跳至主要内容
临床试验/NCT02765334
NCT02765334已完成不适用

A Pilot Feasibility Clinical Trial of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) for postStroke Arm Paresis

Tan Tock Seng Hospital1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2015年12月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
13
试验地点
1
主要终点
Change in Upper extremity Fugl-Meyer motor score post training

研究概览

简要总结

A feasibility trial of Neurostyle Brain Exercise Therapy Towards Enhanced Recovery (nBETTER) system for Brain Computer Interface (BCI) neurofeedback for rehabilitation of the subacute and chronic hemiplegic upper limb aimed at improving upper limb recovery for subacute to chronic stroke patients.

详细描述

Stroke remains the 4th cause of death in Singapore and despite advances in neuro-medical care and rehabilitation, 40-50% of stroke survivors are left with permanent neuro-disability and a reduced quality of life. The previous 2 decades has seen exponential leaps in the development of rehabilitation technologies which enhance neuroplasticity and rehabilitation outcome. One of these potentially useful technologies is nBETTER System, was developed by Institute for Infocomm Research, Agency for Science, Technology and Research (A*STAR). nBETTER is a portable, internet-connected device that detects the imagination of movement of stroke-affected limb using a Electroencephalography (EEG)-based Brain-Computer Interface (BCI) thus delivering visually engaging feedback for directed neurofeedback aimed at improving upper limb recovery for subacute to chronic stroke patients. The pilot study aims to recruit 13 patients using a multi centre trial design to investigate nBETTER system feasibility and safety for rehabilitation of subacute to chronic stroke patients with upper limb motor impairment and to determine clinical efficacy, safety and feasibility of such a system when it is delivered with standard occupational therapy.

The investigators primary hypothesis is that nBETTER is a feasible and safe prototype in stroke survivors (> 3 months) with moderate to severe arm impairment (FMMA 10-50). The primary outcome is a gain of 15% in Fugl-Meyer motor scores at 6 weeks after 18 sessions (total of 27 hours) of supervised training by occupational therapists and bioengineers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged 21-80 years with first-ever clinical stroke diagnosed on CT or MRI brain imaging.
  • •Stroke duration of 3-24 months.
  • •Stroke type: ischemic or haemorrhagic
  • •Fugl-Meyer motor score of the upper limb range from 10-50
  • •Ability to pay attention and maintain supported sitting for 1.5 hours continuously
  • •Able to give own consent and understand simple instructions
  • •Fulfils BCI resting brain states on initial screening.

排除标准

  • •Recurrent clinical stroke
  • •Functional status: severe aphasia or inattention, unstable medical conditions which may affect participation (e.g. unresolved sepsis, postural hypotension, end stage renal failure) or anticipated life expectancy of <1 year due to malignancy or neurodegenerative disorder)
  • •Hemispatial neglect (visual or sensory) or severe visual impairment despite visual aids
  • •History of epilepsy, severe depression or active psychiatric disorder
  • •Skull defect or previous cranial surgery as this would affect physical fit of EEG cap interface
  • •Local arm factors: severe spasticity Modified Ashworth scale >2 in any region, visual analogue scale (VAS score) >4/10, fixed joint contractures or joint replacements, patients with poor skin conditions which would contraindicate repetitive arm training.
  • •TMS contraindications: females with reproductive potential not on reliable contraception; pregnancy; cardiac pacemakers; orthodontics (braces); metal implants.

研究组 & 干预措施

nBETTER and Conventional Therapy

Experimental

Intervention: nBetter therapy

干预措施: nBETTER (Device)

结局指标

主要结局

Change in Upper extremity Fugl-Meyer motor score post training

时间窗: Baseline and week 6

As above

次要结局

  • Change in Frenchay Arm Test of Function (FAT)(Baseline and week 6)
  • Change in Modified Ashworth Scale score (MAS)(Baseline and week 6)
  • Change in Visual Analogue Scale (VAS)(Baseline and week 6)
  • Change in Transcranial Magnetic Stimulation Assessment (TMS)(Baseline and week 6)
  • Change in Grip Strength(Baseline and week 6)

研究者

发起方
Tan Tock Seng Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验