About this trial
Antiretroviral therapy (ART) has significantly decreased the morbidity and mortality of HIV infection. However, adherence challenges in taking daily oral ART persist. A retrospective cohort study across 31 countries from 2010-19 reported that only 65% of people with HIV (PWH) on ART exhibited virologic suppression (VS) three years after starting ART;1 the rate of VS in South Africa among PWH on ART is 60-65%. Adherence barriers span individual and structural factors, such as stigma, recall difficulties, housing and/or food insecurity, mental illness, substance use, transportation, stock-outs, and other factors that vary by country and population.
Adherence interventions can benefit from direct objective adherence monitoring. Pharmacologic metrics of adherence assess drug levels in plasma, dried blood spots, hair (a metric our group pioneered) or urine and predict outcomes more accurately than self-reported adherence. However, most of these metrics preclude real-time assessment, requiring expensive laboratory equipment and trained laboratory personnel. Thus, few adherence interventions have successfully incorporated objective metrics, likely due to laboratory and shipping delays. A low-cost (\<$2/test) point-of-care adherence metric - developed by our group - should allow for real-time biofeedback and improve the impact of metric-driven adherence interventions.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
Currently enrolled in another ART adherence intervention
Patients on ART regimen that does not include Tenofovir
HIV care providers from non-study sites Failure to provide written consent
Trial design
Parallel
Treatments tested in this trial
POC urine assay informed enhanced ART adherence counselling for viral suppression
BehavioralCollect urine on intervention participants and screen for presence of TFV. Feedback will be provided to the participant based on the results on their ART adherence with provision of enhanced ART adherence counseling for viral suppression.
Treatment groups
Trial outcomes
Primary outcomes
Viral Suppression at 6 months
The primary outcome of effectiveness will be viral suppression at 6 months.
Secondary outcomes
Viral suppression at 9, 12, and 18months
Durability of the 6-month intervention on viral suppression at 9, 12, and 18months
Resistance testing and genotype results @ 6 and 18 months
The effect of the intervention on need for resistance testing and genotype results @ 6 and 18 months
Feasibility and Acceptability of the intervention
Assess the feasibility and acceptability of the intervention using a survey and in-depth interviews
Cost-effectiveness of the intervention
Assess the cost per patient, cost per additional patient with VS, and cost per disability-adjusted life-year averted from a society perspective with using the urine-based TFV adherence assay to inform adherence counseling vs. standard of care counseling.
Sponsors and contacts
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University of California, San Francisco
Lead sponsor
Desmond Tutu HIV Foundation
Collaborator
University of Cape Town
Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborator