Partnered implementation of the veteran sponsorship initiative: protocol for a randomized hybrid type 2 effectiveness-implementation trial.

Joseph C Geraci, Erin P Finley, Emily R Edwards, Sheila Frankfurt, A Solomon Kurz, Nipa Kamdar, Megan E Vanneman, Leonard M Lopoo, Hannah Patnaik, Jean Yoon, Nicholas Armstrong, Ashley L Greene, Gilly Cantor, Joseph Wrobleski, Erin Young, Matthew Goldsmith, Richard W Seim, Marianne Goodman
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引用次数: 4

Abstract

Background: The USA is undergoing a suicide epidemic for its youngest Veterans (18-to-34-years-old) as their suicide rate has almost doubled since 2001. Veterans are at the highest risk during their first-year post-discharge, thus creating a "deadly gap." In response, the nation has developed strategies that emphasize a preventive, universal, and public health approach and embrace the value of community interventions. The three-step theory of suicide suggests that community interventions that reduce reintegration difficulties and promote connectedness for Veterans as they transition to civilian life have the greatest likelihood of reducing suicide. Recent research shows that the effectiveness of community interventions can be enhanced when augmented by volunteer and certified sponsors (1-on-1) who actively engage with Veterans, as part of the Veteran Sponsorship Initiative (VSI).

Method/design: The purpose of this randomized hybrid type 2 effectiveness-implementation trial is to evaluate the implementation of the VSI in six cities in Texas in collaboration with the US Departments of Defense, Labor and Veterans Affairs, Texas government, and local stakeholders. Texas is an optimal location for this large-scale implementation as it has the second largest population of these young Veterans and is home to the largest US military installation, Fort Hood. The first aim is to determine the effectiveness of the VSI, as evidenced by measures of reintegration difficulties, health/psychological distress, VA healthcare utilization, connectedness, and suicidal risk. The second aim is to determine the feasibility and potential utility of a stakeholder-engaged plan for implementing the VSI in Texas with the intent of future expansion in more states. The evaluators will use a stepped wedge design with a sequential roll-out to participating cities over time. Participants (n=630) will be enrolled on military installations six months prior to discharge. Implementation efforts will draw upon a bundled implementation strategy that includes strategies such as ongoing training, implementation facilitation, and audit and feedback. Formative and summative evaluations will be guided by the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework and will include interviews with participants and periodic reflections with key stakeholders to longitudinally identify barriers and facilitators to implementation.

Discussion: This evaluation will have important implications for the national implementation of community interventions that address the epidemic of Veteran suicide. Aligned with the Evidence Act, it is the first large-scale implementation of an evidence-based practice that conducts a thorough assessment of TSMVs during the "deadly gap."

Trial registration: ClinicalTrials.gov ID number: NCT05224440 . Registered on 04 February 2022.

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老兵赞助计划的合作实施:随机混合2型有效性实施试验的方案。
背景:自2001年以来,美国最年轻的退伍军人(18- 34岁)的自杀率几乎翻了一番。退伍军人在退伍后的第一年患病风险最高,因此形成了一个“致命的缺口”。为此,国家制定了战略,强调预防、普及和公共卫生方法,并接受社区干预的价值。自杀的三步理论表明,在退伍军人过渡到平民生活时,减少重返社会困难和促进联系的社区干预最有可能减少自杀。最近的研究表明,如果作为退伍军人赞助倡议(VSI)的一部分,志愿者和认证赞助商(1对1)积极参与退伍军人活动,社区干预的有效性可以得到提高。方法/设计:与美国国防部、劳工和退伍军人事务部、德克萨斯州政府和当地利益相关者合作,这项随机混合2型有效性实施试验的目的是评估VSI在德克萨斯州六个城市的实施情况。德克萨斯州是这一大规模实施的最佳地点,因为它拥有这些年轻退伍军人的第二大人口,并且是美国最大的军事设施胡德堡的所在地。第一个目标是确定VSI的有效性,如重新融入社会困难、健康/心理困扰、退伍军人保健利用、连通性和自杀风险等措施所证明的那样。第二个目标是确定在德克萨斯州实施VSI的利益相关者参与计划的可行性和潜在效用,并打算在未来扩展到更多的州。评估人员将采用楔形设计,随着时间的推移,逐步向参与城市推出。参与者(n=630)将在退伍前6个月在军事设施登记。实施工作将借鉴捆绑实施战略,其中包括持续培训、促进实施以及审计和反馈等战略。形成性和总结性评估将在Reach、有效性、采用、实施和维护(RE-AIM)框架的指导下进行,并将包括与参与者的访谈和与主要利益相关者的定期反思,以纵向识别实施的障碍和促进因素。讨论:这一评估将对解决退伍军人自杀流行病的国家实施社区干预具有重要意义。根据《证据法》,这是第一次大规模实施以证据为基础的实践,在“致命空白期”对tsmv进行彻底评估。试验注册:ClinicalTrials.gov ID号:NCT05224440。注册于2022年2月4日
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