ArticlePLOS mental health2025
Standardized effect sizes are far from "Standardized": A primer and empirical illustration in depression psychotherapy meta-analyses.
Article in PLOS mental health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Long-term clinical and cost-effectiveness of a fully automated digital cognitive behavioural therapy for insomnia: 2-year follow-up of a single-blind, superiority, randomised controlled trial.The Lancet regional health. Europe · 2026Article
- Identifying what works in mental health apps through meta-regression analyses of 169 trials.NPJ digital medicine · 2026Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Standardized mean differences (SMDs) are frequently used to appraise the effects of psychological treatments, and to combine them in meta-analyses. Yet, there is no consensus on how exactly SMDs should be computed from randomized trials. In this study, we show that different SMD variants can heavily diverge in aggregate-data meta-analyses, subverting the original purpose of standardization. We investigate the impact this has on the estimated benefits of depression psychotherapies. Different SMD versions using endpoint or change scores were calculated from a comprehensive database of randomized trials, comparing depression psychotherapy against pharmacotherapy and inactive controls. Pooled treatment effects were obtained for each variant, assuming correlations between baseline and endpoint scores of 0.2 through 0.8, and their relationship was examined using bivariate meta-analyses. We also investigated which study characteristics predicted divergent effect estimates. A total of k = 443 trials with 48,221 participants were analyzed. The pooled effect of psychotherapy versus controls varied heavily depending on the calculation methods (SMD = 0.65-1.24), even though the same studies were used. Divergences were less pronounced for psychotherapies compared to pharmacotherapy (SMD = 0.05-0.14). Change score SMDs deviated from endpoint SMDs especially when high (r = 0.8) or low (r = 0.2) pre-post correlations were assumed. This difference was largest in subfields with high treatment effects. Different SMD calculation methods can lead to strongly diverging effect estimates of psychological treatment; especially when change scores are used and pre-post correlations are very high or low. This could have a profound impact on how treatment benefits are interpreted within and across meta-analyses. Researchers could prioritize endpoint SMDs of randomized trials, and should consider standardization using population-level estimates to improve the comparability of meta-analytic effects in the field. Open Material; Registration: htpps://doi.org/10.5281/zenodo.10694719; https://osf.io/yx5jg; https://osf.io/4j23t.
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.