- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07621510
Integrating iSYV Within HIV Clinical Care for Youth Living With HIV in Tanzania
27 maja 2026 zaktualizowane przez: 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.
Przegląd badań
Status
Jeszcze nie rekrutacja
Interwencja / Leczenie
Szczegółowy opis
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.
Typ studiów
Interwencyjne
Zapisy (Szacowany)
5000
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Stuart T Carr, BA
- Numer telefonu: (919) 668-4849
- E-mail: stuart.carr@duke.edu
Kopia zapasowa kontaktu do badania
- Nazwa: Sandy Askew, MPh
- E-mail: sandy.askew@duke.edu
Lokalizacje studiów
-
-
-
Moshi, Tanzania
- Elizabeth Glaser Pediatric AIDS Foundation implementing partner sites in Tanzania
-
Główny śledczy:
- Akwila Temu, MD, MMED
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
- Dorosły
Akceptuje zdrowych ochotników
Nie
Opis
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 studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Aktywny komparator: 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.
|
mental health screening and referral within the standard of care for moderate to severe symptoms
|
|
Eksperymentalny: 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.
|
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.
|
|
Eksperymentalny: 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
|
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.
|
|
Eksperymentalny: 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.
|
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.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
viral load
Ramy czasowe: at 6-months
|
HIV RNA <50 copies/mL considered suppression (per National guidelines)
|
at 6-months
|
|
retention in care
Ramy czasowe: at 6-months
|
clinical follow up as prescribed within 30 days of scheduled 6-month appointment
|
at 6-months
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
changes in self-reported antiretroviral therapy (ART) regarding adherence
Ramy czasowe: 6-months, 12-months, 18-months
|
Self-reported adherence on a 3 question survey (Wilson) 0-100 range, higher scores indicate greater adherence
|
6-months, 12-months, 18-months
|
|
change in self-reported mental health difficulties related to depression
Ramy czasowe: 6-months, 12-months, 18-months
|
self-report of the Patient Health Questionnaire-9 (PHQ-9 ) range is 0-27, higher scores indicate greater depression
|
6-months, 12-months, 18-months
|
|
change in self-reported mental health difficulties related to anxiety
Ramy czasowe: 6-months, 12-months, 18-months
|
self-report on the Generalized Anxiety Disorder-7 (GAD-7) range 0-21 with higher scores indicating greater anxiety
|
6-months, 12-months, 18-months
|
|
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
Ramy czasowe: 6-months, 12-months, 18-months
|
self reported knowledge on the HIV-KQ18 (HIV Knowledge questionnaire 18) range 0-18.
higher score indicates more HIV knowledge
|
6-months, 12-months, 18-months
|
|
viral load
Ramy czasowe: 12-months, 18-months as drawn per standard of care
|
HIV RNA
|
12-months, 18-months as drawn per standard of care
|
|
retention in care
Ramy czasowe: 12-months and 18-months
|
follow up in routine HIV care within 30 days of scheduled 12-month and 18-month appointments
|
12-months and 18-months
|
|
change in coping and self efficacy on the Coping and Self-Efficacy Scale (CSES)
Ramy czasowe: 6-months, 12-months, 18-months
|
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
|
6-months, 12-months, 18-months
|
|
change in resilience on People Living with HIV (PLHIV) Resilience Scale
Ramy czasowe: 6-months, 12-months, 18-months
|
10 items, scale 0 to 2 (range 0 to 20), higher number means more resilience and a better outcome
|
6-months, 12-months, 18-months
|
|
SYV risk behaviors scale
Ramy czasowe: 6-months, 12-months, 18-months
|
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.
|
6-months, 12-months, 18-months
|
|
interpersonal violence on the World Health Organization intimate partner violence (WHO IPV) scale
Ramy czasowe: 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.
|
6-months, 12-months, 18-months
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Śledczy
- Główny śledczy: Dorothy Dow, MD, MSc, Duke Universtiy
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
10 stycznia 2027
Zakończenie podstawowe (Szacowany)
31 marca 2029
Ukończenie studiów (Szacowany)
30 września 2030
Daty rejestracji na studia
Pierwszy przesłany
13 maja 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
27 maja 2026
Pierwszy wysłany (Rzeczywisty)
2 czerwca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
2 czerwca 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
27 maja 2026
Ostatnia weryfikacja
1 marca 2026
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- Pro00119752
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
TAK
Opis planu IPD
de-identified data
Ramy czasowe udostępniania IPD
at the conclusion of trial analysis
Kryteria dostępu do udostępniania 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.
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ANALITYCZNY_KOD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .