Comparing Pain and Kinematic Outcomes of Two Gait-Modifying Shoe Interventions
Status: | Not yet recruiting |
---|---|
Healthy: | No |
Age Range: | 45 - 75 |
Updated: | 3/23/2019 |
Start Date: | April 16, 2019 |
End Date: | November 1, 2020 |
Contact: | Michelle Bruner, MS |
Email: | bruneml@ortho.ufl.edu |
Phone: | 352-273-7337 |
Pilot Study: Comparing Pain and Kinematic Outcomes of Two Gait-Modifying Shoe Interventions on Knee Osteoarthritis Acutely and Over a 12 Week Period
This study involves the use of a newly designed shoe device for knee arthritis patients that
may help reduce knee pain and improve function.
may help reduce knee pain and improve function.
This study involves the use of a newly designed shoe device for knee arthritis patients that
may help reduce knee pain and improve function. This is a 2-phase study designed to evaluate
knee pain and function in healthy participants with a history of medial knee arthritis.
The purpose of this study is to evaluate: 1. how using the shoe device will affect a person's
walking gait and balance over a single day; and 2. how using the shoe device over the course
of a 12-week period will affect a person's walking gait and balance.
may help reduce knee pain and improve function. This is a 2-phase study designed to evaluate
knee pain and function in healthy participants with a history of medial knee arthritis.
The purpose of this study is to evaluate: 1. how using the shoe device will affect a person's
walking gait and balance over a single day; and 2. how using the shoe device over the course
of a 12-week period will affect a person's walking gait and balance.
Inclusion Criteria:
- Chronic, OA-related knee pain
- Diagnosis of medial compartment knee OA (unilateral or bilateral)
- Moderate pain of ≥4 out of 10 points while performing a weight-bearing activity
- Kellgren and Lawrence score of 2, 3, or 4 evidenced on routine, standard-of-care x-ray
within the last 2 years prior to enrollment
- Able to walk unassisted for at least 10 minutes at a time
- Wear a Women's shoe size of 6.5 to 13 or a Men's shoe size of 5 to 12.
Exclusion Criteria:
- Patients suffering from acute septic or inflammatory arthritis
- Unstable cardiovascular, orthopaedic, or neurological conditions, uncontrolled
diabetes, or any condition that would preclude exercise in moderate duration, moderate
workload trials
- Received a corticosteroid injection or invasive procedures within prior 6 months of
the study
- History of avascular necrosis in the knee
- History of knee buckling
- Joint replacement in any lower extremity joint that has not optimally recovered (e.g.
still causes significant pain or affects mobility) as determined by the PI.
- Experienced more than 3 falls within the last year
- Currently using any knee brace on a regular basis for the knee pain, with the
exception of basic knee sleeves
- Pathological osteoporotic fracture
- Severe symptomatic degenerative arthritis in lower limb joints other than the knees
- Severe back pain, prior spinal fusion or spinal deformity that would affect gait
- Major cardiac or pulmonary conditions and any orthopedic limitation that precludes
their ability to independently walk for 10 minutes or longer
- Knee flexion contracture greater than 15°
- Knee flexion of less than 90°
- Any major injury to either knee within the prior 12 months
- Currently enrolled in a supervised physical therapy program
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