PrEP2Prevent An Online PrEP Navigation and Activation Intervention
NCT05281393 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150
Last updated 2024-02-09
Summary
* The goal of this clinical trial entitled, PrEP2Prevent: An Online PrEP Navigation and Activation Intervention for YMSM, is to develop and test a method for supporting access to an HIV prevention medication called Pre-Exposure Prophylaxis (PrEP) in young men who have sex with men and young transgender and non-binary individuals. The main questions it aims to answer are:
* What are some of the experiences and barriers providers have seen regarding this population accessing PrEP
* Using information gathered from PrEP providers and navigators, develop a mobile health platform and PrEP related content that will be tested by members of the population to see if the features are usable and the content is understandable.
* Enroll 150 study participants to see if utilizing the mobile health platform and receiving supportive sessions related to motivation and barriers to accessing PrEP is achievable.
* Participants will
* Be given access to the mobile health Platform called PrEPresent, which provides them with access to prevention related content, the ability to schedule with a patient navigator and create customizable goals
* Complete a baseline, 3 month and 6 month assessment about personal health, health history and technology, along with a PrEP adherence rapid urine test
* Complete up to 4 sessions to assist participants in the intervention group with discussing any barriers to accessing PrEP
Conditions
- HIV Infections
Interventions
- BEHAVIORAL
-
PrEPresent
PrEP2Prevent is being done in several phases (parts) to develop and pilot test a PrEP activation, navigation and support intervention for young men who have sex with men (YMSM), trans youth and non-binary youth in Los Angeles. It targets an intervention for these young people where they need it most - on PrEP uptake. PrEP stands for pre-exposure prophylaxis.
Sponsors & Collaborators
-
Florida State University
collaborator OTHER -
Children's Hospital Los Angeles
lead OTHER
Principal Investigators
-
Michele D Kipke, PhD · Children's Hospital Los Angeles
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 16 Years
- Max Age
- 26 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-01-28
- Primary Completion
- 2023-06-20
- Completion
- 2024-01-03
Countries
- United States
Study Locations
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