Pre-Exposure Prophylaxis (PrEP)

2

Review clinical trials related to Pre-Exposure Prophylaxis (PrEP). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Peer-led Community-based PrEP Delivery Among Youth in Brazil

The goal of this project is to conduct a series of studies to refine, test, and understand experiences with a peer-led community-based intervention in which youth will be integrated into health care teams and trained to deliver HIV pre-exposure prophylaxis (PrEP) to their peers. The study team will conduct a randomized trial to determine if peer delivery of PrEP to youth aged 15-24 in Brazil will increase PrEP uptake, persistence, and adherence compared to standard PrEP care provided in health facilities.

Participants needed: 1,400
Trial details
Age: 15-24Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Mar 5, 2026Locations: 2
Eligibility criteria

Aged 15-24 years [+5]

HIV positive test result [+2]

Status: Not yet recruiting

Filling Gaps in the HIV Pre-exposure Prophylaxis Cascade Through Counseling

This study s objective is to test the acceptability and feasibility of a guide to facilitate counseling about HIV prevention, focusing on HIV pre-exposure prophylaxis (PrEP). PrEP is a medication taken by HIV-negative persons to avoid an HIV infection. Healthcare providers (including but not limited to physicians and nurses) who see gay, bisexual and other men who have sex with men (GBM) will be randomly assigned to completing a short online training versus continuing their usual activities. The online training consists of modules containing brief information about PrEP, and about how to address concerns and difficulties that GBM face to get PrEP and to take care of their sexual health. The investigators will ask healthcare providers to answer questionnaires before and after the research activities take place, and a member of the research team will interview some of them at the end. Every time a healthcare provider has a counseling session with a GBM, they will facilitate putting a research coordinator in touch with the person receiving the counseling. Those GBM will also be asked to fill out questionnaires. These activities will take place in the province of Ontario, Canada.

Participants needed: 200
Trial details
Age: 19+Biological sex: AllType: InterventionalSponsor: Unity Health TorontoUpdated: Nov 29, 2024Locations: 1
Eligibility criteria

For practicing health-care professionals, hold a valid license to practice in On... [+1]

Anticipate to stop working at their current practice site before the end of the... [+9]