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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48358
Enrollment
76
Registered
2019-04-18
Start date
2019-08-07
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

knee replacement surgery Total Knee arthroplasty

Interventions

A pre-operative and a post-operative educational session of respectively 45 and 30 minutes by a physical therapist about the neuroscience of pain, accompanied by an evidence-based booklet.

Sponsors

Tergooiziekenhuizen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

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 outcome will be the change in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain scale score 3 months following surgery.

Secondary

MeasureTime frame
Secundary study parameters are the level of pain catastrophizing thoughts, assessed with the Pain Catastrophizing Scale Dutch Version (PCS-DV), preoccupation with pain, assessed with the Pain Vigilance and Attention Questionnaire (PVAQ) and presence and severity of anxiety and depression are determined with the *Hospital Anxiety and Depression Scale*. Disease specific and general health related quality of life is assessed with the RAND-36 and WOMAC, subscale stiffness and physical functioning. Patient parameters are gathered and include demographic information, BMI, duration of kneepain, osteoarthiritis severity graded by Kellgren-Lawrence 0*4 grading scale, the number of visits to healthcare providers, other than the visits related to the TKA and use of analgesic medication.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)