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临床试验/NCT02098265
NCT02098265招募中不适用

A Closed Loop Neural Activity Triggered Stroke Rehabilitation Device

University of Wisconsin, Madison2 个研究点 分布在 1 个国家目标入组 288 人开始时间: 2010年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
288
试验地点
2
主要终点
Action Research Arm Test Scores

研究概览

简要总结

The purpose of this research is to determine if two non-invasive brain stimulation techniques, muscle stimulation of the arm and neuro-stimulation through the tongue, can increase the extent of stroke recovery.

详细描述

The aim of this study is to determine if functional muscle stimulation, in addition to non-invasive neurostimulation through the tongue (TDU), directed by electroencephalogram (EEG) output, can increase the extent of stroke recovery on behavioral measures and induce brain plasticity as measured by functional magnetic resonance imaging (fMRI).

Adult stroke patients with upper extremity motor impairments (henceforth "experimental group"), healthy controls, and participants with risk factors for stroke, without upper extremity impairment (allowing them to serve as controls for patients with upper extremity impairments (henceforth "control group")), will be recruited in this study. Half of the participants in the experimental group will be randomly assigned to the EEG-BCI (brain-computer interface) training ("closed-loop") group and will receive training on the BCI task along with muscle and tongue stimulation. The other half of the participants in the experimental group receiving traditional rehab will not receive any kind of FES or tongue stimulation for the first 8-10 weeks of study period and then will start receiving BCI-FES-tongue stimulation rehab therapy.

All participants without UE impairment in Control group 1 will receive 4-6 (minimum 4, up to a maximum of 6) sessions of training on the BCI system and pre- and post MRI and 2 behavioral testing sessions.

Addition of a Control group 2 is consistent with the AHA grants - Twenty four ischemic stroke patients with moderate upper extremity (dominant right hand affected) impairment (score of 1 or 2 on the motor sub-component of the NIH stroke scale (NIHSS) and ARAT score 20-45); no upper extremity injury or conditions that limited use prior to the stroke; and pre-stroke independence with a Modified Rankin Score of 0 or 1), will be recruited in this arm. All participants in this group will receive MR sessions and behavioral testing similar to the Experimental group.

Addition of an Experimental group receiving EEG-BCI-bilateral FES intervention using the recoveriX system: recoveriX is a brain driven rehabilitation system for stroke patients that pairs mental activities with motor functions. Through the EEG-based recoveriX BCI system, the brain receives visual and tactile feedback in real-time, making rehabilitation more effective. A stroke patient imagines a hand movement while receiving visual feedback through a virtual avatar, and tactile feedback through electrical muscle stimulation paired to the patient's imagined movement, with the aim that these patients might regain the volitional ability to grasp following therapy. Unlike the current EEG-BCI-FES intervention that involves stimulation of only the impaired arm, with recoveriX, both arms are simultaneously stimulated during the course of the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • (Experimental Group):
  • Stroke patients with persistent upper extremity (UE) deficits
  • Inclusion Criteria (Control Group 1)
  • Stroke patients without UE impairments
  • Participants with risk factors for stroke
  • healthy controls
  • No known neurologic, psychiatric or developmental disability
  • Inclusion Criteria (Control Group 2)
  • Stroke patients with persistent upper extremity (UE) deficits
  • Moderate upper extremity (dominant right hand affected) impairment (score of 1 or 2 on the motor sub-component of the NIH stroke scale (NIHSS) and ARAT score 20-45)
  • No upper extremity injury or conditions that limited use prior to the stroke
  • Pre-stroke independence with a Modified Rankin Score of 0 or 1, for the standard FES only intervention.

排除标准

  • (for all participants):
  • Allergic to electrode gel, surgical tape and metals
  • Participants under treatment for infectious diseases or having apparent oral lesions or inflammation will be excluded from the study
  • Women who are pregnant or may become pregnant during the course of the study will be excluded
  • Participants with contraindications for MRI will be offered the opportunity to participate in the interventions study only (e.g. EEG-BCI-FES and behavioral testing)
  • Exclusion Criteria (for healthy controls)
  • Contraindications for MRI
  • Allergic to electrode gel, surgical tape, and metals.

研究组 & 干预措施

Experimental Group - RecoveriX

Experimental

Recruited from participants who have completed the study intervention

干预措施: RecoveriX (Other)

Experimental Group - Immediate BCI Therapy

Experimental

EEG - BCI training (closed loop)

干预措施: BCI-FES (Device)

Experimental Group - Immediate BCI Therapy

Experimental

EEG - BCI training (closed loop)

干预措施: Behavioral Assessments (Behavioral)

Experimental Group - Immediate BCI Therapy

Experimental

EEG - BCI training (closed loop)

干预措施: Magnetic Resonance Imaging (Other)

Experimental Group - Immediate BCI Therapy

Experimental

EEG - BCI training (closed loop)

干预措施: EEG (Other)

Experimental Group - Delayed BCI Therapy

Experimental

Scanned and tested 4 times over a 10-week period before EEG-BCI training

干预措施: Behavioral Assessments (Behavioral)

Experimental Group - Delayed BCI Therapy

Experimental

Scanned and tested 4 times over a 10-week period before EEG-BCI training

干预措施: Magnetic Resonance Imaging (Other)

Experimental Group - Delayed BCI Therapy

Experimental

Scanned and tested 4 times over a 10-week period before EEG-BCI training

干预措施: EEG (Other)

Experimental Group - Delayed BCI Therapy

Experimental

Scanned and tested 4 times over a 10-week period before EEG-BCI training

干预措施: Delay (Other)

Experimental Group - Delayed BCI Therapy

Experimental

Scanned and tested 4 times over a 10-week period before EEG-BCI training

干预措施: BCI-FES (Device)

Control Group 1

Active Comparator

48 stroke patients, 48 participants with risk factors for stroke, 48 healthy controls receiving 4-6 training sessions on the EEG-BCI, pre- and post- behavioral testing, and MRI

干预措施: Behavioral Assessments (Behavioral)

Control Group 1

Active Comparator

48 stroke patients, 48 participants with risk factors for stroke, 48 healthy controls receiving 4-6 training sessions on the EEG-BCI, pre- and post- behavioral testing, and MRI

干预措施: Magnetic Resonance Imaging (Other)

Control Group 1

Active Comparator

48 stroke patients, 48 participants with risk factors for stroke, 48 healthy controls receiving 4-6 training sessions on the EEG-BCI, pre- and post- behavioral testing, and MRI

干预措施: EEG (Other)

Control Group 1

Active Comparator

48 stroke patients, 48 participants with risk factors for stroke, 48 healthy controls receiving 4-6 training sessions on the EEG-BCI, pre- and post- behavioral testing, and MRI

干预措施: BCI-FES (Device)

Control Group 2

Active Comparator

24 Stroke Patients with UE impairment receiving standard FES only therapy

干预措施: Functional Electric Stimulation (FES) (Device)

结局指标

主要结局

Action Research Arm Test Scores

时间窗: 4 months

The Action Research Arm Test (ARAT) is designed for evaluation of upper extremity function. This test consists of sections for Grasp, Grip, Pinch and Gross Movements and comprise a total of 19 tests. Each test is scored 0-3 where 0 is 'no movement' and 3 is 'the movement is performed normally'. Each section is scored separately and the scores added for a total possible range of scores from 0-57 where the higher the score, the complete and efficient the movement. ARAT will be assessed at baseline and end of study (approximately 4 months)

次要结局

  • Signal change in functional MRI(4 months)
  • Change in Electroencephalogram (EEG) Response Strength(4 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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