Actively Recruiting
Intervention to Enhance PrEP Persistence
Led by Brown University · Updated on 2025-03-12
300
Participants Needed
3
Research Sites
199 weeks
Total Duration
On this page
Sponsors
B
Brown University
Lead Sponsor
W
Whitman-Walker Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
The investigators will conduct a fully powered randomized controlled trial (RCT) to test the effect of a patient navigation intervention for Black/African American (B/AA) men who have sex with men (MSM) on PrEP initiation, adherence and retention in care. B/AA men who have sex with men (MSM) are disproportionately impacted by the HIV/AIDS epidemic in the United States. Pre-exposure prophylaxis (PrEP), a once daily medication, can dramatically reduce HIV acquisition risk. However, social and structural barriers have contributed to suboptimal PrEP initiation, adherence, and retention in care among B/AA MSM. Our prior NIH-funded pilot study (R34MH109371; MPI: Nunn, Chan, Mena) developed and evaluated an Intervention to Retain and Adhere MSM in PrEP (RAMP-IT-UP), a brief strengths-based patient navigation program to enhance PrEP care outcomes among young B/AA MSM. The intervention was found to be highly acceptable among B/AA MSM and demonstrated preliminary effectiveness. Compared to control participants, RAMP-IT-UP participants were statistically more likely to initiate PrEP and adhere to PrEP based on pharmacy fill data and PrEP blood levels. Additionally, RAMP-IT-UP participants were more likely to be retained in PrEP care at the 3-month and 6-month clinical visits. Specific Aim #1 of this study will conduct a fully powered randomized controlled trial (RCT to estimate the effectiveness of RAMP-IT-UP in improving PrEP adherence and care outcomes among B/AA MSM in real-world community health center settings (CHCs). Specific Aim #2 will estimate the cost-effectiveness of RAMP-IT-UP among B/AA MSM attending CHCs compared to standard of care. The investigators will also determine the cost-effectiveness of differing levels of intensity of navigation services to prevent HIV based on data collected in Specific Aim #1. Our goal is to develop a cost-effective intervention that enhances PrEP care outcomes and reduces HIV incidence for B/AA MSM which will be relevant for CHCs across the US. The long-term goal of this work is to decrease HIV incidence among B/AA MSM, which aligns with federal Ending the HIV Epidemic and National HIV/AIDS Strategy goals. This application is led by an experienced team of investigators with a proven track record conducting HIV, PrEP and disparities research in real-world clinical settings.
CONDITIONS
Official Title
Intervention to Enhance PrEP Persistence
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years and older
- Assigned male sex at birth
- Identify as Black/African American
- Report at least one male sex partner in the past 12 months
- Meet the CDC eligibility criteria for PrEP
- Have not taken PrEP for at least 30 days
- Are HIV-negative based on antibody testing at the time of enrollment
- Understand and speak English
- Able to provide informed consent
- Agree to authorize study access to their EHR and pharmacy fill data
You will not qualify if you...
- Under the age of 18
- Assigned female sex at birth
- Does not identify as Black/African American
- Has not had a male sex partner in the past 12 months
- Does not meet CDC eligibility criteria for PrEP
- Has taken PrEP within the last 30 days
- HIV-positive or inconclusive HIV status based on antibody testing at the time of enrollment
- Does not understand or speak English
- Unable to provide informed consent
- Does not agree to authorize study access to their EHR and pharmacy fill data
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
Whitman Walker Health
Washington D.C., District of Columbia, United States, 20005
Actively Recruiting
2
University of Mississippi Medical Center
Jackson, Mississippi, United States, 39216
Actively Recruiting
3
The Rhode Island Public Health Institute
Providence, Rhode Island, United States, 02907
Actively Recruiting
Research Team
D
Dr. Amy Nunn, ScD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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