Psilocybin-assisted psychotherapy for treatment resistant depression: A randomized clinical trial evaluating repeated doses of psilocybin

灵霉素 难治性抑郁症 随机对照试验 心理治疗师 萧条(经济学) 致幻剂 心理学 医学 抑郁症状 精神科 临床心理学 重性抑郁障碍 内科学 认知 经济 宏观经济学
作者
Joshua D. Rosenblat,Shakila Meshkat,Zoe Doyle,Erica Kaczmarek,Ryan M. Brudner,Kevin Kratiuk,Rodrigo B. Mansur,Christian Schulz,Rickinder Sethi,A. Abate,Shaun Ali,Jordan Bawks,Marc G. Blainey,Elisa Brietzke,Victoria Cronin,Jessica Danilewitz,Shalini Dhawan,Anthony Di Fonzo,M. Di Fonzo,Pawel Drzadzewski,William Dunlop,Hajnalka Fiszter,Fabiano A. Gomes,Smrita Grewal,Marisa Leon-Carlyle,Marilyn McCallum,Niki Mofidi,Hilary Offman,Jeremy Riva-Cambrin,Joel E. Schmidt,Mark E. Smolkin,Joan M. Quinn,Andrea Zumrova,Michelle Marlborough,Roger S. McIntyre
出处
期刊:Med [Elsevier BV]
卷期号:5 (3): 190-200.e5 被引量:6
标识
DOI:10.1016/j.medj.2024.01.005
摘要

Summary

Background

Psilocybin-assisted psychotherapy (PAP) has been associated with antidepressant effects. Trials to date have typically excluded participants with complex presentations. Our aim was to determine the feasibility of PAP in a complex population, including high levels of treatment resistance in major depressive and bipolar disorder and patients with baseline suicidality and significant comorbidity. We also evaluated flexible repeated doses over a 6-month period.

Methods

Adults with treatment-resistant depression as part of major depressive or bipolar II disorder without psychosis or a substance use disorder were eligible to participate. Subjects were randomized to immediate treatment or waitlist control, with all eventually receiving PAP. Participants had one, two, or three psilocybin sessions with a fixed dose of 25 mg. Each dose was accompanied by preparation and integration psychotherapy sessions. Acceptability, safety, tolerability, and efficacy were evaluated (this study was registered at ClinicalTrials.gov: NCT05029466).

Findings

Participants were randomized to immediate treatment (n = 16) or delayed treatment (n = 14). 29/30 were retained to the week-2 primary endpoint. Adverse events were transient, with no serious adverse events. Greater reductions in depression severity as measured by the Montgomery-Åsberg Depression Rating Scale (MADRS) were observed in the immediate treatment arm compared to the waitlist period arm with a large hedge's g effect size of 1.07 (p < 0.01). Repeated doses were associated with further reductions in MADRS scores compared to baseline.

Conclusions

PAP was feasible in complex patients with preliminary antidepressant efficacy and adequate safety and tolerability. Repeated doses were associated with greater reductions in depression severity.

Funding

This work was funded by Brain and Cognition Discovery Foundation (BCDF), Usona, and Braxia Scientific.
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