Feasibility of Resting Intervals During Exercise Programs for Individuals With Knee Osteoarthritis
Recruiting · NCT06857123 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Pittsburgh
View the official record on ClinicalTrials.gov →Interventions studied
Exercise with RestExercise without Rest
What this trial is about
This pilot randomize trial tests the feasibility of administering two different exercise programs in people with knee osteoarthritis. One group receives the exercise program administered as usual, and the other group received the exercise program with resting intervals.
Who can take part
Age range
45 Years to 79 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Age between 45 and 79 yo.
- Clinical diagnosis of primary, early to moderate stage knee osteoarthritis.
- BMI range \< 35 kg/m2.
- Sedentary lifestyle
- Knee joint is the most painful joint in the body.
- Ability to speak and understand English.
- Willingness to comply with all study procedures and be available for the duration of the study.
Exclusion criteria
- Non-OA disease of the knee.
- Advanced knee osteoarthritis
- Knee injection in the past 3 months.
- Major knee trauma/surgery in the past 5 years or previous knee surgery with hardware limiting cartilage assessment..
- Participate in regular exercise or physical activity .
- Participation in an intervention study for knee OA.
- Currently using a cane, walker or crutches to walk.
- History of cardiovascular disease or hypertension not controlled by medication.
- Two or more unexplained falls in the past year.
- Inflammatory, autoimmune disorders, neurological, systemic, muscular, or connective tissue conditions that affect walking or ability to exercise.
- Contraindication to MRI.
- Medical condition or characteristic of the participant that could place the individual at increased risk or preclude s/he from complying with study procedures.
- Pregnant female.
- Acute or terminal illness.
Where it is running
1 location listed across 1 US state.
- University of Pittsburgh - Pittsburgh, Pennsylvania, United States