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Effects of brain-computer interface technology based on motor imagery on motor function and neural regeneration mechanism of patients with spinal cord injury

Effects of brain-computer interface technology based on motor imagery on motor function and neural regeneration mechanism of patients with spinal cord injury

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056740
Enrollment
Unknown
Registered
2022-02-12
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

Spinal cord injury

Interventions

BCI-Treadmill:BCI-Treadmill
Motomed:Motomed

Sponsors

Jiangsu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Stable vital signs, suitable for exercise testing; 2. Age: 18-75 years old, no gender restrictions; 3. Trauma that conforms to the International Diagnostic Criteria for Neurological Classification of Spinal Cord Injury revised by the American Spinal Cord Injury Association in 2019 and diagnosed by CT or MRI Spinal cord injury (including surgical trauma); 4. The motor level of spinal nerve injury is T2-T12, AIS spinal cord injury grades A and B; 5. The course of disease is more than 3 months, less than 12 months (the spinal shock period has passed); 6. Good cognitive function, can understand and actively participate in the training program, agree and sign the informed consent form for this clinical study.

Exclusion criteria

Exclusion criteria: 1. Comorbidities that limit the patient's exercise capacity include deep vein thrombosis in the lower extremities, diabetes, hypertension, coronary heart disease, severe osteoporosis, and female pregnancy; 2. Patients with severe anxiety and depression (SAS>50 points, SDS>70 points); 3. The range of motion of the lower limbs is limited or the flexion and extension of the lower limbs are restricted due to other factors; 4. Improved Ashworth of lower extremity muscle tone > grade 2; 5. Diseases that are not suitable for wearing the device, such as scalp and skull injury, skin injury or infection of the lower extremities, which make the device unable to be worn; 6. The investigator judges that the patient has poor compliance or does not understand the test, and cannot complete the study as required; 7. Participated in other clinical trials of drugs or medical devices during the same period; 8. Other conditions judged by the investigator to be unsuitable for inclusion and unable to tolerate rehabilitation training.

Design outcomes

Secondary

MeasureTime frame
Extremity surface electromyography assessment;Sensory score;

Primary

MeasureTime frame
Lower extremity motor score;Transcranial Magnetic Stimulation Motor Evoked Potentials;

Countries

China

Contacts

Public ContactYongqiang Li

Jiangsu Provincial People's Hospital

liyongqiang_1980@163.com+86 13327829260

Outcome results

None listed

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