- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03901677
Tai Chi Exercise on Balance and Awereeness
April 29, 2020 updated by: Ayça Aytar TIĞLI, Baskent University
Effects of Tai Chi Exercise on Balance and Body Awareness of Younger Adults
The aim of this study is to determine the effect of Tai chi exercises on balance and body awareness in younger adults.
Forty-two healthy subjects between the ages of 18-25 who do not have any restriction to exercise participate in our study.
After recording the sociodemographic characteristics of the subjects, static and dynamic balance and body awareness will be evaluated.
Kinesthetic Ability Trainer will be used to assess static and dynamic balance and body awareness will be evulated with Body Awareness Questionnaire.
All assessments will be done before and 12 weeks after the tai chi exercise.
Tai-chi training will be performed as a group exercise.
Duration for tai chi exercise will be 60 minutes for 2 days per week totally 12 weeks.
Study Overview
Detailed Description
Tai-chi training was performed as a group exercise.
Duration for tai chi exercise was 60 minutes for 2 days per week for 12 weeks.
Each session includes 10 min warm-up and cool-down and 40 min Tai Chi exercises.
During exercises, attention was paid to correct positioning of the upper and lower extremity joints, and mentally concentration was achieved.
Slow and controlled movements were carried out by a specialized physiotherapist
Study Type
Interventional
Enrollment (Actual)
42
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
-
-
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Ankara, Turkey, 06790
- Başkent University
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-
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
18 years to 25 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects between the ages of 18-25,
- Subjects who had lack of disease.
Exclusion Criteria:
- Subjects with neurological symptoms,
- Subjects with orthopedic problems,
- Subjects with heart failure,
- Subjects with respiratory distress.
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: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Tai-chi training
Tai-chi training performe as a group exercise.
Duration for tai chi exercise will be 60 minutes for 2 days per week for 12 weeks.
Each session includes 10 min warm-up and cool-down and 40 min Tai Chi exercises.
During exercises, attention paid to correct positioning of the upper and lower extremity joints, and mentally concentration achieve.
Slow and controlled movements will carry out by a specialized physiotherapist.
|
Group exercise apply with physiotherapist
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body Awareness Questionnaire
Time Frame: 12 week
|
Body awareness will be evaluated with Body Awareness Questionnaire (BAQ).
It is a questionnaire composed of 4 subgroups (changes in the body process, sleep-wake cycle, estimation of the onset of the disease, estimation of the body reactions) and a total of 18 expressions to determine the normal or non-normal sensitivity level of the body composition.
Subjects assess each item from 1 to 7. Higher scores on the BAQ indicates higher awareness.
|
12 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Balance Test
Time Frame: 12 week
|
Kinesthetic Ability Trainer (KAT) 3000 (KAT 3000, Berg, Vista, CA, USA) will be used to assess static and dynamic balance.
The KAT 3000 consists of a movable platform supported on a central point by a small pivot.
A tilt sensor on the platform is connected to a computer, which registers the deviation of the platform from a reference position 18.2 times each second.
The distance from the central point to the reference position is measured at every registration.
From the summation of these distances, a score, the balance index (BI), can be calculated (a low BI implies good ability to perform the balance test).
|
12 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: ayca tigli, Phd, Başkent University
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)
January 8, 2019
Primary Completion (ACTUAL)
April 2, 2019
Study Completion (ACTUAL)
May 2, 2019
Study Registration Dates
First Submitted
April 2, 2019
First Submitted That Met QC Criteria
April 2, 2019
First Posted (ACTUAL)
April 3, 2019
Study Record Updates
Last Update Posted (ACTUAL)
April 30, 2020
Last Update Submitted That Met QC Criteria
April 29, 2020
Last Verified
April 1, 2019
More Information
Terms related to this study
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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