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Completed

NCT Number: NCT03378440

Psychosocial Predictors of Poor Outcomes After a Knee Arthroplasty

The purpose of this study is to explore the association between the psychosocial variables: pain catastrophizing, fear of movement, coping skills, pain attitudes, anxiety and depression with postoperative outcomes (pain, health functioning, physical performance, and quality of life) after a knee arthroplasty (KA). The prevalence of KA 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 them 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 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.

This study is a single centre, prospective observational study of subjects undergoing primary KA. The study is designed and aimed to examine the relationship between postoperative psychosocial factors and the development of post-operative persistent pain and disability.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Iriteb S.L.

Badalona, Barcelona, 08912, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 or unicompartimental knee arthroplasty.
  • Knee osteoarthritis diagnosis.
  • Patients 18 years old or more.

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 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.

Treatment and study plan

Primary outcomes

  1. Self-reported Pain

    Time frame: Change from baseline to 1, 3 and 6 months after surgical intervention

    Participants will be asked to rate their pain at resting, walking and flexing their knee 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.

  2. Disability / Limitations

    Time frame: Change from baseline to 1, 3 and 6 months after surgical intervention

    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.

Secondary outcomes

  1. Self-reported Quality of life

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    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).

  2. Kinesiophobia

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    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.

  3. Pain Attitudes

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    Participants will be asked to complete the Spanish version of Survey of Pain Attitudes - Brief (SOPA-B). The SOPA-B is a 30 item self-administered questionnaire which evaluates the pain attitudes and is composed of 7 subscales: solicitude, emotion, medical cure, control, physical harm, disability and medication. This questionnaire uses a 5-point Likert scale with responses ranging from 0 = very false to 4 = very true.

  4. Depression and anxiety

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    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.

  5. Range of Motion

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    Goniometric assessments of knee will be carried out to assess flexion and extension range of motion.

  6. Pain Catastrophism

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    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.

  7. Function

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    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.

  8. Walking Speed

    Time frame: 1 week, 1 month, 3 months and 6 months after surgical intervention

    4 Meters Walking Test (4MWT) will be used to evaluate patient's walking speed.

Sponsors and collaborators

Lead sponsor

University of Barcelona

Other

Collaborators

  • Hector Beltran-Alacreu, PhD

Registry information

Official study title

Psychosocial Predictors of Poor Outcomes After a Knee Arthroplasty: Prospective Observational Study.

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Dec 19, 2017
Registry last updated
Nov 3, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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