Psilocybin with psychotherapeutic support for treatment-resistant depression: a pilot clinical trial.

IF 4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Therapeutic Advances in Psychopharmacology Pub Date : 2025-10-02 eCollection Date: 2025-01-01 DOI:10.1177/20451253251377187
Sally Meikle, Olivia Carter, Paul Liknaitzky, Lauren Johansen, Ravi Iyer, Nigel Strauss, Martin Williams, David Castle, Susan L Rossell
{"title":"Psilocybin with psychotherapeutic support for treatment-resistant depression: a pilot clinical trial.","authors":"Sally Meikle, Olivia Carter, Paul Liknaitzky, Lauren Johansen, Ravi Iyer, Nigel Strauss, Martin Williams, David Castle, Susan L Rossell","doi":"10.1177/20451253251377187","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Depressive disorders are a major global health challenge, with many individuals unresponsive to existing treatments. Novel psychedelic therapies show promise but require further research.</p><p><strong>Objectives: </strong>This study aimed to evaluate the feasibility, safety and effectiveness of psilocybin with psychotherapeutic support for treatment-resistant depression (TRD), investigate predictors of treatment outcomes and deepen understanding of individual variability in response.</p><p><strong>Design: </strong>Open-label, single-arm pilot trial with mixed-methods assessment.</p><p><strong>Methods: </strong>Treatment consisted of two 25 mg psilocybin sessions, alongside three preparatory and six integration sessions. Depression severity was assessed using the self-rated Quick Inventory of Depressive Symptomatology at 3 weeks (primary endpoint) and at 20 weeks post-dose 2 (long-term follow-up). Potential predictors of clinical outcomes were evaluated using questionnaires, and qualitative interviews were used to capture individual experiences.</p><p><strong>Results: </strong>At the aggregate level, a clinically meaningful reduction in depressive symptoms was observed at the primary endpoint (mean change = -7.14; <i>p</i> = 0.02; Hedges' g = -1.27; 95% CI [-2.40, -0.37]) and maintained long-term. Individual participant data revealed diverse response patterns. Two participants displayed a sustained treatment response, three relapsed, and two exhibited no substantial improvement. Exploratory analyses identified mindset prior to dosing, spiritual experiences and perceptual shifts during dosing as predictors of treatment trajectory, while treatment expectations were not a reliable predictor. Adverse events were largely consistent with previous studies, with no serious adverse events.</p><p><strong>Conclusion: </strong>Findings add to the growing evidence base for psilocybin therapy and provide direction for further research on individual variability in response to better tailor treatments and enhance efficacy.</p><p><strong>Trial registration: </strong>Australian New Zealand Clinical Trials Registry (ACTRN12621001097831).</p>","PeriodicalId":23127,"journal":{"name":"Therapeutic Advances in Psychopharmacology","volume":"15 ","pages":"20451253251377187"},"PeriodicalIF":4.0000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12491823/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Advances in Psychopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/20451253251377187","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Depressive disorders are a major global health challenge, with many individuals unresponsive to existing treatments. Novel psychedelic therapies show promise but require further research.

Objectives: This study aimed to evaluate the feasibility, safety and effectiveness of psilocybin with psychotherapeutic support for treatment-resistant depression (TRD), investigate predictors of treatment outcomes and deepen understanding of individual variability in response.

Design: Open-label, single-arm pilot trial with mixed-methods assessment.

Methods: Treatment consisted of two 25 mg psilocybin sessions, alongside three preparatory and six integration sessions. Depression severity was assessed using the self-rated Quick Inventory of Depressive Symptomatology at 3 weeks (primary endpoint) and at 20 weeks post-dose 2 (long-term follow-up). Potential predictors of clinical outcomes were evaluated using questionnaires, and qualitative interviews were used to capture individual experiences.

Results: At the aggregate level, a clinically meaningful reduction in depressive symptoms was observed at the primary endpoint (mean change = -7.14; p = 0.02; Hedges' g = -1.27; 95% CI [-2.40, -0.37]) and maintained long-term. Individual participant data revealed diverse response patterns. Two participants displayed a sustained treatment response, three relapsed, and two exhibited no substantial improvement. Exploratory analyses identified mindset prior to dosing, spiritual experiences and perceptual shifts during dosing as predictors of treatment trajectory, while treatment expectations were not a reliable predictor. Adverse events were largely consistent with previous studies, with no serious adverse events.

Conclusion: Findings add to the growing evidence base for psilocybin therapy and provide direction for further research on individual variability in response to better tailor treatments and enhance efficacy.

Trial registration: Australian New Zealand Clinical Trials Registry (ACTRN12621001097831).

Abstract Image

Abstract Image

Abstract Image

心理治疗支持裸盖菇素治疗难治性抑郁症:一项试点临床试验。
背景:抑郁症是一项重大的全球健康挑战,许多个体对现有治疗无反应。新的迷幻疗法显示出希望,但需要进一步的研究。目的:本研究旨在评价裸盖菇素联合心理治疗支持治疗难治性抑郁症(TRD)的可行性、安全性和有效性,探讨治疗结果的预测因素,加深对个体反应差异的理解。设计:开放标签,单臂试验,混合方法评估。方法:治疗包括2个25mg裸盖菇素疗程,3个预备疗程和6个整合疗程。在第2次给药后3周(主要终点)和20周(长期随访)使用自评抑郁症状快速量表评估抑郁严重程度。使用问卷评估临床结果的潜在预测因素,并使用定性访谈来捕捉个人经验。结果:在总体水平上,在主要终点观察到有临床意义的抑郁症状减轻(平均变化= -7.14;p = 0.02; Hedges' g = -1.27; 95% CI[-2.40, -0.37])并长期维持。个体参与者的数据显示了不同的反应模式。两名参与者表现出持续的治疗反应,三名复发,两名没有实质性的改善。探索性分析发现,给药前的心态、给药期间的精神体验和感知变化是治疗轨迹的预测因子,而治疗预期不是可靠的预测因子。不良事件与以往的研究基本一致,未发生严重的不良事件。结论:研究结果为裸盖菇素治疗提供了越来越多的证据基础,并为进一步研究裸盖菇素治疗的个体差异提供了方向,从而更好地定制治疗方案,提高疗效。试验注册:澳大利亚新西兰临床试验注册中心(ACTRN12621001097831)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.90
自引率
2.40%
发文量
35
审稿时长
10 weeks
期刊介绍: Therapeutic Advances in Psychopharmacology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of psychopharmacology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in psychopharmacology, providing a forum in print and online for publishing the highest quality articles in this area.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信