Intervention for Virologic Suppression in Youth (iVY)
HIV/AIDS, Young Adult, Mobile Health
About this trial
This is an interventional health services research trial for HIV/AIDS focused on measuring Young Adults, Telehealth, Health Disparity, HIV, Mobile App
Eligibility Criteria
Inclusion Criteria: Receive care at an AIDS Healthcare Foundation (AHF) California or Florida-based healthcare center HIV seropositive 18-29 years of age Have an unsuppressed HIV viral load in the past 3 months. Able to speak English Have access to smartphone Exclusion Criteria: Unable or unwilling to provide consent. Evidence of severe cognitive impairment, active psychosis, or substance use that may impede ability to provide informed consent during the consent process. Those with a history of hemophilia or unable to conduct finger prick at home for the HIV viral load testing.
Sites / Locations
- Division of Prevention Science, Center for AIDS Prevention Studies (CAPS)
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard of Care Arm
Intervention Arm: Video-Counseling+app
The Standard of Care (SOC) arm will include the current care delivery model: regularly scheduled visits with a healthcare provider and lab testing every 3-6 months or more/less frequently depending on the individual's HIV health outcomes (e.g., VL suppression) . At each assessment, the investigators will review participant responses to examine acute need for referral for medical, psychological, or substance use services. In between assessments, researchers will also do monthly check-ins to improve retention and check contact information.
The video-counseling+app arm will receive 12 brief weekly counseling sessions (given over 16 weeks) with a social worker, along with access to the WYZ app to use based on their needs. After 16 weeks, participants receive another assessment and based on VL, those in the video-counseling+app arm will be categorized as intervention responders or non-responders (responder= virologically suppressed; non-responder= virologically unsuppressed. Responders in video-counseling+app arm will continue to use the app only. Non-responders in the intervention arm will continue with intensified video-counseling+app for 16 more weeks.