using virtual reality | NA | NA | TAU (medication) | Short | ✓ | ✓ | ✗ | ✗ |
Hajihasani 2018187 | Chronic pain | NA | Low | 8 (404) | Adults | NR | Individual CBT + physical therapy | NA | Physical therapy | NA | NR | ✓ | ✓ | ✗ | ✓ |
Hall 2018188 | Chronic pain | NA | Moderate | 4 (1128) | Adults | UK | NA | Individual CBT, group CBT, mixed individual + group CBT (all physiotherapist led) | Spinal stability, physiotherapy, advice, advice + exercises | NA | Long | ✓ | ✗ | ✗ | ✓ |
Harris 2015194 | Chronic pain | NA | Low | 5 (305) | Adults, older adults | Germany, Australia, USA, Canada | Individual CBT + relaxation, group CBT + relaxation | NA | Relaxation, biofeedback, self-management CBT | WLC | Short–long | ✗ | ✗ | ✗ | ✓ |
Hjorth 2014210 | Excessive weight gain | Schizophrenia | Critically low | 1 (15) | Adults | NR | Group CBT | NA | NA | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Ho 2019211 | Chronic pain | NA | Moderate | 4 (457) | Adults | USA, UK, Canada | Individual CBT or group CBT for pain and/or insomnia | NA | Education, behavioural desensitisation (placebo) | Symptom monitoring, WLC | Short | ≤ | ✓ | ✓ | ✓ |
Iwasaki 2018222 | Chronic pain | NA | Critically low | 2 (256) | Adults | USA | Intensive individual CBT, brief individual CBT | N | NA | TAU | Long | ✗ | ✗ | ✗ | ✓ |
Jacob 2018225 | Excessive weight gain | NA | Low | 1 (18) | Adults | Portugal | Individual CBT | NA | NA | WLC | Short | ✗ | ′ | ✓ | ′ |
Kisely 2015251 | Chronic pain | NA | Moderate | 8 (422) | NR | NR | Group CBT, individual CBT | Brief CBT (delivered by nurses) | Paroxetine only | TAU, WLC, placebo, assessment | Short | ′ | ′ | ✓ | ✓ |
Larkin 2014265 | Fatigue | Prostate cancer | Critically low | 2 (85) | Adults | The Netherlands, Scotland | Individual CBT (delivered by therapists) | CBT (delivered by nurses) | Brief nursing intervention | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Liu 2012281 | Chronic pain | NA | Low | 2 (275) | Adults | NR | NR | NA | NA | TAU, attention control | Long | ✗ | ✓ | ✗ | ✓ |
Lonergan 2016285 | Chronic pain | NA | Critically low | 6 (501) | Children, adolescents | Australia, the Netherlands, Germany, USA | Family CBT | NA | Education, education + drug | TAU, WLC | Short–long | ✗ | ✗ | ✗ | ✓ |
Macea 2010129 | Chronic pain | NA | Critically low | 1 (51) | Adults | Sweden | NA | Internet-based CBT | NA | WLC | Short | ✗ | ✗ | ✗ | ✓ |
McMahon 2013302 | Chronic pain | NA | Moderate | 1 (29) | Adults | NR | Individual CBT | NA | Education | NA | Short | ✓ | ✓ | ✓ | ✓ |
Mehta 2018306 | Chronic pain | NA | Low | 22 (3014) | Adults | USA, Sweden, Australia, Spain, Germany, Canada, the Netherlands | NA | Internet-based CBT | High-intensity face-to-face CBT, positive psychology therapy, internet-based acceptance and commitment therapy | WLC, TAU, attention control, discussion groups, information | Short | ✗ | ✓ | ✓ | ✓ |
Monticone 2015317 | Chronic pain | NA | Moderate | 4 (226) | Adults | NR | Individual CBT (delivered by psychologist) | CBT ([delivered by health-care professional) | Physiotherapy or medication | WLC | Short | ✓ | ≤ | ≤ | ✓ |
Niknejad 2018330 | Chronic pain | NA | Critically low | 2 (370) | Older adults | NR | Group CBT or individual CBT for pain | NA | Education | Symptom monitoring | Short | ✗ | ′ | ′ | ✓ |
O’Keeffe 2016341 | Chronic pain | NA | Low | 1 (80) | Adults | NR | NR | NA | Neck exercises | NA | Long | ✗ | ✗ | ✗ | ✓ |
Palermo 2010354 | Chronic pain | NA | Low | 2 (68) | Children, adolescents | NR | NA | Internet-based CBT and CD-ROM CBT | NA | WLC | Short | ≤ | ✗ | ✗ | ✓ |
Raggi 2018374 | Chronic pain | NA | Critically low | 4 (391) | Children, adolescents, adults | NR | NR | NA | Education, education + drug | NA | Short | ≤ | ✓ | ✗ | ✓ |
Ramond-Roquin 2014375 | Chronic pain | NA | Moderate | 3 (348) | Adults | USA, Sweden | NR | NA | Education | TAU, NR | Long | ✓ | ✗ | ✗ | ✓ |
