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Prognostic Risk Factors in Randomized Clinical Trials of Face-to-Face and Internet-Based Psychotherapy for
Mariia Merzhvynska1, Markus Wolf1, Tobias Krieger2
1Department of Psychology, University of Zurich, Zurich, Switzerland.
Randomized controlled trials (RCTs) for face-to-face therapy (FTF) include patients with poorer prognoses than those for internet-based therapy (IBT). This highlights the need for more representative samples in internet-based depression treatment research.
Area of Science:
- Psychiatry and Mental Health
- Clinical Psychology
- Health Services Research
Background:
- Adults with severe depressive symptoms, comorbidities, or socioeconomic disadvantages often have poorer prognoses.
- Excluding these patients from randomized controlled trials (RCTs) limits the generalizability of research findings.
- Understanding prognostic risk factors (PRFs) in different therapy modalities is crucial for evidence-based practice.
Purpose of the Study:
- To compare PRFs in patient samples of RCTs for face-to-face therapy (FTF) versus internet-based therapy (IBT) for depression.
- To assess the impact of PRFs on treatment effectiveness in different delivery formats.
- To inform future research and clinical guidelines for depression treatment.
Main Methods:
- Systematic review and meta-regression analysis of RCTs comparing FTF and IBT for depression (2000-2021).
- Searched PsycINFO, Cochrane CENTRAL, and meta-analysis reference lists.
- Utilized a prognostic risk index (PROG) to quantify PRFs in study samples.
Main Results:
- 105 RCTs with 18,363 patients were included; 48 examined FTF and 57 examined IBT.
- RCTs for FTF had significantly higher PROG scores (poorer prognosis) than RCTs for IBT (mean PROG FTF=3.55 vs IBT=2.27).
- No significant association was found between PROG and treatment effect size, though sensitivity analyses yielded mixed results.
Conclusions:
- Patient samples in FTF therapy RCTs exhibit poorer prognostic risk factors compared to those in IBT RCTs.
- This difference impacts the generalizability of current evidence on IBT for depression.
- Future research should prioritize clinically representative samples for IBT trials and improve PRF reporting.
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