Hybrid Type I Effectiveness-Implementation Trial of Project nGage

Description

The goal of this Hybrid Type I effectiveness-implementation trial is to test Project nGage, an evidence-based, flexible, and tailored intervention that leverages existing social network members to promote retention in care and viral suppression among young Black men and women ages 18-49.

Conditions

HIV Seropositivity

Study Overview

Study Details

Study overview

The goal of this Hybrid Type I effectiveness-implementation trial is to test Project nGage, an evidence-based, flexible, and tailored intervention that leverages existing social network members to promote retention in care and viral suppression among young Black men and women ages 18-49.

Harnessing Social Network Support to Improve Retention in Care and Viral Suppression Among Young Black Men in Chicago and Alabama: A Hybrid Type I Effectiveness-implementation Trial of Project nGage

Hybrid Type I Effectiveness-Implementation Trial of Project nGage

Condition
HIV Seropositivity
Intervention / Treatment

-

Contacts and Locations

Birmingham

University of Alabama at Birmingham 1917 Clinic, Birmingham, Alabama, United States, 35205

Birmingham

Birmingham AIDS Outreach, Birmingham, Alabama, United States, 35233

Huntsville

Thrive Alabama, Huntsville, Alabama, United States, 65801

Chicago

Howard Brown Health, Chicago, Illinois, United States, 60613

Chicago

Chicago Center for HIV Elimination, Chicago, Illinois, United States, 60637

Chicago

Crown Family School of Social Work, Policy, and Practice at the University of Chicago, Chicago, Illinois, United States, 60637

New Orleans

Tulane University, New Orleans, Louisiana, United States, 70118

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

  • * Romantic/Sexual partners of Index participant
  • * Relationship strain or abuse present in Index-SC relationship

Ages Eligible for Study

18 Years to 49 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of Chicago,

Alida Bouris, PhD, PRINCIPAL_INVESTIGATOR, University of Chicago

David S Batey, PhD, PRINCIPAL_INVESTIGATOR, Tulane University

Study Record Dates

2027-12-31