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Biomedical and Engineering approaches form a key element to neurological rehabilitation of upper limbs. Brain Computer Interface (BCI) using Motor execution and Motor Imagery are known to aid motor recovery in stroke. The purpose of this study is to demonstrate that Noninvasive Sensorimotor Rhythm (SMR) based EEG based BCI using motor execution and Motor Imagery tasks can aid in rehabilitation of upper limb movements in chronic stroke.
The project aims to explore an SMR-based BCI system that can exploit the sensorimotor rhythm voluntary modulation to play a virtual game as neurofeedback using motor executory tasks and imagined hand movements by stroke patients, who suffer from upper limb disability.
Full description
Brain Computer Interface (BCI) using Motor execution and Motor Imagery are known to aid motor recovery in stroke. The purpose of this study is to demonstrate that Noninvasive Sensorimotor Rhythm (SMR) based EEG based BCI using motor execution and Motor Imagery tasks can aid in rehabilitation of upper limb movements in chronic stroke.
The project aims to explore an SMR-based BCI system that can exploit the sensorimotor rhythm voluntary modulation to play a virtual game as neurofeedback using motor executory tasks and imagined hand movements by stroke patients, who suffer from upper limb disability. Studies have shown that movement and motor imagery (MI) (i.e., the mental rehearsal of a movement without any activation of the muscles) induce similar EEG patterns over the motor cortex.
Movement execution, preparation and even observation are usually accompanied by a decrease in µ- and β-rhythm in the cortical area representing the involved body segment. Such a reduction is called event-related desynchronization (ERD).The increase in µ-rhythm, i.e. event-related synchronization (ERS), is observed in the regions of the brain representing body segments, which are not involved in the task.This study is a pilot study to examine the feasibility of a SMR based EEG BCI using motor task and motor imagery and involve a gaming feedback for same.
The first two days will be used for calibrating the BMI using commands in computer screen followed by further two days for testing the BMI and feedback control during gaming in computer to move the ball in the computer screen.
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Inclusion criteria
• age: 21-75 years
Subacute or chronic stroke; interval of at least 3 months and interval of at least 6 months from stroke to time of enrollment, respectively.
no cerebellar signs or bilateral motor deficit
Cognitive ability to consent, assimilate, and participate actively in the treatment protocol (Mini Mental State Examination score > 24 points, out of a total 30 indicating normal cognitive ability);
Modified Rankin scale scores 1-3 (Mild-Moderate functional disability post-stroke);
Modified Ashworth Scale of Spasticity score <= 3 (ranges from 0-4 with 4 reflecting maximum spasticity)
No epilepsy /usage of antiepileptic drug
◦ Subjects with Stroke will be included if they have:
unilateral impaired upper limb
Able to initiate hand movements like opening and closing fist and no joint contracture or severe spasticity in the affected upper limbs.
Sufficient sitting balance to participate in experimental activities.
No condition (e.g. severe arthritis, central pain) that would interfere with the administration of motor function tests.
English-language comprehension and cognitive ability sufficient to give informed consent (MMSE >=24) and to cooperate with the intervention.
Exclusion criteria
• Orthopedic conditions of either upper or lower extremity that would affect performance on the study
untreated depression that may affect motivation to participate in the study
vascular cognitive impairment interfering with comprehending the tasks
Individuals with stroke who have been diagnosed with cognitive or severe visual deficits, hemineglect, uncontrolled angina, or pregnancy
no psychiatric or neurological condition other than stroke
◦ Stroke will be excluded if they have:
Pregnancy (Self -reported)
Dementia (MMSE score less than 24)
Recurrence of stroke (Occurrence of new focal deficits reported by patient or detected by PI on examination during visits)
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10 participants in 1 patient group
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Central trial contact
Jose CL Vidal; Subasree R
Data sourced from clinicaltrials.gov
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