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Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty

Primary Purpose

Osteo Arthritis Knee, Knee Arthroplasty, Catastrophizing

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Pain Neuroscience Education
Multimodal Physiotherapy
Usual Care
Sponsored by
University of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Osteo Arthritis Knee

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • To have sufficient Spanish or Catalan reading, writing and speaking skills to comprehend all explanations and to complete the assessment tools.
  • Be able to provide the informed consent.
  • Be scheduled to undergo in a total knee arthroplasty.
  • Primary knee osteoarthritis diagnosis.
  • Score more than 20 points in the Pain Catastrophizing Scale (PCS).
  • Score more than 4 over 10 on pain Visual Analogue Scale (VAS)
  • Patients older than 18 years old.

Exclusion Criteria:

  • Patients scheduled to undergo in a total knee arthroplasty because of prostheses replacement, tumor, infection or fracture.
  • Patients scheduled to undergo in a bilateral total knee arthroplasty.
  • Patients that will need another total knee or hip replacement surgery in less than a year regarding the current intervention.
  • Patients scheduled for unicompartmental knee arthroplasty.
  • Patients with other pathologies with characteristic features of a central sensitization. (i.e. Fibromyalgia)
  • Co-existing other inflammatory or rheumatic conditions (i.e. rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus or ankylosing spondylitis)
  • Co-existing other mental condition and/or major depression.

Sites / Locations

  • Hospital Germans Trias i Pujol

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Usual Care

PNE

Multimodal Physiotherapy

Arm Description

Group-based preoperative biomedical education, postoperative hospital and home rehabilitation.

Usual care + Preoperative Pain Neuroscience Education

Usual care + Preoperative Multimodal physiotherapy

Outcomes

Primary Outcome Measures

Pain. Changes from baseline 6 months post-surgery.
Participants will be asked to rate their pain intensity on a horizontal 100-mm Visual Analogue Scale (VAS), ranging from 0 = no pain to 100 = 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.

Secondary Outcome Measures

Range of Motion
Goniometric assessments of knee will be carried out to assess flexion and extension range of motion.
Walking Speed
4 Meters Walking Test (4MWT) will be used to evaluate patient's walking speed.
Function
30-Second Chair Stand Test (30sCST) will be use to evaluate patient's functionality on standing, because it is a well-recognized test to detect early declines in functional independence.
Dynamic Balance
Y Balance Test (YBT) will be use to evaluate patient's dynamic balance.
Disability / Limitation
Western Ontario and McMaster University Osteoarthritis Index (WOMAC) (Spanish version) will be used to assess patient´s physical function. This questionnaire 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.
Health-related Quality of Life
The spanish version of the Euro Quality of Life 5D-5L (EQ-5D-5L) was used to assess the health related quality of life (HRQL).(10) The EQ-5D-5L consists in two pages: the first one is based on a descriptive system that defines health in terms of five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five response categories: no problems, slight problems, moderate problems, severe problems, extreme problems.(10) A health state is composed by taking one level for each dimension, and a preference-based scoring function is used to convert the descriptive system to a summary index score (ranging from states worse than dead <0 to full health 1).
Pain Catastrophism
The Spanish version of Pain Catastrophizing Scale (PCS) was used to asses thoughts and feelings related to pain experiences.(9) The PCS is a 13 item self-administered questionnaire composed of 3 subscales: rumination, magnification and helplessness. The PCS uses a 5-point Likert scale with responses ranging from 0 = not at all to 4 = all the time. Overall scores range from 0 to 52 points, the higher the score, the higher is the pain catastrophism level.
Depression and anxiety
Participants will be asked to complete the Hospital Anxiety and Depression Scale (HADS) (Spanish version) will be used. The HADS is a 14 item self-administered questionnaire comprised of 2 subscales: depression and anxiety, both composed with 7 items. Each item use a 4-point Likert scale with responses ranging from 0 to 4. Overall scores range from 0 to 21 points for each subscales, and final score is presented using each subscale scores separately. The higher the score, the higher are the anxiety or depression levels.
Kinesiophobia
Participants will be asked to complete the Tampa Scale for Kinesiophobia (TSK-11) (Spanish version). TSK-11 is a 11 item self-administered questionnaire used to assess the pain-related fear of movement. The TSK-11 uses a 4-point Likert scale with responses ranging from 1 = totally disagree, to 4 = totally agree. Overall scores range from 11 to 44 indicating a higher degree of pain-related fear of movement when the score is higher.
Self-efficacy
Participants will be asked to complete the Chronic Pain Self-Efficacy Scale (Spanish version). The Chronic Pain Self-Efficacy Scale is a 19 item self-administered questionnaire used to asses pain-related self-efficacy. It uses a visual analog scale for each item, ranging from 0 = totally uncapable to 10 = totally capable. Overall score ranges from 0 to 190. The higher the score, the higher is the subjects' self-efficacy.

