Actively Recruiting
StereoEEG Motor Neuronal Potentials Decoding
Led by Research Center of Neurology, Russia · Updated on 2025-07-24
30
Participants Needed
1
Research Sites
133 weeks
Total Duration
On this page
Sponsors
R
Research Center of Neurology, Russia
Lead Sponsor
I
Institute of Higher Nervous Activity and Neurophysiology of RAS
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goals of this study are (1) to evaluate the rate of stereoEEG brain-computer interface (BCI) classification accuracy and (2) to collect the dataset of neuronal signals recorded from stereoEEG electrodes during motor performance, motor imagery or brain-computer interface control. The study enrolls hospitalised patients suffering from resistant epilepsy with already implanted intracranial stereoEEG electrodes for medical reasons (i.e. for preoperative localization of the epileptogenic foci). The number and location of electrodes are determined solely for the clinical purposes of stereoEEG monitoring and are not related to the protocol of the current study. After obtaining informed consent to participate in the study, each patient will participate in one experimental session lasting no more than 60 minutes, recording brain signals associated with hand movement, motor imagery, and BCI control. All tasks and instructions presented during the study session are not pro-epileptogenic and cannot provoke an epileptic attack. The experiments will take place in the patient's room, without interruption of observation by the department's medical staff. The data recorded in this study will be used to improve or develop new algorithms for decoding motor signals from deep brain structures for their potential use in invasive BCIs.
CONDITIONS
Official Title
StereoEEG Motor Neuronal Potentials Decoding
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female patients who have had stereoEEG electrodes implanted for medical reasons
- Voluntary informed consent to participate in the study
- Age from 18 to 70 years
You will not qualify if you...
- Patient refusal to participate in the study
- Cognitive impairment that prevents following the study instructions
- Severe visual impairment that does not allow viewing visual instructions on a computer screen
- Upper limb paresis or other motor disorders
- Pain in the hand of any etiology
- Any acute diseases, exacerbation of chronic diseases, acute life-threatening conditions
- Occurrence of an epileptic attack during the experiment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Research center of neurology, Department of neurorehabilitation and physiotherapy
Moscow, Russia, 125367
Actively Recruiting
Research Team
O
Olesya A Mokienko, MD PhD
CONTACT
R
Roman Kh Lyukmanov, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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