实施 "全球共识 "以防止大学男性遭受性暴力的战略(SCALE):全国实施试验的研究方案。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-08-29 DOI:10.1186/s13063-024-08401-5
Kathryn M Yount, Daniel J Whitaker, Xiangming Fang, Quach Thu Trang, Meghan Macaulay, Tran Hung Minh
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引用次数: 0

摘要

背景:在全球范围内,15-24 岁的女性遭受性暴力侵害的风险较高,这是导致不良心理、生理和行为健康后果的一个风险因素。性暴力在大学中很常见,最常见的施暴者是男性,但在低收入和中等收入国家中,针对男性的循证预防策略很少经过测试。GlobalConsent 是一个由六个模块组成的网络教育项目,改编自美国的一个有效项目。在越南进行的一项随机试验中,GlobalConsent 在治疗后九个月内减少了男性的性暴力行为(几率比 [OR] = 0.71,95%CI 0.50-1.00),并增加了亲社会干预行为(几率比 = 1.51,1.00-2.28)。关于扩大规模的最佳实施策略还需要证据:我们将对越南北部、中部和南部的六所医科大学进行随机分组,采用两套不同强度的实施策略来实施 GlobalConsent。强度较高的策略将包括:(1) 加强与大学领导和教师在实施前和实施后的接触;(2) 加强实施前的宣传、跟踪和对学生的激励,以促进学生参与和完成 GlobalConsent。强度较高的大学将获得额外的培训和支持,以开展更多的活动。我们将比较两种实施方式的实施动力和结果、干预效果和成本效益。我们的混合方法比较中断时间序列设计包括:(1)对大学领导和实施团队进行定性访谈和定量调查,以评估实施障碍和促进因素;(2)对领导和教师、实施团队和男生进行重复调查,以评估多层次的实施驱动因素和结果;(3)对男生进行重复调查,以评估行为结果(性暴力和干预行为)和中介变量(知识、态度、情感和能力);以及(4)时间日记和成本跟踪,以评估两个实施策略捆绑包的成本效益:该项目首次评估了在越南所有地区为大学生男性提供有效的基于网络的性暴力预防计划的一揽子实施策略,并与一项预防暴力培训计划(D43TW012188)进行了协同。这种方法将为如何在全国范围内推广 GlobalConsent 提供严谨的证据,随着 GlobalConsent 规模的扩大,有望减少与性暴力相关的基于性别的健康不平等现象:试验注册:NCT06443541。在 ClinicalTrials.gov 进行了追溯注册。注册日期:2024 年 6 月 05 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men (SCALE): study protocol for a national implementation trial.

Background: Globally, women 15-24 years are at heightened risk of sexual violence victimization, a risk factor for adverse mental, physical, and behavioral health outcomes. Sexual violence is common at universities and most often perpetrated by men, yet few evidence-based prevention strategies targeting men have been tested in low- and middle-income countries. GlobalConsent is a six-module, web-based educational program adapted from an efficacious U.S.-based program. Nine months post-treatment in a randomized trial in Vietnam, GlobalConsent reduced men's sexually violent behavior (odds ratio [OR] = 0.71, 95%CI 0.50-1.00) and increased prosocial intervening behavior (OR = 1.51, 1.00-2.28) relative to an attention-control. Evidence regarding optimal implementation strategies for scale up is needed.

Methods: We will randomize six medical universities in North, Central, and South Vietnam to deliver GlobalConsent using two different packages of implementation strategies that vary in intensity. Higher-intensity strategies will include greater (1) pre- and post-implementation engagement with university leaders and faculty and (2) greater pre-implementation outreach, follow-up, and incentives for students to promote engagement and completion of GlobalConsent. Higher intensity universities will receive additional training and support for their added activities. We will compare implementation drivers and outcomes, intervention effectiveness, and cost-effectiveness across the two implementation bundles. Our mixed-methods comparative interrupted time series design includes (1) qualitative interviews and quantitative surveys with university leaders and implementation teams to assess implementation barriers and facilitators; (2) repeated surveys with leaders and faculty, implementation teams, and male students to assess multilevel implementation drivers and outcomes; (3) repeated surveys with male students to assess behavioral outcomes (sexual violence and intervening behavior) and mediating variables (knowledge, attitudes, affect, and capacities); and (4) time diaries and cost tracking to assess cost-effectiveness of the two implementation-strategies bundles.

Discussion: This project is the first to assess packages of implementation strategies to deliver an efficacious web-based sexual violence prevention program for undergraduate men across all regions of Vietnam and synergizes with a violence-prevention training initiative (D43TW012188). This approach will produce rigorous evidence about how to disseminate GlobalConsent nationally, which holds promise to reduce gender-based health inequities linked to sexual violence as GlobalConsent is brought to scale.

Trial registration: NCT06443541. Retrospectively registered with ClinicalTrials.gov. Registered on June 05, 2024.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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