It was well known that the mirror therapy could decrease pain of upper-limb amputated patients. The mirror therapy is known to make a plastic change some parts of the brain perceiving the painful body part and modulating its signal by feedback of visual information mirrored with the corresponding contra-lateral normal parts. In this study, post-operative analgesic efficiency of the virtual reality using a mirror therapy after total knee arthroplasty will be evaluated. This clinical trial will be performed in the form of prospective, single-blind (i.e. assessor-blind), parallel group, randomized (allocation ratio 1:1), single cohort.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
Patients are required to look at the images of both lower extremities ranged from the perineal area to the foot. Virtual reality system records in real-time method both lower extremities. Following the validity assessement mirrored image of the surgeried lower extremity is re-formed using the virtusal reality system flipping the image of lower extremity not-surgeried and being calibration for the symmetricity.
Ulsan University Hospital
Ulsan, South Korea
6 minute walk test
The distance walked at a self-selected speed along a 40 cm corridor in 6 min. The distance was measured in meters, and more the meters better the result. A walking aid was used if needed.
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Visual analogue scale (VAS) while resting
checking the VAS while resting
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Visual analogue scale (VAS) while moving
checking the VAS while resting
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Active ROM of flexion and extension on the knee
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Tridol consumption per week
Time frame: after the 1st and 2nd session (5 days) intervention
WOMAC index
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Graded ambulation distances
Grade 1: able to ambulate ≤5 feet Grade 2: able to ambulate \>5 feet but \<10 feet Grade 3: able to ambulate \>10 feet but \<30 feet Grade 4: able to ambulate ≥30 feet
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Timed-stands test
The patients were asked to rise from and sit down on a chair with a height of 45 cm, 10 times and as quickly as possible, without using the armrests. The time spent was recorded.
Time frame: shortly after the 1st and 2nd session (5 days) intervention, and after 6 weeks after intervention
Side effects
Time frame: after the 1st and 2nd session (5 days) intervention
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