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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04870528
Adjunctive Effect of Pulsed Electromagnetic Field on Quadriceps Muscle Strength After Burn Injury
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
• Subjects: Sixty patients with lower limb burn, subdivided into two groups each one has 30 patients.
- Group (A) = Pulsed Electromagnetic Field therapy and quadriceps strengthening exercises group.
Group (B) = quadriceps strengthening exercises group. • Equipment and tools:
Measurements tools:
Isokinetic dynamometer : to measure the quadriceps muscle peak torque before the treatment and after 8 weeks of treatment for both groups.
- Therapeutic tools:
Pulsed Electromagnetic Field therapy device and free weights for strengthening of quadriceps muscle.
Tipo de estudio
Inscripción (Anticipado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Walaa A Abd Elaziz, master
- Número de teléfono: 020 01099386825
- Correo electrónico: walaaamr106@gmail.com
Ubicaciones de estudio
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Giza
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Dokki, Giza, Egipto, 12613
- Reclutamiento
- Cairo university
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Contacto:
- Walaa A Abd Elaziz, master
- Número de teléfono: 020 01099386825
- Correo electrónico: walaaamr106@gmail.com
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- - Patients are males.
- Their age will range from (25-40) years.
- Patients will suffer from second-degree burn ( Partial thickness of thermal injury).
- Total body surface area (TBSA) for the burns will be ranged from 20% to 35% .
- They will be selected from Outpatient Clinic of Faculty of Physical Therapy and Burn Unit at Om El-Obour Hospital.
- Patients will begin the training program after complete wound healing.
- All patients will receive traditional physical therapy program in the form of range of motion exercise, stretching, splinting, massage, functional training for ambulation and activities of daily living.
- Patients will be given their informed consent.
Exclusion Criteria:
- - Patients who participate in any rehabilitation program to improve muscle strength prior to the study.
- Musculoskeletal disorders that will impair performance during training and tests.
- Equilibrium disorders.
- Uncontrolled cardiovascular or pulmonary diseases .
- Neurological and renal disorders.
- metabolic or vascular disease with a neurological component such as diabetes,
- Malignant conditions.
- Psychiatric illness, severe behavior or cognitive disorders.
- Subjects with burn to the posterior thigh with knee flexion contracture, which affected the function of the quadriceps muscle.
- Lower limb lymphedema or lipoedema.
- Athletic subjects.
- Subjects with morbid obesity.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Experimental group
- This group will be composed of 30 patients with lower limb burn of second-degree.
Subjects will receive pulsed magnetic field over thigh areas for 24 sessions over a period of 8 weeks (3sessions/week) with receiving strengthening exercises for quadriceps muscle and traditional physical therapy program in the form of range of motion exercise, stretching, splinting, massage, functional training for ambulation and activities of daily living.
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the pulsed electromagnetic field device treatment parameters will be set as 15 Hz frequency, 20 gauss amplitude, and 20 minutes as total treatment duration.
• Parameters of the exercise program: Intensity : The weight or load the patients lifted is set at 50-60% of their individual 1RM , 3 sets of 10 repetitions during the first week. During the second week, the lifting load is increased to 70-75% (3 sets of 10 repetitions) of their individual 1RM and continued for weeks 2-6. After this, training intensity is increased to 80-85% of the 1 RM and implemented from weeks 7-8. Frequency: 3 sessions per week for 8 weeks. Number of repetitions: 3 sets,10 repetitions in each set. Total treatment duration: 8 weeks |
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Comparador activo: control group
Subjects will receive strengthening exercises for quadriceps muscle and traditional physical therapy program in the form of range of motion exercise, stretching, splinting, massage, functional training for ambulation and activities of daily living for 24 sessions over a period of 8 weeks (3sessions/week)
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• Parameters of the exercise program: Intensity : The weight or load the patients lifted is set at 50-60% of their individual 1RM , 3 sets of 10 repetitions during the first week. During the second week, the lifting load is increased to 70-75% (3 sets of 10 repetitions) of their individual 1RM and continued for weeks 2-6. After this, training intensity is increased to 80-85% of the 1 RM and implemented from weeks 7-8. Frequency: 3 sessions per week for 8 weeks. Number of repetitions: 3 sets,10 repetitions in each set. Total treatment duration: 8 weeks |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Isokinetic dynamometer for measuring The peak torque of the quadriceps muscle
Periodo de tiempo: 8 weeks
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8 weeks
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Walaa A Elaziz, master, lecturer assistant at faculty of physical therapy, Cairo University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- P.T.REC/012/002906
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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