- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07621510
Integrating iSYV Within HIV Clinical Care for Youth Living With HIV in Tanzania
27 de maio de 2026 atualizado 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.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
Descrição detalhada
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 estudo
Intervencional
Inscrição (Estimado)
5000
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Stuart T Carr, BA
- Número de telefone: (919) 668-4849
- E-mail: stuart.carr@duke.edu
Estude backup de contato
- Nome: Sandy Askew, MPh
- E-mail: sandy.askew@duke.edu
Locais de estudo
-
-
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Moshi, Tanzânia
- Elizabeth Glaser Pediatric AIDS Foundation implementing partner sites in Tanzania
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Investigador principal:
- Akwila Temu, MD, MMED
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Não
Descrição
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.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Comparador Ativo: 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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
viral load
Prazo: 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
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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changes in self-reported antiretroviral therapy (ART) regarding adherence
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 6-months, 12-months, 18-months
|
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
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Dorothy Dow, MD, MSc, Duke Universtiy
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Estimado)
10 de janeiro de 2027
Conclusão Primária (Estimado)
31 de março de 2029
Conclusão do estudo (Estimado)
30 de setembro de 2030
Datas de inscrição no estudo
Enviado pela primeira vez
13 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
27 de maio de 2026
Primeira postagem (Real)
2 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
2 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
27 de maio de 2026
Última verificação
1 de março de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- Pro00119752
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
SIM
Descrição do plano IPD
de-identified data
Prazo de Compartilhamento de IPD
at the conclusion of trial analysis
Critérios de acesso de compartilhamento 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 informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
- ANALYTIC_CODE
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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