Hofmann Stefan G, Carpenter Joseph K, Otto Michael W, Rosenfield David, Smits Jasper A J, Pollack Mark H
Department of Psychological and Brain Sciences, Boston University, 648 Beacon Street, 6th, Floor Boston, MA 02215, United States.
Department of Psychology, Southern Methodist Univeristy, Expressway Tower 1100N, Dallas, TX 75275, United States.
Contemp Clin Trials. 2015 Jul;43:223-30. doi: 10.1016/j.cct.2015.06.015. Epub 2015 Jun 23.
The use of D-cycloserine (DCS) as a cognitive enhancer to augment exposure-based cognitive-behavioral therapy (CBT) represents a promising new translational research direction with the goal to accelerate and optimize treatment response for anxiety disorders. Some studies suggest that DCS may not only augment extinction learning but could also facilitate fear memory reconsolidation. Therefore, the effect of DCS may depend on fear levels reported at the end of exposure sessions. This paper presents the rationale and design for a randomized controlled trial examining the relative efficacy of tailoring DCS administration based on exposure success (i.e. end fear levels) during a 5-session group CBT protocol for social anxiety disorder (n = 156). Specifically, tailored post-session DCS administration will be compared against untailored post-session DCS, untailored pre-session DCS, and pill placebo in terms of reduction in social anxiety symptoms and responder status. In addition, a subset of participants (n = 96) will undergo a fear extinction retention experiment prior to the clinical trial in which they will be randomly assigned to receive either DCS or placebo prior to extinguishing a conditioned fear. The results from this experimental paradigm will clarify the mechanism of the effects of DCS on exposure procedures. This study aims to serve as the first step toward developing an algorithm for the personalized use of DCS during CBT for social anxiety disorder, with the ultimate goal of optimizing treatment outcome for anxiety disorders.
使用D-环丝氨酸(DCS)作为认知增强剂来强化基于暴露的认知行为疗法(CBT),代表了一个有前景的新转化研究方向,其目标是加速并优化对焦虑症的治疗反应。一些研究表明,DCS不仅可能增强消退学习,还可能促进恐惧记忆的重新巩固。因此,DCS的效果可能取决于暴露疗程结束时报告的恐惧水平。本文介绍了一项随机对照试验的基本原理和设计,该试验在一项针对社交焦虑症的5节小组CBT方案(n = 156)中,检验根据暴露成功率(即最终恐惧水平)调整DCS给药的相对疗效。具体而言,将在社交焦虑症状减轻和反应者状态方面,将针对性的疗程后DCS给药与非针对性的疗程后DCS、非针对性的疗程前DCS以及药丸安慰剂进行比较。此外,一部分参与者(n = 96)将在临床试验前进行一次恐惧消退保持实验,在该实验中,他们将在消除条件性恐惧之前被随机分配接受DCS或安慰剂。这个实验范式的结果将阐明DCS对暴露程序影响的机制。本研究旨在作为朝着开发一种在社交焦虑症的CBT期间个性化使用DCS的算法迈出的第一步,最终目标是优化焦虑症的治疗结果。