Assessing the effects of methodological differences on outcomes in the use of psychedelics in the treatment of anxiety and depressive disorders: A systematic review and meta-analysis
This systematic review and meta-analysis of nine clinical trials found that psilocybin, ayahuasca and LSD produced large, rapid and sustained reductions in anxiety (Cohen’s d = 1.26) and depression (Cohen’s d = 1.38) with no serious adverse reactions reported. Methodological differences in agent type did not significantly affect outcomes, but trials using multiple dosing sessions showed significantly greater efficacy than single‑session protocols.
7 cited-by links indexed in Blossom
Authors
- Leger, R. F.
- Unterwald, E. M.
Published
Abstract
Background
Classical psychedelics are a group of drugs which act as agonists on the serotonin-2A (5-HT2A) receptor. Evidence suggests they may have a uniquely rapid and enduring positive effect on mood. However, marked heterogeneity between methodological designs in this emerging field remains a significant concern.
Aims
To determine how differences in the type of psychedelic agent used and the number of dosing sessions administered affect subjects’ depression and anxiety outcomes and adverse drug reactions (ADR).
Methods
This review collected and screened 1591 records from the MEDLINE and Web of Science databases for clinical trials reporting objective data on mood for subjects with a known anxiety or depression.
Results
After screening, nine clinical trials met inclusion criteria. Meta-analysis of these studies showed significant, large positive effect sizes for measures of anxiety (Cohen’s d = 1.26) and depression (Cohen’s d = 1.38) overall. These positive effects were also significant at acute (⩽1 week) and extended (>1 week) time points. No significant differences were observed between trials using different psychedelic agents (psilocybin, ayahuasca or lysergic acid diethylamide (LSD)), however, a significant difference was observed in favour of trials with multiple dosing sessions. No serious ADR were reported.
Conclusion
Psilocybin, ayahuasca and LSD all appear to be effective and relatively safe agents capable of producing rapid and sustained improvements in anxiety and depression. Moreover, the findings of the present analysis suggest that they may show a greater efficacy when given to patients over multiple sessions as compared to the more common single session used in many of the existing trials.
Research Summary of 'Assessing the effects of methodological differences on outcomes in the use of psychedelics in the treatment of anxiety and depressive disorders: A systematic review and meta-analysis'
βBlossom's Take
Multiple dosing sessions were linked to greater symptom improvement in psychedelic trials
SourcedHow did psychedelics perform in trials of anxiety and depression, and did design matter?
- 9 trials
- Clinical trials included
- d = 1.26
- Anxiety effect size
- d = 1.38
- Depression effect size
- No serious ADR
- Serious adverse drug reactions
Psychedelic agents compared in the review
Systematic review and meta-analysis of nine clinical trials. The figures are pooled effect sizes and reported safety findings from the paper’s own synthesis, not individual patient-level outcomes, and the review notes no significant agent differences but greater efficacy with multiple dosing sessions.
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Study Details
- Study Typemeta
- Populationhumans
- Characteristicsliterature review
- Journal
- Compounds
- Topics
- APA Citation
- Citation FormatsExport citation
Cited By (7)
Papers indexed in Blossom that reference this study.
Vizeli, P., Studerus, E., Holze, F. et al. · Translational Psychiatry (2024)
Jacobs, E., Murphy-Beiner, A., Rouiller, I. et al. · Neuroethics (2023)
Simonsson, O., Carhart-Harris, R., Davis, A. K. et al. · Psychiatry Research (2023)
Gold, N. D., Goldway, N., Gerlach-Houck, H. et al. · Biorxiv (2023)
Kopra, E., Ferris, J. A., Winstock, A. R. et al. · Journal of Psychopharmacology (2023)
Kopra, E., Cleare, A. J., Rucker, J. et al. · Journal of Affective Disorders (2022)
Aday, J. S., Heifets, B. D., Pratscher, S. D. et al. · Psychopharmacology (2021)
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