None listed
Conditions
Interventions
Others : The inertial measurement unit (IMU) sensors are attached to the patients' sternum, shoulder, upper arm, lower arm, and hand muscles for collecting kinematic data. The evaluation is performed
Sponsors
National Rehabilitation Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients with stroke due to one-sided infarction or hemorrhagic 2) One-sided upper extremity dysfunction 3) A person who has understood the description of the experiment and has agreed to participate by himself
Exclusion criteria
Exclusion criteria: 1)having neurological pain or muscle atrophy before the stroke 2) Severe spasticity (more than 3 grade in Modified Ashworth Scale) 3) Unable to communicate such as aphasia 4) Having a skin-related disease or open wounded. 5) Fracture or osteoporosis. 6) Diseases or injuries related soft tissue or amputation in upper limb. 7) Unable to maintain seating position for 10 minutes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| THe kinematic data from the SMART Board System | — |
Secondary
| Measure | Time frame |
|---|---|
| Fugl-Meyer Assessment Upper extremity ;Action research arm test ;Active Range of motion(Shoulder flexion/extension, abduction/adduction, internal/external rotation, Elbow flexion/extension);Modified Ashworth Scale (Elbow flexion/extension);Brunnstrom stage of upper extremity;Stroke Impact Scale 3.0 | — |
Countries
Korea, Republic of
Contacts
Public ContactYeajin Ham
National Rehabilitation Center
Outcome results
None listed