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Effect of Mulligan Medial/Lateral Glide w/wo Compression/Decompression Technique on Pain ROM and Function KO

Not Applicable
Active, not recruiting
Conditions
Knee Osteoarthritis
Registration Number
NCT06757946
Lead Sponsor
Superior University
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.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
54
Inclusion Criteria

Not provided

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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pain Rating Scale (NPRS)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)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 Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Services Hospital, Shadman 1

🇵🇰

Lahore, Punjab, Pakistan

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