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NCT07292584Recruiting

Evaluating an Interactive Digital Toolkit for Women's PrEP Implementation

Source: ClinicalTrials.gov · Last updated 23 Jun 2026

Brief summary (registry, in English)

The goal of this study is to test if a Digital PrEP Toolkit helps cisgender women learn about and access PrEP in Alabama and Mississippi. PrEP is a medication that prevents HIV infection. The main questions it aims to answer are: Can participants complete the Digital PrEP Toolkit in under 10 minutes? Do participants find the Digital PrEP Toolkit useful and easy to use? Does the Digital PrEP Toolkit increase the number of women who start taking PrEP? Investigators will work with up to 125 women at 3 HIV and STI clinics in Alabama and Mississippi. Participants will use the Digital PrEP Toolkit on a tablet at the clinic. They will answer questions about their HIV knowledge before and after using the Toolkit. Participants will then discuss PrEP options with a healthcare staff member and decide if they want to start PrEP. Participants will answer follow-up questions at 3 months. Investigators will also review participants' medical records at 6 months to see if they started PrEP and are still taking it.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
125 (estimated)
First submitted
24 Nov 2025
Start date
20 Apr 2026
Primary completion date
Dec 2027
Lead sponsor
University of Alabama at Birmingham
Diseases
HIV
NCT number
NCT07292584

What you commit to

  • Study type: Interventional
  • Planned participants: 125
  • From 20 Apr 2026 to the primary completion date, Dec 2027
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Living with HIV

Age

  • Younger than 18 years of age

Other

  • Do not identify as female and/or were not biologically assigned female at birth
  • Report no sexual activity in the past six months and no anticipated sexual activity in the next six months
  • Unable or unwilling to provide informed consent

Who the study is looking for

  • HIV-negative
  • Cisgender women
  • 18 years or older
  • English-speaking
  • Report sexual activity in the last six months or anticipate sexual activity in the next six months.

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesRecruiting
Five Horizons Health Services
Coordinator of this site? Confirm its status
MontgomeryUnited StatesRecruiting
Five Horizons Health Services
Coordinator of this site? Confirm its status
StarkvilleUnited StatesRecruiting
Five Horizons Health Services
Coordinator of this site? Confirm its status
TuscaloosaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.