对同时患有酒精使用障碍和创伤后应激障碍的退伍军人进行行为激活:随机对照试验的基础和方法。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Shannon M. Blakey , Amber K. Alsobrooks , Antonio A. Morgan-López , Nicholas Kruskamp , Tracy L. Simpson , Stacey B. Daughters , Chase M. DuBois , Jovin S. Huang , Janequia Evans , Bethzaida N. Serrano , Patrick S. Calhoun , Jean C. Beckham , Eric B. Elbogen
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引用次数: 0

摘要

背景:近 200 万美国退伍军人同时患有酒精使用障碍和创伤后应激障碍(AUD/PTSD)。现有的 AUD/PTSD 治疗方法强调减轻症状,有时忽略了社会心理功能的改善,辍学率高达 50%。此外,目前测量社会心理功能的方法仅限于自我报告。本研究方案描述了一项1:1平行、双臂、试验性随机对照试验,比较了行为激活(BA)心理疗法和复发预防(RP)心理疗法对患有AUD/PTSD的退伍军人的治疗效果:方法:46 名患有 AUD/PTSD 的退伍军人将被随机分配到每周八次、每次一小时的 BA 或 RP 虚拟个人治疗中。将在治疗前和治疗后进行临床访谈、自我报告和地理空间评估。在治疗过程中还将进行部分结果和探索性测量。分析重点将放在试验可行性、BA 可接受性和初步疗效上。地理空间分析将探讨从治疗前到治疗后地理空间运动的变化是否可用于客观衡量治疗反应。研究机构和独立的数据与安全监控委员会将对试验的进展、安全性和质量进行监控。来自同意参与者的去身份化数据将提交给赞助商指定的数据存储库:如果试验成功,将有助于为患有 AUD/PTSD 的退伍军人提供一种更易接受的治疗方案。积极的研究结果还将为在患有 AUD/PTSD 的平民中测试 BA 奠定基础。最后,通过采用新颖的地理空间方法和技术,本研究有可能产生一种客观测量 AUD/PTSD 恢复情况的新方法,可用于其他临床试验。本研究已在 ClinicalTrials.gov (NCT06249386) 上注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behavioral activation for veterans with co-occurring alcohol use disorder and posttraumatic stress disorder: Basis and methodology for a pilot randomized controlled trial

Background

Nearly 2 million U.S. veterans live with co-occurring alcohol use disorder and posttraumatic stress disorder (AUD/PTSD). Extant AUD/PTSD treatments emphasize symptom reduction, sometimes overlooking psychosocial functioning improvements, and have dropout rates as high as 50 %. Additionally, current approaches to measuring psychosocial functioning are limited to self-report. This study protocol describes a 1:1 parallel, two-arm, pilot randomized controlled trial comparing Behavioral Activation (BA) psychotherapy to Relapse Prevention (RP) psychotherapy for veterans with AUD/PTSD.

Methods

Forty-six veterans with AUD/PTSD will be block-randomized to eight weekly, virtual, hour-long individual sessions of BA or RP. Clinical interview, self-report, and geospatial assessments will be administered at pre- and post-treatment. Select outcome and exploratory measures will be administered during treatment. Analyses will focus on trial feasibility, BA acceptability, and preliminary efficacy. Geospatial analyses will explore whether pre- to post-treatment changes in geospatial movement can be used to objectively measure treatment response. The study site and an independent Data and Safety Monitoring Board will monitor trial progress, safety, and quality. De-identified data from consenting participants will be submitted to a sponsor-designated data repository.

Conclusion

If successful, this trial could help to provide veterans with AUD/PTSD with a more acceptable treatment option. Positive findings would also lay groundwork for testing BA in civilians with AUD/PTSD. Finally, by incorporating novel geospatial methods and technologies, this study could potentially yield a new approach to objectively measuring AUD/PTSD recovery that could be used in other clinical trials. This study was registered in ClinicalTrials.gov (NCT06249386).

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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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