Rapid HIV Viral Load Monitoring in High Risk Patients In Uganda
NCT03553693 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2443
Last updated 2021-03-30
Summary
The RAPID-VL study will take place in 20 HIV care health facilities in Southwestern Uganda. The study will test the hypothesis that a multi-component intervention package that targets barriers to efficient and timely HIV viral load (VL) testing will improve test ordering, speed up result turnaround times, and improve the quality of VL results counseling to patients. Phase 1 of the study will consist of a 1-year retrospective medical record review in all participating health facilities. In Phase 2 the intervention will be introduced in 10 randomly chosen health facilities, while the remaining 10 sites will continue with standard VL testing and counseling operations. The study will measure the speed and efficiency of VL testing, experiences of patients and clinicians with the intervention, and the cost of the intervention.
Conditions
Interventions
- OTHER
-
RAPID-VL study intervention
* Viral load (VL) ordering flowsheet with periodic health facility performance feedback * Rapid near-point-of-care VL testing and telephone delivery of results * Structured VL counseling package
Sponsors & Collaborators
-
Centers for Disease Control and Prevention
collaborator FED -
Infectious Diseases Research Collaboration, Uganda
collaborator OTHER -
Makerere University
collaborator OTHER -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Vivek Jain, MD, MAS · University of California, San Francisco
-
Moses R Kamya, MBChB, MMed · Makerere University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 2 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-07-16
- Primary Completion
- 2020-11-16
- Completion
- 2020-11-16
Countries
- Uganda
Study Locations
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