SR-WBV Training for Frail Elderly in the Skilling up Stage
Effects of Whole Body Vibration With Stochastic Resonance and Dance Therapy in the Elderly: Effects on Physical Functional Performance
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This study is based on the guideline of falls management exercise programs (FaME; from Skelton and Dinan).
The goals:
Skilling up: improvement in neuromuscular control, postural control and strengthening of large muscle groups of the lower extremity.
Training Gain: improvement of functional abilities. Maintaining the Gains: muscle growth, improvement of bone density and multi-sensory exercises.
First, a pilot study was conducted with untrained elderly ("Effects of stochastic resonance therapy on postural control in the elderly population" (KEK Bern: No.228/09, Clinical Trial Registry: NCT01045746). Following, a second pilot study was conducted with frail elderly (Application of Whole-body Vibration With Stochastic Resonance in Frail Elderly: The Effects on Postural Control Clinical Trial Registry:NCT01543243).
It was found that the selected chosen form of recruitment (presentation and advertisement) and the measurements methods are suitable for untrained elderly. But for frail elderly the chosen form of recruitment and the measurement methods are not sufficient.
For this study, measurement parameters for functional performance and strength will be used.
Goals of the study in the skilling up phase:
- Feasibility
- Study the effect on physical functional performance
- Study the effects on muscle strength.
The participants will be recruited in Canton Bern - Swizerland and will be randomly allocated to an intervention group or sham group.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Bern, Suiza, 3008
- Slavko Rogan
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- RAI (Resident Assessment Instrument) >0
- live in canton Bern
- in terms of training load be resistant.
Exclusion Criteria:
- acut joint disease, acut thrombosis, acute fractures, acute infections, acute tissue damage, or acute -- surgical scars
- seniors with prosthesis.
- alcoholic
- acute joint disease, activated osteoarthritis, rheumatoid arthritis, acute lower limb
- acute inflammation or infection tumors
- fresh surgical wounds
- severe migraine
- epilepsy
- acute severe pain
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Intervention
T0 - intervention over 4 weeks with stochastic resonance whole-body vibration (SR-WBV) (5 Hz, noise 4) - T1
|
Participants will undergo a training program set over four weeks, three times a week with 3 to 6 Hz, Noise 4.
Otros nombres:
Participants will undergo a training program set over four weeks three times a week with 1 Hz, Noise 1.
Otros nombres:
|
|
Comparador falso: Sham group
T0 - intervention over 4 weeks with stochastic resonance whole-body vibration (SR-WBV) (1 Hz, noise 1) - T1
|
Participants will undergo a training program set over four weeks, three times a week with 3 to 6 Hz, Noise 4.
Otros nombres:
Participants will undergo a training program set over four weeks three times a week with 1 Hz, Noise 1.
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Physical Functional Performance
Periodo de tiempo: after 4 weeks
|
Short physical performance battery (SPBB): The SPBB examines 3 areas of lower extremity function: standing balance (semi-tandem stand, side-by-side stand, full tandem stand), usual walking speed and ability to stand from a chair. These areas represent essential tasks important for independent living. The scores range from 0 (worst performance) to 12 (best performance). SPPB 0-6 is "Poor performance"; SPPB 7-9 is "Intermediate performance; SPPB 10-12 is "High Performance". |
after 4 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Isometric Maximum Voluntary Contraction (IMCV) in Newton (N) Right Knee-extensor
Periodo de tiempo: after 4 weeks
|
It will be evaluated by isometric MCV (Newton) at 90 degree angle in the knee joint.
|
after 4 weeks
|
|
Ismometric Maximal Voluntary Contraction (IMVC) Left Knee-extension
Periodo de tiempo: after 4 weeks
|
It will be evaluated by isometric MCV (Newton) at 90 degree angle in the knee joint.
|
after 4 weeks
|
|
Isometric Rate of Force Development (IRFD) Right Knee-extensor
Periodo de tiempo: after 4 weeks
|
It will be evaluated by isometric RFD (Newton/seconds) at 90 degree angle in the knee joint.
|
after 4 weeks
|
|
Isometric Rate of Force Development (IRFD) Left Knee-extensor
Periodo de tiempo: after 4 weeks
|
It will be evaluated by isometric RFD (Newton/seconds) at 90 degree angle in the knee joint.
|
after 4 weeks
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Silla de estudio: Rogan Slavko, MSc, Bern University of Applied Science, Department WGS
- Director de estudio: Radlinger Lorenz, PhD, Bern University of Applied Science, Department WGS
- Silla de estudio: Jessica Kessler, MSc, BUAS
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MSc-study (Biel)
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. .