spinal cord injury
Conditions
Interventions
control group:The control group underwent the treatment of functional electrical stimulation, physical therapy: professional physical therapists performed passive activity training, auxiliary training
experimental group:Experimental group of brain-computer interface-functional electrical stimulation system treatment, physical therapy: by professional physical therapist according to the specific pat
Sponsors
China Rehabilitation Research Center Beijing Boai Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1: Compliance with the International Standard for neurological Classification of Spinal Cord Injury , revised by the American Spinal Injury Committee, with clinical manifestations of spinal cord injury, and imaging support such as CT or MRI; 2: In accordance with the American Spinal cord Injury Association (American Spinal Injury Association, ASIA), the neurological and functional grade of spinal cord injury is grade A SCI, and the plane of injury is C5; 3: Age was 18 – 65 years old 4: The disease duration was more than 6 months 5: Good vision or corrected visual acuity 6: Good mental state, conscious, have a certain cognitive ability to understand the instructions 7: Volunteer to participate in this study and sign the informed consent form 8: After the assessment of the Kinaesthesia-Visual Imagery Questionnaire (the kinesthetic and visualimagery questionnaire, KVIQ), the subjects had some motor imagery ability
Exclusion criteria
Exclusion criteria: 1: Hearing impairment, unable to communicate; extreme restlessness or moderate to severe cognitive impairment 2: Hearing impairment, unable to communicate; extreme restlessness or moderate to severe cognitive impairment 3: Visual defect, unilateral neglect and so on can not see the computer screen 4: Serious complications, cardiopulmonary diseases, uncontrollable hypertension, serious body deformity, multiple organ damage or important organ insufficiency, serious spasm, etc 5: Patients with brain trauma, wound recovery period after craniocerebral surgery, unable to place electrodes or may be caused by brain electrode placement; skull defect or metal skull repair; metal such as cardiac pacemaker in the inner body; 6: Patients without healed upper limb or hand fractures 7: Unwilling to sign the informed consent form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional near-infrared spectroscopy;GRASSP Scale scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Muscle bone ultrasound;Muscle tone tester;protractor;Spinal cord injury independence assessment scale; | — |
Countries
China
Contacts
Public ContactFubiao Huang
China Rehabilitation Research Center
Outcome results
None listed