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Clinical Trials/NL-OMON27550
NL-OMON27550
Recruiting
Not Applicable

Effectiveness of pain neuroscience education on pain after total knee arthroplasty: a randomised controlled trial

Tergooi hospital, department of Orthopaedics0 sites76 target enrollmentTBD
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ConditionsPatients with a primary diagnosis of osteoarthritis and scheduled for an elective unilateral total knee arthroplasty (TKA)

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patients with a primary diagnosis of osteoarthritis and scheduled for an elective unilateral total knee arthroplasty (TKA)
Sponsor
Tergooi hospital, department of Orthopaedics
Enrollment
76
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

.A.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Tergooi hospital, department of Orthopaedics

Eligibility Criteria

Inclusion Criteria

  • •Patients 18 years or older
  • •Symptomatic knee osteoarthritis according to the American College of Rheumatology classification criteria (Wu et al, 2005\). Radiographic disease severity will be evaluated for each participant (Kellgren\-Lawrence 0\-4 grading scale).
  • •Scheduled for an elective unilateral total knee arthroplasty (TKA) no sooner than 2 weeks from the time of recruitment
  • •Be able to understand and speak Dutch language
  • •Patient is willing and able to complete scheduled study procedures and follow\-up evaluations.
  • •Provide written informed consent

Exclusion Criteria

  • •Scheduled for revision arthroplasty
  • •Diagnosis of inflammatory arthritis (i.e. rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosis, ankylosing spondylitis)
  • •Scheduled for TKA because of a fracture, malignancy or an infection;
  • •Patient is currently participating in any other surgical intervention studies or pain management studies
  • •Previous total knee arthroplasty or any other lower limb surgery within the past six months
  • •Cognitive impairment

Outcomes

Primary Outcomes

Not specified

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