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A Waist Circumference and Body Fat Percentage Dual-Dimension Nine-Square Grid Model for Precision Obesity Management: A Randomized Controlled Trial in Overweight/Obese University Students

H

Hainan Normal University

Status

Completed

Conditions

Overweight and/or Obesity

Treatments

Behavioral: Dynamic Matrix Management for Weight Control (DMM-WC)
Behavioral: Standard Aerobic Prescription

Study type

Interventional

Funder types

Other

Identifiers

NCT07133542
AQNU2024111

Details and patient eligibility

About

The goal of this randomized controlled trial is to test whether a dual-dimensional 9-grid matrix intervention improves body composition and exercise adherence compared to standard aerobic exercise in overweight/obese college students. The main questions it aims to answer are:

Does the 9-grid model optimize fat distribution (measured by waist-hip ratio) and sustain body fat reduction better than traditional exercise?

Does dynamic risk stratification in the 9-grid system enhance long-term exercise adherence?

How does spatial migration of participants within the grid (quantified by centroid index G) reflect intervention efficacy?

Researchers will compare the 9-grid management group (receiving dynamic positioning + 5-tier personalized strategies) to the control group (receiving standardized aerobic exercise) to see if the 9-grid model:

Reduces waist-hip ratio more effectively

Delays intervention plateau in body fat loss

Increases exercise adherence at 8 weeks

Participants will:

Undergo body measurements (weight, body mass index (BMI), body fat percentage, waist/hip circumference) at baseline, 4 weeks, and 8 weeks

Complete the Exercise Adherence Rating Scale (EARS) at 4 and 8 weeks

If in 9-grid group:

  • Be classified into 1 of 9 grid zones every 2 weeks based on waist circumference risk + body fat status
  • Receive zone-specific interventions (nutrition/exercise/behavioral guidance)

If in control group:

  • Perform progressive aerobic exercise (40-90% heart rate reserve (HR) 3×/week
  • Use heart rate monitors for intensity tracking

Enrollment

50 patients

Sex

All

Ages

18 to 36 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age & Status:

    • Full-time university students aged 18-36 years
  2. Overweight/Obesity Diagnosis (per Chinese criteria):

    • Males: Body Mass Index (BMI) ≥24 kg/m² AND waist circumference ≥85 cm
    • Females: Body Mass Index (BMI) ≥24 kg/m² AND waist circumference ≥80 cm
  3. Exercise Capacity:

    • Able to safely perform moderate-intensity exercise (confirmed by Physical Activity Readiness Questionnaire [PAR-Q], all items "No")
  4. Tech Compliance:

    • Own smartphone with proficiency in health apps (e.g., WeChat Sport)
  5. Informed Consent:

    • Signed written consent with commitment to complete 12-week intervention

Exclusion criteria

  1. Metabolic Diseases:

    • Diagnosed diabetes, thyroid dysfunction, or history of cardiovascular disease
  2. Exercise Contraindications:

    • Orthopedic/neurological conditions limiting exercise
  3. Confounding Medications:

    • Use of weight/metabolism-affecting drugs in past 3 months
  4. Special Physiological Status:

    • Pregnancy or lactation
  5. Conflicting Participation:

    • Concurrent enrollment in other weight-management trials

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups, including a placebo group

Dynamic Nine-Grid Matrix Group
Experimental group
Description:
Tiered management via waist-risk/body-fat matrix. Participants receive bi-weekly health positioning and one of five precision strategies (e.g., high-intensity exercise + dietary control for Grid-I; low-intensity maintenance for Grid-IX). Real-time feedback via digital dashboard.
Treatment:
Behavioral: Dynamic Matrix Management for Weight Control (DMM-WC)
Standard Aerobic Prescription Group
Placebo Comparator group
Description:
Standardized progressive aerobic exercise at 40-90% heart rate reserve. Intensity/volume are personalized at baseline but remain static afterward. Adherence monitored using Huawei wearables (no dynamic adjustments or tiered feedback).
Treatment:
Behavioral: Standard Aerobic Prescription

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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