- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03733613
Reliability and Validity of Kinect Detector for Fitness Tests and Gait Performance Analysis
To Verify the Reliability and Validity of Kinect Detector While Apply to Physical Fitness Tests and Gait Performance Analysis
Study Overview
Detailed Description
Background: Depending on nature and needs, physical fitness can be divided into healthy fitness and physical fitness (also known as competitive fitness). Healthy fitness includes cardio-respiratory fitness, muscle fitness, muscular endurance, flexibility, and body composition. Physical fitness includes coordination, speed, explosiveness, balance, agility, and reaction time. Although the monitoring of fitness is very important, most of the tests need to be assisted by professionally trained fitness inspectors, so that the public who wants to regularly check their fitness status will facing a dilemma-- insufficient of inspectors. In the face of such a situation, the somatosensory detector may be a choice which is relatively objective, convenient and no need to rely on the inspectors. Therefore, the validity and retest reliability of the somatosensory detector need to be verified in order to achieve accurate and objective measurement results.
Research purposes: To verify the retest reliability and validity of the somatosensory detector on physical fitness and gait performance.
Methods: The trial will enroll 60 subjects, 30 of them were healthy individuals between the ages of 20 and 65, and 30 are healthy elderly than 65 years of age. The exclusion criteria including: (1) those who are unable to follow the instructions and who have orthopedic, nervous system or cardiopulmonary system disorders, or who have abnormal gait pattern, or who are affected by the above physiological system disorders. Subjects will receive two tests, there's a one-week interval between each test. In the first test, the fitness assessment of the fitness inspector and the somatosensory detector was performed simultaneously, and the fitness evaluation of the somatosensory detector was performed only for the second time. And use statistical software to analyze the reliability and validity of the somatosensory detector.
Statistical Analysis: Using SPSS 20.0 for data archiving and statistical analysis, the reliability and validity of the test will be detected by intraclass correlation one-way random model, and presenting by the intraclass correlation coefficient and 95% confidence interval.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Yea-Ru Yang, Ph.D.
- Phone Number: +88628267279
- Email: yryang@ym.edu.tw
Study Locations
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Taipei, Taiwan
- Recruiting
- National Yang-Ming University
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Principal Investigator:
- Yea-Ru Yang, PhD
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Contact:
- Yea-Ru Yang, PhD
- Phone Number: +886228267279
- Email: yryang@ym.edu.tw
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- healthy adults
Exclusion Criteria:
- those unable to follow to instructions
- those have abnormal gait pattern which caused by orthopedics system disorders, nervous system disorders or cardio-respiratory disorders
- those with abnormal movement performance which caused by physiological system obstacles
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Healthy adults
Subjects will receive pre and post-test, in order to verify the test-retest reliability of the Somatosensory detector
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no intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gait speed
Time Frame: Change from baseline at one week
|
Gait speed is calculated using distance in meters and time in seconds.
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Change from baseline at one week
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Gait cadence
Time Frame: Change from baseline at one week
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Cadence is the rate at which a person walk, expressed in steps per minute.
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Change from baseline at one week
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Gait stride length
Time Frame: Change from baseline at one week
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The stride length is the distance between two successive placements of the same foot.
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Change from baseline at one week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
One leg standing test
Time Frame: Change from baseline at one week
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To test balance ability
|
Change from baseline at one week
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Functional forward reach test
Time Frame: Change from baseline at one week
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To test functional balance performance
|
Change from baseline at one week
|
Timed up and go test
Time Frame: Change from baseline at one week
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To test functional balance performance
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Change from baseline at one week
|
Upper arm curl test
Time Frame: Change from baseline at one week
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To test functional muscle strength of upper extremities
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Change from baseline at one week
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30 seconds sit-stand-sit test
Time Frame: Change from baseline at one week
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To test functional muscle strength of lower extremities
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Change from baseline at one week
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2 minutes stepping test
Time Frame: Change from baseline at one week
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To test cardiopulmonary ability
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Change from baseline at one week
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- YM106054E
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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