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NCT Number: NCT06423612

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

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Desmond Tutu HIV Foundation

East London, South Africa

Location status: Recruiting

Location contact

Andrew Marino, PhD

PRINCIPAL_INVESTIGATOR

Sammy Nena

CONTACT

[email protected]

+27715153785

About this study

This is a randomized hybrid type 1 effectiveness study design to assess the factors related to implementation of a point-of-care urine TFV assay test into routine HIV clinical care. We plan to recruit a total of 500 adults living with HIV who received primary HIV care from one of the selected study clinics in BCM, Eastern Cape. Individuals who have been prescribed ART for at least 6 months who have not achieved VS will be randomized in a 1:1 fashion at the baseline visit to the intervention arm vs. the SoC arm.

Total duration of the study is 18 months from the time of enrollment.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Aim 1: Individuals ≥18 years of age at the initial screening visit living with HIV, prescribed ART for at least three months, and are not virally suppressed.

Aim 2: Same as Aim 1 for the acceptability survey and in-depth interviews. HIV care providers in the selected clinic sites for the feasibility survey and in-depth interviews.

Aim 3: Same as Aim 1 for the cost-effectiveness study.

Exclusion criteria

  • 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

Treatment and study plan

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.

Primary outcomes

  1. Viral Suppression at 6 months

    Time frame: 18 months

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

Secondary outcomes

  1. Viral suppression at 9, 12, and 18months

    Time frame: 18 months

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

  2. Resistance testing and genotype results @ 6 and 18 months

    Time frame: 18 months

    The effect of the intervention on need for resistance testing and genotype results @ 6 and 18 months

  3. Feasibility and Acceptability of the intervention

    Time frame: 18 months

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

  4. Cost-effectiveness of the intervention

    Time frame: 18 months

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Monica Gandhi

CONTACT

[email protected]

415 476 4082 ext. 127

Purba Chatterjee

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • Desmond Tutu HIV Foundation
  • National Institute of Allergy and Infectious Diseases (NIAID)
  • University of Cape Town

Registry information

Acronym: ROVING-PUMA

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 21, 2024
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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