- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02156453
Functional Recovery After Total Knee Arthroplasty
The Evaluation of Short-term Functional Recovery of Total Knee Arthroplasty Patients
Total knee replacement is one of the most successful surgical procedures in Orthopaedics. However, 10-20% of the patients are still dissatisfied with the results of the surgery. In general, the evaluation of postoperative functional outcomes are usually measured by self-report questionnaires, such as the Western Ontario and Mcmaster Universities osteoarthritic Index (WOMAC) and the Short Form-36 health survey (SF-36). Another method to evaluate functional outcome of the patients is to use the performance-based tests such as the two-minute walk test, but there is still little information regarding its use for evaluating functional recovery in patients receiving total knee arthroplasty.
The objectives this study are: 1) to assess the relationship between self-report questionnaires and performance-based tests among patients scheduling for TKA; and 2) to identify clinical variables that are associated with pre- and postoperative functional performance of the patients.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Osteoarthritis (OA) of the knee is one of the most prevalent age-related musculoskeletal conditions, resulting in significant impairment in patients' abilities to perform activities and adversely impacting their quality of life. The level of impairment in patients with knee OA can be measured using validated self-report questionnaires, such as the disease-specific Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the generic Medical Outcomes Study Short Form-36 (SF-36). Self-report questionnaires have been recommended by some investigators for their high internal consistency and ease of administration. Another method to evaluate physical function in patients with knee OA is to use performance-based tests. These tests are tools that assess patients' ability to execute a task in a standardized environment, and include the 2-minute walk test (2MWT) and the timed get-up-and-go test (TUG).
Among all the self-reported questionnaires for knee OA, the WOMAC is one of the most commonly used for baseline assessment and for measurement of treatment outcome, and has been validated for patients undergoing total knee arthroplasty (TKA). Although the WOMAC provides information on how individuals perceive their physical function in their own environment, it does not describe their ability to perform a specific task or action. In addition, some investigators showed that scores from self-report questionnaires before and after arthroplasty can overestimate patients' actual functional capacity. For example, Parent et al demonstrated that total knee arthroplasty patients had a dramatic improvement at 2 months as assessed by the WOMAC function subscale, however there were no significant changes when measured with performance-based tests assessing gait speed and stair ascent duration. Therefore, clinicians should be cautious when interpreting findings from studies that provide only self-report questionnaire scores. Given that self-report questionnaires may over-estimate functional status after joint replacement, some authors advocate performance-based tests as measures of outcome, and recommend their use during the preoperative period as baseline measurements followed by subsequent comparison with postoperative measurements.
The objectives of this study are: 1) to assess the relationship between self-reported questionnaires (WOMAC and SF-36) and performance-based tests (2MWT, TUG) among patients scheduling for TKA; and 2) to identify clinical variables that are associated with pre- and post-operative performance of the 2MWT and TUG. Our hypothesis is that correlations between self-report questionnaires and performance-based tests would be low to moderate, and thus these two types of measurements evaluate distinct domains of functional status in patients undergoing TKA.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Bangkok
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Bangkoknoi, Bangkok, Thailand, 10700
- Siriraj Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients who aged between 40-100 years
- Patients who diagnosed with end-stage osteoarthritis of the knee
Exclusion Criteria:
- Patients who receive total knee replacement on the contralateral side during the past 6 months
- Patients with diseases or conditions that may affect postoperative functional recovery such as severe cardiopulmonary disease
- Unable to participate in postoperative follow-up visits
- Prior surgery on the affected knee, such as high tibial osteotomy
- Patients with complex deformity who require bone grafting or metal augments
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Total knee arthroplasty
Patients undergoing uncomplicated total knee replacement
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All patients will undergo total knee replacement using midvastus approach by single surgeon.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change of the 2-minute walk test (2MWT) from baseline to at 1 year after surgery
Time Frame: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change of the Timed get-up-and-go test (TUG) from baseline to 1 year after surgery
Time Frame: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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Change of the pain scores on the Visual Analog Scale from baseline to 1 year after surgery
Time Frame: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
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Change of the functional scores on the WOMAC index (Thai version) from baseline to 1 year after surgery
Time Frame: baseline, 3 months, 6 months and 1 year after surgery
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baseline, 3 months, 6 months and 1 year after surgery
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Change of the physical function domain of the SF-36 Health Survey from baseline to 1 year after surgery
Time Frame: baseline, 3 months, 6 months and 1 year after surgery
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baseline, 3 months, 6 months and 1 year after surgery
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aasis Unnanuntana, M.D., Siriraj Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 126/2556(EC2)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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