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开发和测试一种新型的、计算机化的失眠和焦虑干预措施,以减少高危学生样本中安全辅助手段的使用:一项随机对照试验。

Developing and Testing a Novel, Computerized Insomnia and Anxiety Intervention to Reduce Safety Aids Among an at-Risk Student Sample: A Randomized Controlled Trial.

机构信息

Florida State University; Medical University of South Carolina.

Florida State University.

出版信息

Behav Ther. 2020 Jan;51(1):149-161. doi: 10.1016/j.beth.2019.05.012. Epub 2019 Jun 3.

DOI:10.1016/j.beth.2019.05.012
PMID:32005332
Abstract

Anxiety and insomnia disorders are two of the most common and costly mental health conditions. They are frequently comorbid, but current treatments do not target both. To streamline treatment, we developed a computerized intervention targeting a transdiagnostic factor, safety aids (cognitive or behavioral strategies used to cope with distress that paradoxically exacerbate symptoms). We conducted a randomized controlled trial to determine the acceptability and efficacy of this brief one-session intervention. Young adult undergraduates (N = 61) with elevated subclinical anxiety and insomnia were randomized to receive the anxiety-insomnia intervention or a physical health control condition. Participants were followed for 1 month and completed self-report measures. Analyses indicated that participants found the intervention acceptable, credible, and engaging. Analyses revealed the active intervention reduced sleep- and anxiety-related safety aids, with medium to large effect sizes. Findings suggest that targeting safety aids for anxiety and insomnia is acceptable and effective in reducing the target mechanism, safety aids, as well as worry. Future research should replicate these findings within a clinical sample and with a longer-term follow-up.

摘要

焦虑和失眠障碍是最常见和代价最高的心理健康问题之一。它们经常同时存在,但目前的治疗方法并不能同时针对这两种疾病。为了简化治疗,我们开发了一种针对共病因素(用于应对痛苦但反而加重症状的认知或行为策略)的计算机干预措施。我们进行了一项随机对照试验,以确定这种简短的一次性干预措施的可接受性和疗效。有轻度临床焦虑和失眠的年轻成年大学生(N=61)被随机分配接受焦虑-失眠干预或身体健康对照组。参与者随访了 1 个月,并完成了自我报告的测量。分析表明,参与者认为该干预措施是可以接受的、可信的和吸引人的。分析显示,积极的干预措施减少了与睡眠和焦虑相关的安全辅助工具,具有中等至较大的效果大小。研究结果表明,针对焦虑和失眠的安全辅助工具是可以接受的,并且可以有效地减少目标机制、安全辅助工具和担忧。未来的研究应该在临床样本中并进行更长时间的随访来复制这些发现。

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