Randhawa 2016376 | Chronic pain | NA | Low | 1 (117) | Adults | USA | Individual CBT | NA | NA | TAU | Long | ≤ | ✓ | ≤ | ✓ |
Richmond 2015382 | Chronic pain | NA | Moderate | 14 (2706) | Adults | NR | Individual or group CBT (delivered by psychologists) | Individual CBT or goup CBT (delivered by physiotherapist or other health-care professionals) | NA | TAU, WLC | Long | ✓ | ✗ | ✗ | ✓ |
Sakamoto 2016392 | Chronic pain | NA | Moderate | 2 (127) | Adults | USA, UK | NR | NA | NA | No intervention | Short | ✓ | ✗ | ✓ | ′ |
Schofield 2006396 | Chronic pain | NA | Critically low | 1 (28) | Older adults | Canada | Individual CBT | NR | Attention support | NA | Short | ✗ | ✗ | ✗ | ✓ |
Shamliyan 2013404 | Chronic pain | NA | Low | 1 (158) | Adults | Germany | Individual CBT minimal contact programme | NA | NA | Brochures | NR | ≤ | ✓ | ✓ | ✓ |
Shearer 2016406 | Chronic pain | NA | Low | 1 (80) | Adults | Italy | NA | CBT (delivered by physiotherapist) | Multimodal physiotherapy | NA | Long | ✓ | ✗ | ✗ | ✓ |
Skelly 2018413 | Chronic pain | NA | Low | 9 (1708) | Adults | Spain, USA, UK, Finland, NR | Group CBT, individual CBT, mixed group + individual CBT | Group CBT, individual CBT, mixed group + individual CBT (delivered by health-care professionals) | Drug, exercise | TAU, attention control, active management | Short–long | ✓ | ✓ | ✓ | ✓ |
Sprenger 2011426 | Chronic pain | NA | Critically low | 5 (225) | Children, adolescents | NR | Individual CBT, family CBT | Internet-based CBT | NR | NR | Short | ✗ | ✗ | ✗ | ✓ |
Tang 2018440 | Chronic pain | NA | Low | 3 (404) | Children, adolescents | USA | NA | Internet-based CBT, family internet-based CBT | Internet-based education, specialised headache treatment programme | WLC | Short | ✗ | ✓ | ✓ | ✓ |
Veehof 2016473 | Chronic pain | NA | Low | 2 (190) | Adults | NR | Group CBT | NA | Acceptance and commitment therapy, mindfulness-based stress reduction | NA | Short | ≤ | ✓ | ≤ | ✓ |
Velleman 2010475 | Chronic pain | NA | Critically low | 4 (179) | Children, adolescents | NR | NA | Computerised CBT | Computerised education programme | WLC | Short | ✗ | ✗ | ✗ | ✓ |
Verhagen 2009480 | Chronic pain | NA | Moderate | 2 (68) | Adults | NR | Individual CBT | NA | Drug, relaxation | NA | Short | ✗ | ✓ | ✓ | ✓ |
Wendebourg 2017495 | Fatigue | Multiple sclerosis | Low | 3 (152) | Adults | UK, New Zealand, USA | Face-to-face individual CBT, face-to-face individual CBT + telephone contact | Internet-based CBT + telephone contact | Group intervention (not CBT), relaxation | No intervention | Short | ′ | ′ | ✗ | ✓ |
Xu 2017508 | Fatigue | Traumatic brain injury | Low | 1 (12) | Adults | Australia | Individual CBT | NA | NA | WLC | Short | ✗ | ✗ | ✗ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Al Sayegh 201038 | Injuries to the head | Head injury | Low | 1 (16) | Adults | NR | Individual CBT adapted to account for difficulties with attention, concentration, fatigue and memory, single session individual CBT + manual | NA | NA | WLC, TAU | Short | ≤ | ✓ | ✓ | ✓ |
Gómara-Toldrà 2014172 | Spinal cord injury | NA | Low | 1 (61) | Adults | The Netherlands | Multidisciplinary individual CBT for coping with neuropathic pain | NA | NA | WLC | Short | ✓ | ✗ | ✗ | ✓ |
Sullivan 2018437 | Intracranial injury | NA | Low | 1 (58) | Adults | USA | Single session individual CBT with therapist | NA | NA | TAU | Short | ✗ | ✗ | ✗ | ✓ |
Thomas 2017449 | Intracranial injury | Depression | Moderate | 1 (77) | Adults | USA | Individual CBT | NA | Supportive psychotherapy | NA | Short | ✓ | ′ | ′ | ✗ |
Reviews falling under primary ICD-11 code 24 (Table 31) have been subdivided into those with mental conditions and those with physical conditions. The reviews are listed under each of their respective categories.
