Center for Alcohol and Addiction Studies, Brown University, Providence, RI, USA.
Department of Neuroscience, Brown University, Providence, RI, USA.
Psychopharmacology (Berl). 2024 Jun;241(6):1101-1110. doi: 10.1007/s00213-024-06598-6. Epub 2024 Apr 29.
Recent years have seen a resurgence in randomized, placebo controlled trials (RCTs) utilizing non-classical psychedelics (e.g. 3,4-methyl enedioxy methamphetamine [MDMA]), and classical psychedelics (e.g. psilocybin, lysergic acid diethylamide [LSD], and N,N-dimethyltryptamine [DMT/ayahuasca]) in conjunction with assisted therapy (AT) for psychiatric disorders. A notable methodological challenge in psychedelic AT, however, is the complexity of blinding procedures. The lack of efficacious blinding can introduce considerable response bias, reduce internal validity, and compromise participant retention. This systematic review examines design and blinding techniques in RCTs utilizing psychedelics and placebo for the treatment of psychiatric disorders. The aim of this work is to identify factors that may inform future RTC design for conducting psychedelics research. We conducted a systematic review of PubMed, MEDLINE, CINAHL, Cochrane Central Register of Controlled Trials (CENTRAL), Psycinfo, Embase, and Web of Science Core Collection to examine: (1) placebo selection, (2) study design, and (3) integrity of blinding measures. Sixteen publications were identified as meeting the criteria for a systematic review. Our findings suggest that traditional placebo administration is insufficient to control for expectancy confounds. Consequently, experimental methodology that limits personnel unblinding and the use of an active placebo are important considerations when designing prospective clinical studies involving psychedelics.
近年来,随机、安慰剂对照试验(RCTs)利用非经典迷幻剂(例如 3,4-亚甲二氧基甲基苯丙胺 [MDMA])和经典迷幻剂(例如裸盖菇素、麦角酸二乙酰胺 [LSD] 和 N,N-二甲基色胺 [DMT/ayahuasca])结合辅助治疗(AT)治疗精神疾病的数量有所增加。然而,迷幻 AT 中一个显著的方法学挑战是盲法程序的复杂性。缺乏有效的盲法可能会引入相当大的反应偏差,降低内部有效性,并损害参与者的保留率。本系统评价检查了使用迷幻药和安慰剂治疗精神疾病的 RCT 中的设计和盲法技术。这项工作的目的是确定可能为未来进行迷幻药研究的 RCT 设计提供信息的因素。我们对 PubMed、MEDLINE、CINAHL、Cochrane 中央对照试验注册中心(CENTRAL)、Psycinfo、Embase 和 Web of Science Core Collection 进行了系统评价,以检查:(1)安慰剂选择,(2)研究设计,和(3)盲法措施的完整性。确定了 16 篇符合系统评价标准的出版物。我们的研究结果表明,传统的安慰剂给药不足以控制预期混淆。因此,当设计涉及迷幻药的前瞻性临床研究时,限制人员揭盲和使用活性安慰剂的实验方法是重要的考虑因素。