Actively Recruiting
High-Intensity Interval Training(HIIT) on Cardio-metabolic Risk in School-age Children
Led by Children's Hospital of Fudan University · Updated on 2025-12-16
336
Participants Needed
1
Research Sites
215 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate the health promotion effects of high-intensity interval training (HIIT) intervention on school-age children who are at high risk for cardiovascular disease (CVD), as well as the long-term adherence and acceptability of HIIT in this population for future application.
CONDITIONS
Official Title
High-Intensity Interval Training(HIIT) on Cardio-metabolic Risk in School-age Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
-
Aged 7-18 years at baseline.
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At least one of the following cardio-metabolic abnormalities:
- Prediabetes (Impaired fasting glucose: 5.6 ≤ fasting blood glucose level ≤ 6.9 mmol/L; or Impaired glucose tolerance: 7.8 ≤ blood glucose level after 2 hours postprandial ≤ 11.0 mmol/L).
- Lipid abnormalities (High-density lipoprotein cholesterol ≤ 1.04 mmol/L; or Low-density lipoprotein cholesterol ≥ 3.37 mmol/L; or Triglycerides ≥ 1.70 mmol/L, or Total cholesterol ≥ 5.18 mmol/L).
- Elevated blood pressure (Systolic/diastolic blood pressure consistently higher than the 90th percentile for gender, age, and height; or systolic/diastolic blood pressure ≥ 120/80 mmHg).
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Written consent from participants and their guardians.
You will not qualify if you...
- Previously diagnosed with heart failure, severe malnutrition, immune deficiency, liver or kidney disease, cancer, or other diseases deemed unsuitable for participation.
- Taking weight loss drugs, or undergone weight loss surgery.
- Attending behavior-based intervention programs (exercise or diet) within a year.
- Regular HIIT (at least once per week).
- Secondary obesity, such as neuropsychiatric disorders, endocrine disorders, sleep apnea syndrome, or other conditions.
- Unable to take interventions due to health conditions, such as joint diseases, fractures, injuries.
- Other situations unsuitable for participation.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Children's Hospital of Fudan University
Shanghai, Shanghai Municipality, China, 021
Actively Recruiting
Research Team
W
Wennan He
CONTACT
W
Weili Yan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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