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Dietary Intervention for Low Free Sugars in Children With Non-alcoholic Fatty Liver Disease

Dietary Intervention for Low Free Sugars in Children With Non-alcoholic Fatty Liver Disease: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06579729
Enrollment
146
Registered
2024-08-30
Start date
2018-10-01
Completion date
2022-04-01
Last updated
2024-08-30

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

Conditions

Child Obesity, Low-free Sugar Dietary, NAFLD

Brief summary

A 48-week dietary intervention program was conducted in children aged 5-14 years with a diagnosis of NAFLD, who were randomized into a low free sugar diet group and a regular diet group. The primary objective of this study is to determine whether a low free sugar dietary intervention program improves liver function, fasting glucose, fasting insulin, lipid profile and hepatic steatosis in children with NAFLD. The effects of the intervention will be analyzed and compared at weeks 12, 24 and 48.

Interventions

BEHAVIORALDietary intervention for low free sugars

After baseline data collection, the intervention group received a 30-60 minute educational session with a dietitian and clinicians, including a health education prescription. Interventions occurred at weeks 1, 12 and 24, with routine evaluations of disease, diet, physical activity, and adherence. Follow-ups at 48 weeks assessed NAFLD extent, dietary profile, and health knowledge for both subjects and guardians.

Sponsors

China Medical University, China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* Age: above 5 years old and below 14 years old; * Guardian's consent and signing of informed consent; * WHO growth and development curves as the reference standard, overweight is defined as BMI greater than or equal to the 85th percentile of the WHO growth curves for children, and obesity is defined as BMI greater than or equal to the 95th percentile of the WHO growth curves for children; * Liver imaging performance meets the diagnostic criteria of diffuse fatty liver.

Exclusion criteria

* Age \<5 years or \>14 years; * Previous history of alcohol consumption; * Non-cooperation with the study, inability to comply with the study treatment or study visit. * Past or active hepatitis B virus infection; * Past or active hepatitis C virus infection; * Chronic or acute liver failure; * Cholestasis; * Hepatomegaly; * Cystic fibrosis; * α1-antitrypsin deficiency; * Autoimmune hepatitis; * Tyrosinemia; * Galactosemia or any recognized liver disease, any physical condition deemed by a physician to be unable to complete the trial. Physical Condition.

Design outcomes

Primary

MeasureTime frameDescription
NAFLDAt weeks 1, 12 and 24NAFLD was diagnosed using liver ultrasonography with a Phillip IU Elite color Doppler ultrasound after a fasting period to reduce gastrointestinal interference.
DietaryAt weeks 1, 12 and 24The dietary habits of the subjects were evaluated by a semi-quantitative Food Frequency Questionnaire (FFQ), which was recalled over the past month and included food items, frequency, and amount of intake. The FFQ used in this study covered 72 food items from 11 food groups and 4 frequency categories, including 'average daily, weekly, monthly intake or hardly eat'.
Physical activity levelAt weeks 1, 12 and 24Physical Activity Questionnaire for Children (PAQ-C) was answered by subjects. The PAQ-C reflects the overall physical activity level of children in the past 7 days.The scale consists of 10 items, .and a 1-5 scale was used to obtain a total score by summing the scores of the individual items. The PAQ-C scale scores \< 2.33 defined as low physical activity levels, 2.33-3.66 as moderate physical activity levels, and \>3.66 as high physical activity levels.

Secondary

MeasureTime frameDescription
Waist circumferenceAt weeks 1, 12 and 24Waist circumference was measured with circumference measuring tape.
HeightAt weeks 1, 12 and 24Height was measured using Height Measuring Ruler (Selcom, Germany) .
Blood pressureAt weeks 1, 12 and 24Blood pressure was measured using an Omron electronic blood pressure monitor (HBP-1300).
Waist-to-height ratioAt weeks 1, 12 and 24Waist-to-height ratio (WHtR) = waist circumference (cm)/height (cm).
Body weightAt weeks 1, 12 and 24Body weight was measured using Body Composition Analyzer (DC-13, Parade, Japan).
BMIAt weeks 1, 12 and 24BMI (kg/m2) = body weight (kg)/height2 (m2).

Countries

China

Outcome results

None listed

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