Effect of robot–assist gait rehabilitation (experiment #2) after applying a gait rehabilitation robot according to gait level and preference (experiment #1) in acute or subacute stroke patients
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0008211
- Lead Sponsor
- Hallym University Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 55
Patients with the first stroke among patients diagnosed with stroke within 6 months and patients with a functional walking index of 2 or less at the time of evaluation are included.
Patients with other diseases that causes restrictions on gait function, with difficulties in cooperation due to severe delirium and cognitive impairment, and patients who are contraindications of applying robot therapy were excluded.
Contraindications are as follows:
- Wearing spinal orthosis
- Pressure sore
- Patients with severe joint construction and stiffness
- Severe orthostatic hypotension
- Craniotomy
- PEG, abdominal and thoracic surgery, etc.
- Unable to do weight-bearing exercises
- Severe neurogenic bladder/intestinal tract and Foley catheter
- Patients whose body size exceeds the robot's acceptable range
- Patients who need to maintain intravenous treatment during gait training
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional Ambulatory Category
- Secondary Outcome Measures
Name Time Method Berg balance scale;Manual Muscle Testing ;10 meter walk test;Hamilton Anxiety Rating Scale;Hamilton Depression Rating Scale