Leveraging mHealth to Enable and Adapt CHW Strategies to Improve TB/HIV Patient Outcomes in SA
NCT ID: NCT04298905
Last Updated: 2026-01-29
Study Results
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Basic Information
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ACTIVE_NOT_RECRUITING
NA
62 participants
INTERVENTIONAL
2022-03-10
2026-12-31
Brief Summary
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Investigators have demonstrated the feasibility of mHealth and human resource solutions in South Africa and shown marked improvements in screening, linkage and treatment initiation as well as supporting patient adherence through video DOT (vDOT) and early identification of treatment related toxicity. Investigators' strategies have evaluated solutions for individual cascade steps through TB and HIV smartphone and tablet-based m-health applications implemented by a CHW. This study combines these individual cascade step approaches into an innovative TB/HIV cascade intervention study entitled, "Leveraging mHealth to enable and adapt community health worker strategies to improve TB/HIV patient outcomes in South Africa (LEAP-TB-SA) Trial."
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Detailed Description
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Studies addressing the TB or HIV care cascades are increasingly common, yet few offer an integrated, sustainable approach to TB/HIV co-infection and, to date, no intervention spans the entire cascade. The TB/HIV care cascade begins with diagnosis of TB in a PLWH or in a person newly diagnosed with both diseases. Patients newly diagnosed with TB and HIV face a burdensome model of care influenced by: a) timing of HIV treatment initiation; b) worsened symptom profiles associated with immune reconstitution syndrome; c) higher pill burden; d) differential adherence challenges; e) and more frequent care visits for directly observed therapy (DOT) and laboratory evaluations. Many, have struggled with adherence to HIV regimen, prior to the TB diagnosis. Data found that 44% of PLWH on anti-retroviral therapy (ART) present with viral suppression to first TB visit, suggesting the need to further intensify adherence interventions in this group.
Hypothesis: The intervention will have fewer composite negative TB outcomes (i.e. treatment failure, loss to follow-up, and death) compared to attention controls.
Primary Aims:
1\. to determine the feasibility, acceptability and impact of a mHealth triggered, escalating adherence intervention by community health workers (CHW) to improve rif-resistant (RR)-TB treatment outcomes among PLWH in Kwa-Zulu Natal, Province of South Africa through a pilot randomized controlled trial. H1. the mHealth triggered, escalating adherence intervention by CHW's will improve treatment success for RR-TB and HIV co-infected patients compared to attention control participants.
Secondary Aims:
1. to conduct a time-limited prospective screening cohort of close contacts of persons diagnosed with RR-TB using respondent driven sampling.
2. to evaluate willingness to participate in the trial and determine who screen fails for any reason.
3. to evaluate study process indicators to further refine the behavioral and technological components of the intervention (patient symptom reporting; vDOT submission compliance; CHW adherence coaching sessions; intervention theoretical models; and mHealth application feature enhancements to support care coordination).
4. to characterize the emergence of resistance among patients with non-adherence to RR-TB treatment, by obtaining two additional sputum specimens (i.e., 1) on treatment initiation for all patients and 2) among participants with a 30-day period of less than optimal adherence (defined as \<90% of vDOT submissions or patient/provider report non-adherence) and/or treatment failure (defined as positive culture with evidence of additional antimicrobial resistance) to fully characterize resistance patterns through genotypic and phenotypic resistance testing as well as next generation molecular sequencing.
5. to characterize HIV genotypic resistance patterns among participants with a detectable viral load.
6. to determine, retrospectively, the impact of HIV resistance patterns on RR-TB treatment outcomes.
7. to assess stigma throughout the RR-TB care continuum and evaluate whether the level of stigma changes through different phases of treatment.
8. to pilot test the psychometric properties of four novel indicators of intersectional RR- TB-HIV stigma.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Standard of Care
Individuals randomized to standard of care will receive a standardized adherence education session and provided with a paper-based diary to track appointments and adherence. Instructions will be provided on the importance of daily adherence in the primary health care facility closest to patients' residence, as per standard of care. Directly observed therapy (DOT) is recommended for all patients at patients' nearest clinic. All patients are seen face-to-face monthly for adherence monitoring, monthly symptom reports and laboratory evaluations per standard of care treatment guidelines. All research participants will also receive a clinic visit quality checklist to ensure completeness of standard of care procedures.
No interventions assigned to this group
mHealth intervention
Individuals randomized to the intervention arm will receive the same standardized adherence education, followed by an orientation session to the study intervention. This orientation will include education on basic smartphone operations and use. The CHW will set up appointment reminders for clinic visits as well as daily adherence reminders for submission of the video DOT sessions and symptom reports. A smartphone capable of downloading apps, receiving short message service (SMS) and access wifi and cellular connectivity will be provided to intervention patients. All patients are seen face-to-face monthly for adherence monitoring, monthly symptom reports and laboratory evaluations per standard of care treatment guidelines. All research participants will also receive a clinic visit quality checklist to ensure completeness of standard of care procedures.
CHW mHealth patient intervention for trigger escalation
The CHW dashboard is a tablet-based, per-patient summary of the patient intervention. It is this dashboard that identifies a trigger to escalate the adherence intervention. This dashboard is created by receiving information from the patient's smartphone application as well as the National Health Laboratory Service (NHLS) data feed of laboratory results. The monitoring features included in this dashboard:
1. NHLS laboratory results: Dashboard receives and flags NHLS results for any positive smear or culture (new positive after prior negative results) or detectable viral load (with prior viral suppression)
1. Triggered, escalating adherence coaching:
2. Safety monitoring: reports all abnormal laboratory values to provider
2. Appointment keeping (RETAIN):
a. Triggered, escalating adherence coaching
3. vDOT submissions:
a. Triggered, escalating adherence coaching
4. Symptom reports:
1. Triggered, escalating adherence coaching
Interventions
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CHW mHealth patient intervention for trigger escalation
The CHW dashboard is a tablet-based, per-patient summary of the patient intervention. It is this dashboard that identifies a trigger to escalate the adherence intervention. This dashboard is created by receiving information from the patient's smartphone application as well as the National Health Laboratory Service (NHLS) data feed of laboratory results. The monitoring features included in this dashboard:
1. NHLS laboratory results: Dashboard receives and flags NHLS results for any positive smear or culture (new positive after prior negative results) or detectable viral load (with prior viral suppression)
1. Triggered, escalating adherence coaching:
2. Safety monitoring: reports all abnormal laboratory values to provider
2. Appointment keeping (RETAIN):
a. Triggered, escalating adherence coaching
3. vDOT submissions:
a. Triggered, escalating adherence coaching
4. Symptom reports:
1. Triggered, escalating adherence coaching
Eligibility Criteria
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Inclusion Criteria
* HIV positive
* Outpatient TB treatment (including short course RR-TB treatment) or admission \< 30 days is expected
Exclusion Criteria
* Patients who require hospitalization for TB treatment at treatment initiation
* Extrapulmonary or disseminated TB disease
* Severe clinical presentation: BMI \< 18 kg/m2 or a person unable to stand/walk
18 Years
ALL
No
Sponsors
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Johns Hopkins University
OTHER
University of Witwatersrand, South Africa
OTHER
Responsible Party
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Principal Investigators
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Jason E Farley, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins University School of Nursing
Locations
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Kelly Lowensen
Baltimore, Maryland, United States
Countries
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References
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Other Identifiers
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IRB00211518
Identifier Type: -
Identifier Source: org_study_id
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