- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06523790
The Impact of Exercise Methods on Human Body Functions and Metabolism (EXMET-BW&Y)
Comparative Study on the Effects of Brisk Walking and Yoga on Glucose and Lipid Metabolism and Neurocognitive Function in Adults: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial aims to investigate the differential impacts of yoga and walking exercise training on weight-related body fat and metabolic biomarkers in women over an 8-month period. The study will recruit women aged 18-65 years, who will be randomly assigned to either a yoga group or a walking group.
Yoga Group: Participants in the yoga group will attend 90-minute yoga sessions, 3 times per week.
Walking Group: Participants in the walking group will engage in one-hour fast-paced walking sessions, 6 times per week.
Outcome Measures: Physical and metabolic markers will be assessed at baseline and after 8 months of exercise intervention. The primary outcomes will include changes in body weight, BMI, visceral fat, and basal metabolism. Metabolic biomarkers such as serum leptin, glucose, total cholesterol (TC), apolipoprotein A (APOA), and apolipoprotein B (APOB) will also be measured.
Participants will be monitored for adherence to the exercise protocol and any adverse events throughout the study. Data will be collected during the intervention, and analyzed to determine the differential effects of yoga and walking on the measured outcomes.
The study aims to provide insights into the relative benefits of yoga and walking exercise regimens on women's health, particularly in terms of body composition and metabolic health, thereby informing future exercise recommendations and health interventions.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: jin li
- Phone Number: (86)18438175639
- Email: lijin0213@126.com
Study Locations
-
-
Henan
-
Zhoukou, Henan, China
- Recruiting
- Zhou Kou Normal University
-
Contact:
- Jin Li
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Female participants aged 18-65 years; Willing and able to participate in an 8-month exercise program; Generally healthy with no contraindications to physical activity; Ability to provide informed consent
Exclusion Criteria:
Current participation in a structured exercise program; Known cardiovascular, respiratory, or metabolic disorders that contraindicate exercise; Pregnancy or planning to become pregnant during the study period; Use of medications affecting metabolism or physical activity levels; Any other condition that, in the opinion of the investigators, would make participation unsafe or not feasible
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Yoga Group
Participants in this group will undergo 90-minute yoga sessions, 3 times per week, for 8 months.
The yoga intervention includes a combination of asanas (postures), pranayama (breathing exercises), and meditation designed to improve flexibility, strength, and mental well-being.
|
Participants in the yoga group will attend 90-minute yoga sessions, 3 times per week, for 8 months.
The sessions will include a combination of asanas (postures), pranayama (breathing exercises), and meditation.
|
|
Experimental: Walking Group
Participants in this group will engage in one-hour fast-paced walking sessions, 6 times per week, for 8 months.
The walking intervention is designed to improve cardiovascular fitness, endurance, and support weight loss.
|
Participants in the brisk walking group will engage in one-hour fast-paced walking sessions, 6 times per week, for 8 months.
The walking regimen is designed to improve cardiovascular fitness, endurance, and support weight loss.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Body Weight
Time Frame: Baseline, 8 months
|
Measurement of body weight changes in kilograms from baseline to 8 months.
|
Baseline, 8 months
|
|
Change in Body Mass Index (BMI)
Time Frame: Baseline, 8 months
|
Measurement of BMI changes calculated as weight in kilograms divided by height in meters squared from baseline to 8 months.
|
Baseline, 8 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Serum Leptin Levels
Time Frame: Baseline, 8 months
|
Measurement of serum leptin levels in ng/mL from baseline to 8 months.
|
Baseline, 8 months
|
|
Change in Fasting Blood Glucose Levels
Time Frame: Baseline, 8 months
|
Measurement of fasting blood glucose levels in mg/dL from baseline to 8 months.
|
Baseline, 8 months
|
|
Change in Total Cholesterol (TC) Levels
Time Frame: Baseline, 8 months
|
Measurement of total cholesterol levels in mg/dL from baseline to 8 months.
|
Baseline, 8 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: xiaomeng liu, Zhoukou Normal University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZhoukouNU-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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