- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07569211
Simplified HCV Integrated Management Model in Methadone Clinics in Ukraine (SHIM)
The goal of this pragmatic, quasi-experimental cluster trial is to evaluate whether simplified, onsite hepatitis C virus (HCV) treatment integrated into opioid agonist maintenance therapy (OAMT) clinics improves cure rates compared with referral-based care in Ukraine . The study includes adults (18 years and older) receiving OAMT with confirmed chronic HCV infection and no prior HCV treatment.
The main questions it aims to answer are:
- Does onsite Simplified HCV Integrated Management (SHIM) increase the proportion of patients achieving sustained virologic response 12 weeks after treatment completion (SVR12) compared with case management and referral (CMR) to specialist clinics?
- Does adding provider pay-for-performance (P4P) incentives to SHIM further improve progression along the HCV treatment cascade and SVR12 rates?
Researchers compared three models of care across 13 OAMT clinics in 12 Ukrainian cities:
- Case Management and Referral (CMR): structured referral to off-site specialist clinics for HCV treatment
- SHIM: simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians
- SHIM + P4P: SHIM with provider incentives linked to completion of key cascade milestones All SHIM clinics were supported by Project ECHO telementoring to strengthen clinician capacity . The study used nationally procured direct-acting antivirals (DAAs) under routine program conditions and did not reimburse diagnostic costs.
Between February 2023 and December 2024, 616 eligible patients were enrolled .
Participants:
- Completed confirmatory HCV RNA testing
- Underwent simplified pretreatment clinical and laboratory assessment
- Received 12 weeks of pan-genotypic DAA treatment either onsite (SHIM arms) or at specialist clinics (CMR arm)
- Attended follow-up visits during treatment for adherence assessment and counseling
- Were prescribed HCV RNA testing 12 weeks after treatment completion to confirm cure (SVR12) The primary outcome was SVR12. Secondary outcomes included completion of pretreatment evaluation, treatment initiation, treatment completion, and completion of SVR assessment.
This study evaluates HCV care under real-world conditions during ongoing national treatment scale-up in Ukraine. The findings inform whether integrating simplified HCV treatment into OAMT clinics-and aligning provider incentives-can improve cure rates and accelerate progress toward HCV elimination in high-burden populations.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Kyiv, Ucrania, 01054
- Ukrainian Institute on Public Health Policy
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- currently receiving treatment at the selected OAT site (implying a diagnosis of opioid dependence according to ICD 10);
- aged 18 years or older;
- residing within the study catchment area; and
- having a positive HCV antibody test documented in the medical chart
Exclusion Criteria:
- previous HCV treatment history;
- active tuberculosis (assessed using 4-item screening questionnaire and confirmed according to the current national protocol);
- pregnant or planning pregnancy in the next 6 months;
- planning to move to another city in the next 6 months;
- unwillingness to undergo confirmatory HCV RNA PCR test at their own expense and treat HCV
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Investigación de servicios de salud
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador activo: Case Management and Referral
structured referral to off-site specialist clinics for HCV treatment
|
structured referral to off-site specialist clinics for HCV treatment
|
|
Experimental: Simplified HCV Integrated Management
simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians
|
simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians
|
|
Experimental: Simplified HCV Integrated Management + Pay-for-performance
simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians with provider incentives linked to completion of key cascade milestones
|
simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians
provider incentives linked to completion of key cascade milestones
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Sustained virologic response
Periodo de tiempo: Up to 24 weeks after treatment completion
|
Number of participants who have HCV RNA below the limit of quantitation (≤50 IU/mL) based on clinical records
|
Up to 24 weeks after treatment completion
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Completion of all pretreatment diagnostic assessments
Periodo de tiempo: Through study completion, an average of 2 weeks after baseline
|
Number of participants who complete all pretreatment diagnostic assessments according to the SHIM algorithm (complete blood count, basic metabolic panel (including creatinine), hepatic function panel, fibrosis assessment, and HBsAg testing) based on clinical records
|
Through study completion, an average of 2 weeks after baseline
|
|
Treatment initiation
Periodo de tiempo: Through study completion, an average of 4 weeks after baseline
|
Number of participants who are prescribed treatment for HCV infection based on clinical records
|
Through study completion, an average of 4 weeks after baseline
|
|
Treatment completion
Periodo de tiempo: Through study completion, an average of 14 weeks after baseline
|
Number of participants who complete the full course of HCV treatment as prescribed based on clinical records
|
Through study completion, an average of 14 weeks after baseline
|
|
SVR assessment completion
Periodo de tiempo: Up to 24 weeks after treatment completion
|
Number of participants who complete HCV RNA testing for SVR confirmation based on clinical records
|
Up to 24 weeks after treatment completion
|
|
HCV reinfection
Periodo de tiempo: 12 months after treatment completion
|
Number of participants who receive a positive result of HCV RNA test at 12 months after treatment completion, based on clinical records
|
12 months after treatment completion
|
Colaboradores e Investigadores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Infecciones transmitidas por la sangre
- Trastornos relacionados con narcóticos
- Desordenes mentales
- Infecciones
- Infecciones por virus de ARN
- Enfermedades virales
- Enfermedades del Sistema Digestivo
- Enfermedades del HIGADO
- Hepatitis, Viral, Humana
- Enfermedades contagiosas
- Trastornos relacionados con sustancias
- Trastornos inducidos químicamente
- Infecciones por Flaviviridae
- Hepatitis
- Trastornos relacionados con opioides
- Hepatitis C
- Práctica profesional
- Organización y administración
- Administración de Servicios de Salud
- Economía y organizaciones de la atención médica
- Gestión de atención al paciente
- Planificación de atención al paciente
- Atención médica integral
- Financiamiento, organizado
- Ciencias económicas
- Mecanismos de Reembolso
- Seguro, Salud, Reembolso
- Referencia y consulta
- Gestión de casos
- Reimbursement, Incentive
Otros números de identificación del estudio
- 127-2022
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Marco de tiempo para compartir IPD
Criterios de acceso compartido de IPD
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- CIF
Datos del estudio/Documentos
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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