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Идёт набор NCT06599931

Cerebello-motor Neuromodulation After Stroke. CERSTIM.

Без фазы С лечением Stroke Healthy

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: tACS Transcranial alternating stimulation.
Кому может быть актуально
Состояния в реестре: Stroke, Healthy. Базовые параметры: от 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

CEREBELLO-MOTOR NEUROMODULATION AFTER STROKE

Обзор

The CERSTIM study is a physiopatholgical study investigating transcranial alternating current stimulation in stroke patients in the cerebello-motor loop. The design is a cross over design testing two frequencies in the gamma band and one placebo. We will use behavioural data, functional MRI, and Electroencephalography to disentangle the effect of tACS and its frequency. Healthy participants will be also recruited.

Подробное описание

Neuromodulation, by the means of Non-Invasive Brain Stimulation techniques, is a promising method to enhance motor recovery of the upper limb following a stroke. However, none of these techniques have yet been effectively transferred to the patient's bedside. An international group of experts has examined this issue, identifying barriers that need to be overcome for successful transferability. Among their findings, two were particularly emphasized: (i) the insufficient characterization of the mechanisms through which these stimulations are effective, and (ii) the comparison of stimulation parameters before moving on to larger samples. We have decided to use this model to study tACS (transcranial Alternating Current Stimulation) on the cerebellomotor network.

The choice of tACS is justified by (i) its ability to "entrain" a neural network through its oscillations, (ii) its innovative nature, and (iii) its "wearable" characteristic, making it quickly transferable. The choice of the cerebellomotor network is based on literature data showing that (i) the cerebellum plays a crucial role in motor learning in healthy individuals (which is one of the substrates of post-stroke recovery), and (ii) cerebellomotor synchronization is a good prognostic indicator for the recovery of hand motor function.

In light of these findings, we have decided to conduct a pathophysiological, bi-centric study to determine the cerebral mechanisms by which tACS acts on the cerebellomotor network. Three single sessions of tACS, each lasting 20 minutes, will be conducted 7-15 days apart, with a different frequency (50 or 70 Hz, corresponding to gamma oscillations) or a placebo frequency known as "sham." To understand the cerebral mechanisms, we will use Magnetic Resonance Imaging (MRI) and Electroencephalography (EEG). We will also examine a behavioral motor adaptation task on a tablet. The order in which the three frequencies are applied will be randomized This study will include 30 patients and 15 healthy subjects. The patients will be individuals who have suffered a stroke more than 6 months ago, resulting in a hand deficit without complete paralysis. The healthy controls will serve as a reference for mechanisms and imaging/electrophysiology data.

We hypothesize the following: The mechanisms involved following cerebellomotor stimulation could include a modification of brain rhythms in the beta or gamma band during movement, an increase in activity in the primary motor cortex, or a change in the excitation-inhibition balance between the cerebellum and the primary motor cortex, or directly at the level of the primary motor cortex. These different mechanisms may vary depending on the frequency used.

This research is part of the NEUROTECH Impulse Program managed by INSERM.

Вмешательства

  • Устройство tACS Transcranial alternating stimulation
    session of 20 minutes

Первичные конечные точки

  • change in activation in the primary motor cortex and cerebellum using functional magnetic Resonance [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]
Вторичные конечные точки (5)
  • comparison between activation in the primary motor cortex and cerebellum using functional magnetic Resonance with the 50 Htz versus the 70 Htz frequency [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]
  • change in functional connectivity between the primary motor cortex and cerebellum using functional magnetic Resonance [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]
  • change in functional connectivity using EEG after intervention and comparison between frequencies of tACS [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]
  • change in behaviour after intervention and comparison between frequencies of tACS [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]
  • comparison of the prespecified patients outcome with those of healthy subjects [Срок оценки: [Time Frame: within 1 hour before and after the intervention]]

Критерии участия

PATIENTS

Критерии включения

  • Male or female aged 18 years or older on the day of inclusion.
  • Affiliated with a social security system, Universal Health Coverage (CMU), or any equivalent scheme.
  • Ischemic stroke or intraparenchymal hematoma that occurred more than 6 months ago, with no upper time limit.
  • Motor deficit of the upper limb confirmed by the ARAT scale, with the ability to grip and press on a tablet.
  • stroke lesion not affecting the motor cortex in the hand knob area.

Критерии исключения

\-- Pregnant and breastfeeding women

  • Total paralysis of the affected hand
  • Conditions that are life-threatening or could compromise follow-up during the study period
  • Contraindications to MRI and tACS (ferromagnetic surgical clips, ocular implants, intraocular or nervous system metallic foreign bodies, implants or metallic objects likely to concentrate the radiofrequency field, cochlear implants, brain or cardiac stimulators, presence of a craniotomy scar)
  • Participation in another biomedical study focused on motor or overall recovery during the same period, or current exclusion period from another biomedical study

HEALTHY

Критерии включения

  • Male or female aged 18 years or older on the day of inclusion.
  • Affiliated with a social security system, Universal Health Coverage (CMU), or any equivalent scheme.

Non inclusion criteria

\-- Pregnant and breastfeeding women

  • Conditions that are life-threatening or could compromise follow-up during the study period
  • Contraindications to MRI and tACS (ferromagnetic surgical clips, ocular implants, intraocular or nervous system metallic foreign bodies, implants or metallic objects likely to concentrate the radiofrequency field, cochlear implants, brain or cardiac stimulators, presence of a craniotomy scar)
  • Participation in another biomedical study during the same period, or current exclusion period from another biomedical study

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Перекрёстный дизайн
Маскирование
Двойное слепое
Основная цель
Фундаментальное исследование

Центры проведения

Франция · 2 центра
  • ICM_ Institut du Cerveau et de la Moelle épinière, Hôpital Pitié, 47 Bd de l'Hôpital — Paris
  • ToNIC - Toulouse neuro Imaging center (Inserm)Pavillon Baudot — Toulouse

Идентификаторы

NCT: NCT06599931 · C23-100 · 2024-A00623-44

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