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Mental conditions | |||||||||||||||
McDaid 2008300 | Bereavement | NA | Moderate | 1 (134) | Adolescents, adults | The Netherlands | Family CBT | NA | NA | TAU | Long | ✗ | ✓ | ✗ | ✗ |
Physical conditions | |||||||||||||||
Moraes 2018319 | Care involving peritoneal dialysis | NA | Critically low | 1 (24) | NR | NR | Individual CBT | NA | NR | NR | Short | ✗ | ≤ | ≤ | ✓ |
ICD-11 primary/secondary | Condition description | Study | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | ||||||||
|
|
Andersson 201445 | NA | Low | 11 (934) | Adults | Australia, the Netherlands, Spain, Sweden, Switzerland, USA | NA | Internet-based CBT | High-intensity CBT | NA | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Barrett 201658 | Substance abuse | Critically low | 1 (66) | Adults | USA | Integrated individual CBT for substance abuse disorder, depression and pain | NA | Twelve-step facilitation | NA | Long | ✗ | ✓ | ✗ | ✗ |
|
|
Carlbring 201887 | NA | Low | 16 (914) | Adults | Australia, the Netherlands, Spain, Sweden, Germany, USA | NA | Internet-based CBT | High-intensity CBT | NA | Short | ✗ | ′ | ✓ | ✓ |
|
|
Farrand 2013142 | NA | Low | 35 (2977) | Adults | NR | NA | Guided self-help CBT, minimal contact CBT, self-administered CBT | NA | WLC TAU Attention control | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Kolubinski 2018256 | Psychosis, bipolar, cognitive deficit, brain injury, learning disability, autism | Critically low | 2 (562) | Adults | UK | Group CBT | NA | NA | WLC | Short | ✗ | ✓ | ✗ | ✗ |
|
|
Osborn 2006348 | Cancer survivors | Critically low | 1 (34) | Adults | NR | Individual CBT | NA | NR | NR | Short | ✗ | ✓ | ✓ | ✓ |
|
|
Ruiz 2012389 | NA | Critically low | 3 (258) | Adults | NR | Group CBT, individual CBT | NA | Acceptance and commitment therapy | NA | Short–long | ✓ | ✓ | ✓ | ✓ |
|
|
Yoshinaga 2015515 | NA | Critically low | 2 (68) | NR | NR | Group CBT, individual CBT | NA | Group occupational therapy | TAU | Short | ✓ | ✓ | ✓ | ✓ |
Study | Condition description | Comorbid/specific symptoms | AMSTAR-2 quality rating | Number of RCTs (number of participants) | Age | Country of RCTs | CBT intervention group | Comparator group | Outcome | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
High intensity (description) | Low intensity (description) | Active (description) | Non-active (description) | Follow-up time | HRQoL | Depression | Anxiety | Condition specific | |||||||
Bernard 201862 | COPD, heart failure, cancer, chronic pain | NA | Critically low | 8 (NR) | Adults | Brazil, the Netherlands, Pakistan, USA, international | CBT + exercise therapy (some group) | NA | Exercise therapy | NA | Short | ✗ | ✓ | ✓ | ✓ |
van Beugen 2014467 | Tinnitus, diabetes, chronic pain, cancer, headache, epilepsy, fatigue, functional gastrointestinal | NA | Low | 19 (3974) | Adults | NR | NA | Internet-based CBT | NA | TAU, WLC | Short | ✓ | ✓ | ✓ | ✓ |
Appendix 8 Gap maps of included systematic reviews grouped according to the condition each targeted, as per the ICD-11
Secondary ICD-11 (number of reviews, RCTs, participants) | Who: severity | What: intensity | When: delivered | Where: participants recruited | Follow-up | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Subclinical | Clinical | Chronic | Severe | Not reported | High | Low | Not reported | Preventative | Standard | Relapse prevention | Not reported | Community | GP primary | Outpatients | Inpatients | School/university | Institution | Not reported | Short | Long | Not reported | |
