None listed
Conditions
Interventions
Medical Device : - Experimental group: 15 patients receive 30 minutes of upper limb rehabilitation training using the U30R.
- Control group: 15 patients receive 30 minutes of conventional upper limb r
Sponsors
Asan Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Stroke patients aged 19 years or older 2. Patients with hemiparesis 3. Patients with upper limb spasticity graded less than 3 on the Modified Ashworth Scale (MAS) 4. Patients with a Brunnstrom recovery stage of 4 or higher
Exclusion criteria
Exclusion criteria: 1. Patients taller than 190 cm or shorter than 150 cm 2. Patients weighing more than 135 kg 3. Patients whose seated shoulder height (from the seat to the shoulder) is less than 53 cm 4. Patients with severe communication difficulties due to cognitive impairment or aphasia 5. Patients with serious internal medical conditions that may affect training 6. Patients with neurological or musculoskeletal disorders that may interfere with training 7. Patients who are otherwise unable to perform upper limb rehabilitation training 8. Patients who have participated in another medical device study for the same indication (stroke) within 30 days of the final visit of that study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer Assessment of the Upper Extremity (FMA-UE) | — |
Secondary
| Measure | Time frame |
|---|---|
| Modified Barthel Index (MBI);Modified Ashworth Scale (MAS);Range of Motion (ROM);Motricity Index (MI)_Upper | — |
Countries
Korea, Republic of
Contacts
Public ContactMin Ho Chun
Asan Medical Center
Outcome results
None listed