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Clinical Trials/ACTRN12611001184965
ACTRN12611001184965Completed未知

Mindfulness, cognitive processes and coping in chronic illness: a randomised controlled trial to evaluate the effect of mindfulness training prior to total joint arthroplasty on post-operative pain and physical function

Professor Peter Choong0 sites145 target enrollmentStarted: November 15, 2011Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
145

Study Overview

Brief Summary

The main purpose of this study was to determine if participating in a mindfulness-based stress reduction program improved patient pain, function and psychological wellbeing following hip or knee joint replacement surgery. To answer this question, researchers compared two groups of patients with hip or knee osteoarthritis, with 127 patients randomly allocated to either a ‘test group’ or ‘control group’: • Test group: 65 patients completed an 8-week mindfulness-based stress reduction course prior to joint replacement. • Control group: 62 were provided with the usual standard of care for patients undergoing joint replacement surgery. Patients in both groups completed questionnaires that measured their pain, function and psychological well-being on 3 occasions: before surgery, at 3-months after surgery and again at 12-months after surgery. MAIN RESULTS Patients in the test group who completed the mindfulness training had greater improvements in pain and function 12-months after their surgery compared to the treatment as usual group. Another finding was that a higher proportion of patients who underwent the mindfulness training decided to not proceed with surgery based on symptom improvement.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Treatment
Masking
Blinded (masking used)

Eligibility Criteria

Ages
20 Years to 80 Years (—)
Sex
All

Inclusion Criteria

  • On the surgical waiting list for primary total joint replacement for end stage osteoarthritis at the study institution

Exclusion Criteria

  • (i) Revision surgery or surgery for neoplastic disease; (ii) Inability to provide informed consent due to mental incompetence (e.g., intellectual disability, dementia) (mild cognitive impairment (MCI) would not be cause for exclusion); (iii) active drug or alcohol use disorder which in the opinion of the investigators makes the patient unsuitable for participation in the trial (iv) limited English language fluency (v) evidence at interview or on the Memory Complaints Questionnaire (MCQ) of presumptive cognitive impairment requiring clinical assessment.

Investigators

Sponsor
Professor Peter Choong

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