- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02778009
Fit Physicians: Use of Activity Monitors and Activity Integration Program in First Year Medical Students (FitPhysician)
Fit Physicians: A Novel Physical Activity Integration Program to Improve Fitness and Activity in Medical Students: A Randomized Pilot Study
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Using fitness trackers and exercise testing, it will determine if participating in a novel program that incorporates wellness into the academic term will improve fitness.
An estimate, 120 students will enroll in this study. Men and women aged 18-55 years of age that are just entering medical school. Students who are currently pregnant will not be allowed to participate in this study.
Participation will involve 2 visits at the start of the academic school year, and two visits at the end of the academic school year.
These visits will entail you undergoing a body composition scan measured by an duel energy x-ray absorptiometry (iDEXA) machine. The scan takes approximately 15 minutes. Subjects may be asked to perform an exercise stress test on a treadmill. The exercise test is approximately 40 minutes. Subjects may be asked to participate in a fitness program 2x a week, and may be asked to wear a Fitbit Flex™ activity tracker on the wrist for the duration of the school year. Investigators will be accessing academic grades to use for statistical purposes only. Subject names will never be given to any other party other than the investigators involved.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
New York
-
Old Westbury, New York, Estados Unidos, 11568568
- NYIT
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- First year medical students
- Must have smartphone
Exclusion Criteria:
- Medical conditions that prohibit exercise
- pregnancy
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Fit Physician Group
Subjects will receive activity monitor and will be required to attend monthly wellness lectures and weekly exercise intervention. Every subject will undergo an iDEXA scan to measure body mass composition |
Subjects will receive pre study and post study scans to assess body mass composition
Subjects in the Fit Physician Arm will be required to attend monthly wellness lectures
Subjects in the Fit Physician Arm will be required to attend weekly exercise interventions
Subjects in the Fit physician arm and the activity monitor arm will receive activity monitors to assess their activity level throughout the academic year
|
|
Comparador activo: Activity Monitor Only Group
Subjects will receive an activity monitor without any intervention Every subject will undergo an iDEXA scan to measure body mass composition ) |
Subjects will receive pre study and post study scans to assess body mass composition
Subjects in the Fit physician arm and the activity monitor arm will receive activity monitors to assess their activity level throughout the academic year
|
|
Otro: Control Group
Subjects will not an activity monitor nor will they receive any intervention Every subject will undergo an iDEXA scan to measure body mass composition
|
Subjects will receive pre study and post study scans to assess body mass composition
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Steps per day measured daily by FitBit Flex
Periodo de tiempo: 10 months
|
10 months
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Body Mass Composition assessed by iDEXA scan
Periodo de tiempo: 10 months
|
10 months
|
|
Academic Performance assessed by numeric grade point average
Periodo de tiempo: 10 months
|
10 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Silla de estudio: Brian Harper, MD, NYIT College of Osteopathic Medicine
Publicaciones y enlaces útiles
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
- BHS-1153
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
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. .