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The efcacy of family-based interventions for preventing overweight or obesity among children adolescents

The efcacy of family-based interventions for preventing overweight or obesity among children adolescents

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098762
Enrollment
Unknown
Registered
2025-03-13
Start date
2025-03-31
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Obesity

Interventions

Usual care:Follows the standard treatment recommendations
Family-based treatment :Family-based treatment

Sponsors

Tongde Hospital of Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Target children aged >= 6 years and<18 years old; 2. Referring to the "Screening for Overweight and Obesity in School aged Children and Adolescents (WS/T586-208)", the target child's BMI is greater than the obesity threshold for the corresponding gender and age; 3. If a family has more than one child aged 6-18 years with overweight or obesity, the oldest child is designated as the targeted child. 4. At least one parent or legal guardian with a BMI of 24.0 kg/m² or higher who is willing to participate. 5. Targeted child resides with targeted parent at least 50% of the time. 6. Informed consent to accept this study.

Exclusion criteria

Exclusion criteria: Families are excluded from the study if either the child/ adolescent or parents: 1. Those who do not meet the diagnostic and inclusion criteria 2. Participation to any degree in weight management/weight-loss program. 3. Weight-related surgeries within the last 2 years. 4. Weight-affecting medications known to cause weight gain or loss. 5. Medications affecting growth. 6. Severe heart, lung, liver, and kidney dysfunction. 7. Musculoskeletal system injuries, patients with limited activity due to surgery or with other contraindications to exercise. 8. Pregnant or is planning on becoming pregnant during the 2 years study period. 9. Unwilling to participate in this study or not cooperate with the researchers.

Design outcomes

Primary

MeasureTime frame
Body composition;Height;Weight;Deitary survey;Waist circumference;Hip circumference;

Countries

China

Contacts

Public ContactLuo Xi

Tongde Hospital of Zhejiang Province

luoxi0571@sina.com+86 571 8997 2108

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026