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Psilocybin for depression: Considerations for clinical trial design

Kelley C. O’donnell, Sarah E. Mennenga, Michael P. Bogenschutz

Journal of Psychedelic Studies September 1, 2019 DOI: 10.1556/2054.2019.026 via OpenAlex

Summary

AI-generated from the abstract

Designing rigorous clinical trials of psilocybin for major depressive disorder requires careful attention to participant selection, placebo control, blinding, dosing, non-pharmacological support, outcome measures, and safety. Transparent methods and analysis maximize the chance of obtaining meaningful, reproducible results and help gain broader scientific acceptance for psychedelic research.

Study at a glance

Characteristics Review Peer reviewed
Topics Anxiety Depression Psilocybin
Keywords Blinding Clinical trial Protocol science
Citations 15
Key finding Careful and transparent study design and data analysis will maximize the likelihood of generating meaningful, reproducible results and identifying a treatment-specific effect for psilocybin in major depressive disorder.

Abstract

Background and aims Given the enormous global burden of depressive illness, there is an urgent need to develop novel and more effective treatments for major depressive disorder (MDD). Recent findings have suggested that psychedelic drugs may have a role in the treatment of depressive symptoms, and a number of groups are in the process of developing protocols to study this question systematically. Given the subjective quality of both the psychedelic experience and depressive symptomatology, great care must be taken when designing a protocol to study the clinical efficacy of psychedelic drugs. This study will discuss many factors to consider when designing a clinical trial of psilocybin for MDD. Methods We provide a thorough review of pertinent research into antidepressant clinical trial methodology and review practical considerations that are relevant to the study of psychedelic-assisted treatment for depression. Results We discuss participant selection (including diagnostic accuracy, exclusion criteria, characteristics of the depressive episode, and the use of concurrent medications), study interventions (including dosing regimens, placebo selection, non-pharmacological components of treatment, and the importance of blinding), trial duration, outcome measures, and safety considerations. Conclusions Careful and transparent study design and data analysis will maximize the likelihood of generating meaningful, reproducible results, and identifying a treatment-specific effect. Meeting the highest standards for contemporary trial design may also broaden the acceptance of psychedelic research in the scientific community at large.

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