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Effectiveness of PNE on pain after TKA

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON27550
Enrollment
76
Registered
2019-05-29
Start date
2019-08-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with a primary diagnosis of osteoarthritis and scheduled for an elective unilateral total knee arthroplasty (TKA)

Interventions

PNE is an educational strategy used by physical therapists that provides information regarding the underlying neurophysiology and neurobiology processes involved in pain experience. In longer lasting

Sponsors

Tergooi hospital, department of Orthopaedics
Lead Sponsor

Eligibility

Inclusion 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

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

Design outcomes

Primary

MeasureTime frame
The primary clinical outcome is pain at 3 months after TKA surgery. The Western Ontario and McMaster Universities Osteoarthirits Index (WOMAC-DV), subscale pain, will be used as pain specific instrument.

Secondary

MeasureTime frame
1. Pain levels 12 months after surgery in patiens undergoing TKA 2. Physical functioning 3 and 12 months post-operative 3. Stiffness 3 and 12 months post-operative 4. Health related quality of life 3 and 12 months post-operative 5. Attention to pain 3 and 12 months post-operative 6. Pain catastrophizing 3 and 12 months post-operative 7. Anxiety and depression 3 and 12 months post-operative

Contacts

Public ContactDominique Baas

Tergooi Hospital

researchorthopedie@tergooi.nl+31 88 753 50 23

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)