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促通器,一种基于脑机接口的干预手段,用于促进脑卒中后上肢运动功能的恢复:一项随机对照试验的研究方案,旨在测试早期和长期疗效,并确定反应的决定因素。

The Promotoer, a brain-computer interface-assisted intervention to promote upper limb functional motor recovery after stroke: a study protocol for a randomized controlled trial to test early and long-term efficacy and to identify determinants of response.

机构信息

Fondazione Santa Lucia, IRCCS, Rome, Italy.

Department of Computer, Control, and Management Engineering "Antonio Ruberti", Sapienza University of Rome, Rome, Italy.

出版信息

BMC Neurol. 2020 Jun 27;20(1):254. doi: 10.1186/s12883-020-01826-w.

Abstract

BACKGROUND

Stroke is a leading cause of long-term disability. Cost-effective post-stroke rehabilitation programs for upper limb are critically needed. Brain-Computer Interfaces (BCIs) which enable the modulation of Electroencephalography (EEG) sensorimotor rhythms are promising tools to promote post-stroke recovery of upper limb motor function. The "Promotoer" study intends to boost the application of the EEG-based BCIs in clinical practice providing evidence for a short/long-term efficacy in enhancing post-stroke hand functional motor recovery and quantifiable indices of the participants response to a BCI-based intervention. To these aims, a longitudinal study will be performed in which subacute stroke participants will undergo a hand motor imagery (MI) training assisted by the Promotoer system, an EEG-based BCI system fully compliant with rehabilitation requirements.

METHODS

This longitudinal 2-arm randomized controlled superiority trial will include 48 first ever, unilateral, subacute stroke participants, randomly assigned to 2 intervention groups: the BCI-assisted hand MI training and a hand MI training not supported by BCI. Both interventions are delivered (3 weekly session; 6 weeks) as add-on regimen to standard intensive rehabilitation. A multidimensional assessment will be performed at: randomization/pre-intervention, 48 h post-intervention, and at 1, 3 and 6 month/s after end of intervention. Primary outcome measure is the Fugl-Meyer Assessment (FMA, upper extremity) at 48 h post-intervention. Secondary outcome measures include: the upper extremity FMA at follow-up, the Modified Ashworth Scale, the Numeric Rating Scale for pain, the Action Research Arm Test, the National Institute of Health Stroke Scale, the Manual Muscle Test, all collected at the different timepoints as well as neurophysiological and neuroimaging measures.

DISCUSSION

We expect the BCI-based rewarding of hand MI practice to promote long-lasting retention of the early induced improvement in hand motor outcome and also, this clinical improvement to be sustained by a long-lasting neuroplasticity changes harnessed by the BCI-based intervention. Furthermore, the longitudinal multidimensional assessment will address the selection of those stroke participants who best benefit of a BCI-assisted therapy, consistently advancing the transfer of BCIs to a best clinical practice.

TRIAL REGISTRATION

Name of registry: BCI-assisted MI Intervention in Subacute Stroke (Promotoer).

TRIAL REGISTRATION NUMBER

NCT04353297 ; registration date on the ClinicalTrial.gov platform: April, 15/2020.

摘要

背景

中风是长期残疾的主要原因。急需具有成本效益的上肢卒中后康复计划。脑-机接口(BCI)可以调节脑电图(EEG)感觉运动节律,是促进上肢运动功能恢复的有前途的工具。“Promotoer”研究旨在促进基于脑电图的 BCI 在临床实践中的应用,为短期/长期增强卒中后手功能运动恢复和参与者对基于 BCI 的干预的反应的可量化指标提供证据。为此,将进行一项纵向研究,其中亚急性中风参与者将在手运动想象(MI)训练中接受 Promotoer 系统的辅助,这是一种完全符合康复要求的基于脑电图的 BCI 系统。

方法

这项纵向 2 臂随机对照优势试验将纳入 48 名首次单侧亚急性中风参与者,随机分为 2 个干预组:BCI 辅助手 MI 训练和不支持 BCI 的手 MI 训练。这两种干预措施都作为标准强化康复的附加方案进行(每周 3 次疗程;6 周)。将在以下时间点进行多维评估:随机分组/干预前、干预后 48 小时、干预结束后 1、3 和 6 个月:主要观察指标是干预后 48 小时的 Fugl-Meyer 评估(上肢)。次要观察指标包括:随访时的上肢 Fugl-Meyer 评估、改良 Ashworth 量表、疼痛数字评分量表、动作研究上肢测试、国立卫生研究院卒中量表、手动肌肉测试,所有这些都在不同时间点进行测量,以及神经生理和神经影像学测量。

讨论

我们预计基于 BCI 的对手部 MI 练习的奖励将促进手部运动结果的早期改善的长期保留,并且这种临床改善将通过基于 BCI 的干预产生的长期神经可塑性变化来维持。此外,纵向多维评估将解决那些最受益于基于 BCI 治疗的中风参与者的选择问题,从而不断推进 BCI 向最佳临床实践的转移。

试验注册

登记名称:亚急性中风中的基于 BCI 的 MI 干预(Promotoer)。

试验注册号

NCT04353297;在 ClinicalTrial.gov 平台上的注册日期:2020 年 4 月 15 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ea/7320550/875e9cd72d86/12883_2020_1826_Fig1_HTML.jpg

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