- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07621510
Integrating iSYV Within HIV Clinical Care for Youth Living With HIV in Tanzania
27 de mayo de 2026 actualizado por: Duke University
Youth living with HIV (YLWH) experience mental health (MH) challenges that compromise their HIV care.
Though the MH gap is well described, MH service delivery to YLWH is rare, especially in low resource settings.
MH professionals are few and interventions tailored to the needs of this population are scarce.
This project proposes a way to bridge the gap by streamlining the Sauti ya Vijana (SYV, The Voice of Youth) intervention redesigned to integrate into the differentiated HIV clinical care model in Tanzania.
SYV is a peer-led, group-based treatment designed with and for YLWH to address their self-reported MH challenges and stressors living with HIV.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Descripción detallada
SYV incorporates components of existing evidence-based models: Trauma Focused-Cognitive Behavioral Therapy, Interpersonal Psychotherapy, and Motivational Interviewing to address the needs youth described in formative interviews.
Preliminary data indicates implementation success with estimated effects towards improved MH, antiretroviral therapy adherence, and a 10% greater increase in viral suppression in the intervention arm compared to standard of care.
The central hypothesis here is that the new integrated "i" SYV will be acceptable, feasible, and effective to improve virologic suppression and improve retention in care.
The mechanism of change is that improved MH leads to better medication adherence, viral suppression, and care engagement.
The rationale is twofold: 1) Tanzania is planning to initiate MH screening in HIV clinical visits, but the MH treatment gap persists; 2) the iSYV stepped-care package could be an effective approach to support integrated MH care for YLWH.
The central hypothesis will be tested in a hybrid type-2 effectiveness-implementation trial.
The first aim will leverage the Fit to Context Framework, using an iterative Designing for Dissemination and Sustainability approach.
Current SYV peer-group leaders with extensive experience delivering SYV will co-design the new iSYV package.
The iSYV in-person sessions will be delivered by trained peer youth leaders and be aligned to the Tanzanian differentiated care model: stable youth (those fully suppressed) attend clinic every 6 months; and unstable youth (those with HIV RNA > 50 copies/mL) attend enhanced adherence counseling monthly.
Youth with symptoms of MH difficulties on screening (PHQ9-depression, GAD7-anxiety, Trauma-related stress) will join the unstable group.
To support engagement between visits, iSYV will explore use of a mHealth gamification strategy.
The second aim includes a pilot and a four-arm cluster randomized trial.
Two large implementing partners of PEPFAR clinics will support testing of the iSYV care package.
The primary outcome is powered to show an increase in viral suppression (HIV RNA <50 copies/mL) in the unstable group and improved retention in care among the stable group.
Change in MH is measured as a secondary outcome.
The third aim will evaluate implementation determinants and outcomes, including acceptability, feasibility, fidelity, and cost informed by the Consolidated Framework for Implementation Research.
The proposal is significant because it is expected to help address the MH gap for YLWH with implications for HIV care in Tanzania and other low income areas.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
5000
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Stuart T Carr, BA
- Número de teléfono: (919) 668-4849
- Correo electrónico: stuart.carr@duke.edu
Copia de seguridad de contactos de estudio
- Nombre: Sandy Askew, MPh
- Correo electrónico: sandy.askew@duke.edu
Ubicaciones de estudio
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Moshi, Tanzania
- Elizabeth Glaser Pediatric AIDS Foundation implementing partner sites in Tanzania
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Investigador principal:
- Akwila Temu, MD, MMED
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- youth living with HIV (YLWH) 15-24 years;
- have understanding of their HIV status;
- able to attend iSYV sessions if site is randomized to the intervention.
Exclusion Criteria:
- inability to provide informed consent/assent or participate meaningfully in the intervention due to cognitive impairment, psychosis, or other disability;
- enrollment in any other MH, stigma-related, or adherence intervention research study.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: eSOC (enhanced Standard of Care)
Currently mental health screening is not part of routine care.
Youth at all trial clinics who report moderate to severe symptoms will be referred for care within the local standard.
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mental health screening and referral within the standard of care for moderate to severe symptoms
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Experimental: eSOC (enhanced Standard of Care) + iSYV (integrated Sauti ya Vijana or The voice of youth)
iSYV is an intervention that will be peer-led and group based in six monthly sessions.
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mental health screening and referral within the standard of care for moderate to severe symptoms
Integrated "i"SYV is a streamlined version of the original intervention SYV that is adapted for integration into routine clinical care.
The original SYV intervention included 10 group weekly sessions (2 incorporating caregivers) and 2 individual sessions with adaptation to fit without routine adolescent HIV care based on Tanzanian National HIV Guidelines for HIV care follow up visits.
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Experimental: eSOC (enhanced Standard of Care) + iSYV + mHealth (mobile Health)
mHealth will be an additional experimental intervention exploring the boosting effect of gamification of intervention content to boost participant knowledge and understanding of iSYV content
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mental health screening and referral within the standard of care for moderate to severe symptoms
Integrated "i"SYV is a streamlined version of the original intervention SYV that is adapted for integration into routine clinical care.
