Social anxiety and MDMA-assisted therapy investigation: a novel clinical trial protocol

被引:5
作者
Lear, M. Kati [1 ]
Smith, Sarah M. [1 ]
Pilecki, Brian [1 ]
Stauffer, Chris S. [2 ]
Luoma, Jason B. [1 ]
机构
[1] Portland Psychotherapy Clin Res & Training Ctr, Portland, OR 97227 USA
[2] Oregon Hlth & Sci Univ, Dept Psychiat, Portland, OR USA
来源
FRONTIERS IN PSYCHIATRY | 2023年 / 14卷
关键词
MDMA; social anxiety disorder; psychedelic research; clinical trial protocol; psychedelic assisted therapy; EMOTION-FOCUSED THERAPY; HEART-RATE-VARIABILITY; 3,4-METHYLENEDIOXYMETHAMPHETAMINE MDMA; ATTENTIONAL BIAS; ECSTASY MDMA; TRUE SELF; DISORDER; AUTHENTICITY; COMPLEMENTARITY; AVOIDANCE;
D O I
10.3389/fpsyt.2023.1083354
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
BackgroundSocial anxiety disorder (SAD) is a serious and prevalent psychiatric condition that heavily impacts social functioning and quality of life. Though efficacious treatments exist for SAD, remission rates remain elevated and a significant portion of those affected do not access effective treatment, suggesting the need for additional evidence-based treatment options. This paper presents a protocol for an open-label pilot study of MDMA-assisted therapy (MDMA-AT) for social anxiety disorder. The study aims to assess preliminary treatment outcomes, feasibility and safety, and psychological and physiological processes of change in the treatment of SAD with MDMA-AT. A secondary aim includes the development of a treatment manual for MDMA-AT for SAD. MethodThe outlined protocol is a randomized, open-label delayed treatment study. We will recruit 20 participants who meet criteria with moderate-to-severe social anxiety disorder (SAD) of the generalized subtype. Participants will be randomly assigned to an immediate treatment (n = 10) or delayed treatment condition (n = 10). Those in the immediate treatment condition will proceed immediately to active MDMA-AT consisting of three preparation sessions, two medicine sessions in which they receive oral doses of MDMA, and six integration sessions over approximately a 16-week period. The delayed treatment condition will receive the same intervention after a 16-week delay. Our primary outcome is SAD symptom reduction as measured by the Liebowitz Social Anxiety Scale administered by blinded raters at post-treatment and 6 month follow up. Secondary outcomes include changes in functional impairment, feasibility and safety measures, and novel therapeutic processes of change including shame and shame-related coping, belongingness, self-concealment, and self-compassion at post-treatment. Exploratory outcomes are also discussed. DiscussionThe results of this pilot trial advance the field's understanding of the acceptability and potential effectiveness of MDMA-AT for social anxiety disorder and provide an overview of relevant therapeutic mechanisms unique to SAD. We hope findings from this protocol will inform the design of subsequent larger-scale randomized controlled trials (RCT) examining the efficacy of MDMA-AT for SAD.
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页数:15
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