Tai Chi Exercise on Balance and Awereeness
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| ClinicalTrials.gov Identifier: NCT03901677 |
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Recruitment Status :
Completed
First Posted : April 3, 2019
Last Update Posted : April 30, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Young Adult | Other: Tai-chi training | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 42 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Masking Description: | All assessments done by masked therapist to avoid bias who have no idea about intervention before and 12 weeks after the tai chi exercise. |
| Primary Purpose: | Treatment |
| Official Title: | Effects of Tai Chi Exercise on Balance and Body Awareness of Younger Adults |
| Actual Study Start Date : | January 8, 2019 |
| Actual Primary Completion Date : | April 2, 2019 |
| Actual Study Completion Date : | May 2, 2019 |
| Arm | Intervention/treatment |
|---|---|
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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.
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Other: Tai-chi training
Group exercise apply with physiotherapist |
- 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.
- 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).
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| Ages Eligible for Study: | 18 Years to 25 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03901677
| Turkey | |
| Baskent University | |
| Ankara, Turkey, 06790 | |
| Principal Investigator: | ayca tigli, Phd | Baskent University |
| Responsible Party: | Ayça Aytar TIĞLI, Principal Investigator, Baskent University |
| ClinicalTrials.gov Identifier: | NCT03901677 |
| Other Study ID Numbers: |
KA19/10 |
| First Posted: | April 3, 2019 Key Record Dates |
| Last Update Posted: | April 30, 2020 |
| Last Verified: | April 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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exercise Awareness posture |