Full Information

First Posted
February 18, 2019
Last Updated
May 10, 2023
Sponsor
University of Barcelona
Collaborators
Hector Beltran-Alacreu, PhD
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1. Study Identification

Unique Protocol Identification Number
NCT03847324
Brief Title
Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty
Official Title
Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
September 18, 2019 (Actual)
Primary Completion Date
March 14, 2023 (Actual)
Study Completion Date
March 14, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Barcelona
Collaborators
Hector Beltran-Alacreu, PhD

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to test whether adding a treatment using pain neuroscience education (PNE) and multimodal physiotherapy to usual care, in subjects with knee osteoarthritis and pain catastrophizing, who are scheduled for a total knee arthroplasty (TKA), is more effective than only usual care. There is a high evidence level of different systematic reviews, which support the efficacy of physiotherapy treatments combined with behavioural/educational techniques aimed to reduce pain catastrophism, pain and disability in other pathologies. The primary aim of that kind of interventions is to help the subjects to reconceptualise its own pain understanding and its role on the recovery process, as well as promoting an increase of activity and encourage the subject to resume its usual activity instead of continuing to avoid it.
Detailed Description
The prevalence of TKA has increased dramatically during the last two decades, its popularity can be attributed to its evident success regarding pain improvement, deformity correction and disability reduction in knee osteoarthritis subjects. However, only a third of the patients report no functional problems after surgery, the 20% of then are unsatisfied with its functional skills and around a 20% are experiencing pain, high disability degrees and a significant quality of life reduction. This results cannot be fully explained by mechanical processes, surgical procedures or surgery variations, but it seems to be related to other psychological aspects. Chronic pain subjects often develop maladaptive thoughts and behaviours (i.e. pain catastrophism, Kinesiophobia, activity avoidance) which contribute to make the subject suffer physically as well as emotionally, and affect on the intensity and persistency of pain. Although many psychosocial factors have been studied, pain catastrophism has emerged as one of the most important predictors for persistent pain after a total knee arthroplasty, as well as its severity and duration, that's why it is getting more importance when it comes to study chronic pain in this subjects. Reducing pain catastrophism has become a key factor to determine the success in the rehabilitation of some maladies accompanied by pain, considering that its reduction has been associated with the clinical improvement of pain itself. It has been observed that treatments using psychological and psychosocial interventions, therapeutic education and coping skills training, or physical therapy and therapeutic exercise, are effective techniques to reduce pain catastrophism. Nevertheless, it's still necessary to determine whether the maladaptive pain related thoughts approach, using physical therapy and behavioural techniques, are able to reduce the risk of suffering postoperative chronic pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteo Arthritis Knee, Knee Arthroplasty, Catastrophizing, Pain

