- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06393686
The Effect of Yoga on the Fitness of Children
Impact of Yoga Intervention on Physical Fitness Parameters in Preadolescent Children: A Randomized Controlled Trial
This study aims to evaluate the effect of yoga on physical fitness among healthy primary school children using a randomized control design. A total of 52 children, ages 8-13, will be randomly assigned to either the Yoga Group or the Control Group. Participants will be assessed using the EUROFIT Test Battery as the primary outcome measure.
The Yoga Group will do 45-minute yoga sessions twice a week for 10 weeks, while the Control Group will not receive any intervention. Outcome assessments will be repeated at the end of the 10-week intervention period.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Nicosia, Cyprus
- Near East University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants who do not have any mental or physical disabilities
- Participants who have not participated in any exercise regime for the previous six months
Exclusion Criteria:
• Individuals who do not participate in 90 percent of the 10-week yoga training program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Yoga Group
The yoga intervention will be implemented every two weeks, with each session lasting 45 minutes and implemented for 10 weeks.
Sessions will always be led by the same certified yoga instructor.
Each session will include a variety of different yoga poses, as well as breathing techniques and deep relaxation methods.
|
The yoga intervention will be implemented every two weeks, with each session lasting 45 minutes and implemented for 10 weeks.
Sessions will always be led by the same certified yoga instructor.
Each session will include a variety of different yoga poses, as well as breathing techniques and deep relaxation methods.
|
No Intervention: Control Group
There will be no intervention in the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
EUROFIT Test Battery
Time Frame: 12 weeks
|
The 10 tests for the Eurofit Test Battery are used as standards in the measurements of school-aged children. Anthropometry: Height, Weight, BMI, Skinfold thickness
|
12 weeks
|
Anthropometric measurements
Time Frame: 12 weeks
|
Anthropometric measurements involved determining participants' height using a non-elastic measuring tape (SECA brand), affixed to a wall.
The Tanita MC-180MA III device facilitated weight analysis, and Body Mass Index (BMI) (kg/m2) was calculated by dividing body weight (in kilograms) by the square of height (in meters).
|
12 weeks
|
Body Mass Index
Time Frame: 12 weeks
|
Weight in kilograms and height in meters will been calculated and, weight and height will be combined to report BMI in kg/m2.
|
12 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- YDU/2019/74-938
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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