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Clinical Trials/NCT06751095
NCT06751095
Not yet recruiting
Not Applicable

Effects Of Maitland's Mobilization At Mid Versus End Range On Pain, Range Of Motion And Functional Disability In Patients With Knee Osteoarthritis.

Riphah International University0 sites44 target enrollmentJanuary 10, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Riphah International University
Enrollment
44
Primary Endpoint
Numeric Pain Rating Scale
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Knee Osteoarthritis (OA) is the most common form of arthritis affecting mostly elderly people contributing to major cause of disability worldwide.In knee osteoarthritis Maitland's manual therapy technique could be the most effective technique among all in decreasing pain sensitivity and increasing range of motion in knee OA.The aim of this study to compare effects of Maitland's mobilization at mid range versus end range on pain. range of motion and functional disability in patients with knee OA, providing useful insights for healthcare professionals to optimize treatment strategies and enhance outcomes in this context.

Detailed Description

Knee Osteoarthritis (OA) is the most common form of arthritis affecting mostly elderly people contributing to major cause of disability worldwide.In knee osteoarthritis Maitland's manual therapy technique could be the most effective technique among all in decreasing pain sensitivity and increasing range of motion in knee OA.The aim of this study to compare effects of Maitland's mobilization at mid range versus end range on pain. range of motion and functional disability in patients with knee OA, providing useful insights for healthcare professionals to optimize treatment strategies and enhance outcomes in this context. This Randomized Clinical Trial will be conducted at DHQ Gujrat through consecutive sampling technique on 44 patients which will be allocated using simple random sampling through sealed opaque enveloped into (Group A and Group B).Maitland's mobilization at end range(Group A) incorporates the end range Maitland's mobilization,strengthening exercises, knee isometrics, transcutaneous electrical stimulation(TENS) and heating pad . Maitland's mobilization in Mid range (Group B) will be treated with Mid range Maitland's mobilization, TENS,strengthening exercises,knee isometrics and heating pad.Outcomes, encompassing pain levels, range of motion(ROM), and functional disability will be evaluated through Visual analogue scale (VAS),Goniometer and WOMAC scale.The treatment plan spans 4 weeks, comprising 3 sessions per week. Data will be analyzed during SPSS software version 25. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups. Data will be collected at baseline and after 4 weeks of follow up.

Registry
clinicaltrials.gov
Start Date
January 10, 2025
End Date
June 30, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participants with age between 40 to 60 years.
  • Participants of both genders will be included.
  • Patient with unilateral/bilateral symptomatic tibiofemoral knee OA.
  • Patient suffering from stiffness less than 30 minutes
  • Patients with radiologically diagnosed case of grade 2 knee OA according to the Kellgren and Lawrence scale
  • Patients with reported peak knee pain of \>3 on visual analogue scale (VAS)

Exclusion Criteria

  • Participants with acute inflammation of knee
  • Participants with severe degenerative lumbar spine disease e.g spondylolisthesis
  • Participants with systemic inflammatory arthritic or neurological conditions
  • Participants with intraarticular injection in the prior 3 months
  • Participants with unstable heart condition
  • Participants with received physical therapy of knee in last 3 months

Outcomes

Primary Outcomes

Numeric Pain Rating Scale

Time Frame: 4 Weeks

The Numerical Pain Rating Scale (NPRS) is a commonly used self-report measure to assess the intensity of pain experienced by individuals. Participants rate their pain on a numerical scale, typically ranging from 0 (no pain) to 10 (worst possible pain).

Secondary Outcomes

  • WOMAC Osteoarthritis INDEX(4 weeks)
  • Universal Goniometer(4 weeks)

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