Acute Effects of Blood Flow Restriction Training to Failure on Hypoalgesia in Patients With Severe Knee Osteoarthritis Using Dynamic or Fixed Occlusion Pressure
Recruiting · NCT07300384 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Valencia
View the official record on ClinicalTrials.gov →Interventions studied
Low-intensity resistance exercise to failure with moderate arterial occlusion pressure and dynamic pressure.Low-intensity resistance exercise to failure with moderate arterial occlusion pressure and fixed pressure.
What this trial is about
This study aims to compare the acute effects on hypoalgesia of training to failure using blood flow restriction (BFR) with dynamic occlusion versus BFR with fixed occlusion in patients with severe gonarthrosis. Two different training conditions will be performed with varying levels of blood flow occlusion (%BFR) and percentage of load (%RM): 1) 30% RM and 50% BFR with dynamic pressure; 2) 30% RM and 50% BFR with fixed pressure. Each participant will complete two individual sessions under different training conditions, randomly assigned with a 72-hour interval between sessions.
Who can take part
Age range
50 Years to 85 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 50 and 85 years
- Diagnosis of severe gonarthrosis according to the clinical and radiographic criteria of the American College of Rheumatology guidelines.
- On the waiting list for unilateral total knee replacement (TKR) surgery
Exclusion criteria
- Pain in the contralateral leg with an intensity ≥80/100 mm on the visual analog scale (VAS) during daily activities.
- Previous hip or knee replacement surgery and osteotomy within the last year.
- Autoimmune arthritis
- Medical conditions that contraindicate exercise.
- Participation in exercise programs (\>2 days/week with training at intensities of 10-15 1RM) in the previous six months.
- History of stroke, brain surgery, major depression, or self-reported cognitive impairment that could affect performance in the study.
- Cardiovascular, thrombotic, or vascular risk factors (uncontrolled hypertension, peripheral arterial disease, history of deep vein thrombosis or pulmonary embolism, heart failure, severe varicose veins, or uncontrolled anticoagulant therapy).
- Skin or local alterations at the cuff application site (ulcers, open wounds, infections, lymphedema, or severe edema).
- Inability to communicate normally or with impaired communication skills.
Where it is running
2 locations listed.
- Faculty of Physiotherapy, University of Valencia - Valencia, Valencia, Spain
- University of Valencia - Valencia, Valencia, Spain