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RECRUITINGINTERVENTIONAL

Closing -TB GAPs - for People Living With HIV: TB Guidance for Adaptable Patient-Centered Service

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Tuberculosis (TB) is the world's leading infectious cause of mortality and responsible for 1/3 of deaths in people living with human immunodeficiency virus (PLHIV). Children and adolescents living with HIV (CALHIV) are disproportionately affected due to inadequate preventive services, large case detection gaps, treatment and adherence challenges, and knowledge gaps. This project will generate evidence to inform interventions targeting several of these weaknesses in the TB/HIV cascade of care. Early detection and treatment of TB improve outcomes in people living with HIV (PLHIV). A key challenge in the detection of HIV-associated TB has been the implementation of screening that identifies the correct population for diagnostic testing. Increasing evidence demonstrates the poor performance of recommended symptom screens and diagnostic approaches. Hence, the investigators aim to define a more accurate TB screening and testing strategy among PLHIV (Objective 1 and Objective 2). TB preventive treatment (TPT) averts HIV-associated TB. Nevertheless, among PLHIV, TPT initiation and completion rates are sub-optimal and effective delivery strategies are not defined. As such, the investigators aim to identify the most effective TPT delivery strategy through shared decision making and by integrating approaches proven to be effective at improving HIV treatment adherence (Objective 3). Although evidence demonstrates that isoniazid preventive therapy (IPT) is cost-effective in young children living in TB/HIV high burden settings, the cost-effectiveness of newer short-course TPT has primarily been studied in the context of a TB low-burden, high-income setting. The investigators aim to generate evidence to fill this knowledge gap and inform policy for PLHIV living in TB/HIV high burden settings (Objective 4). This study is supported by the Centers for Disease Control and Prevention of the U.S. Department of Health and Human Services (HHS) as part of a financial assistance award totaling an anticipated $5,000,000 over five years with 100 percent funded by CDC/HHS.

Who May Be Eligible (Plain English)

OBJECTIVES 1 and 2: Who May Qualify: - HIV positive or HIV exposed and presumptively positive while awaiting confirmatory testing in infants Who Should NOT Join This Trial: - do not provide willing to sign a consent form or assent as appropriate or are currently being treated for TB OBJECTIVE 3: Who May Qualify: - negative TB symptom screen OR for whom TB disease has been ruled out in accordance with WHO Guidelines in adults and according to consensus definitions for child TB Who Should NOT Join This Trial: - do not provide willing to sign a consent form or assent as appropriate or are currently being treated for TB Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
OBJECTIVES 1 and 2: Inclusion Criteria: * HIV positive or HIV exposed and presumptively positive while awaiting confirmatory testing in infants Exclusion Criteria: * do not provide informed consent or assent as appropriate or are currently being treated for TB OBJECTIVE 3: Inclusion Criteria: * negative TB symptom screen OR for whom TB disease has been ruled out in accordance with WHO Guidelines in adults and according to consensus definitions for child TB Exclusion Criteria: * do not provide informed consent or assent as appropriate or are currently being treated for TB

Treatments Being Tested

OTHER

patient-centered TB preventive therapy

The intervention phase includes i) enrolling participants who have had TB disease excluded and allowing participant selection of a preferred TPT regimen, and ii) randomizing participants to one of two participant adherence support modalities.

OTHER

TB preventive therapy adherence support

As part of this study, enhanced adherence support will be provided via bi-directional messaging and/or via clinic phone calls. All participants randomized to enhanced adherence support will receive a weekly text reminder beginning seven days after the initiation. Each message will ask participants if they would like to be contacted to discuss any questions and will prompt participants to ask questions by text if more convenient or preferable. All text-based questions from participants will be answered by a trained nurse with back up from a physician.

Locations (5)

Baylor College of Medicine Children's Foundation
Mbabane, Eswatini
Baylor College of Medicine Children's Foundation
Maseru, Lesotho
Baylor College of Medicine Children's Foundation
Lilongwe, Malawi
Baylor College of Medicine Children's Foundation
Mbeya, Tanzania
Baylor College of Medicine Children's Foundation
Kampala, Uganda