- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02320747
Immediate Effect of Tai Chi Exercise in Healthy Volunteers
Immediate Effect of Tai Chi Exercise in Healthy Volunteers:Randomized Controlled Study
Tai Chi has been widely practiced as a Chinese martial art that focuses on slow sequential movements, providing a smooth, continuous and low intensity activity. It has been promoted to improve balance and strength and to reduce falls in the elderly, especially those 'at risk'. The potential benefits in healthy younger age cohorts and for wider aspects of health have received less attention.
The present study documented prospective changes in balance and vascular responses for a community sample of adults.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Rajasthan
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Jaipur, Rajasthan, India, 302019
- Gyansanjeevani
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18 to 25 years old
- Have given written informed consent
- Have a high school level of education
- Be healthy and psychologically stable as determined by screening for medical and psychiatric problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis laboratory tests.
- Have an active interest in exploring and developing their spiritual lives
- Cigarette smokers must agree to abstain from smoking on session days
- Agree to refrain from using any psychoactive drugs, including alcoholic beverages, within 24 hours
- Agree that for one week before each session, refrain from taking any nonprescription medication, nutritional supplement, or herbal supplement except when approved by the study investigators.
Exclusion Criteria:
- Women who are pregnant or nursing
- Cardiovascular conditions: coronary artery disease, stroke, angina, uncontrolled hypertension, a clinically significant ECG abnormality
- Epilepsy with history of seizures
- Insulin-dependent diabetes
- Currently taking psychoactive prescription medication on a regular (e.g., daily) basis
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control Group
|
|
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Experimental: Tai Chi Group
Experienced instructor at teaching tai chi delivered in a group setting in the community lasted approximately 40 minutes.
Participants in the program served as an active control group that matched to the program and delivered.The class comprised mainly seated exercises including stretching, low-level strength, and low-level cardiovascular exercise.
Participants walked (warm-up and cool-down) for 7 min in class, remaining seated or standing with arm support the rest of the time.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate (HR)
Time Frame: 40 Minutes
|
Heart rate was recorded before and after the session.
|
40 Minutes
|
|
Systolic Pressure (SP)
Time Frame: 40 minutes
|
40 minutes
|
|
|
Diastolic Pressure (DP)
Time Frame: 40 Minutes
|
40 Minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Avinash Mishra, MSc, Shanghai University of Sport
- Study Director: Dinghai Yu, Shanghai University of Sport
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Adwin009
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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