EFFECTIVENESS OF BFRT ON PATIENTS WITH KNEE OSTEOARTHRITIS GRADE 2
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2023/05/052454
- Lead Sponsor
- ONE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Age between 40-60 years
Diagnosed with unilateral knee OA according to the American College of Rheumatology criteria
Moderate to very severe (scores between 5 and 13 on the Lequesne Questionnaire)
History of surgery or any invasive procedure on the knee(s) with OA;
Undergone a physical therapy or muscle strengthening program for lower limb in the past 3 months;
Planned events, such as knee replacement or travel, which may interfere with the adherence of individuals during the trial period
History of acute myocardial infarction and/or stroke;
History of peripheral arterial disease or deep vein thrombosis;
History of cancer that has generated limitations or restrictions to physical exercise;
Decompensated systemic blood pressure without medical supervision
Changes in the dose or type of anti-inflammatory or analgesic drugs in the last 3 months
Morbid obese patients
Uncontrolled Diabetes
Neuropathy
Positive Homanâ??s sign
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1-RM knee extension and flexion for strength <br/ ><br>WOMAC and The Lequesne Algofunctional Index for pain <br/ ><br>The multidimensional fatigue inventory for fatigue <br/ ><br>The Time Get Up and Go Test (TUG), 30-second Chair Stand Test (30-sCST), and 40m Fast Paced Walk Test (40mFPWT) for physical function and risk of fall <br/ ><br>WHO BREF QOL for quality of life <br/ ><br>Timepoint: Pre interventional assessment and post interventional assessment will be taken of the outcome measures between the time period of 4 weeks <br/ ><br>
- Secondary Outcome Measures
Name Time Method oneTimepoint: N/A