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Group Alcohol Interventions for College Men

2020年3月3日 更新者:Ohio University

Examining an Integrated Bystander and Alcohol Program for Sexual Assault Perpetration: A Preliminary Randomized Controlled Trial

The objective of the proposed project is to conduct a randomized controlled trial (RCT) comparing sexual assault perpetration and related outcomes (i.e., bystander behavior; rape myth acceptance) for men who receive a group alcohol intervention only to men who receive a group integrated alcohol and sexual assault intervention.

研究概览

详细说明

Although research suggests that sexual assault interventions based on Bystander and Social Norms theory help to reduce sexual assault among college men, these programs do not completely eliminate sexual assault and their effects tend to fade over time. Unfortunately, there is minimal research on whether (1) decreasing alcohol use concurrently decreases sexual assault perpetration among college men and (2) whether alcohol interventions can be incorporated into existing sexual assault programs for college men (i.e., Bystander/Social Norms programs). Therefore, the objective of the proposed project is to conduct a randomized controlled trial (RCT) comparing sexual assault perpetration and related outcomes (i.e., bystander behavior; rape myth acceptance) for men who receive a group alcohol intervention only to men who receive a group integrated alcohol and sexual assault intervention. Specifically, the alcohol only intervention will consist of the Brief Alcohol Screening and Intervention for College Students (BASICS), an empirically-supported intervention for college student drinking. The integrated alcohol and sexual assault intervention, which we have termed Ohio University's Combined Alcohol and Normative Intervention program (OU CAN), will be modeled after BASICS and empirically-supported Bystander and Social Norms interventions for sexual assault. The current study will recruit 100 college men who are sanctioned by their university to receive an alcohol intervention for violating a campus alcohol policy: by definition an indicated and at-risk population for sexual assault perpetration. Men will be followed for 6 months to determine the effects of the intervention on sexual assault perpetration and other primary outcomes (e.g., bystander behavior).

研究类型

介入性

注册 (实际的)

93

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

男性

描述

Inclusion Criteria:

  • Must be 18 or older; must be an Ohio University student; must be male; must be sanctioned to receive an alcohol intervention by Ohio University

Exclusion Criteria:

  • Under the age of 18

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
有源比较器:Alcohol and Relaxation
This arm will receive a brief (2-hour) alcohol intervention based on motivational interviewing termed BASICS and a brief (1.5 hour) relaxation intervention
A one session intervention focused on reducing drinking with motivational interviewing
A one session intervention focused on increasing relaxation skills
有源比较器:Alcohol and Relationships
This arm will receive a brief (4-hour), two session, integrated alcohol and relationship intervention based on motivational interviewing designed to increase healthy alcohol use and sexual behavior. The interventions are based on an integrated BASICS and integrated Bystander protocols
A one session intervention focused on reducing drinking and sexual behavior while drinking
A one session intervention focused on reducing sexual assault with a focus on the role of alcohol

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Sexual Experiences Survey
大体时间:6 months post-intervention
A self-report measure that examines potential sexual assault behaviors
6 months post-intervention

次要结果测量

结果测量
措施说明
大体时间
Bystander Behavior Scale
大体时间:6 months post-intervention
A self-report measure that examines opportunities and engagement in prosocial bystander behavior.
6 months post-intervention
Illinois Rape Myth Acceptance Scale
大体时间:6 months post-intervention
A self-report measure that examines rape supportive beliefs
6 months post-intervention
Sexual Social Norms Inventory
大体时间:6 months post-intervention
A self-report measure that examines sexual normative beliefs
6 months post-intervention
Alcohol use Disorders Identification Test
大体时间:6 months post-intervention
A self-report measure that examines alcohol use
6 months post-intervention
Comprehensive Effects of Alcohol
大体时间:6 months post-intervention
A self-report measure that examines expectancies of alcohol use
6 months post-intervention

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Brian T Wymbs, PhD、Ohio University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2017年1月1日

初级完成 (实际的)

2019年11月1日

研究完成 (实际的)

2019年11月1日

研究注册日期

首次提交

2016年12月1日

首先提交符合 QC 标准的

2016年12月2日

首次发布 (估计)

2016年12月6日

研究记录更新

最后更新发布 (实际的)

2020年3月5日

上次提交的符合 QC 标准的更新

2020年3月3日

最后验证

2020年3月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 16-F-33

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

BASICS的临床试验

3
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