Health TrialsbyHealthPanel

Integrating Supports to Promote PrEP for Black Adolescents Working With Apps- Atlanta

ConditionHIV Infections
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14-21
SponsorEmory University

About this trial

This study applies Social Cognitive Theory to develop behavioral interventions promoting PrEP adherence. It seeks to adapt and test the enhanced HMP app for feasibility and acceptability among Black adolescents and young adults (AYAs) and adult supports.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

African Americans

Living in metropolitan Atlanta counties- Cobb, DeKalb, Fulton, Gwinnett

Have a PrEP indication (e.g., sex with a partner living with HIV, condomless sex, sex with multiple partners, engagement in transactional sex, or at least one sexually transmitted infection in the past 6 months)

self-reported provision of instrumental, informational, or emotional support for a Black AYA 14-21 years old

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Health MPowerment App

    Behavioral

    A mobile health app designed to facilitate increased PrEP use and adherence among AYAs

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: AYA groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Acceptability/Usability

The study evaluates an app's impact through post-intervention interviews, focusing on user experience, ethical concerns, and future usage intentions. It explores burden, satisfaction, attitudes, and how the app influences communication and adherence. Sekhon's Theoretical Framework of Acceptability will be utilized to measure this outcome.

Time frame
1 month, 3 months, and 6 months
2

Feasibility: Communication

Communication between adolescents and young adults (AYA) and support person (i.e., Experience using chat features; Experience using forums). A modified version of Structured Assessment of FEasibility (SAFE) will be utilized to measure this outcome.

Time frame
1 month, 3 months, and 6 months

Secondary outcomes

1

Medication Adherence Tracker

This will be measured by analyzing the percent of dates with data entered into the medication tracker and correlating that data with reasons why participants did not take their medication (when applicable)

Time frame
1 month, 3 months, and 6 months
2

Data Usage

This will be measured by comparing the amount of time (minutes) spent using distinct features of the app (e.g. forums, educational resources, avatars, side effect trackers, chat features)

Time frame
1 month, 3 months, and 6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Emory University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: