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COMPLETED
NCT04168008
NA

A Peer-Led Intervention to Improve Postpartum Retention in HIV Care

Sponsor: University of Pennsylvania

View on ClinicalTrials.gov

Summary

The purpose of this study is to test the efficacy of a theory-driven peer intervention for pregnant and postpartum women living HIV. The peer intervention is designed to increase self-efficacy, social support, self-regulatory behaviors, and outcome expectancy in order to improve retention in care and viral suppression postpartum. The intervention will consist of face-to-face prenatal educational sessions, starting in early third trimester, and postpartum sessions scheduled up to three months postpartum.

Official title: A Randomized Controlled Trial of Women Involved in Supporting Health (WISH), a Peer-Led Intervention to Improve Postpartum Retention in HIV Care

Key Details

Gender

FEMALE

Age Range

16 Years - Any

Study Type

INTERVENTIONAL

Enrollment

151

Start Date

2020-03-03

Completion Date

2025-09-08

Last Updated

2026-10-09

Healthy Volunteers

No

Conditions

Interventions

BEHAVIORAL

WISH Adherence

The educational sessions will consist of an adherence-centered curriculum.

BEHAVIORAL

WISH Parenting

The educational sessions will focus on parenting and baby care.

Locations (7)

University of Alabama at Birmingham

Birmingham, Alabama, United States

MedStar Health Research Institute

Washington D.C., District of Columbia, United States

Emory University

Atlanta, Georgia, United States

Montefiore Medical Center/Albert Einstein College of Medicine

The Bronx, New York, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

Medical University of South Carolina

Charleston, South Carolina, United States

Baylor College of Medicine

Houston, Texas, United States