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Pain Neuroscience Education in Patients With Total Knee Arthroplasty

Investigation of the Efficacy of Neuroscience Pain Education in Patients With Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05928351
Enrollment
34
Registered
2023-07-03
Start date
2023-06-01
Completion date
2023-12-01
Last updated
2024-01-17

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

Conditions

Osteoarthritis, Knee

Keywords

pain neuroscience education, knee, osteoarthritis

Brief summary

The aim of Pain Neuroscience Education (PNE) is to explain to patients the biological and physiological processes involved in a pain experience and, more importantly, defocus the issues associated with the anatomical structures. PNE provides compelling evidence in reducing pain, disability, pain catastrophization, and limited physical movement in musculoskeletal problems. Knee osteoarthritis (KOA) is a very common painful musculoskeletal problem, especially in people over 50 years old, and lead to decrease in knee range of motion. Despite costly arthroscopic surgeries and long-term physiotherapy treatments, poor outcomes are common. The lack of satisfactory results suggests that some practices should be revised. Although PNE could be useful as an intervention, to our knowledge, there is no randomized controlled trial in the literature investigating the effects of PNE in patients with a KOA. Therefore, we aimed to examine the effectiveness of PNE on clinical outcomes in patients with KOA.

Interventions

OTHERPain Neuroscience Education

The experimental group will follow a PNE protocol based on previous procedure for 6 weeks in addition to the standard physiotherapy program (SPP) in postoperative period. Each PNE session will take 45-60 min. PNE will be conducted in line with international guidelines and covered the neurophysiology of pain, transition from acute to chronic pain, and the nervous system ability to modulate the pain experience.

OTHERStandard Physiotherapy Program (SPP)

The control group will follow a SPP. The 45-minute-long treatment sessions will be held 5 days per week. The treatment program will be organized in 3 periods as 0-2 weeks, 3-4 weeks and 5-6 weeks. The overall treatment program will include scar massage, patellar mobilization, coldpack, ankle pump, quadriceps and hamstring strengthening, hip range of motion, hip strengthening exercises, squat, ascending and descending stairs, walking training. All exercises will be 10 repetitions x 2 sets.

Sponsors

Ahi Evran University Education and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

the blinded assessor

Intervention model description

Randomized

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Having a body mass index between 19-40 kg/m2, * Having had a unilateral TKA, * Knee pain score to be 4 and above daily according to the visual analog scale, * Ability to read, speak and understand Turkish.

Exclusion criteria

* Prosthesis disorders requiring re-surgery, * Having visual, auditory and cognitive impairment, * Secondary TKA such as rheumatoid arthritis, * Acute pain, * Pregnancy, drug and alcohol use, * Having bilateral TKA, * Not volunteering to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Pain severityBaselineVisual Analogue Scale (0-10, higher means worse)
Pain severity change is being assessed6 weekVisual Analogue Scale (0-10, higher means worse)
Pain and FunctionBaselineKnee Injury and Osteoarthritis Outcome Score (0-100, higher means better)
Pain and Function change are being assessed6 weekKnee Injury and Osteoarthritis Outcome Score (0-100, higher means better)

Secondary

MeasureTime frameDescription
Anxiety and Depression change is being assessed6 weekHospital Anxiety Depression Scale (0-21, higher means worse)
Physical FunctionBaseline40 meter walking test (in seconds, less is better)
KinesiophobiaBaselineTampa Scale of Kinesiophobia (17-68, higher means worse)
Kinesiophobia change is being assessed6 weekTampa Scale of Kinesiophobia (17-68, higher means worse)
Pain Catastrophizing change is being assessed6 weekPain Catastrophizing Scale (0-52, higher means worse)
Physical Function change is being assessed6 week40 meter walking test (in seconds, less is better)
Pain CatastrophizingBaselinePain Catastrophizing Scale (0-52, higher means worse)
Level of quality of lifeBaselineShort Form-12 (0-100, higher means better)
Level of quality of life change is being assessed6 weekShort Form-12 (0-100, higher means better)
Anxiety and DepressionBaselineHospital Anxiety Depression Scale (0-21, higher means worse)

Countries

Turkey (Türkiye)

Outcome results

None listed

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