None listed
Conditions
Interventions
Medical Device : This study is randomly assigned to a control group performing conventional central nervous system rehabilitation and robotic rehabilitation of the lower extremities, and an experiment
Sponsors
Wonkwang University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ? Patients diagnosed with cerebral hemorrhage or cerebral infarction through computed tomography or magnetic resonance imaging ? Patients within 1 week to 6 months of onset due to initial stroke (cerebral infarction + cerebral hemorrhage) ? Men and women over 19 years of age ? Patients who agreed to participate in the study after explanation about the study ? Patients with cognitive function that can safely and accurately perform lower limb robot rehabilitation treatment ? Patients with severe hemiplegia whose strength on the hemiplegic side is grade 2 or higher and less than grade 4 in the manual muscle strength test
Exclusion criteria
Exclusion criteria: ? Those who cannot complete clinical research due to worsening of underlying disease ? Patients who disagree with the study ? When the weight exceeds 135kg ? Insufficient range of motion or pain to perform the lower limb robot rehabilitation treatment ? Patients who are concerned about a fall or fracture during robot rehabilitation due to severe osteoporosis ? Patients with a history of seizure or high risk of seizure ? Patients contraindicated in electroacupuncture treatment (in-body electrical devices such as pacemakers, blood coagulation disorders, immunosuppressed patients, skin disease patients)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Manual muscle strength test, Range of motion test, Functional Ambulation Categories, Fugl-Meyer Assessment | — |
Secondary
| Measure | Time frame |
|---|---|
| Diffusion tensor imaging | — |
Countries
Korea, Republic of
Contacts
Public ContactMin Cheol Joo
Wonkwang University Hospital
Outcome results
None listed