Hassman Research Institute, Marlton, NJ, USA.
Collaborative NeuroScience Research, Garden Grove, CA, USA.
Neuropsychopharmacology. 2021 Mar;46(4):844-850. doi: 10.1038/s41386-020-00911-5. Epub 2020 Nov 26.
The remarkably high and growing placebo response rates in clinical trials for CNS indications, such as depression and schizophrenia, constitute a major challenge for the drug development enterprise. Despite extensive literature on participant expectancies and other potent psychosocial factors that perpetuate placebo response, no empirically validated participant-focused strategies to mitigate this phenomenon have been available. This study evaluated the efficacy of the Placebo-Control Reminder Script (PCRS), a brief interactive procedure that educates participants about factors known to cause placebo response, which was administered prior to the primary outcome assessments to subjects with major depressive or psychotic disorders who had at least moderate depression. Participants were informed they would participate in a 2-week randomized clinical trial with a 50% chance of receiving either an experimental antidepressant medication or placebo. In actuality, all participants received placebo. Participants randomly assigned to receive the PCRS (n = 70) reported significantly smaller reductions (i.e., less placebo response) in depression than those who did not receive the PCRS (n = 67). The magnitude of this effect was medium (Cohen's d = 0.40) and was not significantly impacted by diagnostic status. The number of adverse events (i.e., nocebo effect) was also lower in the PCRS group, particularly in the first week of the study. These findings suggest that briefly educating participants about placebo response factors can help mitigate the large placebo response rates that are increasingly seen in failed CNS drug development programs.
临床试验中中枢神经系统(CNS)适应证(如抑郁症和精神分裂症)的安慰剂反应率显著升高且不断增长,这对药物开发企业构成了重大挑战。尽管有大量关于参与者期望和其他增强安慰剂反应的强大心理社会因素的文献,但没有经过验证的、以参与者为中心的策略来减轻这种现象。本研究评估了安慰剂对照提醒脚本(PCRS)的疗效,这是一种简短的互动程序,可教育参与者了解导致安慰剂反应的因素,该程序在主要结局评估之前用于有中度以上抑郁的重度抑郁或精神障碍患者。告知参与者他们将参加一项为期 2 周的随机临床试验,有 50%的机会接受实验性抗抑郁药物或安慰剂。实际上,所有参与者都接受了安慰剂。随机分配接受 PCRS 的参与者(n=70)报告的抑郁症状减轻幅度(即,安慰剂反应较小)明显小于未接受 PCRS 的参与者(n=67)。这种效果的幅度中等(Cohen's d=0.40),不受诊断状态的影响。PCRS 组的不良事件(即,反安慰剂效应)也较少,特别是在研究的第一周。这些发现表明,简要教育参与者了解安慰剂反应因素有助于减轻在 CNS 药物开发计划失败中越来越常见的高安慰剂反应率。