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Идёт набор NCT06400186

Movement Amplification Gait Training to Enhance Walking Balance Post-Stroke

Без фазы С лечением Chronic Hemiparetic 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: High intensity gait training in varying external environments, Treadmill walking in varying external environments.
Кому может быть актуально
Состояния в реестре: Chronic Hemiparetic Stroke. Базовые параметры: 18 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
США
Следующий шаг
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Обзор

Stroke is a leading cause of disability in the United States, affecting approximately 795,000 people annually. The Veteran's Health Administration provides over 60,000 outpatient visits for stroke-related care annually at a cost of over $250 million. Among ambulatory people with chronic stroke (PwCS), impaired balance is a common health concern that substantially limits mobility (those with the worst balance walk the least). This project will explore adaptive strategies employed by PwCS in balance challenging environments and if a novel gait training intervention using a robotic device to amplify a person's self-generated movements can improve walking balance. The development of effective interventions to increase walking balance among PwCS will positively impact Veterans' health, quality of life, and ability to participate in walking activities.

Подробное описание

Background: There is a pressing need to develop effective methods to enhance walking balance in people with chronic stroke (PwCS). Interventions that amplify self-generated movements may accelerate motor learning by enhancing a person's perception of movement errors. This method could potentially be applied to help PwCS improve walking balance. To this end, the investigators have developed a cable-driven robot to create a Movement Amplification Environment (MAE) during treadmill walking. The MAE challenges walking balance by applying lateral forces to the pelvis that are proportional in magnitude to real-time lateral center of mass (COM) velocity.

Unlike a popular form of balance training that uses unpredictable perturbations to enhance reactive balance, training in a MAE targets anticipatory balance by developing predictive control mechanisms that are likely to persist when the training environment is removed (after-effects). The investigators believe that supplementing high-intensity gait training (the recommended practice to improve walking speed and distance) with a MAE will substantially enhance walking balance. Thus, the purpose is to evaluate the unique effects of MAE training on walking balance in PwCS and determine feasibility of conducting high-intensity gait training in a MAE.

Specific Aims: Aim 1: To evaluate gait patterns PwCS adapt during and immediately following walking practiced in two balance-challenging training environments: MAE and unpredictable lateral perturbations. Aim 2: To establish feasibility of high intensity gait training in MAE the investigators will evaluate cardiovascular intensity during gait training interventions performed in either a natural unmodified environment or a MAE.

Approach: Aims 1: 15 PwCS will participate in a single-day experiment evaluating gait biomechanics (COM dynamics and stepping patterns) during and immediately following treadmill walking performed in a MAE or while receiving frequent unpredictable lateral perturbations. Outcomes will assess if changes in gait patterns to maintain stability persist immediately following exposure to either of the balance-challenging environments. Aim 2: 15 PwCS will participate in two high-intensity gait training sessions. One session will be performed in a natural unmodified environment, the other in a MAE. The investigators will quantify differences in mean heart rate (HR) between the two sessions and whether mean HR is in the target high-intensity range of 70-85% of maximum HR.

Impact: This project will identify if and how PwCS uniquely adapt locomotor strategies following exposure to balance challenging environments and evaluate feasibility of administering high-intensity gait training in a MAE. Training walking balance of PwCS in a MAE by amplifying their own self-generated movements is a radical departure from current practice and could substantially enhance walking balance. Successful outcomes will motivate a future randomized controlled trial assessing the efficacy of MAE training to enhance walking balance in PwCS.

Вмешательства

  • Поведенческое High intensity gait training in varying external environments
    Participants will engage in two 45-minutes treadmill-based gait training sessions. These training sessions will occur on separate days. One session will be performed in a natural unmodified environment. One session will be performed in a movement amplification environment. The goal of each session will be to achieve 40-minutes of walking within a target heart rate range of 70-85% of estimated heart rate max. Each session will begin and end with a 2.5 minute warm-up and cool down respectively. Pa
  • Поведенческое Treadmill walking in varying external environments
    Participants will perform a series of treadmill walking trials. Each trial will consist of 400 total steps. The first 100 steps will be performed in a natural unmodified environment. The next 200 steps will be performed in 1 of 3 external environments (natural unmodified, movement amplification, or unpredictable lateral perturbations). The final 100 steps will be performed in a natural unmodified environment. Participants will be given rest breaks between trials.

