- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02796196
Prescribed Physical Activity in Improving Sleep and Physical Performance in Patients Undergoing Stem Cell Transplant
Effects of Prescribed Physical Activity on Sleep and Performance in Hematopoietic Cell Transplantation Patients
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
PRIMARY OBJECTIVES:
I. Evaluate whether prescribed physical activity, as part of standard care, improves sleep and functional outcomes in hematopoietic cell transplantation (HCT) (stem cell transplantation) patients during a typical 30-day hospitalization period.
OUTLINE:
Data including demographics, type of HCT (e.g., allogeneic or autologous), preexisting physical conditions (e.g., chronic joint injury), chronic renal failure (CRF), steroid use data, Eastern Cooperative Oncology Group (ECOG) and Karnofsky performance status (KPS) scores are collected from patients' medical charts at time of enrollment. Patients are prescribed participation in a primarily self-directed physical activity program which encourages them to spend 6 hours out of bed daily and to perform 30 minutes of light-to-moderate daily aerobic activity. Patients who are able to maintain independent mobility undergo physical therapist assessment 2 times a week until hospital discharge. Patients wear a physical activity monitoring device and daily activity and sleep data are collected continuously during hospital length of stay (LOS).
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
California
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Palo Alto, California, Estados Unidos, 94304
- Stanford University, School of Medicine
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Admitted to Stanford Hospital for HCT
- Able to provide informed consent
- Speaks language supported by interpretative services
- Able to operate and take care of a physical activity monitor
Exclusion Criteria:
- Does not meet inclusion criteria
- Unable to wear a physical activity monitor throughout hospital stay
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
---|---|
Supportive care (monitoring device, medical chart review)
Data including demographics, type of HCT (e.g., allogeneic or autologous), preexisting physical conditions (e.g., chronic joint injury), CRF, steroid use data, ECOG and KPS scores are collected from patients' medical charts at time of enrollment.
Patients are prescribed participation in a primarily self-directed physical activity program which encourages them to spend 6 hours out of bed daily and to perform 30 minutes of light-to-moderate daily aerobic activity.
Patients who are able to maintain independent mobility undergo physical therapist assessment 2 times a week until hospital discharge.
Patients wear a physical activity monitoring device and daily activity and sleep data are collected continuously during hospital LOS.
|
Revisión de expediente médico
Otros nombres:
Wearable physical activity monitoring device
Otros nombres:
Undergo primarily self-directed physical therapy
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
ECOG performance scores
Periodo de tiempo: At baseline
|
Will focus on trends in scores between patients with different durations of activity and sleep.
Results, from both descriptive and inferential analyses, will be presented in table and/or graphical format.
|
At baseline
|
KPS performance scores
Periodo de tiempo: At baseline
|
Will focus on trends in scores between patients with different durations of activity and sleep.
Results, from both descriptive and inferential analyses, will be presented in table and/or graphical format.
|
At baseline
|
Minutes of aerobic activity per day
Periodo de tiempo: Up to time of hospital discharge, or 29 days
|
Will use interval-censored regression to estimate distributions of activity from one day to the next.
This repeated-measures analysis with a polynomial model will generate average curves for activity, each spanning average LOS (i.e., activity duration plotted on day one, day two, day three, etc.).
Will also run diagnostics to verify the assumptions of a linear model (e.g., statistical independence of observations and lack of undue influence of outliers on model fit).
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Up to time of hospital discharge, or 29 days
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Minutes of sleep per day
Periodo de tiempo: Up to time of hospital discharge, or 29 days
|
Will use interval-censored regression to estimate distributions of sleep from one day to the next.
This repeated-measures analysis with a polynomial model will generate average curves for sleep, each spanning average LOS (i.e., sleep duration plotted on day one, day two, day three, etc.).
Will use multiple linear regressions to control for potential confounders in predicting sleep duration.
Will also run diagnostics to verify the assumptions of a linear model (e.g., statistical independence of observations and lack of undue influence of outliers on model fit).
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Up to time of hospital discharge, or 29 days
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: André Valdez, Stanford University
- Investigador principal: Matthew Smuck, Stanford University
- Investigador principal: Kota Reichert, Stanford University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- IRB-35379 (Otro identificador: Stanford IRB)
- NCI-2016-00737 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
- VAR0137 (Otro identificador: Stanford Cancer Institute)
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. .
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