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Motor Imagery BCI Rehabilitation After Stroke

Primary Purpose

Stroke, Hemiparesis

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Motor imagery BCI training
Sponsored by
Mälardalen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

> 6 months since first time stroke onset and with remaining hemiparesis in upper extremity; able to participate fully in the intervention, able to perform Functional Magnetic Resonance Imaging (fMRI); able to passively extend the wrist 15 degrees and extend fingers fully with a neutral position of the wrist.

In addition, participants need to be able to voluntarily control the power of their grip when requested according to the Visuomotor force tracking method and/or according to the clinical assessment of a therapist (while holding the patient´s hand). According to the Fugl- Meyer Upper Extremity (UE) scale participants should accomplish <14 points on the hand subscale and <2 points in finger flexion and extension (C) in addition to < 47 points on the total motor score (equivalent to moderate disability in the upper extremity.

Exclusion Criteria:

  • other neurological or musculoskeletal disease/injury, or contagious disease.
  • If the research person is regularly treated with botulinum toxin in the upper extremity, 3 weeks should have passed before the first baseline assessment.
  • current or history of epilepsy,
  • severe hearing or visual impairments,
  • metal implants in the brain/skull cochlear implants,
  • any implanted neurostimulator, cardiac pacemaker or cardiac implants of metal, infusion device,
  • any other neurological disorder,
  • pregnancy,
  • current or history of severe psychiatric disorder with need for pharmacological treatment

Sites / Locations

  • Stockholn University Brain Imaging Centre
  • Department of rehabilitation medicine at Danderyd UniversityRecruiting
  • Sweden Mälardalen University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Motor Imagery BCI training

Arm Description

Complete intervention with motor imagery BCI training. Patients recruited by physiotherapists who underwent baseline evaluations with clinical tests, fMRI and EEG measurements. Patients will after intervention perform clinical tests, fMRI, and EEG measurements to evaluate outcomes of intervention.

Outcomes

Primary Outcome Measures

Change of Fugl-Meyer Upper Extremity scale score (0-66 points)
Arm and hand function
Change of EEG alpha and beta activity
Brain motor network activity reflected in BCI feedback
Change of fMRI BOLD activity
Brain motor network activity

Secondary Outcome Measures

Change of monofilament test score
Two point discrimination and monofilament test for sensory function
Change of box and block test score (0-150)
Gross manual dexterity
Change of JAMAR® digital Hand Dynamometer scores (0-90)
Grip strength
Change of visuomotor force-tracking task scores
Quantification of timing and precision aspects of force grip modulation
Change of stroke Impact Scale 16 scores (15-80 points)
Activity limitations related to physical function

