- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00519922
A Study of the Effectiveness of Different Types of Exercise for People With Knee Osteoarthritis (KBA Exercise)
Efficacy of Kinesthesia, Balance and Agility Exercise Training as Treatment of Knee Osteoarthritis: A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Radiographic knee OA is present in an estimated 37% of Americans over the age of 60, representing more than 13 million people. Current medical, non-surgical knee OA treatments focus primarily on symptomatic relief and have met with limited, temporary success. Various therapeutic exercise prescriptions have been used to help ameliorate knee OA symptoms and improve function. Leg strength training is most commonly used. However, recent evidence suggests that shorter programs of kinesthesia, balance and agility (KBA) techniques may result in more rapid symptom relief and functional improvements in comparison to traditional therapeutic exercise. These early benefits could potentially lead to greater long term exercise adherence.
In a case study of an elderly female patient with dynamic knee instability related to OA, physical therapists reported success with a combination of KBA training and traditional therapeutic exercise. These findings need to be verified in a controlled clinical trial. This pilot study will help determine the proper testing and exercise training methods for a larger clinical trial, and will indicate if KBA training done without concurrent strength training is a viable intervention.
Research Hypothesis: Among men and women age 50 and over with Kellgren and Lawrence (1957) Grade 2 or higher symptomatic tibiofemoral OA in one or both knees, an 8-week, 3-day per week kinesthesia, balance & agility (KBA) exercise program - designed to increase dynamic neuromuscular knee stability - safely and effectively changes physical function more effectively than standard leg strength training
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Florida
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Clearwater, Florida, United States
- Morton Plant Mease Cheek-Powell Wellness Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: 1
KBA = Kinesthesia, Balance, Agility Exercise Training
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Participants will exercise three times per week 20 to 30 minutes per session. Agility/Active Range of Motion exercises provide warm-up, improve joint range-of-motion & agility, dynamic proprioception,functional strength & endurance. Kinesthesia & Balance Training will challenge the subject's proprioceptive and neuromuscular control mechanisms to adapt and stabilize the knee joints during dynamic ADL activities (walking, climbing, etc); improve static and dynamic balance and sense of stability & confidence in ADL activities. Soft pads will be used to progress some of the kinesthesia & balance challenge training. Thera-Band® balance pads at 3 levels of softness will be used. These balance pads allow both appropriate starting difficulty and progression of difficulty level (i.e., the softer the pad, the greater the difficulty). Subjects will demonstrate safe balance on a stable surface (i.e. one-footed standing on floor) prior to progressing to the first level of the soft pads. |
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Active Comparator: 2
Standard Lower Extremity Strength Training
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Standard therapeutic exercises for knee OA which are widely used.
Body weight and Thera-Band® color coded elastic bands will be used as appropriate to provide resistance.
Exercises will be progressed according to the individual participant's improvement.
All training for the ST condition will be conducted on stable surfaces (e.g.
standing on floor, sitting in chair, lying on floor).
Exercises may include 4-direction straight leg lifts, heel slides, quad sets, internal & external hip rotation, heel raises, toe raises, knee extension, knee flexion, partial squats/wall slides, etc.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
WOMAC Osteoarthritis Scale; Function subscale change pre to post intervention - KBA vs. standard strength training
Time Frame: 8 weeks
|
8 weeks
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
WOMAC subscale change in Pain and in Stiffness pre to post intervention
Time Frame: 8 weeks
|
8 weeks
|
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Walking speed change in a timed Get Up & Go Test pre to post intervention
Time Frame: 8 weeks
|
8 weeks
|
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Stair climbing and descending speed change pre to post intervention
Time Frame: 8 weeks
|
8 weeks
|
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Gait quality measures with the GAITRite walking mat and EMG, pre to post intervention
Time Frame: 8 weeks
|
8 weeks
|
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Spontaneous engagement in physical activity - change pre to post intervention as measured by the Human Activity Profile
Time Frame: 8 weeks
|
8 weeks
|
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Efficacy for exercise change pre to post intervention as measured by the Self-Efficacy for Exercise scale.
Time Frame: 8 weeks
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8 weeks
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Collaborators and Investigators
Investigators
- Principal Investigator: Matthew W Rogers, MS, The Arthritis Research Institute of America
- Study Director: Nauris Tamulevicius, PhD, Morton Plant Mease Cheek-Powell Wellness Center
- Study Chair: Frances V Wilder, PhD, The Arthritis Research Institute of America
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KneeOAExercise-1
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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