6B00-06: Anxiety or fear-related disorders [agoraphobia with panic disorder, GAD, panic, phobia, SAD, selective mutism, mixed anxiety disorders (GAD, panic, phobia, SAD, separation, selective mutism)], n = 50 reviews (346 RCTs; 24,078 participants) | 0 | 30 | 1 | 1 | 20 | 42 | 10 | 1 | 2 | 48 | 0 | 0 | 5 | 2 | 8 | 4 | 6 | 0 | 35 | 41 | 10 | 1 |
6C40-51: Disorders due to substance use or addictive behaviours (gambling, gaming, hallucinogens, stimulants, substance use), n = 6 reviews (7 RCTs; 476 participants) | 0 | 1 | 0 | 0 | 5 | 3 | 2 | 1 | 0 | 6 | 0 | 0 | 2 | 0 | 2 | 0 | 0 | 0 | 2 | 3 | 2 | 1 |
6C20-21: Disorders of bodily distress or bodily experience (somatoform/MUS], n = 2 reviews (5 RCTs; 554 participants) | 0 | 1 | 0 | 0 | 1 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | 1 | 1 | 1 | 0 | 0 | 0 | 1 | 2 | 1 | 0 |
6B40-45: Disorders specifically associated with stress (acute stress disorders, adjustment disorders, post-traumatic stress disorder), n = 39 reviews (89 RCTs; 6110 participants) | 4 | 17 | 0 | 1 | 18 | 37 | 3 | 0 | 3 | 36 | 0 | 0 | 11 | 2 | 6 | 1 | 6 | 1 | 22 | 35 | 7 | 0 |
6B80-85: Feeding or eating disorders [AN, BED, BN, mixed (AN, BN, BED, EDNOS)], n = 25 reviews (87 RCTs; 7132 participants) | 2 | 13 | 1 | 1 | 10 | 20 | 8 | 0 | 1 | 23 | 1 | 0 | 8 | 3 | 8 | 1 | 1 | 0 | 13 | 17 | 10 | 0 |
6B80-85: Mental disorders associated with pregnancy, childbirth or the puerperium (during IVF, antenatal depression, perinatal anxiety and depression, postnatal depression), n = 19 reviews (39 RCTs; 4737 participants) | 0 | 7 | 0 | 0 | 12 | 15 | 6 | 1 | 3 | 16 | 0 | 0 | 4 | 0 | 0 | 2 | 0 | 0 | 13 | 18 | 1 | 1 |
6A60-80: Mood disorders (bipolar or related disorder, depressive disorders, premenstrual dysphoric disorder, subthreshold depression, treatment-resistant depression), n = 92 reviews (272 RCTs; 42,676 participants) | 9 | 43 | 4 | 3 | 39 | 76 | 29 | 2 | 8 | 84 | 4 | 0 | 14 | 11 | 19 | 6 | 7 | 2 | 48 | 72 | 26 | 1 |
6D70-72: Neurocognitive disorders, n = 1 review (1 RCT; 41 participants) | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 |
6A00-06: Neurodevelopmental disorders (attention deficit hyperactive disorder), n = 5 reviews (13 RCTs; 746 participants) | 0 | 3 | 0 | 0 | 2 | 5 | 1 | 0 | 0 | 5 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 4 | 5 | 0 | 0 |
6B20-25: Obsessive–compulsive or related disorders (body dysmorphic disorder, hypochondriasis, OCD), n = 16 reviews (54 RCTs; 3117 participants) | 0 | 9 | 0 | 1 | 7 | 13 | 5 | 0 | 0 | 16 | 0 | 0 | 1 | 4 | 2 | 0 | 1 | 0 | 12 | 16 | 3 | 0 |
6D10-11: Personality disorders and related traits, n = 4 reviews (7 RCTs; 603 participants) | 0 | 2 | 0 | 0 | 2 | 4 | 0 | 0 | 0 | 4 | 0 | 0 | 0 | 0 | 3 | 0 | 0 | 0 | 1 | 3 | 1 | 0 |
6A20-25: Schizophrenia or other primary psychotic disorders (attenuated psychosis syndrome, delusional disorder, early-onset psychosis, psychosis), n = 31 reviews (135 RCTs; 14,924 participants) | 0 | 14 | 0 | 1 | 16 | 31 | 0 | 0 | 6 | 24 | 1 | 0 | 3 | 1 | 10 | 8 | 0 | 0 | 17 | 20 | 14 | 0 |
Mixed mental (anxiety, addictive, bodily distress, depression, eating disorder, obsessive, stress), n = 60 reviews (447 RCTs; 57,213 participants) | 1 | 31 | 1 | 1 | 28 | 40 | 26 | 1 | 2 | 58 | 0 | 0 | 16 | 8 | 18 | 3 | 11 | 0 | 26 | 53 | 13 | 1 |
