Effects of Multimodal Neuro Rehabilitation on Cortical Activity and Muscle Syenergy in Spastic Cerebral Palsy
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Active Anodal Transcranial Direct Current Stimulation (tDCS) + Task-Oriented Training, Sham Active Anodal Transcranial Direct Current Stimulation + Task-Oriented Training, Active Anodal Transcranial Direct Current Stimulation + Virtual Reality, Sham Active Anodal Transcranial Direct Current Stimulation + Virtual Reality.
- Кому может быть актуально
- Состояния в реестре: Cerebral Palsy. Базовые параметры: 6 лет — 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Список центров уточняется — проверьте первичный протокол.
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
* To determine the effects of tDCS in conjunction with task-oriented training (TOT) and virtual reality (VR) as compared with sham stimulation and conventional physiotherapy on cortical activity and muscle synergy. * To determine the retention effects of tDCS in conjunction with task-oriented training (TOT) and virtual reality (VR) as compared with sham stimulation and conventional physiotherapy on cortical activity and muscle synergy, one-month follow-up across the five groups.
Подробное описание
* To determine the effects of tDCS in conjunction with task-oriented training (TOT) and virtual reality (VR) as compared with sham stimulation and conventional physiotherapy on * gross motor function, gait, balance, mobility, dexterity, and spasticity. * executive functions * self-esteem.
Вмешательства
- Устройство Active Anodal Transcranial Direct Current Stimulation (tDCS) + Task-Oriented Training
Active anodal transcranial direct current stimulation is delivered using a certified tDCS device at a low, safe intensity according to pediatric guidelines. Stimulation is applied to the scalp for approximately 20 minutes per session and is delivered concurrently with task-oriented training. Task-oriented activities individualized to motor deficits, emphasizing: * Functional reaching * Grasp-release tasks * Bilateral coordination * Balance and postural activities * Each session includes 10-15 t - Устройство Sham Active Anodal Transcranial Direct Current Stimulation + Task-Oriented Training
Sham stimulation will mimic active tDCS for the first 30 seconds (ramp up/down) and then deliver no current for the remainder of the session, ensuring blinding. TOT protocol is identical to Group 1. - Устройство Active Anodal Transcranial Direct Current Stimulation + Virtual Reality
Active anodal transcranial direct current stimulation is delivered using a certified tDCS device at a low, safe intensity according to pediatric guidelines. Stimulation is applied to the scalp for approximately 20 minutes per session and is delivered concurrently with Virtual Reality. System: Pediatric upper-limb and balance VR rehabilitation system Activities: Interactive tasks including * reaching, * stepping, * virtual object manipulation, * coordination games. * Session duration: 30 to 40 m - Устройство Sham Active Anodal Transcranial Direct Current Stimulation + Virtual Reality
Sham stimulation will mimic active tDCS for the first 30 seconds (ramp up/down) and then deliver no current for the remainder of the session, ensuring blinding. VR protocol identical to Group 3 - Другое Conventional Physiotherapy
* Stretching of spastic muscle groups * Strengthening exercises for weak muscle groups * Balance and gait training * Functional mobility practice * Session duration: 45 minutes. Delivered by a trained pediatric physiotherapist following standard clinical guidelines.
Первичные конечные точки
- Change in Cortical Activity [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Change in Muscle Synergy Patterns [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Measure Gross Motor Function children. [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Measures balance in children. [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Assesses walking speed in children [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Assesses mobility and balance in children [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Measures balance and reach ability in children [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Assesses manual dexterity in children [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Measures spasticity and muscle tone in children [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
- Measures functional performance and disability in children. [Срок оценки: Baseline (pre-intervention), immediately post-intervention (6 weeks), and 1-month follow-up]
Критерии участия
Критерии включения
- Children aged 6-18 years.
- Neurologist-confirmed spastic cerebral palsy.
- GMFCS Levels I-III (mild to moderate motor impairment).
- Ability to understand and follow simple instructions.
- Medically stable (no planned major surgery; no recent adjustment of medications affecting cortical excitability).
- Parental/guardian written informed consent and child assent.
Критерии исключения
- Active uncontrolled epilepsy or history of seizure in the last year.
- Metal implants in the head or implanted medical/electrical devices (e.g., cochlear implants, ventriculoperitoneal shunts, pacemakers).
- Significant visual or auditory impairments that would interfere with task performance.
- Severe behavioral or cognitive difficulties that would prevent safe application of tDCS or training tasks.
- Currently taking medications known to significantly alter cortical excitability (e.g., benzodiazepines, antiepileptics) if dosage is unstable.
- Participation in other experimental neurorehabilitation or brain stimulation interventions within the last 6 months.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Двойное слепое
- Основная цель
- Лечение
Центры проведения
Список центров уточняется — проверьте первичный протокол.
Идентификаторы
NCT: NCT07574996 · PhD/011109