Spinal cord injury
Conditions
Interventions
SCI group:No intervention
Sponsors
China Rehabilitation Research Center
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patient (1) It meets the diagnostic criteria and is a traumatic or non-progressive medical cause; (2) between the ages of 18 and 75; (3) clear awareness, good understanding, patients can understand and cooperate with treatment and evaluation; (4) Able to remain seated for =30 minutes; (5) No visual impairment, international standard eye chart check binocular vision or corrected vision =1.0; (6) have not participated in other clinical studies in the past 1 month; (7) Patients or their family members agree to participate in this experiment and sign informed consent. Healthy person (1) Good health, no circulatory system, nervous system, mental and metabolic disorders and other diseases; (2) between the ages of 18 and 75; (3) clear awareness, good understanding, patients can understand and cooperate with treatment and evaluation; (4) Able to remain seated for =30 minutes; (5) No visual impairment, international standard eye chart check binocular vision or corrected vision =1.0; (6) Having full capacity for civil conduct; (7) The subject agrees to participate in the experiment and signs the informed consent.
Exclusion criteria
Exclusion criteria: SCI: (1) previous history of stroke, brain trauma and other organic brain diseases; (2) Serious complications, cardiopulmonary diseases, uncontrolled hypertension, severe physical deformities, multiple organ injuries or major organ dysfunction, severe spasms, etc.; (3) Patients with severe cognitive impairment, scores <17 on the Montreal Cognitive Assessment Scale, hearing impairment, visual impairment, aphasia and other difficulties in cooperating with training; (4) There is a history of epilepsy or mental illness; (5) Drug or chronic alcohol addiction; (6) Intracranial metal objects, intracranial tumors, intracranial infections, or the presence of any clinically significant or unstable medical disease; (7) Infection; (8) There are contraindications for the use of fNIRS equipment (head defects or abnormalities, etc.). Healthy person (1) Previous history of atrial fibrillation, heart surgery or betaloc; (2) a history of mental illness, drug abuse, or drug dependence; (3) pregnancy test positive or breastfeeding women; (4) Excessive consumption (more than 8 cups per day, 250mL per cup) of tea, coffee or caffeinated beverages in the past 6 months; Had consumed any beverage or food containing caffeine (such as coffee, strong tea, chocolate, etc.) within 48 hours before the trial began; (5) Drug or chronic alcohol addiction; (6) Intracranial metal objects, intracranial tumors, intracranial infections, or the presence of any clinically significant or unstable medical disease; (7) Infection; (8) Defective or abnormal head, unable to collect fNIRS data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Montreal cognitive assessment; | — |
Secondary
| Measure | Time frame |
|---|---|
| Mini-Mental State Examination;digital span tests;2-back tasks;symbol digit modalities test;Stroop color word test;Rey-Osterrieth complex figure test;Digital flash task;Self-rating Depression Scale;Self-rating Anxiety Scale;MOS Sleep Scale;modified Barthel index; fNIRS relevant data ; | — |
Countries
China
Contacts
Public ContactFubiao Huang
China Rehabilitation Research Center
Outcome results
None listed