Actively Recruiting

Phase Not Applicable
Age: 16Years - 25Years
MALE
Healthy Volunteers
NCT06741618

MyPEEPS Mobile Plus: A Multi-Level HIV Prevention Intervention for Young MSM

Led by Columbia University · Updated on 2026-05-07

500

Participants Needed

1

Research Sites

125 weeks

Total Duration

On this page

Sponsors

C

Columbia University

Lead Sponsor

A

Ann & Robert H Lurie Children's Hospital of Chicago

Collaborating Sponsor

AI-Summary

What this Trial Is About

MyPEEPS Mobile Plus, a multi-level intervention for improving HIV prevention outcomes in YMSM, is a novel and evidence-driven approach using mobile technology to deliver HIV prevention information specifically developed for YMSM. Building on strong preliminary work, the proposed research is the next logical step in a body of work designed to assess whether refinement of this mobile intervention used in combination with virtual PrEP Peer Navigation will result in improvements in PrEP uptake and a reduction in HIV-related behavior. This is key to advancing HIV prevention among HIV-negative US persons at extremely high-risk for HIV seroconversion.

CONDITIONS

Official Title

MyPEEPS Mobile Plus: A Multi-Level HIV Prevention Intervention for Young MSM

Who Can Participate

Age: 16Years - 25Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 16 to 25 years of age
  • Identify as male, non-binary, or genderqueer
  • Assigned male sex at birth
  • Able to read and understand English
  • Own a smartphone
  • Report condomless anal sex with a male in the past year
  • Verified HIV-negative status by OraQuick test
Not Eligible

You will not qualify if you...

  • HIV positive
  • Unable to consent due to severe cognitive impairment or being under the influence of drugs or alcohol as determined by study staff
  • Currently using PrEP consistently

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Columbia University

New York, New York, United States, 10032

Actively Recruiting

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Research Team

R

Rebecca Schnall, PhD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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