Comparison of Ambulatory and Functional Improvement by Morning Walk

Comparison of Clinical Efficacy and Safety for Ambulatory and Functional Improvement in Patients After Total Knee Arthroplasty With Morning Walk

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.

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

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