The original SYV intervention included 10 group weekly sessions (2 incorporating caregivers) and 2 individual sessions with adaptation to fit without routine adolescent HIV care based on Tanzanian National HIV Guidelines for HIV care follow up visits.
A gamified version of iSYV that can be played via SMS or Whatsapp messaging.
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Experimental: eSOC (enhanced Standard of Care) + mHealth (mobile Health)
mHealth is evaluated as a stand alone experimental intervention in this arm to evaluate if mHealth alone (without in person iSYV content) can improve mental health and/or HIV RNA outcomes.
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mental health screening and referral within the standard of care for moderate to severe symptoms
A gamified version of iSYV that can be played via SMS or Whatsapp messaging.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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viral load
Periodo de tiempo: at 6-months
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HIV RNA <50 copies/mL considered suppression (per National guidelines)
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at 6-months
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retention in care
Periodo de tiempo: at 6-months
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clinical follow up as prescribed within 30 days of scheduled 6-month appointment
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at 6-months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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changes in self-reported antiretroviral therapy (ART) regarding adherence
Periodo de tiempo: 6-months, 12-months, 18-months
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Self-reported adherence on a 3 question survey (Wilson) 0-100 range, higher scores indicate greater adherence
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6-months, 12-months, 18-months
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change in self-reported mental health difficulties related to depression
Periodo de tiempo: 6-months, 12-months, 18-months
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self-report of the Patient Health Questionnaire-9 (PHQ-9 ) range is 0-27, higher scores indicate greater depression
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6-months, 12-months, 18-months
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change in self-reported mental health difficulties related to anxiety
Periodo de tiempo: 6-months, 12-months, 18-months
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self-report on the Generalized Anxiety Disorder-7 (GAD-7) range 0-21 with higher scores indicating greater anxiety
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6-months, 12-months, 18-months
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change in HIV knowledge in the SOC+iSYV intervention arm compared to SOC arm at 6 month follow-up and at all timepoints in the intervention arm compared to SOC arm
Periodo de tiempo: 6-months, 12-months, 18-months
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self reported knowledge on the HIV-KQ18 (HIV Knowledge questionnaire 18) range 0-18.
higher score indicates more HIV knowledge
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6-months, 12-months, 18-months
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viral load
Periodo de tiempo: 12-months, 18-months as drawn per standard of care
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HIV RNA
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12-months, 18-months as drawn per standard of care
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retention in care
Periodo de tiempo: 12-months and 18-months
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follow up in routine HIV care within 30 days of scheduled 12-month and 18-month appointments
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12-months and 18-months
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change in coping and self efficacy on the Coping and Self-Efficacy Scale (CSES)
Periodo de tiempo: 6-months, 12-months, 18-months
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self-reported, 13 questions with scale of 0 to 2 (range 0 to 26), where a higher number is a better outcome, more coping and self-efficacy
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6-months, 12-months, 18-months
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change in resilience on People Living with HIV (PLHIV) Resilience Scale
Periodo de tiempo: 6-months, 12-months, 18-months
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10 items, scale 0 to 2 (range 0 to 20), higher number means more resilience and a better outcome
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6-months, 12-months, 18-months
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SYV risk behaviors scale
Periodo de tiempo: 6-months, 12-months, 18-months
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5 items assessing sexual activity, number of sexual partners, condom use, consumption of alcohol, cocaine, heroin, or other substances.
These are yes/no response with clarification of rate/amount.
Higher numbers is higher risk.
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6-months, 12-months, 18-months
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interpersonal violence on the World Health Organization intimate partner violence (WHO IPV) scale
Periodo de tiempo: 6-months, 12-months, 18-months
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self report, 15 items with 0=no and 1-yes.
More yes (higher scale) means more experience with IPV.
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6-months, 12-months, 18-months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Dorothy Dow, MD, MSc, Duke Universtiy
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
10 de enero de 2027
Finalización primaria (Estimado)
31 de marzo de 2029
Finalización del estudio (Estimado)
30 de septiembre de 2030
Fechas de registro del estudio
Enviado por primera vez
13 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
27 de mayo de 2026
Publicado por primera vez (Actual)
2 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
2 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
27 de mayo de 2026
Última verificación
1 de marzo de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- Pro00119752
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
SÍ
Descripción del plan IPD
de-identified data
Marco de tiempo para compartir IPD
at the conclusion of trial analysis
Criterios de acceso compartido de IPD
Data sharing is critical to confirm findings, discover important new associations, and to test new ideas that impact health.
Our core quantitative dataset will be archived in the National Institute of Mental Health (NIMH) Data Archive (NDA).
To achieve this we will harmonize our data to NDA common data elements (CDE) as much as possible prior to data collection.
We will follow the standard practices of the NDA for data uploads, submitting data biannually beginning in the second submission cycle following the Notice of Award.
Data will be made publicly available in the data archive at the time of publication.
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CÓDIGO_ANALÍTICO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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