Xo-Motion R Exoskeleton in SCI-Adoption Study
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: XoMotionR- assisted locomotor training.
- Кому может быть актуально
- Состояния в реестре: Spinal Cord Injury. 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
- Канада
- 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
Adoption of the Xo-Motion R in the Subacute and Chronic SCI Populations at the Glenrose Rehabilitation Hospital
Обзор
After spinal cord injury (SCI), many people lose their ability to walk and do not have access to equipment and assistance that could help them regain functional abilities. Furthermore, many who have the potential to regain function are further hindered by a loss of function in their upper body that limits their ability to use a walker or crutches, thus eliminating options for mobility. This study seeks to determine the safety and feasibility of the XoMotion-R, a self-balancing exoskeleton that allows people with American Spinal Injury Association Impairment Scale (AIS) rating of B-D SCI to walk hands-free in inpatient and outpatient settings. This study will examine how use of the XoMotion-R affects functional outcomes and identify setting-specific barriers and facilitators to clinical adoption. This single-arm feasibility study will recruit 8 SCI inpatients and 8 SCI outpatients whose goal is to improve their walking and incorporate the XoMotion-R into their rehabilitation sessions. Participants will work on a variety of gait tasks tailored to their functional level. The goal is to determine whether early robotic gait training can improve functional outcomes and decrease length of stay, secondary complications, and long-term disability burden.
Вмешательства
- Устройство XoMotionR- assisted locomotor training
The XoMotion-R self-balancing exoskeleton will be utilized for locomotor training in both the inpatient and outpatient setting. Inpatient intervention will be focused on promoting early weight-bearing, postural control, and initiation of step cycles. Training includes progressive walking tasks that emphasize symmetrical lower limb loading, upright posture, and engagement of trunk musculature. In addition to forward ambulation, sessions incorporate functional activities such as sit-to-stand trans
Первичные конечные точки
- SCI Standing and Walking Assessment (SWAT) [Срок оценки: Baseline and completion of 6 weeks of locomotor therapy with the XoMotionR]
- 6min Walk Test (6MT) (Outpatient group) [Срок оценки: Baseline and completion of 6 weeks of locomotor therapy with the XoMotionR]
- 10-m Walk Test (10MWT) (Outpatient Group) [Срок оценки: Baseline and completion of 6 weeks of locomotor therapy with the XoMotionR]
- Modified Timed Up and Go (mTUG) (Outpatient Group) [Срок оценки: Baseline and completion of 6 weeks of locomotor therapy with the XoMotionR]
- Berg Balance Scale (BBS) (Outpatient Group) [Срок оценки: Baseline and completion of 6 weeks of locomotor therapy with the XoMotionR]
Вторичные конечные точки (2)
- Device-generated metrics (Number of steps taken) [Срок оценки: Throughout study completion, for an average of 6 weeks]
- Device-generated metrics (Level of assistance provided) [Срок оценки: Throughout study completion, for an average of 6 weeks]
Критерии участия
Критерии включения
- SCI (AIS C or D in inpatient setting, AIS B-D in outpatient setting; inclusive of cervical injuries)
- inpatients who are preambulatory with predicted probability of walking independently 1year after injury >50% (Hicks et al., 2017)
- outpatients with a functional goal of improved locomotion where the XoMotion is clinically suited to support the achievement of their functional goals
Критерии исключения
- SCI AIS A
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Не применимо
- Модель
- Одна группа
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
Канада · 1 центр
- Glenrose Rehabilitation Hospital — Edmonton
Идентификаторы
NCT: NCT07380516 · Pro00159509