Effect of Mulligan Medial/Lateral Glide With and Without Compression/ Decompression Technique on Pain, Range of Motion and Function on Patients With Knee Osteoarthritis
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Superior University
- Enrollment
- 54
- Locations
- 1
- Primary Endpoint
- Pain Rating Scale (NPRS)
Study Overview
Brief Summary
The Effect of Mulligan Medial/Lateral Glide Techniques with and without Compression-Decompression on Pain, Range of Motion and Function in Patients with Knee Osteoarthritis. This study aims to investigate these effects to develop more effective, non-invasive treatment protocols for improving pain, range of motion and overall function in knee OA
Detailed Description
patients, for the better understanding of response by both treatments (i.e Mulligan medial/lateral glide with and without compression/decompression technique). Patient which meet inclusion criteria, gave their consent.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Health Services Research
- Masking
- None
Eligibility Criteria
- Ages
- 30 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Unilateral Knee OA, Males and females between 30 and 60 years of age,
- •Patients with restricted ROM,
- •Patients are having more than grade III strength of knee muscles,
- •l Willingness to take part in the intervention and evaluations
Exclusion Criteria
- •Patients having unstable knee joint after Total Knee Arthroplasty or medical conditions affecting rehabilitation,
- •l Joint infection of hip and knee,
- •l Soft tissue injuries around knee joints,
- •including tendinitis and bursitis,
- •l Any fracture including patellar fracture, femur or tibia
Arms & Interventions
Interventional group I
Intervention: Mulligan Medial/Lateral glide with compression/ decompression technique (Combination Product)
Interventional group II
Intervention: Mulligan Medial/Lateral glide (Combination Product)
Outcomes
Primary Outcomes
Pain Rating Scale (NPRS)
Time Frame: 12 Months
This tool was utilized to assess the intensity of pain. A score of 0 denotes ""having no pain at all,"" while a score of 10 indicates ""the worst pain I've ever experienced."" The participants were asked to choose a number on the scale that accurately represented how much knee discomfort they were experiencing.According to a study conducted on individuals with knee OA, the interclass correlation was 0.95. Higher scores denote more intense pain; scores range from 0 to 10.
Western Ontario and McMaster Osteoarthritis Index (WOMAC)
Time Frame: 12 months
It is commonly used to assess lower extremity functional status, discomfort, and associated stiffness. The questionnaire consists of twenty-four questions: seventeen pertain to physical status, five concern pain status, and two address stiffness. Each question contains five alternatives starting from 0 which signifies no symptom or trouble at all to 4 which represents considerable difficulty in doing activities with severe symptoms. There are subscale scores for stiffness, discomfort, and functional status. The sum of the 24 items that were listed, with scores ranging from 0 to 96, was the definition of the total scores.
Secondary Outcomes
No secondary outcomes reported
Investigators
Muhammad Naveed Babur
Principal Investigator
Superior University