Spinal Cord Injury
Conditions
Interventions
Healthy control group:EEG assessment of "sufficiency" and "defecation" movements
Stroke group:EEG assessment of "sufficiency" and "defecation" movements
Spinal Cord Injury Group:EEG assessment of "sufficiency" and "defecation" movements
Sponsors
Huashan Hospital, Fudan University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Age 18-75 years, gender-neutral; 2.Patients with spinal cord injury experiencing impaired or absent voluntary bowel and bladder control. 3.Patients with spinal cord injury above the sacral region are classified by the American Spinal Injury Association (ASIA) into grades A, B, C, and D, regardless of the time since the onset of the injury. 4.No significant cognitive impairment (MMSE illiteracy > 17 points, primary education > 20 points, junior high school and above > 24 points). 5.Signing the Informed Consent Form; Stroke group: 6.In accordance with the diagnostic criteria outlined in the "Key Points for the Diagnosis of Major Cerebrovascular Diseases in China 2019," the following criteria must be met: 1. Acute onset; 2. Focal neurological deficits or global neurological deficits; 3. Confirmation of cerebral infarction or hemorrhage through CT or MRI. 7.The course of stroke onset is greater than or equal to two weeks; 8.No history of central or peripheral nervous system disorders; 9. Age 18-75 years old, gender is not limited; 10. No obvious cognitive dysfunction (MMSE illiteracy> 17 points, 20 points for primary school >, and 24 points > junior high school and above); 11. Informed consent and voluntary participation in this study. Healthy control group: 1) No history of central and peripheral nervous system disease is required; 2) Age greater than 18-75 years old, gender is not limited; 3) No obvious cognitive impairment (MMSE illiteracy> 17 points, 20 points in primary school >, junior high school and above upper >24 points); 4) Those who have informed consent and are willing to participate in this study
Exclusion criteria
Exclusion criteria: 1.Individuals with scalp and skin surface lesions; 2.Individuals with metallic implants in the cranial cavity; 3.Hemispatial neglect or hemianopia; 4.Pregnant and lactating women; 5.Unstable angina, coronary stent implantation within the past six months, and patients with cardiac pacemaker implantation; 6.The researchers believe that individuals with other conditions deemed unsuitable for participation in this clinical trial; 7.Individuals who have participated in or are currently participating in other clinical trials within the three months prior to signing the informed consent form;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Event-Related Desynchronization (ERD);Event-Related Synchronization (ERS); | — |
Countries
China
Contacts
Public ContactJie Jia
Huashan Hospital, Fudan University
Outcome results
None listed