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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
616
simplified onsite HCV testing, evaluation, treatment, and follow-up delivered by OAMT physicians
provider incentives linked to completion of key cascade milestones
structured referral to off-site specialist clinics for HCV treatment
Ukrainian Institute on Public Health Policy
Kyiv, Ukraine
Sustained virologic response
Number of participants who have HCV RNA below the limit of quantitation (≤50 IU/mL) based on clinical records
Time frame: Up to 24 weeks after treatment completion
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
Time frame: Through study completion, an average of 2 weeks after baseline
Treatment initiation
Number of participants who are prescribed treatment for HCV infection based on clinical records
Time frame: 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
Time frame: 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
Time frame: 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
Time frame: 12 months after treatment completion
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.