Randomized Trial to Optimize Virologic Suppression Rates Using a Point-of-Care Urine Monitoring Assay (ROVING PUMA)

ConditionART Adherence
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of California, San Francisco

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • POC urine assay informed enhanced ART adherence counselling for viral suppression

    Behavioral

    Collect 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

500 Participants
are divided into 2 treatment groups
Group A: POC Urine Test Informed ART Adherence CounsellingExperimental treatment 1 intervention
Group B: Standard-of-care Enhanced Adherence CounsellingNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Viral Suppression at 6 months

The primary outcome of effectiveness will be viral suppression at 6 months.

Time frame
18 months

Secondary outcomes

1

Viral suppression at 9, 12, and 18months

Durability of the 6-month intervention on viral suppression at 9, 12, and 18months

Time frame
18 months
2

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

Time frame
18 months
3

Feasibility and Acceptability of the intervention

Assess the feasibility and acceptability of the intervention using a survey and in-depth interviews

Time frame
18 months
4

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.

Time frame
18 months

Other outcomes

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