None listed
Conditions
Interventions
Medical Device : test group A : optimized tDCS
test group B : tDCS
control group : Sham tDCS
Sponsors
The Catholic University of Korea, St. Vincent's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Stroke patient confirmed by brain imaging 2. Subacute and chronic patients who have had a stroke for more than 4 weeks 3. A person who can listen to and understand the explanation of this clinical trial and who voluntarily decides to participate and agrees in writing to comply with the precautions. 4. Those who do not fall under the exclusion criteria of this study
Exclusion criteria
Exclusion criteria: 1. A person who cannot perform tDCS due to scalp disease 2. A person who has metal (clip, coil, metabolic foreign body) in the brain. 3. A person with a pacemaker or a wow implant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer assessment | — |
Secondary
| Measure | Time frame |
|---|---|
| Fugl-Meyer assessment | — |
Countries
Korea, Republic of
Contacts
Public ContactYunjeong Lee
The Catholic University of Korea, St. Vincent's Hospital
Outcome results
None listed