Stroke
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1)patients who agree to participate in this study and provide their informed consent; (2)since after stroke within 1 weeks; (3)stroke type is only intracranial hemorrhage or ischemic stroke; (4)inpatients; (5)Brunnstrom Recovery stage is II, III, IV, V; (6)stable general condition
Exclusion criteria
Exclusion criteria: (1)severe sensory disturbance or severe ataxia or severe higher brain dysfunction or severe dementia; (2)patients whose impairment severities changed during the study period; (3)contraindicated for the electrical stimulation (e.g. patients with a medical implant or implantable medical electrical equipment such as a cardiac pacemaker)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer Assessment(FMA) | — |
Secondary
| Measure | Time frame |
|---|---|
| Action research arm test(ARAT), active range of motion(AROM), Motor activity log(MAL), Modified Ashworth scale(MAS), Adverse event | — |
Countries
Japan
Contacts
Nippon Medical School Chiba Hokusoh Hospital Dept. of Rehabilitation