Total knee arthroplasty. Presence of artificial knee joint
Conditions
Interventions
Intervention 1: Intervention group:1BFR with Low Intensity Resistance training ( For the first two weeks participants will follow home plan of standard physical therapy. Resistance training will be st
Sponsors
Riphah International University Lahore
Eligibility
Sex/Gender
All
Age
50 Years to 65 Years
Inclusion criteria
Inclusion criteria: Both male and female patients 50 to 65 years of age (27) Post-total knee arthroplasty for osteoarthritis Unilateral joint replacement surgery
Exclusion criteria
Exclusion criteria: Impaired cognitive function and mental disease (e.g., diagnosis of Alzheimer's disease) Paraplegia/extremity amputation End-stage renal disease requiring dialysis Uncontrolled cardiovascular disease or Severe pulmonary disease Active neoplasm Body mass index greater than 40 kg/m² Peripheral vascular disease or deep vein thrombosis Opioid use and Chronic oral steroid use and anticoagulation use Ipsilateral joint disease involving hip, ankle, or spine Neurologic or other etiology of quadriceps wasting
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: baseline , at 4th week and post training at 8th week. Method of measurement: Numeric Pain Rating Scale (NPRS).;Knee range of motion ROM. Timepoint: baseline , at 4th week and post training at 8th week. Method of measurement: Universal Goniometer.;Strength. Timepoint: baseline , at 4th week and post training at 8th week. Method of measurement: Hand-Held Dynamometer.;Quadriceps muscle thickness. Timepoint: baseline & at the end of 8th week. Method of measurement: Ultrasound Imaging.;Functional Performance. Timepoint: baseline , at 4th week and post training at 8th week. Method of measurement: a)Lower Extremity Function Scale b)6-Minute Walk Test. | — |
Countries
Pakistan
Contacts
Public ContactMaira Shahzad
Riphah International University Lahore
Outcome results
None listed