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El ensayo clínico NCT06048419 para Parálisis cerebral, Parálisis cerebral hemipléjica está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí. | ||
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Acceptability and Efficacy of GO MOVE 50 Ejercicio
Los detalles del ensayo clínico están disponibles principalmente en inglés. ¡Sin embargo, IA Trial Radar puede ayudar! Simplemente haga clic en 'Explicar el estudio' para ver y discutir la información del estudio en el idioma que haya seleccionado.
El ensayo clínico NCT06048419 es un estudio intervencionista para Parálisis cerebral, Parálisis cerebral hemipléjica. Su estado actual es: reclutando. El estudio se inició el 20 de febrero de 2024, con el objetivo de reclutar a 50 participantes. Dirigido por Texas Scottish Rite Hospital for Children, se espera que finalice el 1 de diciembre de 2026. Los datos se actualizaron por última vez en ClinicalTrials.gov el 10 de marzo de 2025.
Resumen
The goal of this clinical trial is to learn about the acceptability and efficacy of Go Move, a mobile website developed to assist youth with unilateral cerebral palsy and their caregivers with setting goals and selecting exercises and activities to meet the goals. The main question\[s\] it aims to answer are:
- Is Go Move accepted by youth with unilateral cerebral palsy and their caregivers?
- Does Go Move support g...
Título oficial
Acceptability and Efficacy of GO MOVE: A Mobile Health Technology for Youth With Unilateral Cerebral Palsy
Condiciones médicas
Parálisis cerebralParálisis cerebral hemipléjicaOtros ID del estudio
- STU-2023-0531
Número del NCT
Inicio del estudio (real)
2024-02-20
Última actualización
2025-03-10
Fecha de finalización (estimada)
2026-12
Inscripción (prevista)
50
Tipo de estudio
Intervencionista
FASE
N/A
Estado general
Reclutando
Palabras clave
home program
Objetivo principal
Tratamiento
Método de asignación
N/A
Modelo de intervención
Grupo único
Enmascaramiento
Ninguno (Abierto)
Brazos / Intervenciones
| Grupo de participantes | Intervención/Tratamiento |
|---|---|
ExperimentalGo Move Home Program Goal driven home program | Home Program Home program for 6 weeks (1 hr and 15 minutes per week) |
Resultado primario
Resultado secundario
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Canadian Occupational Performance Measure (COPM) | The Canadian Occupational Performance Measure is a criterion referenced, individualized, client-centered outcome measure designed for use by occupational therapists to detect change in a client's self-perception of occupational performance over time on a scale of 1-10 (1 being the lowest) | within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention) |
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Goal Attainment Scale (GAS) Light | The Goal Attainment Scale is an individualized, functional outcome measure involving goal selection and scaling. The scale ranges from -2 to +2 with -2 representing a decline in function, -1 no change, 0 expected outcome, +1 a little more, +2 a lot more. | within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention) |
Assisting Hand Assessment (AHA) (optional) | The Assisting Hand Assessment is a criterion referenced, valid and reliable 22-item measure that assesses the assisting or affected hand in carrying out bimanual activities for children with cerebral palsy or obstetric brachial plexus palsy measured by AHA units on a scale of 0-100 with 0 being the lowest level of function. | within 2 weeks of start of intervention (pre-intervention), within 2 weeks of end of intervention (post-intervention) |
Asistente de participación
Criterios de elegibilidad
Criterios de edad
Niño
Edad mínima
3 Years
Criterios de sexo
Todos
- Inclusion criteria for participants to enroll in the study include a diagnosis of unilateral CP or a non-progressive brain lesion, injury, or trauma of the developing brain that presents with a unilateral upper limb motor impairment. GMFCS levels 1 or 2. MACS levels 1-3. Age 3-17 years old, ability to follow directions, ability to complete the assessment protocol, and the ability to access the GO MOVE webpage on a personal device. All ethnic/racial groups will be eligible to participate. The ability to participate in everyday activities without restriction from a physician throughout the duration of their participation in the study (does not have restrictions/contraindications following a medical procedure).
- The study will exclude any patients with uncontrolled epilepsy or significant visual impairment. The study will exclude any patient with severe behavioral problems or the inability to complete the assessment protocol or home program.
Texas Scottish Rite Hospital for ChildrenParte responsable del estudio
Angela Shierk, Investigador principal, Clinical Scientist, Texas Scottish Rite Hospital for Children
Contactos centrales del estudio
Contacto: Angela Shierk, PhD, 4694127172, [email protected]
Contacto: Heather Roberts, PhD, 214-794-8117, [email protected]
1 Centros del estudio en 1 países
Texas
Scottish Rite for Children, Frisco, Texas, 75034, United States
Angela Shierk, PhD, Contacto, 469-412-7172, [email protected]
Reclutando