- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04887363
The Comparisons of Effects of Core Stability Exercise and Tai Chi on Core Muscle Performances in Elderly
The Comparisons of Effects of Core Stability Exercise and Tai Chi on Core Muscle Performances, Core Stability and Balance in Community-living Elderly
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In this pretest, posttest design study, elderly adults enrolled and assigned to the core exercise group or Tai Chi exercise group, the core exercise group received core exercise intervention comparing to Tai Chi exercise group participated Tai chi exercise program as a control group.
The young adults group were also enrolled for a reference group, not received any exercise intervention and just only received the measurements once.
Participants in the two elderly group will receive 12-week, 36-session exercise-based core stability training class. The each 60 minutes core exercise class focuses on exercise for improving strength, endurance of core muscles and trunk stability.
Participants need complete baseline assessments of muscle performance, and balance ability measures 1 week prior and 1 week and 12 weeks following the intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Core exercise group and Tai Chi exercise group
- healthy community-dwelling older adults (60-74 years old)
- not received any core stability or Tai Chi Chuan training within the previous 6 months
- independent in basic daily living activities
- able to move freely without any assistance
- Young adults group a. Their age should be ranged between 20 - 59 years
Exclusion Criteria:
All group
- have a history of orthopedic surgery on spine or lower extremity
- have any spine pathology (e.g., spondylolisthesis, disc herniation)
- have a pain over back or lower limbs to affect the ability to perform activities of daily living
- had a history of vestibular disease (e.g., Meniere' s disease)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Core exercise group
The healthy community-dwelling older adults (60-74 years old), who had not received any core stability or Tai Chi Chuan training within the previous 6 months, were recruited in this study.
All the subjects were independent in basic daily living activities and able to move freely without any assistance.
|
Participants will receive12-week, 60 minutes, 36-session exercise-based core stability training class.
Participants need complete baseline assessments of muscle performance, and balance ability measures 1 week prior and 1 week and 12 weeks following the intervention.
All subjects will receive two post-exercise measurements at 13th week and 25th week.
|
|
Experimental: Tai Chi exercise group
The healthy community-dwelling older adults (60-74 years old), who had not received any core stability or Tai Chi Chuan training within the previous 6 months, were recruited in this study.
All the subjects were independent in basic daily living activities and able to move freely without any assistance.
|
Participants will receive 12-week, 60 minutes, 36-session Tai Chi exercise training class.
Participants need complete baseline assessments of muscle performance, and balance ability measures 1 week prior and 1 week and 12 weeks following the intervention.
All subjects will receive two post-exercise measurements at 13th week and 25th week.
|
|
No Intervention: Young adults group
The healthy young adults who have not any neurological, musculoskeletal or rheumatic disease were recruited as a reference group.
They would not receive any training program in the study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in strength of core muscle groups (trunk) at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using a custom-made isometric dynamometer to measure the strength of trunk flexors, extensors and rotators
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in strength of core muscle groups (hip) at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using a hand-held dynamometer to measure the hip muscle strength
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in endurance of core muscle groups at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using the Stabilizer Pressure Biofeedback Unit (PBU) during the leg-loading test to measure the endurance of lumbo-pelvic stability
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in flexibility of the lower back and hamstring muscles at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using the sit and reach test to measure the flexibility of the lower back and hamstring muscles
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in ability of the dynamic balance at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using the Dual-tasking 3m Timed up and go (3m-TUG) to measure dynamic balance and the fall risk.
Mean time to perform 3m-TUG is 11.56 seconds
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in assessment of postural control at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using a force plate to collect the center of pressure (COP) displacement
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in muscle activity of selected core muscles during performing arm-raising tasks at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using a surface electromyography to record the muscle activity of abdominal and trunk muscles during performing arms-raising tasks with hand-holding 1.5-2 kg
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
|
Changes in assessment of postural control during performing arm-raising tasks at 12-week
Time Frame: The assessments will be conducted 1 and 12 weeks following the intervention
|
Using a force plate to collect the center of pressure (COP) displacement during performing arms-raising tasks with hand-holding 1.5-2 kg
|
The assessments will be conducted 1 and 12 weeks following the intervention
|
Collaborators and Investigators
Investigators
- Study Director: Li-Jiun Liaw, Kaohsiung Medical University Department of Physical Therapy Associate Professor
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
- KMUH-IRB-20120427
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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