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Effects of a brain-computer interface exoskeleton robot on neurological reconstruction function in patients with spinal cord injury

Effects of a brain-computer interface exoskeleton robot on neurological reconstruction function in patients with spinal cord injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101223
Enrollment
Unknown
Registered
2025-04-22
Start date
2024-10-21
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Spinal cord injury

Interventions

Conventional treatment + brain-computer interface exoskeleton robot treatment group:On the basis of conventional rehabilitation treatment, brain-computer interface exoskeleton robot therapy is carried
Conventional treatment group:Conventional rehabilitation treatment, 60min a day, once a day, 5 times a week, continuous intervention for 6 weeks.

Sponsors

Affiliated Hospital of Shandong University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Met the diagnostic criteria for incomplete spinal cord injury by MRI or CT examination and rehabilitation assessment; (2) Patients with spinal cord injury caused by trauma for 3 months or more; (3) Partial motor function of the lower limbs is preserved; (4) Agde 18-75 years old; (5) No aphasia, agnosia, apraxia or other functional impairments that would prevent participation in the study; (6) No history of chronic diseases such as hypertension and heart disease; (7) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those who are unconscious, have a score <of 21 on the Mini-Mental State Examination (MMSE) scale, and have sensory aphasia or mental disorders, and cannot cooperate with treatment and evaluation; (2) Patients using any type of implanted electronic device, including pacemakers or similar assistive devices, electronic infusion pumps, and implanted stimulators; (3) skin ulcers in the irritated area; (4) Accompanied by abnormal function of important organs such as heart and lungs; (5) Previous combined use of brain-computer interface exoskeleton robot training + conventional treatment; (6) Patients with peripheral arterial and venous diseases: such as peripheral atherosclerosis, venous thrombosis, etc.

Design outcomes

Primary

MeasureTime frame
Walking Index for Spinal Cord Injury II;

Secondary

MeasureTime frame
Muscle thickness;A portable digital muscle strength tester measures the patient's muscle strength;Surface electromyography signaling;Muscle circumference;Assessment of activities of daily living;Resting and task-state EEG signals;arterial diameter;degree of muscle edema;

Countries

China

Contacts

Public ContactYang Zhang

Affiliated Hospital of Shandong University of Traditional Chinese Medicine

zhangyang982003@163.com+86 135 8903 8230

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026