[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Research Center of Neurology, Russia\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":75},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100599193","brain-computer-interface-with-plantar-pneumoorthoses-for-post-stroke-rehabilitation-100599193",false,"NCT07081308","Brain-computer Interface With Plantar Pneumoorthoses for Post-stroke Rehabilitation","Clinical Evaluation of a Brain-computer Interface Integrated With Plantar Pneumoorthoses for Motor and Cognitive Rehabilitation in Stroke Survivors","BRAIN-WALK","Inclusion Criteria:\n\n* Age 18-80 years\n* Primary or recurrent supratentorial ischemic stroke\n* Stroke onset 7 days to 24 months\n* Moderate to mild post-stroke lower limb motor impairments\n* Clinical stability\n* Voluntary participation and signing of informed consent\n\nExclusion Criteria:\n\n* Severe cognitive impairments preventing instruction compliance\n* Sensory or severe motor aphasia\n* Severe visual impairments\n* Lower limb contractures\n* Inability to maintain sitting position","ALL","18 Years","80 Years",{"count":21,"type":22},30,"ESTIMATED","INTERVENTIONAL",[25],"NA","STUDY PURPOSE The investigators are testing a new rehabilitation system that helps stroke patients recover their ability to walk and think more clearly. This system, called brain-computer interface with plantar pneumorthoses, uses brain signals to control a special device that provides gentle pressure to the feet, similar to what you feel when walking. The goal is to help patients regain walking skills, improve memory and thinking, and feel better emotionally.\n\nSTUDY QUESTIONS\n\nThe main questions the study aims to answer are:\n\nWhether the investigated technology can improve walking in post-stroke patients? Whether the training to control the technology can improve cognitive function in post-stroke patients?\n\nHOW THE STUDY WORKS The investigators compare two groups - one using the new system, another group receiving standard rehabilitation therapy.\n\nUp to 15 patients will try the new system: 10 sessions, each lasting 12 minutes (about 2 weeks, Monday-Friday).\n\nWHAT HAPPENS DURING TREATMENT?\n\nThe equipment includes:\n\nBrain monitoring device: Safe infrared light sensors placed on the patient's head (like a cap) Computer software: Reads brain signals when the patient thinks about walking Foot device: Special pneumatic shoes that provide gentle pressure to the patient's feet Screen: Shows visual feedback during training.\n\nWhat the patient will do:\n\nSit comfortably in a chair with special shoes on their feet, Complete the task: imagine walking or relax when instructed, What the patient will experience: They will see colors change on the screen and feel gentle pressure on their feet.",[28],"Stroke",[30,31,32,33,34],"Brain-computer interface","Near infrared spectroscopy","gait recovery","stroke rehabilitation","Neurobiofeedback","RECRUITING","2025-07-23",{"date":38,"type":39},"2025-07-28","ACTUAL",{"date":41,"type":39},"2024-10-05",{"date":43,"type":22},"2026-12-31",{"name":45,"class":46},"Research Center of Neurology, Russia","OTHER_GOV",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":57,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":47},"100549353","stereoeeg-motor-neuronal-potentials-decoding-100549353","NCT06432907","StereoEEG Motor Neuronal Potentials Decoding","Decoding of Neuronal Potentials Associated With Motor Performance and Motor Imagery Obtained Using Intracranial stereoEEG Electrodes","Inclusion Criteria:\n\n* male and female patients who have had stereoEEG electrodes implanted for medical reasons;\n* voluntary informed consent to participate in the study;\n* age from 18 to 70 years.\n\nExclusion Criteria:\n\n* patient refusal to participate in the study;\n* cognitive impairment that prevents following the study instructions;\n* severe visual impairment that does not allow viewing visual instructions on a computer screen;\n* upper limb paresis or other motor disorders;\n* pain in the hand of any etiology;\n* any acute diseases, exacerbation of chronic diseases, acute life-threatening conditions;\n* occurrence of an epileptic attack during the experiment.","70 Years",{"count":21,"type":22},[25],"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.\n\nAfter 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.\n\nThe 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.",[60,61],"Drug Resistant Epilepsy","Brain-Computer Interfaces",[63,64,65,66],"Brain-Computer Interface","Motor Imagery","Motor Performance","Intracranial Electroencephalography","2025-07-21",{"date":69,"type":39},"2025-07-24",{"date":71,"type":39},"2024-06-06",{"date":73,"type":22},"2026-12-25",{"name":45,"class":46},""]