Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05626452

PrEP Optimization Among Women to Enhance Retention and Uptake

Led by University of Chicago · Updated on 2026-02-10

680

Participants Needed

1

Research Sites

146 weeks

Total Duration

On this page

Sponsors

U

University of Chicago

Lead Sponsor

A

AllianceChicago

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

PrEP Optimization Among Women to Enhance Retention and Uptake

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • HIV-negative
Not Eligible

You will not qualify if you...

  • Younger than age 18 years
  • HIV-positive

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

J

Jessica Ridgway, MD, MS

CONTACT

S

Samantha Devlin Devlin, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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