- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT05034302
Posture Analysis Through Machine Learning (PathML)
Descripción general del estudio
Estado
Condiciones
Descripción detallada
This is a cross-sectional, single observation study. Individuals will be drawn from local surrounding clinics and the general community. All recruitment will include both men and women. Selection criteria include individuals between the ages of 18-85 years, no major chronic illness that impair mobility and able to complete activities of daily living without assistance. Participants will complete one three hour session where there will be one video camera set up within the home (i.e., static cameras). For approximately 30 minutes of the session they will complete a semi-scripted routine that will include sit to stand transitions, a timed up and go test, and scripted activities of daily living.
Researchers will use a video camera to record participant behavior within their daily life. For two of the three hours, researchers will be video recordings the participants normal (unscripted) activities. • For one hour of the session we will use two cameras, one that will be held by a researcher and one that will be set up on a tripod. During this hour we will ask participants to follow a semi-structured protocol:
- 10 minutes recording the empty space
- 10 minutes that include a timed up a go test (sit up from a chair and walk 10 feet), repeat the test 3 times.
- 6 minute walk test (walk continuously for 6 minutes)
- Four stage balance test
- The remainder of the time, participants will complete standard activities of daily living like household chores, eating or drinking.
Data will be annotated using an established behavioral observation software by training research assistants (ground-truth). The image data from videos will be used to train machine learning models to classify physical activities (e.g. ,'walking', 'sitting' or 'standing up"), information about behavior (e.g., location and purpose of the activity), and performance (e.g., walking speed and sit to stand transition times).
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
California
-
San Luis Obispo, California, Estados Unidos, 93407
- CalPoly
-
-
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:
- Age 18-85 years
- No major chronic illness that impair mobility
- Able to complete activities of daily living without assistance.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
|---|
|
Recordings
Selection criteria include individuals between the ages of 18-85 years, no major chronic illness that impair mobility and able to complete activities of daily living without assistance.
We will recruit approximately equal number of men and women and 30% of the sample will be racial or ethnic minorities.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Postural Status
Periodo de tiempo: Upon enrollment (one timepoint)
|
Sitting versus standing versus moving
|
Upon enrollment (one timepoint)
|
|
Activity type
Periodo de tiempo: Upon enrollment (one timepoint)
|
Indoor vs outdoor vs driving
|
Upon enrollment (one timepoint)
|
|
Sit to stand transition time
Periodo de tiempo: Upon enrollment (one timepoint)
|
Time it takes to go from sitting to standing
|
Upon enrollment (one timepoint)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Activity intensity
Periodo de tiempo: Upon enrollment (one timepoint)
|
Sedentary, light, moderate and vigorous intensity
|
Upon enrollment (one timepoint)
|
|
Activity type
Periodo de tiempo: Upon enrollment (one timepoint)
|
lying, sitting, driving, standing, housework or office work, walking, running, sports, other
|
Upon enrollment (one timepoint)
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Sarah Keadle, Cal Poly
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
- PathML2021
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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. .