跳至主要内容
临床试验/NCT07495059
NCT07495059招募中不适用

Adaptation and Implementation of an Evidence-based Approach to Advance HIV Prevention and Care

University of California, Los Angeles1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
80
试验地点
1
主要终点
Placement on HIV prevention/care continua

研究概览

简要总结

Transgender women in the intervention condition will attend TransAction individual risk reduction sessions; skill building and open group support sessions, and social events between baseline and 3-month assessment. Transgender women participants in the control condition will be invited to social events only.

详细描述

80 transgender women will be randomized to either an intervention condition (receiving all TransAction activities) or a control condition (being invited to TransAction social events only). We will evaluate outcomes such as advancement along the HIV prevention/care continua, sexual risks, substance use, self-efficacy in services seeking, social support, stigma, general well-being, and quality of life at baseline, 3-month, and 6-month follow-ups. Furthermore, we will assess implementation outcomes such as fidelity, adaptation, feasibility, acceptability, and sustainability through implementation documentation, investigator evaluation, and survey/focus groups with peer facilitators and TW participants.

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
16 Years 至 —(Child, Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 16 years of age or older
  • being male at birth and currently self-identified as a TW
  • currently living in Ho Chi Minh City adjacent areas and having no plans to move out of the areas in the next 6 months - have the cognitive capacity to participate in study activities as judged by the study recruiter.

排除标准

  • have been involved in intervention adaptation activities previously with the study team
  • inability to give informed consent/assent

研究组 & 干预措施

Intervention

Experimental

Participants in the intervention condition will attend individual risk reduction sessions; skill building and open group support sessions, and social events between baseline and 3-month assessment

干预措施: TransAction (Behavioral)

Control

Placebo Comparator

Participants in the control condition will be invited to social events only.

干预措施: TransAction (Behavioral)

结局指标

主要结局

Placement on HIV prevention/care continua

时间窗: Baseline, 3-, and 6-months

An ordinal outcome from 1) HIV+; not taking ART; 2) HIV+; taking ART but not virally suppressed (including no viral load test in the last 6 months); 3) HIV+; taking ART and virtually suppressed; 4) HIV-, not having regular HIV testing; 5) HIV-, having regular HIV testing but not taking PrEP; and 6) HIV-; currently on PrEP. A higher value indicates better placement in HIV prevention/care continua.

次要结局

  • Self-efficacy(Baseline, 3-, and 6-months)
  • Social support(Baseline, 3-, and 6-months)
  • General wellbeing and quality of life(Baseline, 3-, and 6-months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chunqing Lin, PhD

Associate Professor-in-Residence

University of California, Los Angeles

研究点 (1)

Loading locations...

相似试验

Adaptation and Implementation of an Evidence-based... | 临床试验