跳至主要内容
临床试验/NCT02801760
NCT02801760已完成不适用

Participation in a Biomedical HIV Prevention Clinical Trial: Perspectives of Younger and Older Young Men Who Have Sex With Men (YMSM) and Transgender Women Who Have Sex With Men

University of North Carolina, Chapel Hill11 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2015年11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
58
试验地点
11
主要终点
Retrospective self-assessment of consent competence as assessed by completion of web-based survey

研究概览

简要总结

This study involves a one-time, web-based quantitative structured self-complete ("web-based") survey for all subjects and a qualitative semi-structured ("qualitative") interview for a selected sub-sample of subjects to evaluate the consent processes in association with research outcomes, specifically early adherence to Pre-exposure Prophylaxis (PrEP) and Human Immunodeficiency Virus (HIV) seroconversion at any point during participation in the ATN 110 or ATN 113 study.

详细描述

Decisional autonomy is a foundational, nearly inviolable principle of contemporary human subjects research. "Autonomy" refers to a deliberative outcome reflecting an individual's choice, outside of controlling influences of other agents. From the perspective of research participation decision-making, autonomy incorporates five elements of consent: competence; disclosure; understanding; voluntariness; and, consent. Adequate research consent processes are thought to be challenged by group-level qualities that define a "vulnerable population" in need of protection from coercion or undue influence. Age (typically less than age 18 in the United States) is a widely accepted status-defining vulnerability. Sexual minority identity or same-sex behavior does not define a "vulnerable" population but 45 Code of Federal Regulations (CFR) 46 subpart A (Common Rule) allows appropriate protections for other vulnerable populations as determined by an individual Institutional Review Board (IRB).

The specific aims of this study address issues within a larger domain of questions about the primacy of decisional autonomy, and associations of autonomous research consent and subsequent participation-associated outcomes. This mixed-methods study will enroll young men who have sex with men (YMSM) and transgender women who have sex with men who are currently or were previously enrolled in the ATN 110 or ATN 113 study.

Data from the web-based survey will be used to test hypotheses about the relationships between participant age, elements of the consent process, and two key participation outcomes (early adherence to PrEP, HIV seroconversion) in the ATN 110 or ATN 113 study. Data from the qualitative interview will be used to explore in further depth age-related vulnerability and disclosure vulnerabilities manifested for participants and whether/how they influenced ATN 110 and ATN 113 study outcomes. The interview will also assess decisional support and the benefits or harms associated with participation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
15 Years 至 22 Years(Child, Adult)
性别
Male
接受健康志愿者

入选标准

  • To be considered eligible for enrollment into ATN 137, an individual must meet all of the criteria listed below.
  • Is currently or was previously enrolled in the ATN 110 or ATN 113 study; and
  • Is willing and able to provide informed consent via online informed consent form (ICF).

排除标准

  • To be considered eligible for enrollment, an individual must not meet any of the criteria listed below.
  • Prematurely discontinued from the ATN 110 or ATN 113 study due to withdrawal of consent or inadvertent enrollment.
  • Inability to complete the web-based quantitative structured self-completed survey in its entirety in a single sitting immediately after consent is provided.

结局指标

主要结局

Retrospective self-assessment of consent competence as assessed by completion of web-based survey

时间窗: Day 1

Retrospective self-assessment of consent disclosure as assessed by completion of web-based survey

时间窗: Day 1

Retrospective self-assessment of consent disclosure as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Experienced harms and benefits associated with autonomous research decision-making as assessed by completion of web-based survey

时间窗: Day 1

Experiences with HIV testing and PrEP adherence technologies including home-based HIV testing Wisepill devices and text message adherence reminders as assessed by completion of web-based survey

时间窗: Day 1

Experiences with HIV testing and PrEP adherence technologies including home-based HIV testing Wisepill devices and text message adherence reminders as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Retrospective self-assessment of consent competence as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Retrospective self-assessment of consent understanding as assessed by completion of web-based survey

时间窗: Day 1

Experienced harms and benefits associated with autonomous research decision-making as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Retrospective self-assessment of consent voluntariness as assessed by completion of web-based survey

时间窗: Day 1

Post-ATN 110 or ATN 113 study PrEP use and experiences as assessed by completion of web-based survey

时间窗: Day 1

Post-ATN 110 or ATN 113 study PrEP use and experiences as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Retrospective self-assessment of consent understanding as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Use of social support and information seeking in the consent process as assessed by completion of web-based survey

时间窗: Day 1

Use of social support and information seeking in the consent process as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

Retrospective self-assessment of consent voluntariness as assessed by completion of in-depth interview with selected participants

时间窗: One-time interview completed no more than 60 days after consent

次要结局

  • Self-assessment of adherence as assessed by in-depth interview with selected participants(One-time interview completed no more than 60 days after consent)
  • Benefit or harm from participation as assessed by completion of web-based survey(Day 1)
  • Benefit or harm from participation as assessed by completion of in-depth interview with selected participants(One-time interview completed no more than 60 days after consent)
  • Types of vulnerabilities (i.e., age, sexual identity, sexual behavior, and race-related) that influenced ATN 110 and ATN 113 study outcomes as assessed by completion of web-based survey(Day 1)
  • Types of vulnerabilities (i.e., age, sexual identity, sexual behavior, and race-related) that influenced ATN 110 and ATN 113 study outcomes as assessed by completion of in-depth interview with selected participants(One-time interview completed no more than 60 days after consent)
  • Need for additional support in the decision making process for clinical trial participation as assessed by web-based survey(Day 1)
  • Need for additional support in the decision making process for clinical trial participation as assessed by in-depth interview with selected participants(One-time interview completed no more than 60 days after consent)
  • Self-assessment of adherence as assessed by web-based survey(Day 1)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (11)

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