- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04707755
Motor Imagery Technique on Lower Limb Function Among Stroke Patients.
Effects of Motor Imagery Technique on Lower Limb Function Among Stroke Patients.
To determine the effects of motor imagery technique on lower limb function among stroke patient.
To determine the effects of motor imagery technique on lower limb spasticity among stroke patients.
To determine the effects of motor imagery technique on gait among stroke patients.
To determine the effects of motor imagery technique on quality of life among stroke patients
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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KPK
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Peshawar, KPK, Pakistán, 251900
- Bibi Zahida Memorial Teaching Hospital
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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:
- Adult without ADHD by Adult ADHD Self-Report Scale score.
- History of no more than one stroke.
- Lower limb muscles spasticity with the grade 1+ or 2 on modified Ashworth in scale.
- Mini-mental status score more than 25.
- Patients who are less than 6 months post-stroke.
- Modified Rankin scale score is 4.
Exclusion Criteria:
- Lesion of frontal, parietal and basal ganglia
- Excessive spasticity that is score of>3 on modified Ashworth spasticity scale.
- Any musculoskeletal disorder impeding lower limb function.
- Participating in any experimental rehabilitation or drug studies.
- Bed ridden patient.
- Subjects psychiatric disorder or dementia.
- Any neglect of space on the affected side, or any other neurological disease or auditory or visual.
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 |
|---|---|
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Experimental: Motor imagery technique
Motor Imagery technique Plus Conventional Physical therapy
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The patient will sit on chair in a quiet room. The patients will be observing motor performance in video, motor performance video will consist of (1) knee flexion and extension movement, (2) sitting to standing movement, (3) stepping movement, (4) walking, (5) climbing and descending stairs. Addition to motor imagery, the patients will be provided the passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs. |
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Comparador activo: Conventional Physical therapy
passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs.
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It includes passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Lower Extremity Function scale
Periodo de tiempo: 8 weeks
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It is 20 items questionnaire, measure the lower extremity function scoring from 1 to 4 for each items, in which minimum score is 0 and maximum score of 80 shows the maximum functional status.
It has a valid and reliable tool to measure the lower extremity functional status.
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8 weeks
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Dynamic Gait Index
Periodo de tiempo: 8 weeks
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It assess gait, balance and fall risk, with 24 is the maximum score, in which 19 or less have been related to increase incidence of falls.
It has high reliability and validity in the stroke population.
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8 weeks
|
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Time Up and Go test
Periodo de tiempo: 8 weeks
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It assess a person's mobility and requires both static and dynamic balance.
Score of less than 10 seconds indicate freely mobile,<20 seconds mostly independent, 20-29 seconds variable mobility, >30 seconds Impaired mobility.
It is reliable, valid, and easy to administer clinical tool in stroke patients.
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8 weeks
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Stroke Specific Quality of Life Scale
Periodo de tiempo: 8 Weeks
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It is a self-report questionnaire, measure the quality of life in stroke patients consisting of 49 items in the 12 domains.
Scoring from 1 to 5 , in which 1 shows strongly agreement and 5 shows strongly disagreement.
It is a reliable and valid tool for measuring the quality of life for stroke patients.
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8 Weeks
|
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Modified Ashworth scale
Periodo de tiempo: 8 Weeks
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It measures the spasticity, ranging from 0 means normal tone to 4 shows increased tone to such extent where passive movement is not possible.
It has good intra-rater reliability and validity in stroke patients .
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8 Weeks
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mirza Obaid Baig, MSPT(NMR), Riphah International University
Publicaciones y enlaces útiles
Publicaciones Generales
- Pedersen SG, Heiberg GA, Nielsen JF, Friborg O, Stabel HH, Anke A, Arntzen C. Validity, reliability and Norwegian adaptation of the Stroke-Specific Quality of Life (SS-QOL) scale. SAGE Open Med. 2018 Jan 8;6:2050312117752031. doi: 10.1177/2050312117752031. eCollection 2018.
- Gul I, Malik MS, Halim A, Rauf S. POST STROKE DEPRESSION: EXPERIENCE AT A TERTIARY CARE HOSPITAL OF PAKISTAN. Pakistan Armed Forces Medical Journal. 2019 Aug 27;69(4):779-83.
- Paravlic AH, Pisot R, Marusic U. Specific and general adaptations following motor imagery practice focused on muscle strength in total knee arthroplasty rehabilitation: A randomized controlled trial. PLoS One. 2019 Aug 14;14(8):e0221089. doi: 10.1371/journal.pone.0221089. eCollection 2019.
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- REC00664 Izharuddin
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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