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El ensayo clínico NCT06962618 (THRIVE-CP) para Parálisis cerebral está aún no recluta. 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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Home-Based Training With Feedback to Improve Outcomes in Adolescents and Young Adults With Cerebral Palsy.. (THRIVE-CP) 70 Domiciliario Evidencia mundo real Adolescentes Corto plazo
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 NCT06962618 (THRIVE-CP) es un estudio intervencionista para Parálisis cerebral. Su estado actual es: aún no recluta. Se prevé iniciar el reclutamiento el 1 de diciembre de 2025 hasta completar 70 participantes. Dirigido por la Universidad de Copenhague, se espera que finalice el 1 de febrero de 2029. Los datos se actualizaron por última vez en ClinicalTrials.gov el 8 de mayo de 2025.
Resumen
This clinical trial aims to determine whether extrinsic feedback through music enhances the effects of home-based motor training for adolescents and young adults with cerebral palsy (CP) and whether feedback improves adherence to the training program.
The main questions it aims to answer are:
- Does extrinsic feedback improve real-world movement more than home training alone?
- Do participants receiving extrinsic f...
Título oficial
The THRIVE-CP Trial - Targeted Home-Based Training With Real-Time Feedback to Improve Versatile Movement Behaviors and Enhance Outcomes in Adolescents and Young Adults With Cerebral Palsy: Protocol for a Randomized Controlled Trial.
Condiciones médicas
Parálisis cerebralOtros ID del estudio
- THRIVE-CP
Número del NCT
Inicio del estudio (real)
2025-12-01
Última actualización
2025-05-08
Fecha de finalización (estimada)
2029-02-01
Inscripción (prevista)
70
Tipo de estudio
Intervencionista
FASE
N/A
Estado general
Aún no recluta
Palabras clave
cerebral palsy
Home-based training
Extrinsic feedback
Movement behavior
Motor learning
Home-based training
Extrinsic feedback
Movement behavior
Motor learning
Objetivo principal
Tratamiento
Método de asignación
Aleatorizado
Modelo de intervención
Paralelo
Enmascaramiento
Cuádruple ciego
Brazos / Intervenciones
| Grupo de participantes | Intervención/Tratamiento |
|---|---|
ExperimentalMusic Motion Group | Music Motion Group Participants will engage in personalized, home-based motor training programs tailored to their individual goals. Each will wear a wireless Inertial Measurement Unit (IMU) on the targeted body part, which transmits movement data via Bluetooth to a tablet app. The training emphasizes task specificity and intensity, with five virtual check-ins to review progress and adjust training parameters.
The intervention studied ...Mostrar más |
Comparador activoControl | CONTROL Participants will follow personalized, home-based motor training programs designed like the Music motion group. They will wear a wireless Inertial Measurement Unit (IMU) on the targeted body part, transmitting movement data via Bluetooth to a tablet app. However, unlike the Music Motion Feedback group, participants in the Control group will not receive any extrinsic feedback during their training. |
Resultado primario
Resultado secundario
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Percentage change in daytime movement of the trained extremity (right or left arm or leg) as measured by 3-axis accelerometer and gyroscope data analyzed via deep-learning neural network | Movement data will be collected using seven Inertial Measurement Units (IMUs) worn continuously for 72 hours at three time points: baseline, 12 weeks (end of intervention), and 24 weeks (follow-up).
IMUs will be attached to the sternum, wrists, thighs, and lower legs using adhesive patches and will capture 3-axis accelerometer and gyroscope data. A validated custom neural network (Novosel et al. 2023) will convert signals into images and analyze them using convolutional layers to extract features related to movement behaviors. The primary metric will be the percentage change (minutes a day) in real-world daytime movement of the trained limb, computed relative to baseline.
This outcome reflects changes in functional mobility resulting from the motor training intervention. | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Number of daily logins to the tablet app | Attendance will be measured as the number of times participants log into the tablet app during the intervention.
Unit of Measure: Number of logins | The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Daily session duration recorded in the tablet app | Adherence will be assessed by the average length of each daily training session. This outcome reflects how long participants remain engaged with the motor training program once they log in.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collectedThe app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Time spent moving the targeted extremity during training recorded in the tablet app | This measure reflects adherence by quantifying the active movement time of the trained extremity during each training session.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collected The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Time spent within target movement intensity threshold recorded in the tablet app | For participants in the Music Motion Feedback group, adherence will also be evaluated by measuring the time spent at or above a predefined movement intensity threshold.
Unit of Measure: Minutes | The app stores the data during the intervention period and will be collected The app stores the data during the intervention period and will be collected at 12 weeks (end of intervention period) |
Action Research Arm Test (ARAT) total score - (Upper Extremity) | In participants engaged in upper extremity training, the ARAT will be used to evaluate upper extremity functional capacity. It consists of 19 items assessing grasp, grip, pinch, and gross movement. Scores range from 0 to 57, with higher scores indicating better arm function.
Time Frame: Baseline, 12 weeks (end of intervention), and 24 weeks (follow-up) Unit of Measure: ARAT total score (0-57) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum isometric arm strength - (Upper Extremity) | Participants engaged in upper extremity training will have the isometric strength of the targeted upper extremity measured using a handheld dynamometer. They will perform maximum voluntary contractions against resistance, and the peak force will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum grip strength - (Upper Extremity) | Participants who are engaged in upper extremity training will have their grip strength of the targeted upper limb measured using a hand dynamometer. The highest of three attempts will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Gross Motor Function Measure-66 (GMFM-66) total score - (Lower Extremity) | In participants who are engaged in lower extremity training the GMFM-66 will be used to assess gross motor function. It evaluates activities such as standing, walking, and running. Scores range from 0 to 100, with higher scores indicating better function.
Unit of Measure: GMFM-66 total score (0-100) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Maximum isometric leg strength - (Lower Extremity) | The isometric strength of the trained leg will be assessed using a handheld dynamometer. Participants will perform maximum voluntary contractions, and peak force will be recorded.
Unit of Measure: Kilograms of force (kgf) | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Distance walked during the Six-Minute Walk Test (6MWT) - (Lower Extremity) | The 6MWT will be used to evaluate walking endurance and aerobic capacity. Participants engaged in lower extremity training will walk as far as possible in six minutes along a flat, indoor course.
Time Frame: Baseline, 12 weeks, and 24 weeks Unit of Measure: Meters walked | Baseline, at 12 weeks (end of intervention period), and at 24 weeks (long term follow up) |
Asistente de participación
Criterios de elegibilidad
Criterios de edad
Niño, Adulto
Edad mínima
15 Years
Criterios de sexo
Todos
- Clinical diagnosis of cerebral palsy
- Sensorimotor deficits in at least one limb
- Demonstrated motivation to develop or regain motor skills, indicated by the expression of specific goals
- Ability to follow instructions independently or with caregiver support
- Ability to provide informed consent
- Diagnosis of dyskinetic cerebral palsy
- Presence of significant health risks that could interfere with participation
- Surgery or first Botox injection within one month before the trial or during the trial period
Parte responsable del estudio
Ivana Bardino Novosel, Investigador principal, Principal Investigator, University of Copenhagen
Contactos centrales del estudio
Contacto: Ivana B Novosel, PhD student, 27328961, [email protected]
Contacto: Jakob Lorentzen, Professor, +4531521131, [email protected]
1 Centros del estudio en 1 países
CP Youth Clinic, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark
Jakob Lorentzen, Professor, Contacto, [email protected]