Study of Neurophysiological Markers of Motor Recovery in Post-stroke Patients.

The study involved 40 participants, half of whom had suffered a stroke with hemiparesis and the other half a control group of healthy volunteers. During the experimental session, the participants have to perform a motor task involving reaction speed. A box with two buttons (right and left) is placed in front of the participant. The participant's hands are placed in the box under the buttons. The experimental task is to press one of the two buttons by extending the fingers in response to a visual stimulus - lamps above the buttons. If the degree of damage to the motor function of one of the participant's limbs does not allow a full button to be pressed, the participants is asked to form an intention for this movement and try to perform it. At the same time, one of the buttons has been designated as a 'target' for the patient, and it is in response to its highlighting that a movement is to be performed. The second button is 'non-target'. Its highlighting should be ignored. Throughout the session, each of the buttons was designated as a target several times.

Throughout the session, the electroencephalogram (EEG) signal was recorded in 17 electrodes placed on the scalp according to the international "10-10" registration system. The recording was performed with a medical electroencephalograph NVX-36 ("Medical Computer Systems", Zelenograd, Russia). Electromyographic (EMG) activity of the flexor digitorum superficialis muscles of both hands was also recorded using surface electrodes. The EMG is recorded with the same amplifier as the EEG signal (NVX-36). The participant takes part in the test within 2 weeks. There were two sessions (at the beginning of rehabilitation and before discharge). Each session lasts a maximum of one hour.

Before the study, the participants' motor activity was tested using the Action Research Arm Test (ARAT). The EEG data were analysed for markers such as movement-related potentials and movement-related desynchronisation of alpha and beta rhythms. Some participants were also invited to take part in an additional study using transcranial magnetic stimulation to assess the integrity of corticospinal connections.

For Healthy Volunteers:

Inclusion criteria

• Availability of signed written informed consent. 3. Absence of somatic and psychiatric diseases (more details in the exclusion criteria) 4. Ability and willingness to comply with the requirements of this protocol.

Exclusion criteria

• The presence of superficial injury of head (S00-S09 International Classification of Diseases 10 (ICD-10).
• The presence of mental, behavioural disorders (F00-F99 ICD-10).
• Drug addiction in the past or at the moment.
• The presence of diseases of the nervous system (G00-G99 ICD-10).
• . History of intracranial injury (S06 ICD-10) or stroke (I64 ICD-10).
• The presence of somatoform disorders (F45 ICD-10).
• Any conditions that, in the opinion of the Investigator, meet the exclusion criteria
• Presence of electrical and/or metallic implants or stimulants in the body (eg, implanted deep brain stimulation devices, pacemakers, hearing aids and cochlear implants, intracranial metal implants).
• Pregnancy
• The presence of malignant neoplasms (C00-C97 ICD-10).

For stroke patients:

Inclusion criteria

• Signed written informed consent.
• People after the first acute cerebrovascular accident (CVA), early or late rehabilitation period.
• The level of severity of paresis of the upper limb from 3 points to 0 (according to a 6-point neurological scale)
• The minimum visual acuity is not lower than 0.2 on the Sivtsev scale.
• The ability and willingness of the patient to comply with the requirements of this protocol.
• Expressed patient motivation for rehabilitation.

Exclusion criteria

• Severe cognitive impairment (<10 points according to the Montreal Cognitive Assessment Scale).
• Hamilton score above 18 points.
• The score on the Rankin scale is above 4 points.
• Associated neurological disorders that cause decreased muscle strength or increased muscle tone in the upper limbs (eg, cerebral palsy, brain damage from trauma) or stiffness (eg, Parkinson's disease, contracture).
• Late stages of arthritis or clinically significant limitation of passive range of motion in any of the joints studied in the study due to other reasons.
• The absence of a part of the upper limb due to amputation caused by various reasons.
• Any medical condition, including mental illness or epilepsy, that may affect the interpretation of study results, study conduct, or patient safety.
• Alcohol abuse, medical marijuana use, or recreational drug use in the 12 months prior to Visit 1.
• Use of experimental drugs or medical devices within 30 days prior to Visit 1.
• Lack of ability to follow study procedures, in the opinion of the investigator.
• The severity of the patient's condition according to the neurological or somatic status, which does not allow full rehabilitation.
• Severe visual disturbances, minimal visual acuity less than 0.2 Sivtsev visual acuity table.
• Unstable angina and/or heart attack within the previous month
• Repeated stroke.
• Severe unilateral spatial neglect.
• Uncontrolled arterial hypertension
• Ataxia
• All forms of epilepsy