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Clinical Trials/NCT05459766
NCT05459766
Unknown
Not Applicable

Effects of a Perioperative Action Observation and Motor Imagery Training in Patients Undergoing Total Knee Arthroplasty

Istituto Clinico Humanitas0 sites50 target enrollmentAugust 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Arthoplasty
Sponsor
Istituto Clinico Humanitas
Enrollment
50
Primary Endpoint
Changes in functional mobility
Last Updated
3 years ago

Overview

Brief Summary

The study is aimed at investigating the effects of action observation and motor imagery training in patients undergoing total knee arthroplasty. Fifty participants will be enrolled during hospital admission and randomized into 2 groups (AO+MI and CTRL groups). AO+MI will undergo 12-minute AO+MI intervention for 3 days (preoperative day, first and second postoperartive days), whereas CTRL group will undergo usual care. At baseline, first and third postoperative days, participants will be assessed for mobility, pain, range of motion, quadriceps acrivation failure and patient's bady-pain representation by a blinded operator.

Registry
clinicaltrials.gov
Start Date
August 1, 2022
End Date
January 31, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istituto Clinico Humanitas
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients scheduled for total knee arthroplasty
  • age greater or equal to 18 years old
  • ability to walk independently.

Exclusion Criteria

  • previous total knee arthoplasty on the contralateral side
  • revision surgery
  • musculoskeletal and neurological disorders influencing functional recovery
  • visual or auditory deficits.
  • postoperative complications
  • weight bearing restrictions
  • lack of walking independency within the second postoperative day.

Outcomes

Primary Outcomes

Changes in functional mobility

Time Frame: At baseline, at 1 day and 3 days after surgery

It will be assessed using the Timed Up and Go test

Secondary Outcomes

  • Changes in perceived pain(At baseline and 3 days after surgery)
  • Changes in body pain representation at the level of the knee joint(At baseline and 3 days after surgery)
  • Changes in quadriceps activation failure(At baseline, at 1 day and 3 days after surgery)
  • Changes in active and passive knee range of motion(At baseline, at 1 day and 3 days after surgery)

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