- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07625878
Music Effect on Concentration and Gait in Cerebral Palsy Children During Physical Therapy Sessions (NMT\CP)
Effect of Physiotherapy With Auditory Cueing on Concentration and Gait in Children With Spastic Cerebral Palsy
- To investigate the effect of music therapy as an additional intervention with physical therapy on concentration in children with spastic CP.
- To investigate the effect of music therapy as an additional intervention with physical therapy on gait parameters for the children with spastic CP.
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
Physical therapy only could be not attractive for child if it done by the traditional way; focus on motor part and no need to involve the sensory part through the rehabilitation.
Sense of hearing could be a unique one to stimulate for a better child attention during physical therapy session, even child with blindness could benefit from this idea.
Using music for attracting attention of the child as a therapeutic way so the child can walk properly regarding time and pace.
Singing as a live form of music could be more sensitive and interactive for child-therapist bond which is important to include the child as an active participant as child is being rehabilitated not just treatment.
Rehabilitation means to involve the child as a whole at this complicated process, not to move a passive limb.
Rehabilitation of CP:
- A "temporal axis": Habilitation/rehabilitation should begin early and continuously - a minimum within the first years of child's life - and intensively - individually designed to meet child's needs.
- A "spatial axis": where individual space, family, school, and social affair places must be all considered.
- An "individual axis": Rehabilitation must observe the child as an active participant, not as a passive person of whom needs care.
- A "relational axis": the standard of taking into consideration the relationship of the child and people who take care of him/her in different contexts of their life (Trabacca et al., 2016).
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Shrouk Mahmoud Mohamed researcher at Cairo university faculty of physical therapy, master
- Número de teléfono: +201002952353
- Correo electrónico: shrouk.rere@gmail.com
Copia de seguridad de contactos de estudio
- Nombre: Maya Galal Abd-Alwahab, Doctorate
- Número de teléfono: +201141904589
- Correo electrónico: maya.galal@pt.cu.edu.eg
Ubicaciones de estudio
-
-
Giza Governorate
-
Dokki, Giza Governorate, Egipto, 02
- Faculty of physical therapy cairo university
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
• The children age ranged from 5 to 7 years old (early childhood).
- Spasticity degree ranges from 1 to 1+ as measured by the Modified Ashworth Scale
- Children with lack of concentration according to MARS (Moss Attention Rating Scale)
- Children can stand alone and walk.
Exclusion Criteria:
- • Children with deafness.
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: MT and PT
music and physical therapy
|
Neurologic music therapy (NMT) Listening to music and moving rhythmically.
program for gait improvement ( Standing, balance and gait training)
|
|
Comparador activo: PT
Physical therapy
|
program for gait improvement ( Standing, balance and gait training)
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
concentration as a cognitive function
Periodo de tiempo: pre intervention and 3 months post intervention
|
ability of child to pay attention during physical therapy sessions and be interactive with the therapist, measured by Moss Attention Rating Scale, score of 22 (minimum score) to less than 110 (maximum score), Higher scores indicate better attention.
|
pre intervention and 3 months post intervention
|
|
Gait
Periodo de tiempo: pre intervention and 3 months post intervention
|
improvement measured by Gross motor function measure 88 (gait section), 0 (minimum score) to 100 (maximum score) percentage %
|
pre intervention and 3 months post intervention
|
|
Kinovea, (Spatial and Temporal Parameters)
Periodo de tiempo: pre and 3 months post intervention
|
Kinovea, (Spatial and Temporal Parameters); Step length in centimeters (higher score better)
|
pre and 3 months post intervention
|
|
Kinovea, (Spatial and Temporal Parameters) ; stride length in centimeters (higher score better)
Periodo de tiempo: pre and 3 months post intervention
|
Kinovea, (Spatial and Temporal Parameters); stride length in centimeters (higher score better)
|
pre and 3 months post intervention
|
|
Gait (cadence)
Periodo de tiempo: pre and 3 months post intervention
|
Using Kinovea, cadence measured in steps\minute (lower score better).
|
pre and 3 months post intervention
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Silla de estudio: Kamal El-sayed Shoukry, Doctorate, Professor of Physical Therapy for Pediatrics Faculty of Physical Therapy Cairo University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- P.T.REC/012/002297
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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