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Набор скоро начнётся NCT07423455

Electrotherapeutic Interventions for Glenohumeral Subluxation After Stroke

Без фазы С лечением Glenohumeral Subluxation Stroke

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: Neuromuscular electrical stimulation, Electromyographic (EMG) biofeedback, Conventional physiotherapy.
Кому может быть актуально
Состояния в реестре: Glenohumeral Subluxation, Stroke. 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
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Comparison of the Clinical and Sonographic Outcomes of NMES and EMG Biofeedback Therapies in Stroke Patients With Glenohumeral Subluxation: Randomized Clinical Trial

Обзор

The aim of this single-blind randomized controlled trial is to compare the effects of two therapies-neuromuscular electrical stimulation (NMES) and electromyographic (EMG) biofeedback-in stroke patients with shoulder (glenohumeral) subluxation. The study will evaluate changes in shoulder structure and function by measuring the acromion-greater tuberosity distance, supraspinatus and posterior deltoid muscle thickness, shoulder range of motion, and Brunnstrom stage of the upper extremity and hand. Clinical outcomes such as shoulder pain, stroke-specific quality of life, and the Shoulder Pain and Disability Index (SPADI) will also be assessed. This trial is designed to provide evidence on which therapy may be more effective for improving shoulder stability, reducing pain, and enhancing quality of life in stroke survivors with shoulder subluxation.

Подробное описание

Shoulder (glenohumeral) subluxation is a common complication after stroke and is associated with pain, impaired upper limb function, and decreased quality of life. Despite the availability of different rehabilitation methods, there is still no clear consensus on the most effective approach for managing post-stroke shoulder subluxation.

The aim of this single-blind, randomized controlled trial is to compare the effects of two electrotherapeutic interventions-neuromuscular electrical stimulation (NMES) and electromyographic (EMG) biofeedback-on both structural and functional outcomes in stroke patients with glenohumeral subluxation.

Participants will be randomly assigned to either the NMES group or the EMG biofeedback group, in addition to receiving standard rehabilitation. The study will evaluate structural outcomes using ultrasonographic measures, including the acromion-greater tuberosity distance and supraspinatus and posterior deltoid muscle thickness. Functional outcomes will include shoulder range of motion and Brunnstrom stages of the upper extremity and hand. Clinical outcomes will be assessed using pain scores, the Stroke-Specific Quality of Life Scale, and the Shoulder Pain and Disability Index (SPADI).

This trial is expected to provide evidence regarding the comparative effectiveness of NMES and EMG biofeedback in improving shoulder stability, reducing pain, and enhancing functional recovery and quality of life in stroke survivors with shoulder subluxation.

Вмешательства

  • Устройство Neuromuscular electrical stimulation
    Neuromuscular electrical stimulation (NMES) will be administered to the supraspinatus and posterior deltoid muscles for 20 minutes daily, five days per week, over a period of three weeks, totaling 15 treatment sessions. All groups will undergo a conventional physiotherapy program consisting of 45-minute sessions, five days per week, for three weeks, totaling 15 sessions. The program will comprise range of motion exercises, stretching, progressive resistive exercises, and activities of daily livi
  • Устройство Electromyographic (EMG) biofeedback
    Electromyographic (EMG) biofeedback therapy will be applied to the supraspinatus and posterior deltoid muscles for 20 minutes daily, five days per week, over a period of three weeks, totaling 15 treatment sessions. All groups will undergo a conventional physiotherapy program consisting of 45-minute sessions, five days per week, for three weeks, totaling 15 sessions. The program will comprise range of motion exercises, stretching, progressive resistive exercises, and activities of daily living-or
  • Другое Conventional physiotherapy
    This group will participate exclusively in a conventional physiotherapy program for 45 minutes daily, five days per week, over a period of three weeks, totaling 15 sessions. The conventional program will include range of motion exercises, stretching, progressive resistive exercises, and exercises targeting activities of daily living.

Первичные конечные точки

  • Acromion-Greater Tuberosity Distance (AGT Distance) - Musculoskeletal Ultrasound Measurement [Срок оценки: Baseline and Week 3]
  • Supraspinatus Muscle Thickness Measured by Musculoskeletal Ultrasound [Срок оценки: Baseline (Week 0) and Week 3]
  • Posterior Deltoid Muscle Thickness Measured by Musculoskeletal Ultrasound [Срок оценки: Baseline (Week 0) and Week 3]
  • Motor Function [Срок оценки: Baseline and Week 3]
Вторичные конечные точки (4)
  • Visual Analog Scale [Срок оценки: Baseline and Week 3]
  • Passive Shoulder Range of Motion (ROM) [Срок оценки: Baseline and Week 3]
  • Shoulder Pain and Disability Index (SPADI) [Срок оценки: Baseline and Week 3]
  • Stroke-Specific Quality of Life Scale (SS-QOL) [Срок оценки: Baseline and Week 3]

Критерии участия

Критерии включения

  • ≥18 years of age,
  • Disease duration >3 months,
  • Glenohumeral subluxation (GHS) confirmed by ultrasonography (USG),
  • Upper extremity and hand Brunnstrom motor stages between 2 and 5

Критерии исключения

  • Mini-Mental State Examination (MMSE) score <24,
  • Visual/hearing impairments, or neglect,
  • Steroid injection for shoulder pain within the last 3 months,
  • Unstable systemic disease,
  • Spasticity with Modified Ashworth Scale (MAS) score 3-4,
  • Presence of metal implants or pacemaker

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
Простое слепое
Основная цель
Лечение

Центры проведения

Turkey (Türkiye) · 1 центр
  • Gaziler Physical Therapy and Rehabilitation Training and Research Hospital — Ankara

Публикации

  • Turkkan C, Ozturk GT, Ugurlu FG, Ersoz M. Ultrasonographic assessment of neuromuscular electrical stimulation efficacy on glenohumeral subluxation in patients with hemiplegia: a randomized-controlled study. Turk J Phys Med Rehabil. 2017 May 17;63(4):287-292. doi: 10.5606/tftrd.2017.953. eCollection 2017 Dec. PMID 31453469
  • Whitehair VC, Chae J, Hisel T, Wilson RD. The effect of electrical stimulation on impairment of the painful post-stroke shoulder. Top Stroke Rehabil. 2019 Oct;26(7):544-547. doi: 10.1080/10749357.2019.1633796. Epub 2019 Jul 12. PMID 31298627
  • Chuang LL, Chen YL, Chen CC, Li YC, Wong AM, Hsu AL, Chang YJ. Effect of EMG-triggered neuromuscular electrical stimulation with bilateral arm training on hemiplegic shoulder pain and arm function after stroke: a randomized controlled trial. J Neuroeng Rehabil. 2017 Nov 28;14(1):122. doi: 10.1186/s12984-017-0332-0. PMID 29183339

Идентификаторы

NCT: NCT07423455 · AEŞH-EK-2025-115

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