Primary and secondary ICD-11 (number of reviews, RCTs, participants) | Who: severity | What: intensity | When: delivered | Where: participants recruited | Follow-up | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Subclinical | Clinical | Chronic | Severe | Not reported | High | Low | Not reported | Preventative | Standard | Relapse prevention | Not reported | Community | GP primary | Outpatients | Inpatients | School/university | Institution | Not reported | Short | Long | Not reported | |
21. Symptoms, signs or clinical findings, not elsewhere classified: mental, behavioural symptoms (aggression, caregivers stress, fear of cancer, fear of falling, suicidal behaviour), n = 8 reviews (17 RCTs; 2817 participants) | 0 | 2 | 0 | 1 | 6 | 2 | 5 | 1 | 1 | 7 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 6 | 6 | 1 | 1 |
24. Factors influencing health: associated with absence, loss or death of others (bereavement through suicide), n = 1 review (1 RCT; 134 participants) | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 |
Primary ICD-11 (number of reviews, RCTs, participants) | Who: severity | What: intensity | When: delivered | Where: participants recruited | Follow-up | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Subclinical | Clinical | Chronic | Severe | Not reported | High | Low | Not reported | Preventative | Standard | Relapse prevention | Not reported | Community | GP primary | Outpatients | Inpatients | School/university | Institution | Not reported | Short | Long | Not reported | |
01 Certain infectious or parasitic diseases (HIV/AIDS), n = 1 review (1 RCT; 46 participants) | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 |
02 Neoplasms (chemotherapy, malignant breast), n = 8 reviews (21 RCTs; 3204 participants) | 0 | 6 | 0 | 0 | 2 | 8 | 0 | 0 | 0 | 8 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 7 | 6 | 4 | 0 |
05 Endocrine, nutritional or metabolic diseases (diabetes mellitus, diabetic neuropathy), n = 3 reviews (8 RCTs; 1061 participants) | 0 | 1 | 0 | 0 | 2 | 3 | 1 | 0 | 0 | 3 | 0 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 1 | 2 | 2 | 0 |
07 Sleep–wake disorders (insomnia disorders), n = 22 reviews (125 RCTs; 14,315 participants) | 0 | 8 | 2 | 0 | 12 | 15 | 10 | 0 | 0 | 22 | 0 | 0 | 6 | 1 | 2 | 0 | 1 | 0 | 15 | 19 | 6 | 0 |
08 Diseases of the nervous system (epilepsy or seizure, neuromuscular disorders, non-epileptic seizures, Parkinson’s disease, post-viral fatigue syndrome), n = 14 reviews (54 RCTs; 5883 participants) | 0 | 5 | 0 | 0 | 9 | 14 | 1 | 0 | 0 | 14 | 0 | 0 | 1 | 1 | 4 | 2 | 0 | 0 | 8 | 10 | 5 | 0 |
10 Diseases of the ear or mastoid process (hyperacusis, tinnitus), n = 3 reviews (9 RCTs; 534 participants) | 0 | 0 | 0 | 0 | 3 | 2 | 2 | 0 | 0 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 3 | 3 | 1 | 0 |
12 Diseases of the respiratory system (asthma), n = 2 reviews (7 RCTs; 174 participants] | 0 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 2 | 0 | 0 |
13 Diseases of the digestive system (dentofacial parafunctional disorders, irritable bowel disorder/syndrome, oral mucositis), n = 9 reviews (27 RCTs; 2079 participants) | 0 | 2 | 0 | 0 | 7 | 4 | 6 | 0 | 0 | 9 | 0 | 0 | 1 | 2 | 4 | 0 | 0 | 0 | 5 | 9 | 2 | 0 |
14 Diseases of the skin (atopic eczema, vitiligo), n = 3 reviews (3 RCTs; 87 participants) | 0 | 1 | 0 | 0 | 2 | 3 | 0 | 0 | 0 | 3 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | 1 | 0 |
