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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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07081308
Acronym
BRAIN-WALK
Enrollment
30
Registered
2025-07-23
Start date
2024-10-05
Completion date
2026-12-31
Last updated
2025-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Brain-computer interface, Near infrared spectroscopy, gait recovery, stroke rehabilitation, Neurobiofeedback

Brief summary

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. STUDY QUESTIONS The main questions the study aims to answer are: Whether 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? HOW THE STUDY WORKS The investigators compare two groups - one using the new system, another group receiving standard rehabilitation therapy. Up to 15 patients will try the new system: 10 sessions, each lasting 12 minutes (about 2 weeks, Monday-Friday). WHAT HAPPENS DURING TREATMENT? The equipment includes: Brain 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. What the patient will do: Sit 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.

Detailed description

INTERVENTION NIRS-BCI-Korvit System Components: NIRScout hardware-software complex (16 light sources, 8 detectors); Software for brain activity classification; Korvit pneumoorthesis for plantar support load reproduction; 22-inch monitor for task demonstration Training Procedure: Patient seated with lower limbs fixed in pneumatic orthoses; Task: kinesthetically imagine walking or relax; Feedback: visual (color change on screen) and tactile (support load through orthosis). Training structure: 16 blocks alternating walking imagination and relaxation/ ASSESSMENT Motor Function: * Fugl-Meyer Scale for Lower Extremity (maximum 34 points, clinically significant improvement ≥6 points); * 10-meter Walk Test (clinically significant improvement ≥0.16 m/s); * Timed Up and Go Test (clinically significant improvement ≥3 seconds). Cognitive Functions and Emotional State: * Addenbrooke's Cognitive Examination III (ACE III); * Hospital Anxiety and Depression Scale (HADS). EXPECTED OUTCOMES. The study aims to confirm the effectiveness of NIRS-BCI combined with plantar support load simulator for: * Gait restoration; * Cognitive function improvement; * Emotional state normalization in post-stroke patients SAFETY The procedure is safe and poses no health risks. Possible minor fatigue after sessions. The study can be discontinued at any stage upon patient request or if adverse effects occur. INNOVATION This research represents a novel approach combining non-invasive brain-computer interface technology with proprioceptive feedback systems for comprehensive post-stroke rehabilitation, addressing both motor and cognitive recovery simultaneously

Interventions

DEVICENIRS-BCI-pneumoorthesis

Patients recieve 10 NIRS-BCI-pneumoorthesis trainings of 16 minutes each over 2 weeks. NIRS-BCI-pneumoorthesis Components: NIRScout hardware-software complex (16 light sources, 8 detectors); Software for brain activity classification; Korvit system for plantar support load reproduction; 22-inch monitor for task demonstration. Training Procedure: Patient seated with lower limbs fixed in pneumatic orthoses; Task: kinesthetically imagine walking or relax; Feedback: visual (color change on screen) and tactile (support load through orthosis). Training structure: 16 blocks alternating walking imagination and relaxation

Sponsors

Pirogov Russian National Research Medical University
CollaboratorOTHER
Institute of Higher Nervous Activity and Neurophysiology of RAS
CollaboratorUNKNOWN
Research Center of Neurology, Russia
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-80 years * Primary or recurrent supratentorial ischemic stroke * Stroke onset 7 days to 24 months * Moderate to mild post-stroke lower limb motor impairments * Clinical stability * Voluntary participation and signing of informed consent

Exclusion criteria

* Severe cognitive impairments preventing instruction compliance * Sensory or severe motor aphasia * Severe visual impairments * Lower limb contractures * Inability to maintain sitting position

Design outcomes

Primary

MeasureTime frameDescription
Walking speed change as assessed by the 10-Meter Walk TestFrom enrollment to the end of treatment at 2 weeksBefore and after treatment course
Lower extremity functional improvement as assessed by the Fugl-Meyer AssessmentFrom enrollment to the end of treatment at 2 weeksBefore and after treatment course

Secondary

MeasureTime frameDescription
Lower extremity functional improvement as assessed by the Timed Up and GO testFrom enrollment to the end of treatment at 2 weeksBefore and after treatment course
Cognitive function improvement as assessed by the Addenbrooke's cognitive examination - IIIFrom enrollment to the end of treatment at 2 weeksBefore and after treatment course

Other

MeasureTime frameDescription
Emotional improvement as assessed by the Hospital Anxiety and Depression ScaleFrom enrollment to the end of treatment at 2 weeksBefore and after treatment course

Countries

Russia

Contacts

Primary ContactRoman Kh Lyukmanov, PhD
xarisovich@gmail.com+74953747776
Backup ContactOlesya Al Mokienko, PhD
o.mokienko@ihna.ru+74953747776

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026