Comparison of Ambulatory and Functional Improvement by Morning Walk
Not Applicable
Completed
- Conditions
- Arthroplasty, Replacement, KneeRobotics
- Registration Number
- NCT03183856
- Lead Sponsor
- Ulsan University Hospital
- Brief Summary
The aim of this study is to determine the clinical efficacy and feasability of gait rehabilitation robot through approving functional improvement by an end-effector typed gait robot in patients underwent total knee arthroplasty.
- Detailed Description
pre-interventional evaluation; within 1 day of initiation of the intervention; 5 days after initiation of the intervention; 10 days after intervention after initiation of the intervention; 42 days after intervention start
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 9
Inclusion Criteria
- Patients underwent Unilateral or both Total Knee Arthroplasty
Exclusion Criteria
- brain disease, spinal cord injury, peripheral neuropathy, myopathy
- Inability to ambulate fully due to muscukoskeletal disorders
- MMSE<23
- history of arthroplasty surgery on either of legs
- Cardiac pacemaker
- Refusal of participation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change of WOMAC index 1 day before the initiation of intervention), 5 day, 10 day, and 31 days after the initiation of intervention Western Ontario and McMaster Universities Osteoarthritis Index
- Secondary Outcome Measures
Name Time Method Change of VAS 1 day before the initiation of intervention), 5 day, 10 day, and 31 days after the initiation of intervention visual analogue scale
Trial Locations
- Locations (1)
Ulsan University Hospital
🇰🇷Ulsan, Korea, Republic of
Ulsan University Hospital🇰🇷Ulsan, Korea, Republic of