首页> 美国卫生研究院文献>Frontiers in Neurology >Non-invasive Focal Mechanical Vibrations Delivered by Wearable Devices: An Open-Label Pilot Study in Childhood Ataxia
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Non-invasive Focal Mechanical Vibrations Delivered by Wearable Devices: An Open-Label Pilot Study in Childhood Ataxia

机译:可穿戴设备提供的非侵入性焦点机械振动:儿童共济失调的开放标签试验研究

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摘要

Non-invasive focal mechanical vibrations (NIFMV) now represent a strategy of increasing interest to improve motor control in different neurological diseases. Nanotechnology allowed the creation of wearable devices transforming thermal variations into mechanical energy with focal vibrations. This kind of wearable stimulators (WS) has produced encouraging preliminary results when used in the treatment of movement disorders and ataxia in adults. In this open label pilot study we first evaluated the feasibility, safety and effectiveness of NIFMV by WS in a cohort of 10 patients with childhood ataxia, a phenomenological category including different conditions still lacking of effective symptomatic therapies. Through the assessment of both clinical rating scales and spatio-temporal gait parameters via standardized gait analysis, we observed that a 4 weeks long treatment with WS Equistasi® was safe and provided significantly different effects in stride features of patients with slowon-progressive cerebellar ataxia and Friedreich's Ataxia. Although limited by the sample size, the absence of a placebo-controlled group, the poor compliance of enrolled population to the original experimental design and the partial accuracy of outcome measures in pediatric subjects, we suggest that NIFMV by WS could support locomotion of patients with childhood slowon-progressive cerebellar ataxia with preserved sensory system and no signs of peripheral neuropathy. Future studies are definitely necessary to confirm these preliminary results and define criteria for successful NIFMV-based treatment
机译:现在,非侵入性局灶性机械振动(NIFMV)代表了一种提高人们对改善不同神经疾病中的运动控制的兴趣的策略。纳米技术允许创建可穿戴设备,这些设备将热变化转化为具有聚焦振动的机械能。当用于成人运动障碍和共济失调的治疗时,这种可穿戴刺激器(WS)产生了令人鼓舞的初步结果。在这项开放标签的先导研究中,我们首先评估了WS在一组10例儿童期共济失调患者中的可行性,安全性和有效性,这是一种包括不同情况但仍缺乏有效对症治疗的现象学类别的患者。通过通过标准化步态分析评估临床评估量表和时空步态参数,我们观察到用WSEquistasi®进行为期4周的治疗是安全的,并且对缓慢/非进行性小脑患者的步幅特征有明显不同的影响共济失调和弗雷德里希的共济失调。尽管受样本量的限制,缺乏安慰剂对照组,入组人群对原始实验设计的依从性差以及儿科受试者的结局指标的部分准确性,我们建议通过WS进行NIFMV可以支持患有以下疾病的患者的运动儿童缓慢/非进行性小脑共济失调,感觉系统得以保留,无周围神经病变的迹象。肯定有必要进行进一步的研究以确认这些初步结果并确定成功基于NIFMV的治疗的标准

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