None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged 20 years or older Patients diagnosed with stroke based on clinical or neuroimaging findings Patients in the subacute phase, defined as 14 to 180 days after stroke onset Patients with a baseline Fugl-Meyer Assessment–Upper Extremity (FMA-UE) score of 50 or lower Patients who were able to perform activities of daily living independently before study participation Patients who, in the investigator’s judgment, are able to understand instructions and perform the required tasks
Exclusion criteria
Exclusion criteria: Patients with other neurological or musculoskeletal disorders that may affect upper limb function Patients with severe spasticity, defined as Modified Ashworth Scale (MAS) > 3 Patients with epilepsy, cardiovascular instability, or serious medical conditions Patients who have difficulty participating in training due to severe visual field defects or severe unilateral neglect Patients whom the investigator considers inappropriate for study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| FMA-UE: Fugl-Meyer Assessment–Upper Extremity | — |
Secondary
| Measure | Time frame |
|---|---|
| ARAT: Action Research Arm Test;BBT: Box and Block Test;K-MBI: Korean Modified Barthel Index;MFT: Manual Function Test;MAS: Modified Ashworth Scale;BRS: Brunnstrom Recovery Stage;VAS: Visual Analogue Scale;Adverse Events and Safety Assessment;Compliance and Session Log Assessment | — |
Countries
Korea, Republic of
Contacts
Kyung Hee University Hospital at Gangdong