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Completed

NCT Number: NCT05353283

PrEP Point-of-Care Brief-Intervention for Adherence Among Young Men Who Have Sex With Men

Despite advances in HIV prevention, the HIV incidence among young men who have sex with men (YMSM) is increasing, threatening to derail achievement of the United States End the HIV Epidemic goals. Although, pre-exposure prophylaxis (PrEP) is a highly effective HIV prevention method, adherence was sufficiently low to comprise efficacy among a high proportion of YMSM in multiple clinical trials and demonstration projects. In this study, the investigators will leverage a novel urine point-of-care drug-level test for PrEP adherence, to both enhance and target motivational-interviewing-based adherence counseling among YMSM, with the goal of preventing HIV infections among this critically at-risk group.

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Key information

Age range

18 year–30 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

University of California, San Francisco/San Francisco General Hospital

San Francisco, California, 94110, United States

About this study

Young men who have sex with men (YMSM; ages 15-29 years) have rising HIV incidence in the United States. Pre-exposure prophylaxis (PrEP) is a highly effective medication prevent HIV infection, both at the individual and population level. However, in several clinical trials and demonstration projects among YMSM, a majority of participants had adherence to PrEP sufficiently low to compromise efficacy throughout the study. Unfortunately, pill-counts and self-reported adherence have limitations in this population, and therapeutic drug monitoring using previously available methods requires expensive equipment and specialized staff, meaning it cannot be implemented at the point-of-care (POC). The investigators have developed a novel POC test to measure urine drug-levels to PrEP for the first time, providing the opportunity to target and enhance adherence counseling during a routine clinical visit. Substantial knowledge gaps on the correct counseling approach and framing of the drug-level feedback message must be addressed to use this strategy to improve adherence among YMSM. This study will use a mixed methods approach to test the central hypothesis that an intervention leveraging a POC urine bioassay to detect PrEP adherence can both target and enhance adherence counseling. Brief interventions are a motivational interviewing (MI) counseling approach with wide uptake by primary care providers for substance use prevention and medical therapy adherence. PrEP2-BAY proposes a brief intervention be used as the framework for POC drug-level feedback among YMSM using PrEP. This study will test the acceptability, feasibility, and preliminary impact on long-term adherence, measured through hair tenofovir levels, of the brief intervention in a pilot randomized controlled trial among YMSM. This proposed research plan has the goal of optimizing PrEP's impact through a novel adherence support intervention. The findings of this proposal will lead to a R01 application to test a POC bioassay-enhanced adherence brief intervention among YMSM in a multi-city trial, with the goal of reducing the burden of HIV among MSM.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male sex at birth who has sex with men
  • Age 18-30 years-old
  • Currently receiving tenofovir-based oral PrEP
  • Plans to continue taking daily PrEP over the upcoming 3 months

Exclusion criteria

  • Participant living with HIV
  • Age > 30 years

Treatment and study plan

Motivational Interviewing Counselling

Behavioral

Motivational interviewing-based counseling will be provided to the participant based on the results of the urine test

Point-of-care Urine Tenofovir Measurement

Device

Urine will be collected and the presence or absence of tenofovir will be measured with the point-of-care urine tenofovir test.

Primary outcomes

  1. Number of Participants Indicating the Intervention Was Acceptable

    Time frame: 3 months

    Number of participants reporting the intervention to be "somewhat" or "very" acceptable on a five-point Likert scale

Secondary outcomes

  1. Long-term Adherence Outcomes

    Time frame: 3 months

    Measure change in tenofovir levels in hair samples from baseline to 3 months using liquid chromatography-mass spectrometry assays.

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • University of Miami

Registry information

Acronym: PrEP2-BAY

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Apr 29, 2022
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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