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Dismantling, optimising, and personalising internet cognitive behavioural therapy for depression: a systematic review and component network meta-analysis using individual data

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LANCET PSYCHIATRY
卷 8, 期 6, 页码 500-511

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ELSEVIER SCI LTD
DOI: 10.1016/S2215-0366(21)00077-8

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资金

  1. Japan Society for the Promotion of Science [17K19808]
  2. National Institute for Health Research (NIHR) Oxford Cognitive Health Clinical Research Facility
  3. NIHR Oxford Health Biomedical Research Centre [BRC-1215-20005]
  4. National Institute on Drug Abuse (NIDA) [K23 DA045766]
  5. Canadian Institutes of Health Research [152917]
  6. National Institute of Mental Health [P50 MH119029, R01 MH111610]
  7. NIHR Oxford Cognitive Health Clinical Research Facility
  8. NIHR Research Professorship [RP-201708ST2-006]
  9. NIHR Oxford and Thames Valley Applied Research Collaboration
  10. Swiss National Science Foundation [180083]
  11. Netherlands Organisation for Health Research and Development [019.182SG.001]

向作者/读者索取更多资源

This study identified 76 RCTs, with findings suggesting that behavioral activation may be beneficial and that relaxation may be harmful for treating depression. Baseline severity emerged as the strongest prognostic factor for endpoint depression, and combining human and automated encouragement reduced dropouts from treatment. Bias risk was low for randomization and missing outcome data, uncertain for deviation from intended interventions, and high for outcome measurement.
Findings We identified 76 RCTs, including 48 trials contributing individual participant data (11 704 participants) and 28 trials with aggregate data (6474 participants). The participants' weighted mean age was 42.0 years and 12 406 (71%) of 17 521 reported were women. There was suggestive evidence that behavioural activation might be beneficial (iMD -1.83 [95% credible interval (CrI) -2.90 to -0.80]) and that relaxation might be harmful (1.20 [95% CrI 0.17 to 2.27]). Baseline severity emerged as the strongest prognostic factor for endpoint depression. Combining human and automated encouragement reduced dropouts from treatment (incremental odds ratio, 0.32 [95% CrI 0.13 to 0.93]). The risk of bias was low for the randomisation process, missing outcome data, or selection of reported results in most of the included studies, uncertain for deviation from intended interventions, and high for measurement of outcomes. There was moderate to high heterogeneity among the studies and their components. 511

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