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| Sponsor: | University of Melbourne |
|---|---|
| Collaborators: |
Australian Physiotherapy Research Foundation United Pacific Industries |
| Information provided by: | University of Melbourne |
| ClinicalTrials.gov Identifier: | NCT00414557 |
Purpose
To investigate the effects of quadriceps strengthening on the adductor moment in individuals with medial knee OA and whether quadriceps strengthening has a different effect on the adductor moment in individuals with and without knee malalignment
| Condition | Intervention | Phase |
|---|---|---|
|
Knee Osteoarthritis |
Procedure: Quadriceps strengthening |
Phase II Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Factorial Assignment Masking: Single Blind Primary Purpose: Treatment |
| Official Title: | The Effects of Knee Malalignment and Quadriceps Strengthening on the Adduction Moment in Individuals With Medial Knee Osteoarthritis |
| Estimated Enrollment: | 107 |
| Study Start Date: | May 2004 |
| Estimated Study Completion Date: | December 2006 |
Although quadriceps strengthening is the cornerstone of physiotherapy management, recent evidence suggests that high quadriceps strength in patients with malaligned knees may increase OA progression.
This study investigates the effects of quadriceps strengthening on the adduction moment in patients with medial knee OA with and without malalignment. 107 participants with and without varus knee malalignment were recruited and randomised into an exercise or a control group. Participants in the exercise group were taught five quadriceps strengthening exercises by a project physiotherapist to be performed five days a week for twelve weeks at home. The exercises were:
Each exercise was performed at 2x10 repetitions for the first 2 weeks and 3x10 repetitions thereafter.
Participants visited the physiotherapist 7 times at Week 1, 2, 3, 4, 5, 7 and 10. They were given the ankle weights and elastic band to bring home and instructed about the repetitions and weights to use by the physiotherapist, who also checked and progressed their exercises. The average duration of the physiotherapy sessions was 30 minutes. To monitor compliance, each participant was given an exercise instructions sheet and kept a training diary to record the exercises they had done.
The control group received no intervention.
Eligibility| Ages Eligible for Study: | 50 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Australia, Victoria | |
| The University of Melbourne | |
| Melbourne, Victoria, Australia, 3040 | |
| Principal Investigator: | Kim Bennell, PhD | University of Melbourne |
| Principal Investigator: | Rana Hinman, PhD | University of Melbourne |
| Principal Investigator: | Tim Wrigley, MSc | University of Melbourne |
| Principal Investigator: | Boon W Lim, MSc | University of Melbourne |
| Principal Investigator: | Leena Sharma, MD | Northwestern University Medical School, Chicago |
More Information
| ClinicalTrials.gov Identifier: | NCT00414557 History of Changes |
| Other Study ID Numbers: | 040850 |
| Study First Received: | December 20, 2006 |
| Last Updated: | December 21, 2006 |
| Health Authority: | Australia: Department of Health and Ageing Therapeutic Goods Administration |
|
Musculoskeletal diseases Joint diseases |
|
Osteoarthritis Osteoarthritis, Knee Arthritis |
Joint Diseases Musculoskeletal Diseases Rheumatic Diseases |