- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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
Studieoversikt
Detaljert beskrivelse
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.
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiesteder
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Taipei, Taiwan
- Rekruttering
- National Yang-Ming University
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Hovedetterforsker:
- Yea-Ru Yang, PhD
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Ta kontakt med:
- Yea-Ru Yang, PhD
- Telefonnummer: +886228267279
- E-post: yryang@ym.edu.tw
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
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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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ingen inngrep
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Gait speed
Tidsramme: Change from baseline at one week
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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
Tidsramme: 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
Tidsramme: 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
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
One leg standing test
Tidsramme: Change from baseline at one week
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To test balance ability
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Change from baseline at one week
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Functional forward reach test
Tidsramme: 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
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Timed up and go test
Tidsramme: 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
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Upper arm curl test
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- YM106054E
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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