Knee Osteoarthritis Clinical Trial
— KBA ExerciseOfficial title:
Efficacy of Kinesthesia, Balance and Agility Exercise Training as Treatment of Knee Osteoarthritis: A Pilot Study
This pilot study will test the testing and exercise training protocols for a larger study that is in the desing phase and may be modified based on the findings of this study. Two exercise groups will be compared; one is a stadard treatment group using leg strength exercises that are commonly employed in therapy clinics. The other group will do balance and agility type exercises, but no specific strength exercises. These "KBA" exercises are increasingly common in therapy clinics, but very little research has been conducted on their effectiveness in treating knee osteoarthritis symptoms. Participants in this study will complete three short paper and pencil tests at the beginning and end of the study (8 weeks of exercise) as well as a leg strength test, a leg endurance test, two short walking tests, and a stair climb/descend test. One of the paper and pencil tests will be taken every two weeks in an effort to see how quickly changes to symptoms might occur. The exercise programs will be conducted 3 afternoons per week (Mon-Wed-Fri) and will be lead by an ACSM certified instructor.
Status | Completed |
Enrollment | 30 |
Est. completion date | July 2008 |
Est. primary completion date | June 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 50 Years and older |
Eligibility |
Inclusion Criteria: - Aged 50 years or over of either gender - Radiographic tibiofemoral OA grade 2 or higher, unilateral or bilateral - Demonstrated knee OA related dysfunction per WOMAC score - Not engaged in a regular exercise program for minimum of 6 months Exclusion Criteria: - Inability to obtain physician release for exercise - High risk health status: e.g., uncontrolled medical conditions such as hypertension, diabetes, heart disease, pulmonary disease, high cholesterol, anginal type pain, dizziness or syncope, orthopnea or paroxysmal nocturnal dyspnea, ankle edema, heart palpitations or tachycardia, intermittent claudication, known heart murmur, unusual fatigue or shortness of breath with usual activities. - Unresolved balance disorder - Unresolved neurological disorder - History of knee surgery or major knee trauma injury - Hip or ankle instability, excessive weakness, surgery or major trauma injury - Intra-articular joint injection within 4 weeks of the study |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
United States | Morton Plant Mease Cheek-Powell Wellness Center | Clearwater | Florida |
Lead Sponsor | Collaborator |
---|---|
The Arthritis Research Institute of America |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | WOMAC Osteoarthritis Scale; Function subscale change pre to post intervention - KBA vs. standard strength training | 8 weeks | No | |
Secondary | WOMAC subscale change in Pain and in Stiffness pre to post intervention | 8 weeks | No | |
Secondary | Walking speed change in a timed Get Up & Go Test pre to post intervention | 8 weeks | No | |
Secondary | Stair climbing and descending speed change pre to post intervention | 8 weeks | No | |
Secondary | Gait quality measures with the GAITRite walking mat and EMG, pre to post intervention | 8 weeks | No | |
Secondary | Spontaneous engagement in physical activity - change pre to post intervention as measured by the Human Activity Profile | 8 weeks | No | |
Secondary | Efficacy for exercise change pre to post intervention as measured by the Self-Efficacy for Exercise scale. | 8 weeks | No |
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