TelePrEP for HIV Prevention

AS
RM
Overseen ByRebecca Moges-Banks, MPH
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Emory University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Who Is on the Research Team?

AS

Aaron Siegler, PhD

Principal Investigator

Emory University

Are You a Good Fit for This Trial?

This trial is for people in the US who use MISTR, a telehealth service for HIV prevention (PrEP). Participants should be interested in starting or continuing PrEP through telemedicine. Specific inclusion and exclusion criteria are not detailed.

Inclusion Criteria

Reside in the United States
Individuals who use MISTR services
I am 18 years old or older.

Exclusion Criteria

Individuals who do not use MISTR services
Individuals who do not reside in the United States

What Are the Treatments Tested in This Trial?

Trial Overview

The study compares different ways of delivering digital messages and website designs to improve how people start and stay on PrEP using telehealth. Participants are randomly assigned to receive standard care or new messaging approaches.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Intervention ConditionExperimental Treatment2 Interventions
Group II: Control ConditionActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Emory University

Lead Sponsor

Trials
1,735
Recruited
2,605,000+

National Institute of Allergy and Infectious Diseases (NIAID)

Collaborator

Trials
3,361
Recruited
5,516,000+