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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07780435
Whole-body Vibration Versus Gravity Force Stimulation on Postural Stability in Children With Duchene Muscular Dystrophy
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Duchenne Muscular Dystrophy (DMD) is a progressive X-linked neuromuscular disorder characterized by muscle fiber degeneration due to mutations in the dystrophin gene (Birnkrant et al., 2018). As muscle weakness advances, children with DMD experience impaired postural control, reduced balance function, and increased risk of falls, all of which significantly contribute to limitations in daily activities and loss of independence (Ricotti et al., 2016). Early therapeutic interventions are essential to slow functional decline and promote motor stability for as long as possible.
Whole-body vibration (WBV) has emerged as a potential modality to enhance neuromuscular activation, proprioception, and balance in individuals with muscle weakness or neurological impairments. Studies suggest that low-frequency WBV can improve muscle spindle sensitivity, postural reactions, and balance performance in pediatric and neuromuscular populations (Brunetti et al., 2015; Saquetto et al., 2015). Although research involving children with DMD is limited, preliminary evidence indicates that WBV may transiently enhance motor function without excessive muscle strain.
Gravity-force stimulation (GFS)-often delivered through tilt platforms, vertical acceleration devices, or graded gravitational loading-has been proposed as another means to stimulate proprioceptive pathways and increase postural control. GFS can enhance sensory input from weight-bearing structures and may promote improved equilibrium response strategies in children with neuromotor impairments (Bates & Hanson, 2019). However, its application specifically in DMD remains under-studied, and direct comparisons with WBV have not been adequately explored.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Giza Governorate
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Giza, Giza Governorate, Egipto, 11432
- Cairo University
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Children diagnosed with Duchenne Muscular Dystrophy (DMD).
- Age between 6 and 10 years.
- Lower extremity and trunk muscle strength graded at least 3+, based on the manual muscle testing criteria.
- Ability to move the upper and lower limbs within functional limits without severe joint restriction.
- Ability to walk independently without assistive devices, corresponding to Levels I and II of the Ambulation Function Classification System for DMD (AFCSD).
Exclusion Criteria:
- Presence of cardiopulmonary dysfunction or congenital or acquired skeletal abnormalities that may interfere with participation.
- History of lower-limb surgical procedures.
- Neurological conditions affecting balance or gait, or evidence of poor motor development not attributable to DMD.
- Behavioral disorders that would prevent cooperation during assessment or intervention sessions.
- Overweight status, defined as a body mass index (BMI) greater than 25 kg/m²
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: whole body vibration group
whole body vibration intervention
|
we use vibrating platform •
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Experimental: force gravity stimulation group
force gravity stimulation intervention
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Thirty children received: • Gravity-Force Stimulation (GFS), which included:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
abdominal muscle thickness
Periodo de tiempo: 3 months
|
measure the abdominal muscle thickness
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3 months
|
|
postural stability
Periodo de tiempo: 3 months
|
• BIODEX MEDICAL SYSTEM used for assessment of postural stability and balance
|
3 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mostafa S. Ali, Cairo 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 (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
- P.T.REC/012/006366
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.
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