NCT06739915Completed
Targeted Universal TB Testing With Simultaneous TPT Prescribing Among People Living With HIV in South Africa
TUTT-PT: Targeted Universal TB Testing With Simultaneous TPT Prescribing Among People Living With HIV in South Africa
Source: ClinicalTrials.gov · Last updated 22 Jul 2026
Brief summary (registry, in English)
Background: In 2023, the South African Department of Health introduced targeted universal TB testing (TUTT) at antiretroviral therapy (ART) initiation (irrespective of the presence of TB symptoms). Guidelines regarding TPT initiation in the setting of TUTT are conflicting - recommending either (1) delaying TPT initiation for all patients until a negative TB test result is returned or (2) delaying TPT only for those patients with a positive TB symptom screen. The new TUTT approach along with ambiguity in the timing of TPT initiation has the potential to substantially reduce timely TPT initiation - missing the period of highest TB risk. In modelling approaches for TB screening and TPT delivery, the investigators found that waiting for a sputum result could decrease TPT prescribing from the current level to approximately 17-31%. A novel alternative is to provide TPT at the time of TB testing to all patients initiating or re-initiating ART (TUTT-PT). Those who test positive for TB (5-8% of patients) would be promptly contacted and switched to anti-TB treatment. The investigators model suggests that this strategy could ensure that almost 90% of patients receive TPT and are tested for TB simultaneously. The viability of such an approach depends on demonstrating the safety and effectiveness of TPT for all vs the standard of care. Guiding the optimal implementation strategy for TPT delivery - balancing high-levels of TPT prescribing with rapid diagnosis and treatment initiation for active TB disease - is essential to ensure the continued success of South Africa's TPT program. The investigators are conducting a one-year study built onto Fedisa PreventTB to compare the proposed novel approach of universal TPT to the standard approaches to inform further TPT policy and optimize the effectiveness of the Fedisa PreventTB behavioral economics approach in light of the new TB testing approach. The overall aim is to pilot test the effectiveness and safety of targeted universal TB testing with simultaneous TPT (TUTT-PT) to increase TPT initiation among PLHIV initiating (or re-initiating) ART and to characterize clinic level implementation determinants among health care workers.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 364 (actual)
- First submitted
- 13 Dec 2024
- Start date
- 28 May 2024
- Primary completion date
- 21 Jul 2025
- Lead sponsor
- Johns Hopkins University
- Diseases
- Tuberculosis, HIV
- NCT number
- NCT06739915
What you commit to
- Study type: Interventional
- Participants enrolled: 364
- From 28 May 2024 to the primary completion date, 21 Jul 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Person living with HIV stable on ART
Other
- Not speaking any of the languages spoken by the study team
Who the study is looking for
- Adults 18 years and older
- Person living with HIV newly initiating or re-initiating ART at a participating site
- Residing within the catchment area of the clinic and willing to be followed up telephonically or via a home visit by a study team tracer
- Willing and able to provide written informed consent
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Perinatal HIV Research Unit Coordinator of this site? Confirm its status | Soweto | South Africa | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.