PrEP Optimization Among Women to Enhance Retention and Uptake
NCT05626452 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 680
Last updated 2026-02-10
Summary
Black women experience one of the highest incidences of HIV among all subpopulations in the United States, but pre-exposure prophylaxis (PrEP) use among Black cisgender women is very limited. The investigators will implement four strategies (provider training, patient education, EMR optimization, and PrEP navigation) at 12 community health clinics in the Midwest and South. The investigators predict that PrEP use and other related outcomes will improve for participants after the intervention period.
Conditions
- PrEP Uptake
Interventions
- BEHAVIORAL
-
PrEP Education
Education for participants regarding PrEP
- BEHAVIORAL
-
Provider training
Training for medical providers at CHCs about how to identify participants eligible for PrEP, how to perform behavioral risk assessment and discussion of PrEP, and how to prescribe PrEP and monitor PrEP
- OTHER
-
EMR Optimization
EMR modifications to enhance PrEP care continuum outcomes including HIV risk assessment, identification of participants eligible for PrEP, provision of PrEP education, clinical decision support tools for prescription of PrEP, and tracking of PrEP care continuum outcomes using an electronic population health management tool
- OTHER
-
PrEP Navigation
Use of CHC staff members to assist participants with obtaining PrEP and attending PrEP care appointments
- OTHER
-
Provider Audit and Feedback
Audit of provider rates of PrEP prescription and persistence among participants and regular provision of feedback to providers with their performance on these PrEP measures
Sponsors & Collaborators
-
AllianceChicago
collaborator OTHER -
Howard Brown Health Center
collaborator OTHER -
Ann & Robert H Lurie Children's Hospital of Chicago
collaborator OTHER - collaborator OTHER
-
Rush University
collaborator OTHER -
University of Chicago
lead OTHER
Principal Investigators
-
Jessica Ridgway, MD, MS · University of Chicago
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-08-10
- Primary Completion
- 2026-04-30
- Completion
- 2026-06-30
Countries
- United States
Study Locations
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