- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico 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
Descripción general del estudio
Descripción detallada
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.
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Taipei, Taiwán
- Reclutamiento
- National Yang-Ming University
-
Investigador principal:
- Yea-Ru Yang, PhD
-
Contacto:
- Yea-Ru Yang, PhD
- Número de teléfono: +886228267279
- Correo electrónico: yryang@ym.edu.tw
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
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
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
---|---|
Healthy adults
Subjects will receive pre and post-test, in order to verify the test-retest reliability of the Somatosensory detector
|
Sin intervención
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Gait speed
Periodo de tiempo: Change from baseline at one week
|
Gait speed is calculated using distance in meters and time in seconds.
|
Change from baseline at one week
|
Gait cadence
Periodo de tiempo: Change from baseline at one week
|
Cadence is the rate at which a person walk, expressed in steps per minute.
|
Change from baseline at one week
|
Gait stride length
Periodo de tiempo: Change from baseline at one week
|
The stride length is the distance between two successive placements of the same foot.
|
Change from baseline at one week
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
One leg standing test
Periodo de tiempo: Change from baseline at one week
|
To test balance ability
|
Change from baseline at one week
|
Functional forward reach test
Periodo de tiempo: Change from baseline at one week
|
To test functional balance performance
|
Change from baseline at one week
|
Timed up and go test
Periodo de tiempo: Change from baseline at one week
|
To test functional balance performance
|
Change from baseline at one week
|
Upper arm curl test
Periodo de tiempo: Change from baseline at one week
|
To test functional muscle strength of upper extremities
|
Change from baseline at one week
|
30 seconds sit-stand-sit test
Periodo de tiempo: Change from baseline at one week
|
To test functional muscle strength of lower extremities
|
Change from baseline at one week
|
2 minutes stepping test
Periodo de tiempo: Change from baseline at one week
|
To test cardiopulmonary ability
|
Change from baseline at one week
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- YM106054E
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
Ensayos clínicos sobre Sin intervención
-
University of OxfordOxford University Hospitals NHS TrustDesconocidoSíntomas de comportamientoReino Unido
-
Munich Municipal HospitalTechnical University of Munich; University of RegensburgDesconocido
-
Shiraz University of Medical SciencesTerminado
-
Heidelberg UniversityDesconocidoRetraso de idioma | Trastornos del desarrollo del lenguajeAlemania
-
Ottawa Heart Institute Research CorporationCanadian Institutes of Health Research (CIHR)Activo, no reclutandoDependencia a la nicotina, cigarrillos | Abstinencia de nicotinaCanadá
-
IWK Health CentreCanadian Institutes of Health Research (CIHR)TerminadoTrastorno de oposición desafiante | Trastorno de conductaCanadá
-
The Hospital for Sick ChildrenTerminadoObesidad infantilCanadá
-
VA Office of Research and DevelopmentTerminadoTrastornos de Estrés PostraumáticoEstados Unidos
-
IWK Health CentreMcGill University; Canadian Institutes of Health Research (CIHR); University of... y otros colaboradoresActivo, no reclutandoTrastornos del neurodesarrollo | Trastornos del ComportamientoCanadá
-
Sahlgrenska University Hospital, SwedenKarolinska University Hospital; Skane University Hospital; Karlstad Central Hospital y otros colaboradoresActivo, no reclutandoClaudicación intermitenteSuecia