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Strengthening Hepatitis B Screening, Linkage to Care and Long-Term Monitoring in Phichit Province, Thailand: A Birth Bohort Approach

Strengthening Hepatitis B Screening, Linkage to Care and Long-Term Monitoring in Phichit Province, Thailand: A Birth Bohort Approach

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07258251
Acronym
HBV-PHICHIT
Enrollment
6000
Registered
2025-12-02
Start date
2026-01-01
Completion date
2028-12-31
Last updated
2025-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Hepatitis B, Hepatitis B Virus Infection

Brief summary

This study in Phichit province, Thailand, aims to find and support adults born before 1992 who are at high risk for hepatitis B infection. Many people in this group were born before the universal hepatitis B vaccine was available and may not know they are infected. The study will invite nearly 240,000 eligible adults for free hepatitis B screening. Those who test positive will be linked to care at one of 12 district hospitals. Doctors will use simplified 2024 World Health Organization (WHO) guidelines to decide who needs treatment. Eligible individuals will receive a safe, effective daily medicine (tenofovir alafenamide). The study will use community health volunteers and phone reminders to help patients stay in care and take their medication regularly. Over three years, the study will track improvements in liver health and virus levels, aiming to prevent liver cirrhosis and cancer.

Detailed description

Chronic hepatitis B virus (HBV) infection is a significant cause of liver cirrhosis and hepatocellular carcinoma (HCC) in Thailand. While Thailand's universal infant vaccination program, implemented in 1992, has been successful, adults born before this date remain a high-risk population with an estimated 2-3 million chronic infections. Despite free access to HBsAg screening and treatment (including TAF/TDF), barriers such as the lack of reimbursement for HBV DNA testing and poor linkage to care have hampered progress toward WHO 2030 elimination targets. This study is a pragmatic implementation research project designed to scale up HBsAg screening, linkage to care, and long-term monitoring in Phichit Province. It targets the birth cohort of adults born before 1992 (approx. 238,786 people). The study will develop and evaluate tools to identify unscreened individuals, improve linkage to dedicated viral hepatitis clinics, and support long-term adherence. A key component is the implementation of simplified WHO 2024 treatment criteria, which utilize non-invasive markers like the APRI score as an alternative to HBV DNA testing to determine treatment eligibility.

Interventions

HBsAg-positive individuals meeting WHO 2024 treatment eligibility criteria will receive daily oral TAF. Tenofovir disoproxil fumarate (TDF) may be used if TAF is unavailable.

BEHAVIORALCommunity-Based Support

Interventions to improve linkage to care, retention, and treatment adherence. This includes telephone calls, home visits by community health volunteers, and phone/SMS reminders for appointments.

DIAGNOSTIC_TESTSimplified WHO 2024 Criteria

HBsAg-positive individuals will be evaluated for treatment eligibility using simplified 2024 WHO guidelines, including APRI score, as an alternative to HBV DNA testing.

Sponsors

Phichit Provincial Public Health Office, Ministry of Public Health, Thailand (Host institution)
CollaboratorUNKNOWN
Division of Gastroenterology, Department of Medicine Siriraj Hospital, Mahidol University
CollaboratorUNKNOWN
Ministry of Health, Thailand
CollaboratorOTHER_GOV
Phichit Provincial Hospital
CollaboratorUNKNOWN
Liver Foundation Thailand
CollaboratorUNKNOWN
Thai Association for the Study of the Liver
CollaboratorUNKNOWN
The Task Force for Global Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Adults born before January 1, 1992 * Residing in Phichit Province * Individuals who test positive for HBsAg will be invited to participate in the follow-up cohort * HBsAg positive patients who are already under care will also be invited to participate

Exclusion criteria

* Subjects who withdraw consent

Design outcomes

Primary

MeasureTime frameDescription
HBsAg Screening Uptake36 monthsPercentage of the target population (adults born before Jan 1, 1992, in Phichit province) who are successfully screened for HBsAg. (Target: 90%)
Linkage to Care36 monthsPercentage of individuals who test positive for HBsAg and are successfully linked to care for clinical assessment and treatment evaluation.
Treatment Initiation36 monthsPercentage of HBsAg-positive individuals identified as eligible for treatment (per WHO 2024 guidelines) who successfully initiate antiviral therapy

Secondary

MeasureTime frameDescription
Treatment Eligibility (Simplified Criteria)36 monthsProportion of HBsAg-positive individuals eligible for treatment based on simplified WHO 2024 criteria without HBV DNA results (e.g., using APRI score)
Treatment Adherence12 Months and 24 MonthsProportion of patients on treatment with good compliance, defined as taking & 80% of prescribed medication, measured by pill count and the 8-item Morisky Medication Adherence Scale (MMAS-8)
Effectiveness of Community-Based Support36 MonthsAssessed by measuring the impact of iinterventions (e.g., health volunteers, phone reminders) on linkage and retention rates
Fibrosis/Inflammation ResponseBaseline and every 6 months for 36 monthsChange in APRI score from baseline among treated patients
HBsAg SerometricsBaseline, 12 Months, 24 Months, 36 MonthsChange in quantitative HBsAg (qHBsAg) from baseline
Retention in Care12 Months, 24 Months, and 36 MonthsProportion of all HBsAg-positive individuals (treated and untreated) who maintain scheduled 6-monthly follow-up appointments.
Virologic ResponseBaseline, 12 Months, 24 Months, 36 MonthsChange in HBV DNA viral load from baseline among treated patients
Biochemical ResponseBaseline and every 6 months for 36 monthsProportion of treated patients achieving ALT normalization

Countries

Thailand

Contacts

Primary ContactDr. Gibril Ndow
gndow@taskforce.org+1 404 907 9954
Backup ContactDr. Wisit Apisitwitaya
wisitapisit1@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026