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Clinical Trials/NCT05138406
NCT05138406
Recruiting
Not Applicable

The Effect of Graded Motor Imagery Training on Pain, Functional Performance, Motor Imagery Skill, and Kinesiophobia After Total Knee Arthroplasty.

Inonu University1 site in 1 country18 target enrollmentFebruary 28, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Arthroplasty
Sponsor
Inonu University
Enrollment
18
Locations
1
Primary Endpoint
Pain intensity
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This study was planned to investigate the long-term effectiveness of the early application of graded motor imagery therapy on pain parameters, functional performance, motor imagery skill, and kinesiophobia in individuals who underwent total knee arthroplasty surgery after knee osteoarthritis.

Detailed Description

Participants aged 45-80 who are scheduled for total knee arthroplasty surgery after knee osteoarthritis will be included. Participants will be selected from the relevant population using a nonprobability random sampling method. Participants who agree to participate in the study and meet the inclusion criteria will be assigned to one of the groups (conventional rehabilitation-only or conventional rehabilitation with graded motor imagery) using the closed envelope method. Evaluations will be made one day before surgery, 6 weeks and 6 months after surgery for each group. Pain Visual Analog Scale; pressure pain threshold algometer; central sensitization Central Sensitization Inventory; the joint range of motion goniometer; muscle strength handheld dynamometer; kinesiophobia Tampa Kinesiophobia Scale; functional mobility and mental stopwatch Timed get up and go test; choice task Recognise™ application; motor imagery skill Movement Imagery Questionnaire-3; functional assessment Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC); The catastrophic degree of pain is planned to be evaluated with the Pain Catastrophizing Scale.

Registry
clinicaltrials.gov
Start Date
February 28, 2022
End Date
June 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Burcu Talu

Associate professor

Inonu University

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with knee osteoarthritis and being on the waiting list to receive unilateral total knee arthroplasty
  • Approved by the orthopedist for early physiotherapy treatment after total knee arthroplasty

Exclusion Criteria

  • - Individuals undergoing revision total knee arthroplasty or undergoing bilateral total knee arthroplasty,
  • Contralateral knee osteoarthritis (defined by activity greater than 4/10 pain)
  • Having undergone any physical therapy intervention or other surgery in the last 6 months
  • Any neurological, cardiac, pulmonary or psychiatric disease (eg, uncontrolled diabetes mellitus, neoplasms, uncontrolled blood pressure, neurological conditions) before or after surgery;
  • Fracture, infection in the acute postoperative phase or presence of fever
  • Cognitive impairments that alter the probability of correct understanding of the motor imagery program
  • Body mass index \> 35 kg / m2
  • Difficulties with understanding or communication
  • Insufficient knowledge of Turkish to follow the study instructions.

Outcomes

Primary Outcomes

Pain intensity

Time Frame: 6 months after surgery

Pain at rest and during activity will be evaluated with the help of the Visual Analogue Scale (VAS). The VAS is a 10 cm scale that rates 0 points as "no pain" and 10 points as "worst pain imaginable".

WOMAC

Time Frame: 6 months after surgery

Functional status will be assessed by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). It consists of three subgroups as pain (5 items), stiffness (2 items) and physical function (17 items) and a total of 24 items. Each item has an evaluation score of 0 = none, 1 = mild, 2 = moderate, 3 = severe, 4 = very severe.

Secondary Outcomes

  • Pressure pain threshold(6 months after surgery)
  • Central sensitization(6 months after surgery)
  • Joint Range of Motion(6 months after surgery)
  • Quadriceps muscle strength(6 months after surgery)
  • Kinesiophobia(6 months after surgery)
  • Functional mobility(6 months after surgery)
  • Mental chronometry delta time(6 months after surgery)
  • Laterality task(6 months after surgery)
  • Movement Imagery Questionnaire-3 (MIQ-3)(6 months after surgery)
  • Pain Catastrophizing Scale(6 months after surgery)

Study Sites (1)

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