MyPEEPS LITE Trial

Description

This study will use community-informed advertisements and messages through electronic methods to recruit and retain a large (N=2,500), 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

HIV/AIDS

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Study Overview

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Study Details

Study overview

This study will use community-informed advertisements and messages through electronic methods to recruit and retain a large (N=2,500), 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.

MyPEEPS LITE Trial

MyPEEPS LITE Trial

Condition
HIV/AIDS
Intervention / Treatment

-

Contacts and Locations

Chicago

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United States, 60611

New York

Columbia University, New York, New York, United States, 10032

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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; and
  • * Be HIV-negative or status unknown
  • * Individuals who identify as transgender

Ages Eligible for Study

16 Years to 29 Years

Sexes Eligible for Study

MALE

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Columbia University,

Rebecca Schnall, PhD, MPH, PRINCIPAL_INVESTIGATOR, Columbia University

Robert Garofalo, MD, MPH, PRINCIPAL_INVESTIGATOR, Ann & Robert H Lurie Children's Hospital of Chicago

Dustin Duncan, ScD, PRINCIPAL_INVESTIGATOR, Columbia University

Study Record Dates

2028-12-01