HIV Clinical Trial
Official title:
CombinADO: a Cluster-randomized Controlled Trial to Compare the Efficacy, Uptake, Feasibility and Acceptability of the CombinADO Strategy Versus Optimized Standard of Care on Viral Suppression, ART Adherence and Retention in HIV Care Among Adolescents and Young Adults Living With HIV Ages 10-24yrs in Nampula Province, Mozambique
This is a cluster-randomized trial designed to compare the effectiveness of the CombinADO strategy versus optimized standard of care (SOC) on viral suppression, antiretroviral therapy (ART) adherence and retention in HIV care among adolescents living with HIV (ALHIV) ages 10 to 24 years attending participating health facilities. Clinics are the units of intervention allocation and randomization. The control condition will be implemented at all facilities (n=12) participating in the trial. The enhanced intervention condition will be superadded to this at a randomly selected half (n=6) of facilities. The goal of this study is to learn whether an enhanced, tailored intervention helps AYAHIV do better with their HIV care (take their medications, stay in care) than the usual care that they receive.
Status | Recruiting |
Enrollment | 2400 |
Est. completion date | July 2024 |
Est. primary completion date | July 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 24 Years |
Eligibility | Adolescents and young adults living with HIV (AYAHIV): Inclusion Criteria: 1. HIV-positive, per medical records and confirmed by health facility staff 2. Age 10 to 24 years 3. Registered as a patient at study site 4. Aware of HIV+ status 5. Provision of signed and dated informed consent form 6. For adolescents under 18 years of age, informed assent and parental informed consent to participate in the study 7. Stated willingness to comply with all study procedures Exclusion Criteria: 1. Has an acute medical condition requiring immediate medical care Caregivers of AYAHIV: Inclusion Criteria: 1. Age 18 years and older 2. Attending a caregiver-specific support group 3. Willingness to be audio-recorded Healthcare Workers (HCW) and Key Informants (KI): Inclusion Criteria: 1. Age 18 years and older 2. Involved in the provision, management, or oversight of adolescent-focused HIV services at the 12 specified study sites 3. Willingness to be audio-recorded For all study participants (AYAHIV, caregivers, HCW and KI): Exclusion Criteria: Any other condition, including but not limited to alcohol or substance abuse and uncontrolled medical condition and/or allergies, that, in the opinion of the study team, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives would make the patient unsuitable for the study or unable/unwilling to comply with the study requirements. |
Country | Name | City | State |
---|---|---|---|
Mozambique | Cs 1 de Maio | Nampula | |
Mozambique | Cs 25 Setembro | Nampula | |
Mozambique | Cs Alua | Nampula | |
Mozambique | Cs Anexo Psi | Nampula | |
Mozambique | Cs Malema | Nampula | |
Mozambique | Cs Muhala Expansao | Nampula | |
Mozambique | Cs n1 Nacala Porto | Nampula | |
Mozambique | Cs Nametil | Nampula | |
Mozambique | Cs Namialo | Nampula | |
Mozambique | Cs Namicopo | Nampula | |
Mozambique | HG Marere | Nampula | |
Mozambique | HR Angoche | Nampula |
Lead Sponsor | Collaborator |
---|---|
Columbia University | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of Cape Town |
Mozambique,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of adolescents and young people living with HIV (AYAHIV) with viral suppression (Viral load <50 copies/ml) | Viral suppression among AYAHIV at intervention versus control sites | 12 months post intervention implementation | |
Secondary | Proportion of eligible adolescents and young people living with HIV (AYAHIV) attending clinic in a 90 day window from end of intervention implementation, as assessed at 12 months post intervention. | Retention in HIV care & treatment among AYAHIV at intervention versus control sites | 12 months post intervention implementation | |
Secondary | Self-reported adherence measured using 3-item adherence scale (mean score) | Self-reported ART adherence among adolescents and young people living with HIV at intervention versus control sites will be measured using a three-item adherence scale. The three items include (1) an assessment of the number of days with missed ART doses in the preceding 30 days [0-30 days]; (2) a scale rating of how good a job you did taking your medicines in the preceding 30 days (never/rarely/sometimes/usually/almost always/always) and (3) a scale rating of how often you took your medicines the way you were supposed to in the preceding 30 days (very poor/poor/fair/good/very good/ excellent).
For analyses using raw scores, item responses for the three adherence items will be linearly transformed to a 0-100 scale with zero being the worst adherence, and 100 representing perfect adherence. The mean of the three scores are then taken to get an equally weight aggregate scale score. An overall mean from the scores from all participants will be reported. |
12 months post intervention implementation | |
Secondary | Proportion of participants with detectable antiretroviral (ARV) on dried blood spot (DBS) specimen | ART adherence among among adolescents and young people living with HIV (AYAHIV) at intervention versus control sites, ARV levels | 12 months post intervention implementation |
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