Первичные конечные точки

  • Lateral center of mass (COM) excursion during walking [Срок оценки: Arm 1 only: On Day 1 of the study, participants will perform three 5-minute treadmill walking trials. We will measure Lateral COM excursion every gait cycle during each trial.]
  • Minimum lateral margin of stability [Срок оценки: Arm 1 only: On Day 1 of the study, participants will perform three 5-minute treadmill walking trials. We will measure minimum lateral margin of stability every gait cycle during each trial.]
  • Heart Rate [Срок оценки: Arm 2 only: On Day 1, participants will perform 45 minutes of treadmill walking. Seven days later, participants will perform another 45 minutes of continuous treadmill walking. We will measure average HR during every 3-minutes of treadmill walking.]
  • Perceived Exertion (RPE) [Срок оценки: Arm 2 only: On Day 1, participants will perform 45 minutes of treadmill walking. Seven days later, participants will perform another 45 minutes of continuous treadmill walking. We will measure average RPE during every 3-minutes of treadmill walking]
  • Treadmill walking speed [Срок оценки: Arm 2 only: On Day 1, participants will perform 45 minutes of treadmill walking. Seven days later, participants will perform another 45 minutes of continuous treadmill walking. We will measure average speed during every 3-minutes of treadmill walking]
  • Number of Steps [Срок оценки: Arm 2 only: On Day 1, participants will perform 45 minutes of treadmill walking. Seven days later, participants will perform another 45 minutes of continuous treadmill walking. We will measure the total number of steps during each day.]
Вторичные конечные точки (8)
  • Step Length [Срок оценки: Arm 1 only: On Day 1 of the study, participants will perform three 5-minute treadmill walking trials. We will measure step length every gait cycle during each trial.]
  • Step Width [Срок оценки: Arm 1 only: On Day 1 of the study, participants will perform three 5-minute treadmill walking trials. We will measure step width every gait cycle during each trial.]
  • 10 Meter Walk Test (10MWT) [Срок оценки: The 10MWT will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered.]
  • Timed Up and Go (TUG) [Срок оценки: The TUG will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered.]
  • Berg Balance Scale (BBS) [Срок оценки: The BBS will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered]
  • Activities-specific Balance Confidence (ABC) Scale [Срок оценки: The ABC will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered.]
  • Dynamic Gait Index (DGI) [Срок оценки: The DGI will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered.]
  • Chedoke-McMaster Stroke Assessment (CMSA) scale [Срок оценки: The CMSA will be administered one time only. This test will be administered on Day 1 before the study intervention has been administered.]

Критерии участия

Критерии включения

  • History of chronic stroke (more than 6 months post-stroke) with weakness on one side
  • Ability to ambulate over ground for 10 meters with or without a single cane, and/or ankle-foot orthosis
  • Ability to tolerate 10 minutes of standing

Критерии исключения

  • Presence of cognitive impairment (score of 22/30 on the Montreal Cognitive Assessment scale (MoCA))
  • Presence of aphasia (score of 71/100 on the Mississippi Aphasia Screening Test (MAST))
  • Excessive spasticity in lower limbs (score of > 3 on the Modified Ashworth Scale
  • Severe cardiovascular and pulmonary disease affecting gait and balance
  • History of recurrent fractures or known orthopedic problems in the lower extremities (i.e. heterotopic ossification) affecting gait and balance
  • Concomitant central or peripheral neurological injury (i.e. traumatic head injury or peripheral nerve damage in lower limbs) affecting gait and balance
  • Evidence of cerebellar ataxia
  • Presence of unhealed decubiti or other skin compromise
  • Enrollment in concurrent physical therapy or research involving gait or balance training
  • Use of braces/orthotics crossing the knee joint
  • Known pregnancy

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 2 центра
  • Northwestern University — Chicago
  • Edward Hines Jr. VA Hospital, Hines, IL — Hines

Идентификаторы

NCT: NCT06400186 · B4882-P · 1I21RX004882

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