Osteoarthritis Clinical Trial
Official title:
Knee Stability Training in Individuals With Knee Osteoarthritis
People with knee osteoarthritis (OA) frequently complain of knee instability. This study
will test whether certain exercises can improve knee stability, reduce pain, and improve
physical function in people with knee OA.
Study hypotheses: 1) Participants in the stability training group will demonstrate less pain
and higher levels of physical function, based on self-report measures of pain and function
(WOMAC, Lower Extremity Function Scale), and less time to complete the Get Up and Go test, a
physical performance measure of function. 2) During walking and the step down task,
participants in the stability training group will demonstrate greater knee motion during
weight bearing, greater vertical ground reaction forces and loading rates, and reduced
ratios of co-contraction between quadriceps/hamsting and tibialis anterior/gastrocnemius
muscle pairs compared to the standard group. Participants in the stability group will also
demonstrate greater step lengths, single limb support times, and average walking velocity
compared to the standard group.
Traditional exercise therapy for knee OA primarily focuses on lower limb strength and joint
motion deficits. Recent evidence has suggested that changes in lower limb biomechanical
factors during weight bearing activities may have substantial impact on physical function
and disease progression in individuals with knee OA. The effectiveness of exercise therapy
programs might be improved by incorporating balance and agility training techniques (knee
stability training). The aim of this trial is to test the effectiveness of supplementing
traditional exercise therapy with knee stability training techniques tailored for
individuals with knee OA.
Participants will be randomly assigned to one of two groups. The first group will
participate in a standard rehabilitation program of traditional exercise therapy for knee
OA. The second group will participate in a standard rehabilitation program supplemented with
a knee stability program. Study visits will occur at study entry, 2 months, 6 months, and 1
year. At each study visit, changes in pain, physical function, and biomechanical factors
will be assessed. This study will last for one year.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04657926 -
A Trial of APPA in the Treatment of Knee Osteoarthritis
|
Phase 2 | |
| Completed |
NCT02536833 -
A Study Evaluating the Safety, Tolerability, and Efficacy of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
|
Phase 2 | |
| Completed |
NCT03014037 -
Comparing Mesenchymal Stem Cell Counts in Unilateral vs. Bilateral Posterior Superior Iliac Spine Bone Marrow Aspiration
|
N/A | |
| Recruiting |
NCT05937542 -
A Qualitative Investigation of CLEAT Participants
|
||
| Completed |
NCT03644615 -
A Mindfulness Program (MBSR) in the Management of Symptomatic Hip and Knee Osteoarthritis
|
N/A | |
| Recruiting |
NCT06061367 -
Muscles Strength and Gait Parameteres After TKA
|
||
| Withdrawn |
NCT04976972 -
A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation
|
N/A | |
| Completed |
NCT05496205 -
A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT03850665 -
Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach
|
N/A | |
| Completed |
NCT02826902 -
Effect of Anesthesia on Quality of Recovery in Patients Undergoing Correctional Tibial Osteotomy - A Randomized Controlled Trial
|
N/A | |
| Completed |
NCT04402502 -
Dynamic 4DCT to Examine Wrist Carpal Mechanics
|
N/A | |
| Completed |
NCT02923700 -
Leukocyte-rich PRP vs Leukocyte-poor PRP for the Treatment of Knee Cartilage Degeneration: a Randomized Controlled Trial
|
Phase 4 | |
| Completed |
NCT04564053 -
Study of Safety, Tolerability and Pharmacokinetics of LNA043 in Japanese Osteoarthritis Participants
|
Phase 1 | |
| Completed |
NCT05070871 -
A Clinical Trial Investigating the Effect of Salmon Bone Meal on Osteoarthritis Among Men and Women
|
N/A | |
| Not yet recruiting |
NCT05036174 -
Diphenhydramine Ointment for Knee Osteoarthritis
|
N/A | |
| Recruiting |
NCT02912429 -
Onlay vs. Inlay Patellofemoral Arthroplasty
|
N/A | |
| Recruiting |
NCT02666443 -
Low Dose Dexamethasone in Supraclavicular Blocks
|
N/A | |
| Active, not recruiting |
NCT02723929 -
Effects of tDCS and tUS on Pain Perception in OA of the Knee
|
||
| Withdrawn |
NCT02921594 -
Kinematic Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties
|
N/A | |
| Terminated |
NCT02820766 -
Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting
|
N/A |