Knee Osteoarthritis Clinical Trial
Official title:
Effectiveness of Reduced Frequency Physical Therapy Supplemented With In-home Exercise Equipment Compared to Standard Care Physical Therapy in Total Knee Arthroplasty
NCT number | NCT03302832 |
Other study ID # | 313 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 1, 2017 |
Est. completion date | October 1, 2019 |
Verified date | January 2020 |
Source | Campbell University, Incorporated |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Rehabilitation after Total Knee Arthroplasty surgery involves physical therapy services to address limitations in range of motion, strength, and participation in normal daily activities. This investigation will compare the outcomes from standard physical therapy intervention in comparison to reduced frequency physical therapy sessions supplemented with in-home exercise equipment.
Status | Completed |
Enrollment | 51 |
Est. completion date | October 1, 2019 |
Est. primary completion date | October 1, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A to 65 Years |
Eligibility |
Inclusion Criteria: - Individual is to undergo TKA by a licensed physician at Participating hospital group - Participating primary health insurance provider - Patient is < 64.5 years of age - Willingness to participate in study protocol Exclusion Criteria: - Previous or current history of cancer - High risk for cardiovascular disease as determined by the American College of Sports Medicine - Individuals with documented mental, psychiatric, or emotional disabilities - Inability to read and write in English |
Country | Name | City | State |
---|---|---|---|
United States | EmergeOrtho | Durham | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Campbell University, Incorporated |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Knee Injury and Osteoarthritis Outcome Score (KOOS) | The KOOS measurement is a patient-reported questionnaire that contains 42 questions covering 5 categories (pain, symptoms, activities of daily living, sports and recreation, and quality of life | Pre-surgery to 3 months post-surgery | |
Secondary | Self-reported home exercise compliance/adherence | Basic questions regarding the percent compliance with home exercises, amount of exercise time per week, and amount of days the participant performed exercise each week. | 1 month post-surgery, 2 months post-surgery, 3 months post-surgery | |
Secondary | Change in Knee Active Range of Motion (AROM) | Measurement of the range of motion that the participant can perform (in degrees) when maximally bending and straightening the knee. | Pre-surgery to 3 months post-surgery | |
Secondary | Change in Knee Passive Range of Motion (PROM) | Measurement of the range of motion (in degrees) that the participant's knee can maximally bend and straighten as a result of a manually applied movement. | Pre-surgery to 3 months post-surgery | |
Secondary | Change in Timed Up-and-Go Test (TUG) | The TUG is a physical performance test that consists of the participant rising from a chair, ambulating 9 meters, turning around, returning to the chair and sitting. It is recorded in seconds. | Pre-surgery to 3 months post-surgery | |
Secondary | Change in 6-minute Walk Test (6MWT) | The 6MWT is an assessment of longer duration ambulation and cardiorespiratory endurance. The test measurement is the total amount of distance that the participant ambulates within a 6-minute period. | Pre-surgery to 3 months post-surgery | |
Secondary | Change in 30 second Chair Stand Test (30s-CST) | The 30s-CST is a test of strength, endurance and functional balance. The maximum number of sit to stand repetitions performed over a 30 second period represents the score for this test. Pre-test positioning includes placement of a 44 cm (17 inch) chair, measured from floor to seat surface, against a wall to inhibit movement of the chair during the test. | Pre-surgery to 3 months post-surgery |
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