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Psychosocial Predictors of Poor Outcomes After a Knee Arthroplasty

U

University of Barcelona

Status

Completed

Conditions

Osteoarthritis, Knee

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

115 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. To have sufficient Spanish or Catalan reading, writing and speaking skills to comprehend all explanations and to complete the assessment tools.
  2. Be able to provide the informed consent.
  3. Be scheduled to undergo in a total or unicompartimental knee arthroplasty.
  4. Knee osteoarthritis diagnosis.
  5. Patients 18 years old or more.

Exclusion criteria

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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