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Comparison of Ambulatory and Functional Improvement by Morning Walk

U

Ulsan University Hospital

Status

Completed

Conditions

Arthroplasty, Replacement, Knee
Robotics

Treatments

Device: Morning walk
Other: no Morning walk

Study type

Interventional

Funder types

Other

Identifiers

NCT03183856
chhwang7

Details and patient eligibility

About

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.

Full 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

Enrollment

9 patients

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

9 participants in 2 patient groups

Morning walk
Experimental group
Description:
200 steps of gait rehabilitation using an end-effector typed gait robot with 5 minute break, 3 times a day for 10 weekdays: the end-effector type gait robot (Morning Walk®, Hyundai Heavy Industry, Republic of Korea)
Treatment:
Device: Morning walk
No Morning walk
Active Comparator group
Description:
200 steps by themselves or with a help of a walker on a even floor at a comfortable pace with 5 minute break, three times a day for 10 weekdays
Treatment:
Other: no Morning walk

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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