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Improving TelePrEP Initiation and Retention Outcomes in the US: The MISTR+ Study
Sponsor: Emory University
Summary
This study uses a rapid randomized controlled trial (RCT) design to examine HIV pre-exposure prophylaxis (PrEP) delivered through telehealth. This study will develop a knowledge base of small, effective changes to digital messaging and website design to improve telemedicine PrEP (telePrEP) provision for MISTR users in the United States.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
223165
Start Date
2027-03-01
Completion Date
2031-05-31
Last Updated
2026-09-16
Healthy Volunteers
No
Conditions
Interventions
No Marginal Cost Interventions
The exact intervention types will be determined based on Aim 1 data analyses that seek to identify the areas that could most benefit from intervention. Possible interventions to be tested include message content, message format, message time of day, and website design.
Low-Marginal Cost Interventions
The exact intervention types will be determined based on Aim 1 data analyses that seek to identify the areas that could most benefit from intervention. Possible interventions to be tested include warm handoffs, personalized messages, and enhanced remote laboratory testing.
Standard of Care
MISTR users receive the current standard of care. The standard of care will be updated as impactful interventions are identified.
Locations (1)
Emory University Rollins School of Public Health
Atlanta, Georgia, United States