Arthroplasty, Replacement, Knee Clinical Trial
Official title:
A Prospective Cohort Study of Patients Undergoing Total Knee and Hip Arthroplasty at a Regional Hospital in Denmark
Verified date | January 2018 |
Source | Bornholms Regionskommune |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
This project will be a descriptive, hypothesis-generating study. The aim is to identify risk factors for poor response to rehabilitation programs after TJR and use these to identify patients who are most susceptible to poor outcomes in order to optimise appropriate rehabilitations strategies and rationalising the distribution of health care resources.
Status | Completed |
Enrollment | 110 |
Est. completion date | February 2018 |
Est. primary completion date | February 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - patients undergoing total knee arthroplasty or total hip arthroplasty - must be able to participate in postoperative rehabilitation - must be able to talk and understand Danish or English Exclusion Criteria: |
Country | Name | City | State |
---|---|---|---|
Denmark | Genoptræningen | Rønne | Bornholm |
Lead Sponsor | Collaborator |
---|---|
Bornholms Regionskommune |
Denmark,
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* Note: There are 31 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 30 second chair stand test, to test the patients functional capacity | Change of 30 second chair stand test from baseline to follow up (an average of 3 months) | ||
Secondary | Health-related quality of life questionnaire | Knee injury and Osteoarthritis Outcome Score (KOOS) or Hip disability and Osteoarthritis Outcome Score (HOOS) | Change of health-related quality of life questionnaire from baseline to follow up (an average of 3 months) | |
Secondary | Pain catastrophizing scale questionnaire | Change of pain catastrophizing scale questionnaire from baseline to follow up (an average of 3 months) | ||
Secondary | Use of analgesics and other medication, qualitative assessment | Changes in the use og analgesics and other medication from baseline to follow up (an average of 3 months) | ||
Secondary | Fall history, events as numbers of falls described by the patient | Change within the fall history from baseline to follow up (an average of 3 months) | ||
Secondary | Patient expectations questionnaire | Preoperative (an average 3 weeks before surgery) | ||
Secondary | Patient satisfaction questionnaire | At follow up (an average of 3 months postoperative). | ||
Secondary | The Forgotten Joint Score questionnaire | At follow up (an average of 3 months postoperative). | ||
Secondary | Rehabilitation compliance | Physiotherapist subjective assessment of patient compliance to the rehabilitation program | At the culmination of the rehabilitation program, an average of 10 weeks. |
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