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Effectiveness of automated locomotor training in patients with acute incomplete spinal cord injury: A randomized controlled multicenter trial

机译:自动运动训练对急性不完全性脊髓损伤患者的有效性:一项随机对照多中心试验

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Background A large proportion of patients with spinal cord injury (SCI) regain ambulatory function. However, during the first 3 months most of the patients are not able to walk unsupported. To enable ambulatory training at such an early stage the body weight is partially relieved and the leg movements are assisted by two therapists. A more recent approach is the application of robotic based assistance which allows for longer training duration. From motor learning science and studies including patients with stroke, it is known that training effects depend on the duration of the training. Longer trainings result in a better walking function. The aim of the present study is to evaluate if prolonged robot assisted walking training leads to a better walking outcome in patients with incomplete SCI and whether such training is feasible or has undesirable effects. Methods/Design Patients from multiple sites with a subacute incomplete SCI and who are not able to walk independently will be randomized to either standard training (3-5 sessions per week, session duration maximum 25 minutes) or an intensive training (3-5 sessions per week, session duration minimum 50 minutes). After 8 weeks of training and 4 months later the walking ability, the occurrence of adverse events and the perceived rate of exertion as well as the patients' impression of change will be compared between groups. Trial registration This study is registered at clinicaltrials.gov, identifier: NCT01147185 .
机译:背景脊髓损伤(SCI)的患者中大部分恢复了门诊功能。但是,在最初的3个月中,大多数患者无法在没有支撑的情况下行走。为了在这样的早期阶段进行门诊训练,部分减轻了体重,并由两名治疗师协助了腿部运动。最近的方法是基于机器人的协助的应用,其允许更长的训练持续时间。从运动学习科学和研究(包括中风患者)可以知道,训练效果取决于训练的持续时间。训练时间越长,步行功能越好。本研究的目的是评估长时间的机器人辅助步行训练是否会在SCI不完全的患者中带来更好的步行结果,以及这种训练是否可行或有不良影响。方法/设计来自多个地点的亚急性SCI不完全且无法独立行走的患者将被随机分为标准训练(每周3-5次,每周持续时间最多25分钟)或强化训练(3-5次)每周,会话持续时间至少50分钟)。经过8周的训练和4个月后的步行能力,不良事件的发生,感知的劳累率以及患者对变化的印象,将在两组之间进行比较。试验注册该研究已在Clinicaltrials.gov上注册,标识符:NCT01147185。

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