...
首页> 外文期刊>Biological psychiatry >Yohimbine enhancement of exposure therapy for social anxiety disorder: A randomized controlled trial
【24h】

Yohimbine enhancement of exposure therapy for social anxiety disorder: A randomized controlled trial

机译:育亨宾增强暴露疗法治疗社交焦虑症的随机对照试验

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background Preclinical and clinical trials suggest that yohimbine may augment extinction learning without significant side effects. However, previous clinical trials have only examined adults with specific phobias. Yohimbine has not yet been investigated in the augmentation of exposure therapy for other anxiety disorders. Methods Adults (n = 40) with a DSM-IV diagnosis of social anxiety disorder were randomized to placebo or yohimbine HCl (10.8 mg) 1 hour before each of four exposure sessions. Outcome measures were collected at baseline, each treatment session, posttreatment, and 1-month follow-up. Results Yohimbine was well tolerated. Yohimbine augmentation, relative to placebo augmentation, resulted in faster improvement and better outcomes on self-report measures of social anxiety disorder severity (Liebowitz Social Anxiety Scale, d =.53) and depressed mood severity (Beck Depression Inventory, d =.37) but not on the clinician-rated measures (Clinical Global Impressions-Severity Scale, d =.09; Clinical Global Impressions-Improvement Scale, d =.25). Between-group differences on the Liebowitz Social Anxiety Scale were moderated by the level of fear reported at the end of an exposure exercise (end fear), such that the advantage of yohimbine over placebo was only evident among patients who reported low end fear. Conclusions The results provide moderate support for yohimbine as a therapeutic augmentation strategy for exposure therapy in social anxiety disorder, one that may be especially effective when coupled with successful exposure experiences. Beneficial effects for yohimbine were readily evident for self-report measures but not for clinician-rated outcomes of social anxiety severity and improvement.
机译:背景临床前和临床试验表明育亨宾可以增强灭绝学习而没有明显的副作用。但是,以前的临床试验仅检查了患有特定恐惧症的成年人。育亨宾尚未用于其他焦虑症的暴露疗法的增强研究。方法将40名DSM-IV诊断为社交焦虑症的成年人随机分为四组,每次1小时随机接受安慰剂或盐酸育亨宾(10.8 mg)。在基线,每次治疗,治疗后和1个月的随访中收集结果指标。结果育亨宾耐受性良好。相对于安慰剂增强,育亨宾增强导致社交焦虑障碍严重程度(Liebowitz社交焦虑量表,d = .53)和情绪低落的严重程度(贝克抑郁量表,d = .37)的自我报告指标改善更快,结果更好。但未按临床医生评估的标准(临床总体印象-严重量表,d = .09;临床总体印象-改善量表,d = .25)。利勃维茨社交焦虑量表的组间差异由暴露运动结束时报告的恐惧程度(最终恐惧)缓解,因此育亨宾比安慰剂的优势仅在报告低端恐惧的患者中明显。结论该结果为育亨宾作为社交焦虑症暴露治疗的一种增强治疗策略提供了适度的支持,当成功获得暴露经验后,该策略可能特别有效。育亨宾的有益效果很容易通过自我报告的方法体现出来,但对于临床上评定的社交焦虑严重程度和改善的结果却没有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号