16 Diseases of the genitourinary system (menopausal hot flushes, menopause), n = 4 reviews (5 RCTs; 860 participants) | 0 | 0 | 0 | 0 | 4 | 4 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 | 4 | 0 | 0 |
17 Conditions related to sexual health (male erectile dysfunction), n = 1 review (0 RCTs; 0 participants) | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 1 |
21 General symptoms, signs or clinical findings: fatigue, n = 4 reviews (7 RCTs; 261 participants) | 0 | 0 | 0 | 0 | 4 | 4 | 2 | 0 | 0 | 4 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 3 | 4 | 0 | 0 |
21 General symptoms, signs or clinical findings: pain (back pain, chronic non-cancer pain, chronic pain, headaches and migraines, fibromyalgia, leukaemia, lumbar fusion surgery, neck pain, non-specific chest pain, spinal pain and injury, OA, orthodontic treatment, RA, RAP, sickle cell disease pain, tempro mandibular disorder), n = 42 reviews (156 reviews; 17,105 participants) | 0 | 11 | 9 | 0 | 22 | 30 | 18 | 0 | 2 | 39 | 1 | 0 | 10 | 4 | 15 | 3 | 3 | 1 | 22 | 31 | 16 | 0 |
21 General symptoms, signs or clinical findings: weight gain, n = 4 reviews (4 RCTs; 138 participants) | 0 | 2 | 0 | 0 | 2 | 4 | 0 | 0 | 0 | 4 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 3 | 3 | 1 | 0 |
22 Injury, poisoning or certain other consequences of external causes (intracranial injury, spinal cord injury), n = 4 reviews (4 RCTs; 212 participants) | 0 | 2 | 0 | 1 | 1 | 4 | 0 | 0 | 1 | 3 | 0 | 0 | 1 | 0 | 2 | 3 | 0 | 0 | 1 | 4 | 0 | 0 |
24 Factors influencing health status (peritoneal dialysis), n = 1 review (1 RCT; 24 participants) | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 | 0 |
Mixed physical conditions (COPD, cancer, chronic pain, diabetes, epilepsy, headache, heart failure, fatigue, functional gastrointestinal, tinnitus), n = 2 reviews (27 RCTs; 3974 participants) | 0 | 0 | 1 | 0 | 1 | 1 | 1 | 0 | 0 | 2 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | 0 | 0 |
Primary physical/secondary mental ICD-11 category (number of reviews, RCTs, participants) | Who: severity | What: intensity | When: delivered | Where: participants recruited | Follow-up | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Subclinical | Clinical | Chronic | Severe | Not reported | High | Low | Not reported | Preventative | Standard | Relapse prevention | Not reported | Community | GP primary | Outpatients | Inpatients | School/university | Institution | Not reported | Short | Long | Not reported | |
Physical: brain injury, conditions related to sexual health, chronic pain, diseases of the ear or mastoid process, sleep–wake disorders; mental: anxiety, autism, bipolar, bodily distress, depression, eating disorders, learning disability, psychosis, stress disorders, n = 8 (71 RCTs; 5813 participants) | 0 | 2 | 0 | 0 | 6 | 5 | 3 | 0 | 0 | 8 | 0 | 0 | 3 | 0 | 4 | 1 | 0 | 0 | 3 | 7 | 2 | 0 |
Appendix 9 Health-related quality of life
Sensitivity analysis: review quality
The sensitivity analysis was conducted with an additional 10 reviews that had been rated as being of low or critically low quality on the AMSTAR-2. Therefore, the sensitivity analysis was conducted with 34 reviews (76 RCTs, 7466 participants). 32,39,63,82,165,188,193,219,220,231,235,236,270,275,276,279,286,299,317,329,343,347,356,371,409,413,445,446,464,467,469,513,518,521 Inclusion of lower-quality reviews increased the estimate of effect (SMD 0.28, 95% CI 0.17 to 0.38) and produced higher levels of heterogeneity (I2 = 71%) (Figure 15).
