Department of Psychiatry and Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
RAND, Santa Monica, CA, United States.
JMIR Res Protoc. 2024 Aug 22;13:e59993. doi: 10.2196/59993.
Young adult veterans who served after the September 11 attacks on the United States in 2001 (ie, post-9/11) are at heightened risk for experiencing behavioral health distress and disorders including hazardous drinking, posttraumatic stress disorder, and depression. These veterans often face significant barriers to behavioral health treatment, and reaching them through brief mobile phone-based interventions may help reduce drinking and promote treatment engagement.
Following a successful pilot study, this randomized controlled trial (RCT) aims to further test the efficacy of a brief (ie, single session) mobile phone-delivered personalized normative feedback intervention enhanced with content to promote treatment engagement.
We will conduct an RCT with 800 post-9/11 young adult veterans (aged 18 to 40 years) with potentially hazardous drinking and who have not recently received treatment for any behavioral health problems. Participants will be randomly assigned to the personalized intervention or a control condition with resources for seeking care. The personalized normative feedback module in the intervention focuses on the correction of misperceived norms of peer alcohol use and uses empirically informed approaches to increase motivation to address alcohol use and co-occurring behavioral health problems. Past 30-day drinking, alcohol-related consequences, and treatment-seeking behaviors will be assessed at baseline and 3, 6, 9, and 12 months post intervention. Sex, barriers to care, posttraumatic stress disorder, depression, and severity of alcohol use disorder symptoms will be explored as potential moderators of outcomes.
We expect recruitment to be completed within 6 months, with data collection taking 12 months for each enrolled participant. Analyses will begin within 3 months of the final data collection point (ie, 12 months follow-up).
This RCT will evaluate the efficacy of a novel intervention for non-treatment-seeking veterans who struggle with hazardous drinking and possible co-occurring behavioral health problems. This intervention has the potential to improve veteran health outcomes and overcome significant barriers to treatment.
ClinicalTrials.gov NCT04244461; https://clinicaltrials.gov/study/NCT04244461.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/59993.
在 2001 年美国遭受“9·11”袭击后入伍的年轻成年退伍军人(即“9·11”后入伍),存在更高风险出现行为健康困扰和障碍,包括危险饮酒、创伤后应激障碍和抑郁。这些退伍军人在寻求行为健康治疗方面往往面临重大障碍,通过简短的基于移动电话的干预措施接触他们可能有助于减少饮酒和促进治疗参与。
在一项成功的试点研究之后,这项随机对照试验(RCT)旨在进一步测试一种简短(即单次疗程)的移动电话提供的个性化规范反馈干预措施的效果,该措施通过提供促进治疗参与的内容得到增强。
我们将对 800 名有潜在危险饮酒行为且最近未因任何行为健康问题接受治疗的“9·11”后年轻成年退伍军人(年龄在 18 至 40 岁之间)进行 RCT。参与者将被随机分配到个性化干预组或接受治疗资源的对照组。干预中的个性化规范反馈模块侧重于纠正对同伴酒精使用的错误感知规范,并使用经验证的方法来增加解决饮酒和同时发生的行为健康问题的动机。将在基线和干预后 3、6、9 和 12 个月评估过去 30 天的饮酒量、与酒精相关的后果和治疗寻求行为。将探讨性别、治疗障碍、创伤后应激障碍、抑郁和酒精使用障碍严重程度作为结果的潜在调节因素。
我们预计将在 6 个月内完成招募,每个入组参与者的资料收集将需要 12 个月。分析将在最后数据收集点(即 12 个月随访)后 3 个月内开始。
这项 RCT 将评估一种针对非治疗寻求的退伍军人的新干预措施的效果,这些退伍军人存在危险饮酒和可能同时发生的行为健康问题。该干预措施有可能改善退伍军人的健康结果,并克服治疗的重大障碍。
ClinicalTrials.gov NCT04244461;https://clinicaltrials.gov/study/NCT04244461。
国际注册报告标识符(IRRID):DERR1-10.2196/59993。