The effect of trunk restriction training using an upper limb rehabilitation robot (Rebless planar) in stroke patients
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0008583
- Lead Sponsor
- Asan Medical Center
- Brief Summary
A clinical study was conducted to find out the effectiveness of trunk restriction training using the upper limb rehabilitation robot Rebelless planner® developed by H Robotics Co., Ltd. for stroke patients. A total of 30 subjects were planned, and each of 15 subjects was randomly assigned to the test group and the control group. The test group conducted upper limb rehabilitation training using a Rebelless planar? for 30 minutes with limited trunk, and the control group conducted upper limb rehabilitation training using a Rebelless planar? for 30 minutes without trunk restriction. After the 10th training, the Elbow Flexion and Wrist Extension angles of the test group increased more than the control group, and there were statistically significant differences between and between groups. It has been confirmed that the robot-assisted static exercise device, Rebelless Planar?, developed by H Robotics Co., Ltd., can have a positive effect on the reconstruction of muscles and the recovery of joint movements in patients requiring upper limb rehabilitation treatment due to stroke.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 30
1. Patients aged 19 years and older with stroke
2. Patients with unilateral paralysis(Hemiparesis)
3. Anyone with a Modified Ashworth Scale of 3 or less on the upper arm.
4. Anyone with a score of 2(Poor) or more on the Elbow Manual Muscle Test
1. Patient with severe impairment of communication due to cognitive impairment or aphasia.
2. Patient with serious medical conditions that may affect training.
3. Patient with neurological or musculoskeletal disorders that may affect training.
4. Inability to perform other upper limb rehabilitation training
5. Patient participating in a medical device study with the same indication(stroke) as this study, within 30 days after the end of the visit.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fugl-Meyer Assessment of the Upper Extremity (FMA-UE)
- Secondary Outcome Measures
Name Time Method Motricity Index (MI)_Upper;Modified Barthel Index (MBI);Range of Motion (ROM);Modified Ashworth Scale (MAS)