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临床试验/NCT02359487
NCT02359487已完成不适用

Behavioral Counseling Intervention Trial to Reduce Alcohol-related Sexual Risk Behavior Among HIV-negative Men in Namibia

Centers for Disease Control and Prevention0 个研究点目标入组 550 人开始时间: 2011年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
550
主要终点
Change in frequency of sex after drinking (measured by count data and proportions)

研究概览

简要总结

The overall purpose of this study is to evaluate an intervention that aims to reduce alcohol-related HIV sexual risk behaviors among HIV-negative men in Namibia. The objectives of the study are to determine the effectiveness of an individual counseling intervention in reducing alcohol-related HIV sexual risk behaviors among men, and in reducing harmful and hazardous alcohol use among men.

详细描述

This study involves a randomized controlled trial of 550 HIV-negative adult men recruited from a single Voluntary Counseling and Testing (VCT) center for HIV in Windhoek, Namibia who report harmful or hazardous alcohol consumption and more than one sex partner in the previous three months.

After receiving standard counseling at the VCT center, all men who test HIV-negative will be invited to be screened for eligibility for the study, and if eligible, to consent to enroll. Personnel hired for the study will then administer a baseline survey via Personal Digital Assistant to all enrolled men. Enrolled participants will then be randomized to either an intervention arm, and receive an additional one-hour counseling session and take-home materials plus general alcohol information materials or to a control arm, and receive general alcohol information materials alone. All men enrolled in the study will receive the general alcohol information materials, consisting of a booklet with alcohol health information and a brochure detailing alcohol abuse support services in the local community. Men in the intervention arm will also receive two cellphone text messages one month and four months following enrollment to boost the risk reduction counseling. Follow-up surveys of all participants will be conducted three months and six months after enrollment

Outcomes measured include self-reported data at baseline, three months and six months post-enrollment regarding: 1) Number, proportion of sex acts preceded by alcohol use; 2) Number, proportion of sex acts protected by condoms; 3) Number of sex partners; and 4) Quantity and frequency of alcohol use; 5) Condom use demonstration scores.

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
None

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

  • Self reported HIV negative status after testing at the Council of Churches Namibia (CCN) NewStart VCT center
  • More than 1 sexual partner in the past 6 months
  • AUDIT screen score 8 to 19
  • Able to provide informed consent
  • Access to a cell phone to retrieve private text messages and calls
  • Plans to stay in the local area for 6 months
  • Able to verbally communicate in English, Oshiwambo, or Afrikaans

排除标准

  • Self reported HIV positive status after testing at the CCN NewStart VCT center
  • Less than 1 sexual partner in the past 6 months
  • AUDIT screen score less than 8 or greater than 20
  • Unable to provide informed consent to participate to enroll in the study
  • Unable to retrieve private cell phone text messages and calls
  • Unable to verbally communicate in English, Oshiwambo, or Afrikaans

结局指标

主要结局

Change in frequency of sex after drinking (measured by count data and proportions)

时间窗: 3 months, 6 months after intervention

Sex acts preceded by alcohol use, for up to 4 recent sex partners, measured by count data and proportions

次要结局

  • Change in condom skills (measured by a condom use demonstration score, modified 9-item male condom use score (MCUS)(3 months, 6 months after intervention)
  • Change in frequency of condom use (measured by count data and proportions)(3 months, 6 months after intervention)
  • Change in number of sex partners(3 months, 6 months after intervention)
  • Change in frequency of alcohol use (measured by AUDIT and CAGE screens)(3 months, 6 months after intervention)

研究者

申办方类型
Fed
责任方
Sponsor

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