Comparison of effects of two physiotherapy mobilization interventions as an adjunct to institution-based exercise program on pain, joint motion, strength, ability to perform activities of daily living & quality of life in knee osteoarthritis patients
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecified
- Registration Number
- CTRI/2024/05/066730
- Lead Sponsor
- Sancheti Institute for Orthopaedics and Rehabilitation College of Physiotherapy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Subjects of either gender with an age group of 40-75yrs & having knee pain.
2.Subjects fulfilling American College of Rheumatology clinical criteria. At least one of the following three Age more than 50, morning stiffness less than 30 min,
Crepitus on knee motion, with or without X Ray findings.
3.Subjects with grade I to III knee osteoarthritis on the Kellgren and Lawrence
scale.
4.Subjects able to stand and walk without help.
1.Subjects with history of knee/ lower limb joint replacement surgery.
2.Subjects present with history of any lower limb fracture or ligament injury.
3.Subjects with post-traumatic knee osteoarthritis.
4.Subjects with patellofemoral arthritis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.VAS (Pain) <br/ ><br>2.Universal goniometerTimepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks)
- Secondary Outcome Measures
Name Time Method 30s chair stand testTimepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks);Micro FET3Timepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks);Time up and goTimepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks);WHOQOL-BREFTimepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks);WOMAC CRD PuneTimepoint: At baseline (0 weeks) and <br/ ><br>Post-intervention (4 weeks)