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Preventive Effects of Different Volumes of High-Intensity Interval Training on Risk Factors for MS in Overweight Young Women

Not Applicable
Completed
Conditions
Metabolic Syndrome
Registration Number
NCT06664398
Lead Sponsor
Beijing Sport University
Brief Summary

This study investigates the effects of different volumes of high-intensity interval training on risk factors for metabolic syndrome in overweight young women.

Detailed Description

The sedentary and inactive female overweight subjects, aged 18 to 30 years, were randomly divided into three groups: high volume high-intensity interval training group (4HIIT group), low volume high-intensity interval training group (1HIIT group) and control group (CON group). Human morphological measures, blood pressure, insulin resistance, blood analysis, and cardiorespiratory fitness were measured at baseline and after exercise intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
30
Inclusion Criteria
  • Women aged 18-30 years;
  • BMI≥24kg/m2, indicating overweight and high risk of metabolic syndrome;
  • Maintaining a stable body weight for the three months prior to the study.
Exclusion Criteria
  • Regular participation in physical exercise (≥3 times/week, exercise time≥30min/time);
  • Any respiratory, musculoskeletal, or cardiovascular diseases;
  • Medical or other contraindications for exercise;
  • Taking medications that affect metabolism;
  • Smoking and/or drinking habits.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Weight8 weeks

Changes in Weight before and after intervention.

Body Mass Index (BMI)8 weeks

Changes in BMI before and after intervention.

body fat percentage8 weeks

Changes in body fat percentage before and after intervention.

waist circumference (WC)8 weeks

Changes in WC before and after intervention.

Systolic blood pressure (SBP)8 weeks

Changes in SBP before and after intervention.

Diastolic blood pressure (DBP)8 weeks

Changes in DBP before and after intervention.

Fasting plasma glucose (FPG)8 weeks

Changes in FPG before and after intervention.

Triglyceride (TG)8 weeks

Changes in TG before and after intervention.

High-density lipoprotein cholesterol (HDL-C)8 weeks

Changes in HDL-C before and after intervention.

Secondary Outcome Measures
NameTimeMethod
Non high-density lipoprotein cholesterol (Non HDL-C)8 weeks

Changes in HDL-C before and after intervention.

Insulin8 weeks

Changes in insulin before and after intervention.

Homeostatic model assessment for insulin resistance (HOMA-IR)8 weeks

12、Homeostatic model assessment for insulin resistance (HOMA-IR) Changes in HOMA-IR before and after intervention.

Triglyceride-glucose (TyG) index8 weeks

Changes in TyG index before and after intervention.

Triglyceride-to-high density lipoprotein cholesterol ratio (TG/HDL-C ratio)8 weeks

Changes in TG/HDL-C ratio before and after intervention.

Visceral fat area (VFA)8 weeks

Changes in VFA before and after intervention.

Trial Locations

Locations (1)

School of Sports Medicine and Rehabilitation, Beijing Sport University

🇨🇳

Beijing, China

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