None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Adults aged 19 to 80 years - Those diagnosed with early (first-onset) supratentorial stroke (ischemic/hemorrhagic) - Patients with onset within 3 months at the time of screening - Those with unilateral upper limb paralysis due to stroke (shoulder, elbow, wrist, finger MMT Fair or lower) - Those who can understand and follow the investigator's instructions (MMSE > 17) - Those who voluntarily decided to participate in this clinical trial and gave written consent to the research subject explanation and consent form
Exclusion criteria
Exclusion criteria: - Those with recurrent stroke - Those with communication limitations due to aphasia, etc. - Those with skin lesions in the area to be stimulated - Those with metal objects inserted into the cranial cavity (Coil, pacemaker, etc.) However, those with metal objects that are not affected by magnetic fields are eligible - Those currently participating in other clinical trials - Those diagnosed with cancer - Those who have difficulty receiving regular treatment for paralyzed upper limbs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| fugl-meyer assessement | — |
Secondary
| Measure | Time frame |
|---|---|
| box and block test | — |
Countries
Korea, Republic of
Contacts
Chungnam National University Hospital