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Идёт набор NCT07156955

Proprioceptive Error Correction for Post-Stroke Upper Limb Rehabilitation

Без фазы С лечением Ischemic Stroke Proprioception

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: Electrical stimulation cue, Visual stimulation cue, No cue.
Кому может быть актуально
Состояния в реестре: Ischemic Stroke, Proprioception. Базовые параметры: от 19 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
South Korea
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Proprioceptive Error Correction Technique Development to Promote Post-stroke Upper Limbs Motor Rehabilitation

Обзор

The investigators aim to develop sensory transformation and augmentation technologies that minimize the impact of proprioceptive errors, thereby significantly enhancing motor learning and rehabilitation of the upper limbs. This study is designed to test proprioceptive error compensation techniques in stroke patients. The human nervous system often receives mismatched information from vision and proprioception during upper limb control, resulting in conflicting sensory inputs that limit the effectiveness of motor learning. In other words, real-time sensory feedback - a critical component of motor learning in the nervous system - is not reliably delivered. Therefore, this study seeks to resolve sensory conflicts by providing additional sensory information through electrical stimulation, with the goal of dramatically improving the effectiveness of motor learning.

Вмешательства

  • Поведенческое Electrical stimulation cue
    A single 30-minute session is provided. Electrodes are attached to the cubital fossa, and stimulation is delivered at a frequency that increases up to 70 Hz as the elbow joint approaches the target angle. Target angles are set between 0 degrees and 120 degrees, based on each participant's available range of motion determined during the initial assessment. Participants adjust their elbow joint angle to match the provided target angle using feedback from the electrical stimulation. When the elbow
  • Поведенческое Visual stimulation cue
    A single 30-minute session is provided. The difference between the current elbow joint angle and the pre-set target angle is displayed on a screen using two colored needles (a red needle for the target angle and a black needle for the current elbow joint angle). The target angle is set within each participant's available range of motion based on the initial assessment. Participants continue the intervention by adjusting their elbow angle using the visual feedback. When the elbow joint angle matc
  • Поведенческое No cue
    A single 30-minute session is provided. The target angle is determined within each participant's available range of motion based on the initial assessment. Throughout the session, participants receive verbal feedback from the assessor and adjust their elbow joint angle accordingly to match the target angle.

Первичные конечные точки

  • Improvement in upper limb motor function [Срок оценки: 6 visits over 3 weeks]
Вторичные конечные точки (1)
  • Proprioceptive accuracy [Срок оценки: Baseline before intervention and immediately after the 30-minute training session]

Критерии участия

Критерии включения

  • Diagnosed with ischemic or hemorrhagic stroke
  • Stroke confirmed by CT or MRI
  • Stroke patients with proprioceptive sensory deficits
  • Chronic stroke patients with onset at least 3 months prior
  • Able to voluntarily flex and extend the elbow joint
  • Age 19 years or older
  • Provide written informed consent (participant or legal representative)

Критерии исключения

  • Severe pain during elbow joint movement
  • Elbow joint contracture, spasticity, ataxia, musculoskeletal disorders, fractures, - non-healing ulcers, or open wounds
  • Progressive or unstable stroke
  • Presence of unilateral neglect
  • Coexisting severe neurological disorders
  • Major psychiatric disorders such as major depressive disorder, schizophrenia, bipolar disorder, or dementia Presence of a pacemaker

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Перекрёстный дизайн
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

South Korea · 1 центр
  • Shinchon Severance Rehabilitation Hospital — Seoul

Идентификаторы

NCT: NCT07156955 · 2025-06-075-001

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