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临床试验/NCT07298785
NCT07298785
招募中
不适用

Peer-led Dynamic Choice HIV Prevention for Women: The Peer-led DCP Pilot Study

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年1月27日最近更新:

概览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Biomedical HIV prevention coverage

概览

简要总结

This study will refine and pilot test the Peer-led Dynamic Choice HIV Prevention (DCP) intervention in a single-arm pilot trial. The study will test the hypothesis that the Peer-led Dynamic Choice HIV Prevention intervention will be feasible and increase biomedical HIV prevention coverage in the 6 months after receipt of the Peer-led DCP intervention compared to the standard of care in the 6 months prior to intervention implementation.

详细描述

The overall goal of this study is to refine and pilot test a Peer-led Dynamic Choice HIV Prevention intervention tailored to women at elevated HIV risk in southwestern Uganda. We will conduct a single-arm pilot trial of the intervention enrolling approximately 60 women to assess the feasibility, acceptability, and preliminary effectiveness of the Peer-led Dynamic Choice Prevention intervention.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
15 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age \>=18 years or mature or mature minor \>=15 years;
  • Female sex at birth;
  • HIV negative by country-standard testing algorithm
  • Elevated risk of HIV exposure, defined as at least 1 of the following: a) eligible for PrEP based on Uganda Ministry of Health Guidelines; b) exchange of sex for goods or money in last 6 months; or c) work in bar or guesthouse

排除标准

  • Contraindication to country-recommended PrEP regimen per national guidelines
  • Participation in another HIV prevention study

研究组 & 干预措施

Peer-led Dynamic Choice HIV Prevention (DCP) intervention

Experimental

干预措施: Peer-led Dynamic Choice HIV Prevention (DCP) intervention (Other)

结局指标

主要结局

Biomedical HIV prevention coverage

时间窗: 24 weeks

Percentage of follow-up months that a participant uses a biomedical HIV prevention product

次要结局

  • At-risk biomedical HIV prevention coverage(24 weeks)
  • Feasibility of delivery of the Peer-Led DCP intervention by peers(24 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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