跳至主要内容
临床试验/NCT06558825
NCT06558825招募中不适用

Development and Pilot Testing of a Mental Health Clinic-Based PrEP Uptake and Adherence Intervention for Women in Treatment for Trauma-Related Conditions

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
2
主要终点
Number of participants who uptake PrEP

研究概览

简要总结

The investigators have previously developed an integrated bio-behavioral intervention to promote PrEP uptake and adherence in cisgender women who are undergoing treatment for trauma-related mental health conditions and who are at a higher risk for HIV. The intervention is delivered within the mental health treatment setting and integrates knowledge, behavioral skills, and motivation to engage in and adhere to PrEP care. The purpose of this study is to assess the preliminary efficacy, feasibility, and acceptability of this intervention. The hypothesis is that, compared to standard treatment, the intervention will be feasible, acceptable, and associated with greater PrEP uptake and adherence.

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 (Outcomes Assessor)

入排标准

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

入选标准

  • Currently undergoing mental health treatment;
  • Have a history of trauma;
  • HIV negative;
  • Sexually active with an opposite sex partner within the past 6 months;
  • Not using PrEP for HIV prevention at the time of screening;
  • Eligible for PrEP based on having at least one Centers for Disease Control and Prevention (CDC)-defined criteria for PrEP;
  • Fluent in English;
  • Own or have regular access to a smart phone.

排除标准

  • HIV positive;
  • Concurrently participating in another HIV prevention program;
  • Have severe cognitive impairment that would interfere with their ability to consent, understand study procedures and/or effectively participate in therapy;
  • Have psychological distress that would prohibit them from participating in the study;
  • Be unable or unwilling to meet study requirements.

结局指标

主要结局

Number of participants who uptake PrEP

时间窗: 12 weeks post intervention

PrEP uptake is defined as obtaining a prescription and taking the first dose.

次要结局

  • Number of Participants who adhere to PrEP(12 weeks post PrEP initiation)
  • PrEP adherence as assessed by proportion of videos uploaded(from the time of PrEP initiation to 12 weeks post PrEP initiation)
  • Intervention feasibility as assessed by study retention(15 weeks post enrollment)
  • Intervention feasibility as assessed by number of participants enrolled(at the time of enrollment)
  • Change in PrEP Anticipated Stigma as assessed by the PrEP Anticipated Stigma Scale(baseline, 15 weeks post enrollment)
  • PrEP adherence as assessed by proportion of self-reported daily adherence(from the time of PrEP initiation to 12 weeks post PrEP initiation)
  • Intervention feasibility as assessed by number of sessions attended by participants(15 weeks post enrollment)
  • Change in PrEP attitudes as assessed by PrEP Attitudes Measure(baseline, 15 weeks post enrollment)
  • Intervention acceptability as assessed by score on a satisfaction questionnaire(15 weeks post enrollment)
  • Change in perceived HIV risk as assessed by Perceived Risk of HIV Scale(baseline, 15 weeks post enrollment)
  • Change in PrEP knowledge as assessed by PrEP Knowledge Questionnaire(baseline, 15 weeks post enrollment)

研究者

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

Angela M Heads

Associate Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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