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| Name | Class |
|---|---|
| The Western-Eastern European Partnership Initiative on HIV, Viral Hepatitis and TB | UNKNOWN |
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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:
Researchers compared three models of care across 13 OAMT clinics in 12 Ukrainian cities:
Between February 2023 and December 2024, 616 eligible patients were enrolled .
Participants:
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Case Management and Referral | Active Comparator | structured referral to off-site specialist clinics for HCV treatment |
|
| Simplified HCV Integrated Management | Experimental | simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians |
|
| Simplified HCV Integrated Management + Pay-for-performance | Experimental | simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians with provider incentives linked to completion of key cascade milestones |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Simplified HCV Integrated Management | Other | simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sustained virologic response | 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 |
| Measure | Description | Time Frame |
|---|---|---|
| Completion of all pretreatment diagnostic assessments | 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ukrainian Institute on Public Health Policy | Kyiv | 01054 | Ukraine |
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| ID | Type | URL | Comment |
|---|---|---|---|
| Study Protocol | View IPD |
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January 1, 2026 - June 30, 2029
Reasonable request to the principal investigator
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Apr 1, 2025 | Feb 27, 2026 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D009293 | Opioid-Related Disorders |
| D006526 | Hepatitis C |
| ID | Term |
|---|---|
| D000079524 | Narcotic-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D012052 | Reimbursement, Incentive |
| D019090 | Case Management |
| D012017 | Referral and Consultation |
| ID | Term |
|---|---|
| D012051 | Reimbursement Mechanisms |
| D007349 | Insurance, Health, Reimbursement |
| D005381 | Financing, Organized |
| D004467 | Economics |
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| Pay-for-performance | Other | provider incentives linked to completion of key cascade milestones |
|
| Case Management and Referral | Other | structured referral to off-site specialist clinics for HCV treatment |
|
| Treatment initiation | 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 | 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 | Number of participants who complete HCV RNA testing for SVR confirmation based on clinical records | Up to 24 weeks after treatment completion |
| HCV reinfection | 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 |
| Informed Consent Form | View IPD |
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D006525 | Hepatitis, Viral, Human |
| D014777 | Virus Diseases |
| D018178 | Flaviviridae Infections |
| D012327 | RNA Virus Infections |
| D006505 | Hepatitis |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D004472 | Health Care Economics and Organizations |
| D010347 | Patient Care Planning |
| D003191 | Comprehensive Health Care |
| D010346 | Patient Care Management |
| D006298 | Health Services Administration |
| D011364 | Professional Practice |
| D009934 | Organization and Administration |