The Comprehensive Adaptive Multisite Prevention of University Student Suicide Trial: Protocol for a Randomized Controlled Trial.

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Kyla Blalock, Jacqueline Pistorello, Shireen L Rizvi, John R Seeley, Francesca Kassing, James Sinclair, Linda A Oshin, Robert J Gallop, Cassidy M Fry, Ted Snyderman, David A Jobes, Jennifer Crumlish, Hannah R Krall, Susan Stadelman, Filiz Gözenman-Sapin, Kate Davies, David Steele, David B Goldston, Scott N Compton
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引用次数: 0

Abstract

Background: Suicidal ideation is increasing among university students. Despite growing demand for services, university counseling centers (UCCs) face limited resources to meet the complex needs of students who are suicidal.

Objective: The Comprehensive Adaptive Multisite Prevention of University Student Suicide (CAMPUS) Trial evaluates 4 treatment sequences within UCCs to develop evidence-based treatment guidelines.

Methods: The CAMPUS Trial consists of a feasibility study followed by a sequential multiple-assignment randomized trial (SMART). The original CAMPUS protocol was modified during the COVID-19 pandemic to accommodate new UCC tele-mental health services, including remote treatment, assessments, and monitoring. A smaller-scale feasibility study was conducted to (1) evaluate implementation of hybrid telehealth and in-person interventions and (2) fine-tune online procedures. Following the feasibility study, university students (aged 18-25 years) seeking UCC services with moderate to severe suicidal ideation will enroll in the CAMPUS Trial. Student participants are randomly assigned to 1 of 4 treatment sequences with 2 stages of intervention. In stage 1, students receive 4 to 6 weeks of either (1) a suicide-focused treatment-Collaborative Assessment and Management of Suicidality-or (2) enhanced treatment as usual. Treatment responders enter the maintenance phase. In stage 2, nonresponders are rerandomized for an additional 1 to 8 weeks of (1) Collaborative Assessment and Management of Suicidality or (2) an intensive skills-based treatment-dialectical behavior therapy for UCC settings. UCC counselors will enroll in the CAMPUS Trial to complete measures about their experience working with students who are suicidal. CAMPUS Trial administration includes representation from all sites to facilitate cross-site coordination and an advisory board of stakeholders from all UCCs to facilitate treatment implementation.

Results: Student participant recruitment began on October 25, 2022, and ended on May 16, 2024. As of November 2024, data collection for the SMART was ongoing with active study participants. Data collection was completed in November 2024, and as of April 2025, data analysis is underway. Full results will be available in 2025.

Conclusions: The CAMPUS Trial offers a model for future SMARTs for the treatment of suicidal thoughts or behaviors (or both) across various settings. The results will inform treatment guidelines for students presenting with suicidality at UCCs.

Trial registration: ClinicalTrials.gov NCT04707066; http://clinicaltrials.gov/ct2/show/NCT04707066.

International registered report identifier (irrid): DERR1-10.2196/68441.

综合适应性多地点预防大学生自杀试验:随机对照试验方案。
背景:大学生自杀意念呈上升趋势。尽管对服务的需求不断增长,但大学咨询中心(UCCs)在满足自杀倾向学生的复杂需求方面面临有限的资源。目的:综合适应性多地点预防大学生自杀(CAMPUS)试验评估UCCs内的4种治疗顺序,以制定循证治疗指南。方法:CAMPUS试验包括可行性研究和顺序多任务随机试验(SMART)。在2019冠状病毒病大流行期间,最初的校园协议进行了修改,以适应新的UCC远程精神卫生服务,包括远程治疗、评估和监测。一项规模较小的可行性研究进行了(1)评估实施混合远程医疗和现场干预(2)微调在线程序。可行性研究结束后,有中度至重度自杀意念的大学生(18-25岁)将参加CAMPUS试验。学生参与者被随机分配到4个治疗序列中的1个,有2个干预阶段。在第一阶段,学生们接受4到6周的治疗,或者(1)以自杀为中心的治疗——自杀倾向的协同评估和管理,或者(2)像往常一样加强治疗。治疗应答者进入维持阶段。在第2阶段,无反应者被重新随机分配,进行额外的1至8周的(1)自杀行为的协作评估和管理,或(2)针对UCC环境的强化技能治疗-辩证行为治疗。UCC辅导员将参加CAMPUS试验,以完成关于他们与有自杀倾向的学生一起工作的经验的测量。CAMPUS Trial的管理包括来自所有地点的代表,以促进跨地点的协调,并由来自所有ucc的利益相关者组成咨询委员会,以促进治疗的实施。结果:学生参与者招募从2022年10月25日开始,到2024年5月16日结束。截至2024年11月,SMART的数据收集工作正在积极进行。数据收集于2024年11月完成,截至2025年4月,数据分析正在进行中。全部结果将于2025年公布。结论:CAMPUS试验为未来smart在各种环境下治疗自杀念头或行为(或两者兼而有之)提供了一个模型。研究结果将为UCCs出现自杀倾向的学生提供治疗指南。试验注册:ClinicalTrials.gov NCT04707066;http://clinicaltrials.gov/ct2/show/NCT04707066.International注册报告标识符(irrid): DERR1-10.2196/68441。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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