Sensitivity analysis: prioritisation of mental subscales
We re-ran the PMA, replacing the physical component scores with the mental component scores from the SF-12/SF-36 in the two reviews that presented both the physical and mental component scores. 220,464 The replacement did not change the overall effect or heterogeneity rating for the HRQoL outcome (SMD 0.24, 95% CI 0.14 to 0.33; I2 = 38%) (Figure 16).
Synthesis of reviews reporting change scores
Data were presented as change scores for the HRQoL outcome in four reviews (four RCTs, 185 participants). 158,246,406,523 Each review represented a different condition: digestive system diseases (irritable bowel syndrome), mixed mental problems (anxiety and depression), pain (neck and whiplash) and respiratory system diseases (asthma). Pooled results showed a moderate effect in favour of CBT (SMD 0.58, 95% CI 0.15 to 1.00; I2 = 66%) (Figure 17).
Appendix 10 Depression
Primary analysis
Within-condition heterogeneity varied between 0% (6D10-11: Personality disorders) and 86.3% (6A60-80: Mood disorders) and across-condition heterogeneity was 81%. The across-condition heterogeneity was too high for us to pool across the ICD-11 category subgroups (Figure 19).
Publication bias
No publication bias was detected using funnel plots (Figure 20) and Egger’s test showed no small-study effects (p = 0.87).
Appendix 11 Anxiety
Publication bias
There was no evidence of publication bias, nor of small-study effects (Egger’s test p = 0.70) (Figure 21).
Subgroup analysis
Cognitive–behavioural therapy intensity
The pooling of 28 meta-analyses collected from reviews of high-intensity CBT (face to face with a highly trained CBT therapist) found a modest effect in favour of CBT (SMD 0.28, 95% CI 0.15 to 0.42; I2 = 54.3%) (Figure 22).
We identified five reviews87,306,343,360,521 (11 RCTs, 503 participants) that directly compared high- with low-intensity CBT interventions on anxiety outcomes in 6B00-06: Anxiety, 6A60-80: Mood and pain [tinnitus 21 Symptoms and signs not otherwise specified (MG30 pain)] conditions. In this subset of direct comparisons, there was no difference between high- and low-intensity CBT (SMD 0.03, 95% CI –0.14 to 0.21; I2 = 20%) (Figure 23).
Type of comparators
The pooling of 14 meta-analyses collected from reviews of CBT compared with an active comparator (i.e. another type of therapy) found a non-significant effect of CBT (SMD 0.19, 95% CI –0.00 to 0.37; I2 = 48.6%). The pooling of 20 meta-analyses collected from reviews of CBT compared with a non-active comparator (e.g. WLC) found a modest effect in favour of CBT (SMD 0.37, 95% CI 0.19 to 0.55; I2 = 64.3%) (Figure 24).
Duration of follow-up
The pooling of 10 meta-analyses collected from reviews that collected long-term follow-up data (> 12 months post intervention) found a modest effect of CBT (SMD 0.38, 95% CI 0.15 to 0.60; I2 = 65.9%). The pooling of 26 meta-analyses collected from reviews that collected only short-term follow-up data (< 12 months) found a similar effect in favour of CBT (SMD 0.27, 95% CI 0.12 to 0.43; I2 = 59.4%) (Figure 25).
Age
The pooling of seven meta-analyses collected from child and adolescent populations (aged < 18 years) found an effect in favour of CBT (SMD 0.37, 95% CI 0.12 to 0.62; I2 = 67%). The pooling of 26 meta-analyses collected from adult populations (aged 18–65 years) found a significant effect in favour of CBT (SMD 0.32, 95% CI 0.15 to 0.48; I2 = 64%). The pooling of two meta-analyses collected from older adult populations (aged > 65 years) found a non-significant effect of CBT on anxiety outcomes (SMD 0.06, 95% CI –0.30 to 0.43; I2 = 0%) (Figure 26).