Full Information

First Posted
April 14, 2021
Last Updated
May 16, 2022
Sponsor
Mälardalen University
Collaborators
Danderyd Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04847089
Brief Title
Motor Imagery BCI Rehabilitation After Stroke
Official Title
Motor Imagery and Real-time Feedback in Stroke Rehabilitation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 14, 2022 (Actual)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
February 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mälardalen University
Collaborators
Danderyd Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research project will investigate motor imagery training in stroke rehabilitation during which patients receive feedback in real time from their brain activity measured with ElectroEncephaloGraphy (EEG). The investigators hypothesize that the feedback training allows to internally stimulate brain motor networks in order to promote functional recovery of the hand.
Detailed Description
This study will be carried out as an explorative study in order to investigate the benefits of mental imagery training of hand movements guided through Brain-Computer Interface (BCI) feedback after stroke. Stroke patients will be trained to mentally imagine the opening and closing of the hand (hereafter named MI, Motor Imagery). During the training, the patients will receive visual feedback in real time that reflects the neural activity related to motor processes. The NeuroFeedback (NF) will be projected with minimal time delay to maximize the neural learning. This type of brain training with feedback is thought to have significant importance to stimulate the ability of the brain to reorganize and compensate for a damaged region. Each participant will go through the following data collection procedure (total of 33 measurement sessions per RP): Week 1-3: Clinical baseline evaluations, 1 time/week MRI measurements, 1 time/week during 2 weeks. Baseline EEG recordings, 1 time/week Week 4-7 MI-neurofeedback training 3 times/week Clinical intervention evaluation, 1 time/week Week 8-10 Same as week 1-3 Magnetic Resonance Imaging (MRI) measurements. The MRI exam will be carried out on a Siemens MAGNETOM Prisma 3T scanner (head-coil with 20 channels) at baseline and at final assessment session at Stockholm University Brain Imaging Centre. The MRI protocol comprises i) anatomical whole brain spin-echo T1 and T2 weighted sequences for description of lesion size and location ii) acquisition of T2*-weighted gradient echo EPI-BOLD images of the whole brain for assessment of resting state functional connectivity of sensorimotor networks (resting-state functional MRI (fMRI)), and iii) the same sequence as the previous with rest interleaved by a motor imagery paradigm further described below. Motor Imagery (MI) paradigm. The paradigm consists of instructing RP, by the use of a mirrored computer screen, to either i) rest his/her mind with eyes closed, ii) mentally imagine a hand movement (MI), or ii) execute a hand movement. The hand movements that are instructed are either to close the hand or to open the hand and extend the fingers. RP will perform several repetitions of each hand movement (MI and execution) in order to collect a statistical basis. Baseline EEG recording. During the baseline EEG recordings, RP will be seated in front a computer screen and perform the MI paradigm (described above). During these session, EEG, EOG, EMG, and accelerometer-data will be collected and are further described below. ElectroEncephaloGram (EEG), ElectroOculoGram (EOG), ElectroMyoGram (EMG) and accelerometer equipment. The EEG equipment consists of a 64-electrode scalp EEG acquisition system (Brain Products ActiCHamp). The 64 electrodes (active Ag/AgCl) will be distributed according to the extended 10-20 reference placement system. In addition to the EEG recording, 3 electrodes (passive Ag/AgCl, Brain Products) will be placed on each side of both eyes and on the earlob to measure eye-movements during the experiment (EOG). EMG electrodes (passive Ag/AgCl, Brain Products) will be placed over four muscles controlling the wrist and fingers according to a standardized protocol. Two accelerometer-sensors (Brain Products) will be placed on the hand and the index finger in order to record movement-related activity. EEG, EOG, EMG and accelerometer data analysis. The recorded data will be further analyzed offline in order to evaluate the characteristic features in the data that best describe MI of hand movements. This will be performed in Matlab and Labview combining custom-made scripts with already developed toolboxes (such as EEGLab, Chronux). Features to be evaluated will include the evoked activity, the time-frequency spectra, phase, correlation coefficients, coherency among other. When the feature that best describes MI has been identified different classifier and pattern recognition methods will be evaluated in extracting the information. Intelligent algorithms, Support Vector Machine (SVM), regularized linear regression, naïve Bayes classifiers among others will be evaluated and compared. These are commonly used methods in the field of neurotechnology and a prior comparison-study using neural data from invasive recordings shows the importance of choosing a well-adapted classifier for extracting information. MI-NeuroFeedback Training (NFT). EEG, EOG, EMG and accelerometer-data will be collected as described in the section "EEG, EMG and accelerometer equipment". RP will perform the MI paradigm without the execution of hand movements. Real-time feedback from recorded EEG-activity will be provided to RP during MI. The feedback consists of a virtual hand on a computer screen whose movements reflect the brain activity of RP related to MI. The recorded data will be further analyzed offline with the analytic tools that are described in previous section.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Hemiparesis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Motor Imagery BCI training
Arm Type
Experimental
Arm Description
Complete intervention with motor imagery BCI training. Patients recruited by physiotherapists who underwent baseline evaluations with clinical tests, fMRI and EEG measurements. Patients will after intervention perform clinical tests, fMRI, and EEG measurements to evaluate outcomes of intervention.
Intervention Type
Device
Intervention Name(s)
Motor imagery BCI training
Intervention Description
Motor Imagery (MI)-BCI training, 2-3 hours, 3 times/week for 4 weeks.
Primary Outcome Measure Information:
Title
Change of Fugl-Meyer Upper Extremity scale score (0-66 points)
Description
Arm and hand function
Time Frame
Up to 10 weeks
Title
Change of EEG alpha and beta activity
Description
Brain motor network activity reflected in BCI feedback
Time Frame
Up to 10 weeks
Title
Change of fMRI BOLD activity
Description
Brain motor network activity
Time Frame
Up to 10 weeks
Secondary Outcome Measure Information:
Title
Change of monofilament test score
Description
Two point discrimination and monofilament test for sensory function
Time Frame
Up to 10 weeks
Title
Change of box and block test score (0-150)
Description
Gross manual dexterity
Time Frame
Up to 10 weeks
Title
Change of JAMAR® digital Hand Dynamometer scores (0-90)
Description
Grip strength
Time Frame
Up to 10 weeks
Title
Change of visuomotor force-tracking task scores
Description
Quantification of timing and precision aspects of force grip modulation
Time Frame
Up to 10 weeks
Title
Change of stroke Impact Scale 16 scores (15-80 points)
Description
Activity limitations related to physical function
Time Frame
Up to 10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 6 months since first time stroke onset and with remaining hemiparesis in upper extremity; able to participate fully in the intervention, able to perform Functional Magnetic Resonance Imaging (fMRI); able to passively extend the wrist 15 degrees and extend fingers fully with a neutral position of the wrist. In addition, participants need to be able to voluntarily control the power of their grip when requested according to the Visuomotor force tracking method and/or according to the clinical assessment of a therapist (while holding the patient´s hand). According to the Fugl- Meyer Upper Extremity (UE) scale participants should accomplish <14 points on the hand subscale and <2 points in finger flexion and extension (C) in addition to < 47 points on the total motor score (equivalent to moderate disability in the upper extremity. Exclusion Criteria: other neurological or musculoskeletal disease/injury, or contagious disease. If the research person is regularly treated with botulinum toxin in the upper extremity, 3 weeks should have passed before the first baseline assessment. current or history of epilepsy, severe hearing or visual impairments, metal implants in the brain/skull cochlear implants, any implanted neurostimulator, cardiac pacemaker or cardiac implants of metal, infusion device, any other neurological disorder, pregnancy, current or history of severe psychiatric disorder with need for pharmacological treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elaine Astrand, PhD
Phone
21-103125
Ext
+46
Email
elaine.astrand@mdh.se
First Name & Middle Initial & Last Name or Official Title & Degree
Susanne Palmcrantz, PhD
Phone
709567653
Ext
+46
Email
susanne.palmcrantz@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elaine Astrand, PhD
Organizational Affiliation
Mälardalen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stockholn University Brain Imaging Centre
City
Stockholm
ZIP/Postal Code
11418
Country
Sweden
Individual Site Status
Active, not recruiting
Facility Name
Department of rehabilitation medicine at Danderyd University
City
Stockholm
ZIP/Postal Code
18288
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susanne Palmcrantz, PhD
Phone
709567653
Ext
+46
Email
susanne.palmcrantz@ki.se
Facility Name
Sweden Mälardalen University
City
Västerås
ZIP/Postal Code
72123
Country
Sweden
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Motor Imagery BCI Rehabilitation After Stroke

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