评估基于网络的干预措施(Deprexis),以减轻退伍军人的抑郁情绪并恢复其功能:随机对照试验协议》。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Rahel Pearson, Christopher G Beevers, Joseph Mignogna, Justin Benzer, Paul N Pfeiffer, Edward Post, Suzannah K Creech
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引用次数: 0

摘要

背景:抑郁症状在退伍军人中很常见,这些症状的存在会增加残疾以及自杀念头和行为。然而,有证据表明,这些症状往往得不到治疗。在症状变得严重和根深蒂固之前进行干预与更好的长期治疗效果有关,包括改善功能和减少疾病的慢性化。计算机提供的干预措施可能特别适合那些有轻度至中度抑郁症状的退伍军人,因为这些干预措施所需的资源较少,获得的障碍较低,因此有可能扩大覆盖范围。尽管有这样的潜力,但针对退伍军人样本中抑郁症状的计算机化干预措施的研究还很缺乏:本研究旨在评估Deprexis(GAIA AG)的疗效,这是一种针对抑郁症状和相关功能障碍的计算机化干预方法:退伍军人将通过美国退伍军人事务部的电子病历以及初级保健和专科诊所招募。首先,将对一小部分退伍军人(人数=16-20)进行定性访谈,以评估治疗程序的可接受性。接下来,有轻度至中度抑郁症状的退伍军人(人数=132)将被随机分配到全自动Deprexis干预组或照常治疗对照组。主要结果将是自我报告的抑郁症状和社会心理功能的各个方面:该项目于 2024 年 5 月获得资助,数据收集工作将在 2024 年 10 月至 2029 年 4 月期间进行。截至稿件提交时,共招募了 4 名参与者,预计将于 2029 年 6 月进行数据分析,并于 2029 年 11 月得出初步结果:本研究将为计算机化自我指导干预对退伍军人抑郁症状和功能障碍的疗效提供初步证据。如果效果显著,这类干预措施可以改善退伍军人获得低资源社会心理治疗的机会:试验注册:ClinicalTrials.gov NCT06217198;https://www.clinicaltrials.gov/study/NCT06217198.International 注册报告标识符 (irrid):PRR1-10.2196/59119。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Evaluation of a Web-Based Intervention (Deprexis) to Decrease Depression and Restore Functioning in Veterans: Protocol for a Randomized Controlled Trial.

Background: Depressive symptoms are common in veterans, and the presence of these symptoms increases disability as well as suicidal thoughts and behaviors. However, there is evidence that these symptoms often go untreated. Intervening before symptoms become severe and entrenched is related to better long-term outcomes, including improved functioning and less disease chronicity. Computer-delivered interventions may be especially appropriate for those veterans with mild to moderate depressive symptoms, because these interventions can require fewer resources and have lower barriers to access and thus have potential for wider reach. Despite this potential, there is a dearth of research examining computerized interventions for depressive symptoms in veteran samples.

Objective: The aim of this study is to evaluate the efficacy of Deprexis (GAIA AG), a computerized intervention for depressive symptoms and related functional impairment.

Methods: Veterans will be recruited through the US Department of Veterans Affairs electronic medical record and through primary care and specialty clinics. First, qualitative interviews will be completed with a small subset of veterans (n=16-20) to assess the acceptability of treatment procedures. Next, veterans (n=132) with mild to moderate depressive symptoms will be randomly assigned to the fully automated Deprexis intervention or a treatment-as-usual control group. The primary outcomes will be self-reported depressive symptoms and various dimensions of psychosocial functioning.

Results: This project was funded in May 2024, and data collection will be conducted between October 2024 and April 2029. Overall, 4 participants have been recruited as of the submission of the manuscript, and data analysis is expected in June 2029, with initial results expected in November 2029.

Conclusions: This study will provide initial evidence for the efficacy of self-guided, computerized interventions for depressive symptoms and functional impairment in veterans. If effective, these types of interventions could improve veteran access to low-resource psychosocial treatments.

Trial registration: ClinicalTrials.gov NCT06217198; https://www.clinicaltrials.gov/study/NCT06217198.

International registered report identifier (irrid): PRR1-10.2196/59119.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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