RECRUITING

Patient-provider Decision Aid for HIV Post-exposure Prophylaxis Following Sexual Assault

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Pilot Testing of a Patient-provider Decision Aid for HIV Post-exposure Prophylaxis Following Sexual Assault

Quick Facts

Study Start:2024-10-04
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06139354

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years or older
  2. * seeking care from DCFNE following sexual assault
  3. * able to provide consent and participate in the study in English
  4. * meets CDC criteria for HIV PEP \[a) seeking care within 72 hours of potential exposure, b) potential exposure\]
  1. * \<18 years old
  2. * Does not meet CDC criteria for HIV PEP \[seeking care \>72 hours after assault, assault with minimal/low exposure risk\]
  3. * unable to complete study requirements in English

Contacts and Locations

Study Contact

Melissa Yu
CONTACT
(916) 360-0149
jcandresearch@uams.edu
Hannah Aston
CONTACT
jcandresearch@uams.edu

Principal Investigator

Jocelyn Anderson
PRINCIPAL_INVESTIGATOR
UAMS

Study Locations (Sites)

District of Columbia Forensic Nurse Examiners
Washington, District of Columbia, 20002
United States

Collaborators and Investigators

Sponsor: University of Arkansas

  • Jocelyn Anderson, PRINCIPAL_INVESTIGATOR, UAMS

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10-04
Study Completion Date2025-06

Study Record Updates

Study Start Date2024-10-04
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • sexual assault

Additional Relevant MeSH Terms

  • Hiv