TCTR20170408001招募中未知
Effectiveness and Cost Effectiveness of a Combination HIV Preventive Intervention with and without daily oral Truvada® pre-exposure prophylaxis (PrEP) with adherence support among young men who have sex with men (YMSM) and transgender women (TGW) ag
S National Institutes of Health (NIH)0 个研究点目标入组 1,240 人开始时间: 2017年4月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 1,240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 26 Years（—）
- 性别
- Male
入选标准
- •â€¢Biological male sex at birth
- •â€¢Self-report of having sold or traded sex to another man for money, drugs, or other goods or services in the previous 12 months.
- •â€¢Age 18 through 26 years at enrollment
- •â€¢Self-reported living in the greater Bangkok Metropolitan area or Pattaya City
- •â€¢Willing to complete study instruments, with or without assistance, Thai and/or English.
- •â€¢Thai citizenship
- •â€¢Willing to provide contact and locator information
- •â€¢Self-reported negative or unknown HIV status
- •â€¢Negative rapid HIV test result at the screening visit
排除标准
- •â€¢Unable or unwilling to provide consent for study participation
- •â€¢Rapid HIV test results at the screening visit suggesting HIV infection
- •â€¢Did not complete baseline assessment (Section 3.1 above)
- •â€¢Any condition that would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.
- •â€¢Concurrently enrolled in another PrEP (oral or topical or injectable) intervention trial or preventive HIV vaccine trial.
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