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three armed, parallel groups, single blind, unicentric randomized controlled trial
Masking
Outcomes Assessor
Masking Description
Single blind
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Group-based preoperative biomedical education, postoperative hospital and home rehabilitation.
Arm Title
PNE
Arm Type
Experimental
Arm Description
Usual care + Preoperative Pain Neuroscience Education
Arm Title
Multimodal Physiotherapy
Arm Type
Experimental
Arm Description
Usual care + Preoperative Multimodal physiotherapy
Intervention Type
Other
Intervention Name(s)
Pain Neuroscience Education
Other Intervention Name(s)
Pain Education
Intervention Description
This program is mainly based in "Explain Pain" concept, used in multiple rehabilitation programs. Its aim is to change the subject's pain understanding, teaching them the biological processes underneath the pain construct, as a mechanism to reduce itself and its related maladaptive thoughts and behaviors.
Intervention Type
Other
Intervention Name(s)
Multimodal Physiotherapy
Intervention Description
This intervention will be divided in pain neuroscience education, orthopedic manual therapy and therapeutic exercise.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Usual care will be divided in: preoperative biomedical group-based education, postoperative hospital rehabilitation and home-based postoperative physiotherapy.
Primary Outcome Measure Information:
Title
Pain. Changes from baseline 6 months post-surgery.
Description
Participants will be asked to rate their pain intensity on a horizontal 100-mm Visual Analogue Scale (VAS), ranging from 0 = no pain to 100 = 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.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Secondary Outcome Measure Information:
Title
Range of Motion
Description
Goniometric assessments of knee will be carried out to assess flexion and extension range of motion.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Walking Speed
Description
4 Meters Walking Test (4MWT) will be used to evaluate patient's walking speed.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Function
Description
30-Second Chair Stand Test (30sCST) will be use to evaluate patient's functionality on standing, because it is a well-recognized test to detect early declines in functional independence.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Dynamic Balance
Description
Y Balance Test (YBT) will be use to evaluate patient's dynamic balance.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Disability / Limitation
Description
Western Ontario and McMaster University Osteoarthritis Index (WOMAC) (Spanish version) will be used to assess patient´s physical function. This questionnaire 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.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Health-related Quality of Life
Description
The spanish version of the Euro Quality of Life 5D-5L (EQ-5D-5L) was used to assess the health related quality of life (HRQL).(10) The EQ-5D-5L consists in two pages: the first one is based on a descriptive system that defines health in terms of five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five response categories: no problems, slight problems, moderate problems, severe problems, extreme problems.(10) A health state is composed by taking one level for each dimension, and a preference-based scoring function is used to convert the descriptive system to a summary index score (ranging from states worse than dead <0 to full health 1).
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Pain Catastrophism
Description
The Spanish version of Pain Catastrophizing Scale (PCS) was used to asses thoughts and feelings related to pain experiences.(9) The PCS is a 13 item self-administered questionnaire composed of 3 subscales: rumination, magnification and helplessness. The PCS uses a 5-point Likert scale with responses ranging from 0 = not at all to 4 = all the time. Overall scores range from 0 to 52 points, the higher the score, the higher is the pain catastrophism level.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Depression and anxiety
Description
Participants will be asked to complete the Hospital Anxiety and Depression Scale (HADS) (Spanish version) will be used. The HADS is a 14 item self-administered questionnaire comprised of 2 subscales: depression and anxiety, both composed with 7 items. Each item use a 4-point Likert scale with responses ranging from 0 to 4. Overall scores range from 0 to 21 points for each subscales, and final score is presented using each subscale scores separately. The higher the score, the higher are the anxiety or depression levels.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Kinesiophobia
Description
Participants will be asked to complete the Tampa Scale for Kinesiophobia (TSK-11) (Spanish version). TSK-11 is a 11 item self-administered questionnaire used to assess the pain-related fear of movement. The TSK-11 uses a 4-point Likert scale with responses ranging from 1 = totally disagree, to 4 = totally agree. Overall scores range from 11 to 44 indicating a higher degree of pain-related fear of movement when the score is higher.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.
Title
Self-efficacy
Description
Participants will be asked to complete the Chronic Pain Self-Efficacy Scale (Spanish version). The Chronic Pain Self-Efficacy Scale is a 19 item self-administered questionnaire used to asses pain-related self-efficacy. It uses a visual analog scale for each item, ranging from 0 = totally uncapable to 10 = totally capable. Overall score ranges from 0 to 190. The higher the score, the higher is the subjects' self-efficacy.
Time Frame
Baseline, 2 weeks before surgery, 1, 3 and 6 months after surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: To have sufficient Spanish or Catalan reading, writing and speaking skills to comprehend all explanations and to complete the assessment tools. Be able to provide the informed consent. Be scheduled to undergo in a total knee arthroplasty. Primary knee osteoarthritis diagnosis. Score more than 20 points in the Pain Catastrophizing Scale (PCS). Score more than 4 over 10 on pain Visual Analogue Scale (VAS) Patients older than 18 years old. Exclusion Criteria: Patients scheduled to undergo in a total knee arthroplasty because of prostheses replacement, tumor, infection or fracture. Patients scheduled to undergo in a bilateral total knee arthroplasty. Patients that will need another total knee or hip replacement surgery in less than a year regarding the current intervention. Patients scheduled for unicompartmental knee arthroplasty. Patients with other pathologies with characteristic features of a central sensitization. (i.e. Fibromyalgia) Co-existing other inflammatory or rheumatic conditions (i.e. rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus or ankylosing spondylitis) Co-existing other mental condition and/or major depression.
Facility Information:
Facility Name
Hospital Germans Trias i Pujol
City
Badalona
State/Province
Barcelona
ZIP/Postal Code
08916
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No

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Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty

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