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临床试验/NCT00649701
NCT00649701Unknown1 期

Phase 1 Online Intervention to Reduce Sexual Risk Among Men Who Have Sex With Men

Public Health Solutions1 个研究点 分布在 1 个国家目标入组 3,097 人开始时间: 2008年4月最近更新:
适应症

试验速览

阶段
1 期
入组人数
3,097
试验地点
1
主要终点
HIV disclosure, HIV testing, and condom use

研究概览

简要总结

The purpose of this study is to develop and test the efficacy of online HIV risk reduction interventions among men who have sex with men.

详细描述

This is an Internet-based, five-branch randomized controlled intervention, enrolling 3,000 adult MSM. The five branches include 1) a control condition receiving no intervention content, 2) a standard text-based prevention webpage, 3) an 8 minute dramatic video addressing sexual risk reduction within the context of alcohol use, 4) a 5 minute documentary video addressing HIV disclosure, HIV testing, and condom use with the sub-context of drug use, and 5) both videos. After completing the baseline survey, eligible participants who consent to participate in the intervention will be randomly assigned to the control condition or one of the four intervention conditions. The control condition will not include the delivery of any intervention content. All participants (branches 1-5) will be asked to complete a brief post-intervention survey (to measure intentions). All intervention participants will be invited to complete a final 60-day follow-up survey.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Age 18 and over;
  • Ability to read and respond in English;
  • Reside within the United States;
  • Report oral or anal sex with any male (new partner or not) in the past 60 days AND report oral, anal or vaginal sex for the first time with any partner (male or female) in the past 60 days;
  • Complete baseline survey
  • Provide an email address;

排除标准

  • Women and transgender persons

结局指标

主要结局

HIV disclosure, HIV testing, and condom use

时间窗: 60 days

次要结局

  • drug and/or alcohol use before sex, and depressive and/or anxiety symptomatology (past 2 weeks)(60 days)

研究者

申办方类型
Other

研究点 (1)

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