Actively Recruiting
AURORA Study-A Transformative Approach to Support PrEP Medication Persistence
Led by WV Health Right, Inc. · Updated on 2024-06-25
105
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
Sponsors
W
WV Health Right, Inc.
Lead Sponsor
V
ViiV Healthcare
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is designed to test the hypothesis that, compared to oral PrEP, use of CAB-LA in underserved populations in a real-world setting supported by a digital health companion program will be associated with greater medication adherence, persistence, retention-in-care, and improved PROs. Patients in the study will receive current standard care for HIV prevention and be offered enrollment in the digital health companion program. Goal of the study is to evaluate medication adherence and persistence in patients receiving CAB-LA vs oral PrEP and who engage with a digital health companion program.
CONDITIONS
Official Title
AURORA Study-A Transformative Approach to Support PrEP Medication Persistence
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Initiation of or current use of PrEP with CAB-LA, daily FTC/TDF, or daily FTC/TAF prescribed according to WVHR standard care
- PrEP medication dispensed by WVHR pharmacy
- Access to a smartphone
You will not qualify if you...
- Receiving HIV PrEP care outside of WVHR
- Positive HIV diagnosis
- Contraindication to oral or injectable PrEP therapy
- Receiving oral bridging therapy before injectable PrEP therapy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
West Virginia Health Right
Charleston, West Virginia, United States, 25311
Actively Recruiting
Research Team
A
Angie Settle, DNP, APRN
CONTACT
R
Rhonda Francis, CPhT, Adv
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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