Smits Jasper A J, Abramowitz Jonathan S, Anderson Rebecca A, Arch Joanna J, Badeja Daniel, Barzilay Snir, Belanger Amanda N, Borchert Thomas, Bryant Emma, Burger Alane S, Dixon Laura J, Dutcher Christina D, Fitzgerald Hayley E, Graham Bronwyn M, Haberkamp Anke, Hofmann Stefan G, Hoyer Jürgen, Huppert Jonathan D, Johnson David, Kabha Baraa Q, Kirk Alex, Margraf Jürgen, McEvoy Peter M, McSpadden Bryan, Newby Jill, Otto Michael W, Papini Santiago, Parsons E Marie, Pittig Andre, Pittig Roxana, Rief Winfried, Schaumburg Svenja, Timpano Kiara R, Waltemate Lena, Wannemüller Andre, Weise Cornelia
Department of Psychology, The University of Texas at Austin, USA.
Department of Psychology, The University of North Carolina at Chapel Hill, USA.
J Anxiety Disord. 2025 Jan;109:102962. doi: 10.1016/j.janxdis.2024.102962. Epub 2024 Dec 25.
This paper reports on the outcomes of a proof-of-principle study for the Exposure Therapy Consortium, a global network of researchers and clinicians who work to improve the effectiveness and uptake of exposure therapy. The study aimed to test the feasibility of the consortium's big-team science approach and test the hypothesis that adding post-exposure processing focused on enhancing threat reappraisal would enhance the efficacy of a one-session large-group interoceptive exposure therapy protocol for reducing anxiety sensitivity.
The study involved a multi-site cluster-randomized controlled trial comparing exposure with post-processing (ENHANCED), exposure without post-processing (STANDARD), and a stress management intervention (CONTROL) in students with elevated anxiety sensitivity. Feasibility was assessed using site performance metrics (e.g., timeline, sample size, missing data). Efficacy was assessed up to 1-month follow-up using the Anxiety Sensitivity Index-3.
Despite challenges posed by unforeseen global crises, a standardized protocol for screening, assessment, and treatment at 12 research sites across four continents was successfully implemented, resulting in a total sample size of 400 with minimal missing data. Challenges in recruitment and adherence to the projected timelines were encountered. Significant reductions in anxiety sensitivity were observed in all conditions. Contrary to hypotheses, group differences were only observed at post-treatment, when ENHANCED and CONTROL outperformed STANDARD but were not significantly different from each other.
This study demonstrates the feasibility of the Exposure Therapy Consortium. Findings raise questions regarding the efficacy of large group exposure interventions and underscore the importance of careful research site selection and an iterative approach to treatment development.
本文报告了暴露疗法联盟一项原理验证研究的结果。该联盟是一个由研究人员和临床医生组成的全球网络,致力于提高暴露疗法的有效性和接受度。该研究旨在测试联盟的大团队科学方法的可行性,并检验以下假设:增加专注于增强威胁重新评估的暴露后处理,将提高单节大组内感受性暴露疗法方案降低焦虑敏感性的疗效。
该研究涉及一项多中心整群随机对照试验,比较了在焦虑敏感性较高的学生中进行暴露后处理(增强组)、无暴露后处理(标准组)和压力管理干预(对照组)的效果。使用站点绩效指标(如时间线、样本量、缺失数据)评估可行性。使用焦虑敏感性指数-3在长达1个月的随访中评估疗效。
尽管遇到了不可预见的全球危机带来的挑战,但一项在四大洲12个研究地点进行筛查、评估和治疗的标准化方案得以成功实施,最终样本量为400,缺失数据极少。在招募和遵守预计时间线方面遇到了挑战。在所有条件下均观察到焦虑敏感性显著降低。与假设相反,仅在治疗后观察到组间差异,此时增强组和对照组的表现优于标准组,但彼此之间无显著差异。
本研究证明了暴露疗法联盟的可行性。研究结果引发了关于大组暴露干预疗效的问题,并强调了仔细选择研究地点和采用迭代方法进行治疗开发的重要性。