Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
Healthy Volunteers
NCT06872307

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

Age: 18Years +
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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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

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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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