Osteoarthritis Clinical Trial
Official title:
Effect of Neuroscience Education on Subjects With Chronic Knee Pain Related to Osteoarthritis : a Randomized Controlled Trial
Osteoarthritis (OA) is a frequent chronic musculoskeletal pathology that usually causes
great disability and significant healthcare costs. Substantial scientific evidence indicates
a role for central sensitization in OA pain. Reconceptualization of pain through
Neuroscience Education (NE) is an intervention that has already been used successfully in
some chronic musculoskeletal pain conditions characterized by alteration on CNS pain
processing or central sensitization (i.e. chronic low back pain, chronic fatigue syndrome,
widespread pain and chronic whiplash associate disorders).There is compelling evidence that
NE have a positive effect on pain, disability, catastrophization and physical performance
for chronic musculoskeletal pain disorders, yet studies examining the value of NE for OA
patients are essentially lacking.
The primary aim of this study is to assess the effect of NE on pain, disability and physical
performance in subjects with chronic OA knee pain waiting for replacement surgery. This will
be the first time NE will be addressed specifically to OA pain. To investigate the benefits
of NE on pain related to knee OA, the effect of a manual therapy intervention combined with
NE (MT+NE) will be compared with this same manual intervention plus an educational program
based on a traditional patho-anatomical or biomedical model (MT+E). The following secondary
aims will be addressed as well:
- Examining the effects of the two interventions on the mechanism of central
sensitization in patients with knee OA;
- Examining the effects of the two interventions on pain catastrophizing, illness
perceptions and kinesiophobia in patients with knee OA;
- Finally, it is aimed at identifying effect moderators for NE in patients with knee OA.
| Status | Recruiting |
| Enrollment | 53 |
| Est. completion date | December 2015 |
| Est. primary completion date | December 2015 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
Inclusion Criteria: 1. An established diagnosis of knee OA according to American College of Rheumatology criteria and Kellgreen/Lawrence scale grades. 2. To be in a waiting list and scheduled to undergo primary knee arthroplasty. 3. To have sufficient Spanish language skills to comprehend all explanations and to complete the assessment tools. Exclusion Criteria: 1. Previous knee joint replacement surgery of the affected joint or any other lower limb surgery within the past 6 months. 2. Stated inability to attend or complete the proposed course of intervention and follow-up schedule. 3. Presence of co-morbidities associated with cognitive impairment. 4. Co-existing inflammatory, metabolic, neurological or severe medical conditions, defined as a diagnosis in the medical record severe enough that the patient cannot participate fully in the study procedures (i.e. cardiovascular disease). 5. Functional illiteracy. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Spain | Hospital Universitario de La Ribera | Alcira | Valencia |
| Lead Sponsor | Collaborator |
|---|---|
| University of Valencia | Hospital de la Ribera |
Spain,
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* Note: There are 27 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Endogenous analgesia through the experimental protocol of conditioned pain modulation | For assessing endogenous analgesia, the method examining the influence of the Diffuse Noxious Inhibitory Control system (or spatial summation) on temporal summation will be applied. Recently, the term conditioned pain modulation has been recommended to describe the psychophysical paradigm of Diffuse Noxious Inhibitory Control system in humans | Up to 3 months | Yes |
| Secondary | Pain at rest and in the last 24 hours | Participants will be asked to rate their pain at rest and in the last 24 hours on a horizontal 100-mm visual analogue scale (VAS). The horizontal line anchors will be "no pain" and "worst imaginable pain". The VAS is a valid and reliable instrument compared with other pain rating scales and has been well established in clinical practice and research for measuring pain levels in arthritis populations. | Up to 3 months | Yes |
| Secondary | Pressure Pain Thresholds | Local and distant sites will be chosen for pressure pain threshold measurement. Regarding local sites, two points will be measured from the knee, 3 cm medial and lateral to the midpoint of the medial and lateral edge of patella, respectively. Regarding control site, a distant site will be used to assess systematic analgesic effect of NE at 5 cm distal to lateral epicondyle. | Up to 3 months | Yes |
| Secondary | Western Ontario and McMaster osteoarthritis index (WOMAC scale) | WOMAC assesses pain, stiffness and physical function and can be completed in less than 5 minutes. It's a widely used, reliable, valid and responsive measure of outcome in people with osteoarthritis of the hip or knee. | Up to 3 months | Yes |
| Secondary | Health-related quality of life using the self-reported Spanish version SF-36 questionnaire | Up to 3 months | Yes | |
| Secondary | Tampa Scale of Kinesiophobia (TSK) (Spanish version) | Up to 3 months | Yes | |
| Secondary | Pain Catastrophization Scale (PCS) (Spanish version) | Up to 3 months | Yes | |
| Secondary | Chronic Pain Coping Inventory-42 (Spanish version) | Up to 3 months | Yes | |
| Secondary | Chronic Pain Acceptance Questionnaire (Spanish version) | Up to 3 months | Yes | |
| Secondary | Goniometric assessment of knee flexion and extension range of motion | Up to 3 months | Yes | |
| Secondary | Strength of the hamstrings and quadriceps muscles | Up to 3 months | Yes | |
| Secondary | Timed "Up & Go" (TUG) Test | Participants will be required to rise from a standard arm chair, walk at a safe and comfortable pace to a mark 3 m away and then return to a sitting position in the chair. The outcome of the test will be the time to complete the task. Time will be measured on a stopwatch to the nearest one-hundredth of a second. | Up to 3 months | Yes |
| Secondary | Central Sensitization Inventory | Signs and symptoms suggesting central sensitization will be monitorized using the Central Sensitization Inventory | Up to 3 months | Yes |
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