Actively Recruiting

Phase Not Applicable
Age: 16Years - 29Years
MALE
Healthy Volunteers
NCT06741631

MyPEEPS LITE Trial

Led by Columbia University · Updated on 2026-02-27

3200

Participants Needed

2

Research Sites

203 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

This study will use community-informed advertisements and messages through electronic methods to recruit and retain a large (N=3,200), diverse national sample of high-risk young men who have sex with men (YMSM) and non-binary individuals that are assigned male sex at birth, 16-29 years of age to determine the efficacy of the MyPEEPS Mobile intervention on reduced incident HIV infections in comparison to a standard of care condition and to examine the degree to which reduced incident HIV infections occurs in the context of potential multilevel moderators and conceptual mediators. This is key to advancing HIV prevention among HIV-negative US persons at extremely high-risk for HIV seroconversion.

CONDITIONS

Official Title

MyPEEPS LITE Trial

Who Can Participate

Age: 16Years - 29Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 16-29 years of age
  • Sex assigned at birth is male and identify gender as male or non-binary
  • Understand and read English
  • Live within US and its territories
  • Own or have access to a smartphone
  • Self-report anal sex with someone who has a penis in the last 12 months
  • Be HIV-negative or status unknown
Not Eligible

You will not qualify if you...

  • Individuals who identify as transgender

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Ann & Robert H. Lurie Children's Hospital of Chicago

Chicago, Illinois, United States, 60611

Actively Recruiting

2

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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