IMB-guided Intervention to Encourage PrEP Uptake Among Young Men Who Have Sex With Men - Trial NCT04865341
Access comprehensive clinical trial information for NCT04865341 through Pure Global AI's free database. This phase not specified trial is sponsored by Medical College of Wisconsin and is currently Not yet recruiting. The study focuses on Human Immunodeficiency Virus. Target enrollment is 132 participants.
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Study Focus
Sponsor & Location
Medical College of Wisconsin
Timeline & Enrollment
N/A
Jul 01, 2023
Jan 31, 2024
Primary Outcome
Change in the number of self-reported HIV self-tests
Summary
The proposed study will involve adolescent (17-24 years old) men who have sex with men
 (described as YMSM hereafter) who meet eligibility criteria to participate in each study.
 Prospective study candidates will receive a copy of the IRB-approved informed consent forms
 and, if they choose to participate, will provide consent before enrollment into this study.
 Involvement of human subjects is detailed in the Research Strategy portion of this proposal,
 Recruitment and Retention Plan, and Protection of Human Subjects sections. Briefly,
 investigators will develop and pilot a randomized controlled trial (RCT) to support HIV
 self-testing (HIVST) and pre-exposure prophylaxis (PrEP) uptake. Intervention content will be
 focused on constructs of the Information-Motivation-Behavioral Skills (IMB) model. To reduce
 cost and increase feasibility, investigators plan to incorporate previously developed content
 as much as possible-investigators see integration of this content as a major strength.
 Investigators will include professionally produced videos about HIV testing and PrEP and
 other resources including the geo-targeted directories to find clinic settings that offer HIV
 testing and PrEP, all of which are publicly available. Investigators believe our approach of
 guiding YMSM through intervention modules based on theory will help improve content
 retention/use and ultimately influence constructs posited to result in behavior change.
 Investigators foresee using multiple forms of attention-matched material, media, and
 programming to engage (and retain engagement) of YMSM throughout the brief single-session
 intervention (45-60 minutes). Intervention content is subject to change depending on feedback
 from focus groups, survey results, YAB feedback, and usability testing. Primary endpoints of
 this study include HIVST and PrEP uptake, including stage of change towards HIVST and PrEP
 uptake. Secondary outcomes include changes in IMB model indicators (e.g., HIV prevention
 knowledge).
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT04865341
Non-Device Trial

