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

Not Applicable
Conditions
Total Knee Arthoplasty
Interventions
Behavioral: Usual care
Behavioral: Action observation and motor imagery
Registration Number
NCT05459766
Lead Sponsor
Istituto Clinico Humanitas
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
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
  • dementia
  • 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CTRLUsual careUsual care, consisting of preoperative education.
AO+MIAction observation and motor imageryVideo-clips observation representing motor contents, followed by motor imagery (12 minutes a day per 3 days).
Primary Outcome Measures
NameTimeMethod
Changes in functional mobilityAt baseline, at 1 day and 3 days after surgery

It will be assessed using the Timed Up and Go test

Secondary Outcome Measures
NameTimeMethod
Changes in perceived painAt baseline and 3 days after surgery

It will be assessed using Numerical Rating Scale (0-10 points), where 0 means no pain and 10 means maximum pain.

Changes in body pain representation at the level of the knee jointAt baseline and 3 days after surgery

It will be assessed using the Pain Drawing Body Chart

Changes in quadriceps activation failureAt baseline, at 1 day and 3 days after surgery

It will be assessed using the Quadricpes Activation Battery

Changes in active and passive knee range of motionAt baseline, at 1 day and 3 days after surgery

It will be assessed using an inertial measurement unit

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