Actively Recruiting
Patient-provider Decision Aid for HIV Post-exposure Prophylaxis Following Sexual Assault
Led by University of Arkansas · Updated on 2025-07-18
45
Participants Needed
1
Research Sites
86 weeks
Total Duration
On this page
Sponsors
U
University of Arkansas
Lead Sponsor
U
University of California, Davis
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this trial is to pilot a digital, interactive patient-provider HIV PEP decision aid. The decision aid will incorporate five sections of content: 1) key clinical factors input by providers; 2) tailored multimedia-based HIV risk sharing information; 3) standardized multimedia educational messaging regarding the effectiveness, risks, and benefits of HIV PEP; 4) direct comparisons of priorities (e.g., physical well-being - "I want to do everything I can to prevent HIV," privacy - "I don't want others to know about the exposure," or cost - "I can't afford the pills'') completed by patients; and 5) tailored feedback regarding patient priorities for use in shared clinical decision making.
CONDITIONS
Official Title
Patient-provider Decision Aid for HIV Post-exposure Prophylaxis Following Sexual Assault
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older
- Seeking care from DCFNE following sexual assault
- Able to provide consent and participate in the study in English
- Meets CDC criteria for HIV PEP including seeking care within 72 hours of potential exposure and having a potential exposure
You will not qualify if you...
- Under 18 years old
- Does not meet CDC criteria for HIV PEP such as seeking care more than 72 hours after assault or assault with minimal/low exposure risk
- Unable to complete study requirements in English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
District of Columbia Forensic Nurse Examiners
Washington D.C., District of Columbia, United States, 20002
Actively Recruiting
Research Team
M
Melissa Yu
CONTACT
H
Hannah Aston
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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