stroke
Conditions
Interventions
tDCS group:tDCS and routine treatment in rehabilitation department
Control group:Routine treatment in rehabilitation department
Sponsors
The First Hospital Affiliated to Army Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with first onset and confirmed cerebral hemorrhage and cerebral infarction by CT or MRI examination or patients with previous lacunar cerebral infarction without sequelae; 2. The age ranged from 18 to 70; 3. Course of disease: 2 weeks to 3 months; 4. Hemiplegia was found on one side of the limb, and the modified Ashworth Scale (MAS) grade of muscle tension on the affected side was = stage II on affected side; 6. Consent and sign informed consent for treatment.
Exclusion criteria
Exclusion criteria: 1. Vital signs are not stable; 2. The use of implanted electronic devices (such as pacemakers); 3. Those with metal implants such as stents; 4. Patients in critical condition or with important organ failure; 5. Pregnant women; 6. Electrode patch severe allergy, local skin injury or inflammation, stimulate the area of hyperalgesia; 7. Epilepsy or has been diagnosed with clear secondary epilepsy patients; 8. Tumor patients; 9. Patients with severe cognitive impairment (MMSE score < 24); 10. Past history of mental disorders and medication history causing symptoms of mental disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Montreal Cognitive Assessment, MOCA;Mini-mental State Examination,MMSE;Fugl-Meyer Assessment Scale, FMAS;Berg balance scale;Hamilton Depression Scale;Hamilton Anxiety Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Modified Barthel index scale; | — |
Countries
China
Contacts
Public ContactHongliang Liu
The First Hospital Affiliated to Army Medical University
Outcome results
None listed