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Pain Neuroscience Education in Total Knee Arthroplasty

A Randomized Clinical Trial of Preoperative Pain Neuroscience Education for Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03231566
Enrollment
120
Registered
2017-07-27
Start date
2015-02-28
Completion date
2017-03-20
Last updated
2017-07-27

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

Conditions

Total Knee Replacement

Brief summary

To determine if education about pain given prior to Knee Arthroplasty will result in better outcomes following surgery

Detailed description

To determine if a preoperative pain neuroscience education (PNE) program would result in superior outcomes compared to usual preoperative education for total knee arthroplasty (TKA). Patients will receive traditional hospital preoperative TKA program (usual care group) or receive the same program plus an additional 30-minute PNE program (experimental group). Pre and post measurements at 1, 3 and 6 months for pain, function, fear of movement and pain catastrophization. We will also compare opioid usage, healthcare expenses and patient satisfaction between groups.

Interventions

BEHAVIORALPain Neuroscience Education

See arm/group description

Sponsors

University of Nevada, Las Vegas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Outcome measures were mailed by patients in prepaid envelopes

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* be scheduled to have a TKA and their standard preoperative TKA education program, indicate their willingness to participate in the study, ability to read and understand English, as the study included the use of an educational booklet, and be able and willing to complete outcome data for 6 months after TKA

Exclusion criteria

* Because all potential participants for this study had been screened and cleared for their orthopedic surgery, the only exclusion criterion was an unwillingness to participate in the study and having had a previous TKA or scheduled for a bilateral TKA.

Design outcomes

Primary

MeasureTime frameDescription
PainChange from Baseline to 1 month, 3 months and 6 months post-surgeryNumeric Pain Rating Scale
FunctionChange from Baseline to 1 month, 3 months and 6 months post-surgeryWestern Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Pain CatastrophizationChange from Baseline to 1 month, 3 months and 6 months post-surgeryPain Catastrophization Scale
Fear of movementChange from Baseline to 1 month, 3 months and 6 months post-surgeryTampa Scale of Kinesiophobia

Secondary

MeasureTime frameDescription
Healthcare ExpensesChange from Baseline to 1 month, 3 months and 6 months post-surgeryCosts associated with healthcare utilization
Patient SatisfactionChange at 1 month, 3 months and 6 months post-surgeryLikert questions
Opioid UseChange at 1 monthOral Morphine Dose Equivalents

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026