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Clinical Trials in China / NCT06905795
Active, not recruiting Not applicable

Screening and Intervention of MASLD in Children

NCT06905795 · tracked via the Priya Life Science China tracker
Sponsor
Ningbo No. 1 Hospital
Phase
Not applicable
Started
2025-04-01
Last updated
2026-01-12

Condition(s) studied

MASLD - Metabolic Dysfunction-Associated Steatotic Liver DiseaseChildren

Investigational drug(s) / intervention(s)

Fibroscan testNutrition guidanceIncrease physical activityHealth education

Fibroscan test: Perform Fibroscan testing on the study subjects every six months.

Nutrition guidance: Each family will be matched with a nutritionist, who will provide daily online dietary guidance for parents and students during the first 21 days, followed by weekly sessions thereafter.

Increase physical activity: Increase physical activity time in and out of school by professional sports trainer.

Health education: Knowledge of healthy lifestyle will be delivered in various forms such as health lectures, brochures, posters, etc.

Study summary

Non-alcoholic fatty liver disease (NAFLD) in children and adolescents has recently been renamed metabolic dysfunction-associated steatotic liver disease (MASLD). It has become one of the leading chronic liver diseases in children. The prevalence of MASLD is 6.3% among the general pediatric population and 40.4% among overweight and obese children, with an increasing trend each year. MASLD increases the risk of various metabolic diseases and can eventually lead to liver fibrosis or hepatocellular carcinoma, contributing to the disease burden.

Previous work by our project team using machine learning methods has identified that fasting insulin, alanine aminotransferase (ALT), and waist-to-height ratio (WHtR) have good predictive value in overweight and obese children, with a recommendation that children with a WHtR ≥ 0.48 should undergo further screening. However, external validation is still required to improve the effectiveness and cost-efficiency of this screening approach.

Till now, there are no approved drug treatments for paediatric MASLD, and lifestyle interventions (such as restricting energy intake and increasing physical activity) are the main therapeutic strategies. However, existing studies face limitations, such as small sample sizes, diverse intervention methods, lack of standardization, and short intervention durations, which hinder their clinical application. Therefore, it is essential to explore effective health lifestyle intervention models tailored to children.

This study aims to: First, optimizing the screening and treatment pathway, assess the cost-effectiveness and applicability of WHtR as a screening tool, and develop a tiered screening system suitable for Chinese children; Second, integrating school, clinic, family, and community resources to establish a multifacted lifestyle intervention model and evaluate its efficacy.

Eligibility

Sex
ALL
Min age
7 Years
Max age
11 Years
Healthy volunteers
Accepted
Inclusion Criteria: * parents agree and support their children's weight loss, and students and parents have informed consent; * students in two to four grade aged 7 and 11 years old; * students with WHtR ≥ 0.48. Exclusion Criteria: * medical history of heart disease, hypertension, diabetes, tuberculosis, asthma, virus hepatitis or nephritis; * obesity caused by endocrine diseases or side effects of drugs; * abnormal physical development like dwarfism or gigantism; * physical deformity such as severe scoliosis, pectus carinatum, limp, obvious O-leg or X-leg; * inability to participate in school sport activities; * a loss in weight by vomiting or taking drugs during the past 3 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Ningbo University Ningbo Zhejiang

More Ningbo No. 1 Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06905795 on ClinicalTrials.gov ↗ ← All trials in China