A Self-administered PrEP Decisional Aid for Dissemination With HIV Self-test Kits (DASH)

Enrolling by invitation · Not applicable

Conditions studied: Pre-Exposure Prophylaxis (PrEP), HIV Prevention

In brief

People using HIV self-testing (HIVST) need access to quality HIV-prevention programming, including education and exploration of pre-exposure prophylaxis (PrEP) - an effective biomedical prevention tool that continues to expand in choices and access points in the US. HIVST and PrEP are both central to ending the HIV epidemic, but presently they are not linked together in a systematic way. To address the critical need for PrEP programming to accompany HIV self-testing (HIVST), our study will work with experts and HIVST users to develop and pilot a novel, interactive, mobile friendly PrEP decisional-aid mobile optimized website that helps to raise awareness around PrEP and guides people through a PrEP-decision-making process that matches their needs and values, and links people to resources for local or online PrEP. This PrEP Decisional Aid to accompany Self HIV-test kits (the DASH app) will be in a randomized controlled pilot trial with 120-170 HIV self-test kit users in the CDC's Together TakeMeHome HIV-test kit dissemination program. PrEP uptake at 3-months (primary outcome) will be compared between arms descriptively and with logistic regression models. Change in additional PrEP related factors (knowledge, stigma, decisional conflict, barriers and facilitators) will be assessed as secondary outcomes. Implementation metrics, acceptability and feasibility will also be evaluated quantitatively and qualitatively. Results will inform revisions and recommendations for a decisional aid for raising PrEP awareness and use among self HIV-test users.

Key facts

Study ID
NCT07614165
Run by
University of Michigan
People needed
170
Starts
2026-04-17
Expected to finish
2026-12-31
Last updated by the study team
2026-06-03

Who can join

Age: 18 and older, up to 39. Sex: any. Healthy volunteers: accepted.

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Where it is running

Full record on ClinicalTrials.gov

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