Sensitivity analysis
As the heterogeneity across the conditions’ subgroups was too large, we did not pool effects across conditions (Figure 27).
Synthesis of reviews reporting change scores
Four lower-quality reviews (four RCTs, 255 participants) reported anxiety outcome data as change scores. 56,105,336,457 These included reviews of 6B00-06: Anxiety, 6A60-80: Mood and 08 Diseases of the nervous system. The heterogeneity was too high (I2 = 88%) to pool across reviews (Figure 28).
Synthesis of reviews reporting dichotomous outcomes
The lower-quality review of Noble et al. 332 (one RCT, 27 participants), classified under mixed mental conditions (anxiety and depression), reported anxiety data as risk differences and showed an effect in favour of CBT (SMD 0.36, 95% CI 0.01 to 0.71). The lower-quality review of Stoll et al. 433 (one RCT, 112 participants), targeting anxiety disorders, presented anxiety outcome data as ORs and reported an effect in favour of CBT (SMD 1.01, 95% CI 0.96 to 1.06) (Figure 29).
Appendix 12 Pain
Publication bias
No publication bias was detected using funnel plots (Figure 30), and Egger’s test showed no small-study effects (p = 0.19).
Subgroup analysis
Cognitive–behavioural therapy intensity
The SMD generated across the high-intensity reviews was in favour of CBT (SMD 0.19, 95% CI 0.01 to 0.37; I2 = 18%) (Figure 31).
Type of comparators
We found an effect in favour of CBT across reviews in the non-active comparator group (SMD 0.59, 95% CI 0.07 to 1.11; I2 = 69%), but the effect was much smaller across reviews in the active comparator subgroup (SMD 0.14, 95% CI –0.11 to 0.38; I2 = 73%) (Figure 32).
Duration of follow-up
Both subgroups produced effects in favour of CBT. The effect was larger in the short-term follow-up group (SMD 0.32, 95% CI 0.04 to 0.59; I2 = 71%) than in the long-term follow-up group (SMD 0.19, 95% CI 0.08 to 0.31; I2 = 0%) (Figure 33).
Age
The standardised mean effect across the reviews conducted in adults was in favour of CBT (SMD 0.21, 95% CI 0.12 to 0.31; I2 = 0%) (Figure 34).
Sensitivity analysis
The across-condition pooled effect was in favour of CBT (SMD 0.21, 95% CI 0.11 to 0.31; I2 = 51%) for reducing pain intensity (Figure 35).
Synthesis of reviews reporting dichotomous outcomes
The review of Bernardy et al. 64 (one RCT, 118 participants) reported pain outcome data as risk difference and showed a non-significant effect for CBT (SMD 0.08, 95% CI –0.03 to 0.19) (Figure 36a). One review, Palermo et al. 354 (two RCTs, 68 participants), presented pain outcome data as ORs. This review demonstrated a non-significant effect for CBT (SMD 7.99, 95% CI –2.72 to 18.70) (Figure 36b).
List of abbreviations
- ADHD
- attention deficit hyperactivity disorder
- AMSTAR
- A MeaSurement Tool to Assess systematic Reviews
- BAI
- Beck Anxiety Inventory
- CBT
- cognitive–behavioural therapy
- CI
- confidence interval
- CINAHL
- Cumulative Index to Nursing and Allied Health Literature
- COPD
- chronic obstructive pulmonary disease
- CRD
- Centre for Reviews and Dissemination
- DARE
- Database of Abstracts of Reviews of Effects
- ECG
- expert consultation group
- HRQoL
- health-related quality of life
- HTA
- Health Technology Assessment
- ICD-11
- International Classification of Diseases, Eleventh Revision
- NDORMS
- Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences
- NIHR
- National Institute for Health Research
- OR
- odds ratio
- PMA
- panoramic meta-analysis
- PPI
- patient and public involvement
- PRISMA
- Preferred Reporting Items for Systematic Reviews and Meta-Analyses
- RCT
- randomised controlled trial
- RR
- risk ratio
- SF-12
- Short Form questionnaire-12 items
- SF-36
- Short Form questionnaire-36 items
- SIGN
- Scottish Intercollegiate Guidelines Network
- SMD
- standardised mean difference
- TAU
- treatment as usual
- VAS
- visual analogue scale
- WHO
- World Health Organization
- WLC
- wait-list control