Virtual Reality's Impact on Upper Limb Function in Post-stroke Patients
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: virtual reality (VR) head mounted display.
- Кому может быть актуально
- Состояния в реестре: Stroke. Базовые параметры: 40 лет — 80 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
- Китай
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Effects of Virtual Reality Features on Upper Limb Motor Function in Post-stroke Patients
Обзор
Stroke rank second among the top causes of death, affecting millions of people in the worldwide. Approximately 70-80% survivors of stroke could experience various levels of upper limb motor impairments, which seriously affects the activities of daily life and cause serious physical and mental burden to patients and their families. As bottleneck effect in traditional rehabilitation techniques become apparent, a number of emerging technologies are being used in rehabilitation treatment in an attempt to break down this barrier.Studies have shown that virtual reality (VR) training can effectively promote the remodeling of the central nervous system and has become an important research direction for motor function rehabilitation.However, most current studies still focus on evaluating the overall intervention effect of VR, with little examination of its intrinsic properties and a lack of exploration of the sense of ownership (SOO) and agency (SOA). Hence, this study conducted different VR interventions on stroke patients to evaluate the effects of the intrinsic properties of VR and the body illusion it produces on the rehabilitation of their upper limb motor function. This study is a single-blind randomized controlled trial. A total of 120 participants will be enrolled and divided into a control group, an interactive VR group, and an immersive and interactive VR group. All groups will be tested on the virtual hand illusion before the intervention. The intervention will last for a fortnight, four times a week for one hour each time. Assessment will be conducted before the intervention, at the end of the intervention, and at week 6 for follow-up. The primary outcome measure is the "Fugl-Meyer Assessment of the Upper Extremity (FMA-UE)". The secondary outcome measures are "SOO questionnaire", "proprioceptive drift scale", "action research arm test (ARAT)", "NIH stroke scale (NIHSS)", "mini mental state examination (MMSE)", "electromyography (EMG)", "electroencephalography (EEG)" and "functional Magnetic Resonance Imaging (fMRI)".
Вмешательства
- Устройство virtual reality (VR) head mounted display
This group of subjects received immersive and interactive VR training, which combined rich immersive VR scenes with specific interactive tasks, including two VR scenes. Task selection was based on the subjects' upper limb functional performance, and experienced therapists provided guidance and monitoring, and adjusted the tasks when necessary.
Первичные конечные точки
- Fugl-Meyer Assessment Upper Extremity Scale (FAM-UE) [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
Вторичные конечные точки (8)
- Sense of ownership questionnaire [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- Proprioceptive drift scale [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- Action Research Arm Test [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- National institutes of health stroke scale [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- Mini-mental state examination [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- Surface electromyography [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- Electroencephalography [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
- functional Magnetic Resonance Imaging [Срок оценки: There were 3 time points for evaluation: before intervention, on the day of intervention end, 4 weeks after intervention end]
Критерии участия
Критерии включения
- First episode of stroke, hemorrhagic or ischemic, confirmed by computed tomography or magnetic resonance imaging of the brain;
- Age 40-80 years, either male or female;
- 3-12 months since stroke occurrence;
- Mild-to-moderate or moderate-to-severe upper extremity impairment, with a FMA-UE score between 16 and 53;
- Basic ability to communicate and comprehend the research instructions, with a score of 21 and above on the MMSE scale;
- Agreement to participate in the study, with an informed consent form duly signed by the patient or a family member.
Критерии исключения
- The presence of ferromagnetic metals implanted in the body;
- Visual or hearing deficits;
- Unstable medical conditions;
- History of receiving similar VR training in the past;
- A history of myasthenia gravis, multiple sclerosis, muscular dystrophy, or other diseases that may cause upper limb movement disorders.
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
Китай · 1 центр
- Qilu hospital — Цзинань
Публикации
- Laver KE, Lange B, George S, Deutsch JE, Saposnik G, Crotty M. Virtual reality for stroke rehabilitation. Cochrane Database Syst Rev. 2017 Nov 20;11(11):CD008349. doi: 10.1002/14651858.CD008349.pub4. PMID 29156493
- Ventura S, Tessari A, Castaldini S, Magni E, Turolla A, Banos R, Lullini G. Effectiveness of a Virtual Reality rehabilitation in stroke patients with sensory-motor and proprioception upper limb deficit: A study protocol. PLoS One. 2024 Aug 12;19(8):e0307408. doi: 10.1371/journal.pone.0307408. eCollection 2024. PMID 39133660
- Tambone R, Giachero A, Calati M, Molo MT, Burin D, Pyasik M, Cabria F, Pia L. Using Body Ownership to Modulate the Motor System in Stroke Patients. Psychol Sci. 2021 May;32(5):655-667. doi: 10.1177/0956797620975774. Epub 2021 Apr 7. PMID 33826456
- Bargeri S, Scalea S, Agosta F, Banfi G, Corbetta D, Filippi M, Sarasso E, Turolla A, Castellini G, Gianola S. Effectiveness and safety of virtual reality rehabilitation after stroke: an overview of systematic reviews. EClinicalMedicine. 2023 Sep 14;64:102220. doi: 10.1016/j.eclinm.2023.102220. eCollection 2023 Oct. PMID 37745019
- Goizueta S, Navarro MD, Calvo G, Campos G, Colomer C, Noe E, Llorens R. Touchscreen-based assessment of upper limb kinematics after stroke: Reliability, validity and sensitivity to motor impairment. J Neuroeng Rehabil. 2025 Feb 11;22(1):27. doi: 10.1186/s12984-025-01563-6. PMID 39934877
Идентификаторы
NCT: NCT06881680 · KYLL-202411-013