- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06673758
Effects of Taichi Exercises on Cardiorespiratory Fittness (taichi)
January 22, 2025 updated by: Riphah International University
Effects of Taichi Exercises on Cardiorespiratory Fitness Among School Going Childern
Effects of tai chi exercises on cardiorespiratory fitness among scchool going childern.
sample size is 30 .divided two groups into 15 15 members one group is giving hand and art crafts activity other is giving tai chi basics level exercises then check and compare cardiorespiratory fitness by time up and go test and 6 minutes walk test.
compare the results.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study will be a randomized controlled trial involving 30 participants, with data collected from the Sanai school system in Sargodha.
The study will include school-aged children with normal weight between the ages of 10 and 14.
Children with any cardiorespiratory conditions, hemophilia, muscular dystrophy, or a history of cardiovascular events will be excluded.
The sample of 30 will be divided into two groups of 15 participants each.
Group A will participate in tai chi exercises across three levels, while Group B will engage only in basic arts and crafts activities.
The interventions will consist of 10 sessions, conducted at a rate of 5 sessions per week over 2 weeks.
To assess the respiratory fitness of the children, data will be collected using the 6-minute walk test and the Timed Up and Go test.
Data analysis will be performed using SPSS version 26.0.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Riphah International University
-
Lahore, Punjab, Pakistan, 5400
- Imran Amjad
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- childerns with 10 to 14 years
- childerns with normal weight less than 30kg/m2
Exclusion Criteria:
- Childerns with any cardiorespiratory issues
- Childerns who have gone through CVA,hemophilia, dystrophy and conditions which impact cardiorespiratory status
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
experimental group given tai chi exercises on three levels of two weeks sessions of total 10 session in five days of each week.
|
tai chi exercises of three basic levels will be given with sessions of two weeks five time a day and follow efftects of tai chi exercises by 6minute walk test and time up and go test and check the results before and after exercises
Other Names:
|
|
Other: control group
15 participants are given art and crafts activity of two weeks
|
Art and crafts activity will be given to control group and check cardiorespiratory fitness before and after arts and crafts activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
6 minute walk test
Time Frame: 2 weeks
|
6 minutes walk test is use for diagnosis of cardiorespiratory fitness after tai chi and art andcrafts activity
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
time up and go test
Time Frame: 2 weeks
|
time up and go test will be use after tai chi exercises and art and crafts activity
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Anum Saleem, MS*, Ripah International university
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 29, 2024
Primary Completion (Actual)
December 29, 2024
Study Completion (Actual)
January 15, 2025
Study Registration Dates
First Submitted
November 3, 2024
First Submitted That Met QC Criteria
November 3, 2024
First Posted (Actual)
November 5, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 22, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- REC/RCR & AHS/24/0712
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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