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Effect of Mulligans Mobilization With Movement in Osteoarthritis Knee.

Not Applicable
Completed
Conditions
Osteo Arthritis Knee
Interventions
Behavioral: Mulligan's mobilization with movement MWM added isometric strength training
Registration Number
NCT05577403
Lead Sponsor
Majmaah University
Brief Summary

To evaluate the effect of Mulligan's mobilization with movement in osteoarthritis of the knee.

Detailed Description

Patients with knee OA diagnosed at the orthopaedic clinic of Tumair general hospital and referred to the physiotherapy department who attended the rehabilitation centre of Majmaah university will be recruited.

Patients will be excluded if they had knee or hip injury, sensory deficits in the lower extremity, a history of lower-extremity surgery, or a history of a quadriceps or hamstring muscle injury, had low back-related leg pain, or had any contraindication to manual therapy.

The protocol was submitted to and approved by the Majmaah University Research Ethics committee (MUREC Dec.2/ COM-2021/19-3)

Participants will be requested to sign a written informed consent form approved by the institutional ethics committee. A total of 60 participants were randomly assigned to group A (experimental group): Mulligan's mobilization with movement MWM added isometric strength training, and group B (control group): Sham MWM added isometric strength training. Pre and post-test readings were taken at baseline, week 2, and week 4, respectively. The outcome measures for this study will be maximal voluntary isometric contraction of quadriceps strength (measured by ISOMOVE dynamometer), ROM, and Western Ontario and McMaster universities osteoarthritis (WOMAC) index.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patient with knee OA with radiological evidence of grade 2 or 3 of the Kellgren and Lawrence scale.
  • Age between 40-65 years, unilateral or bilateral involvement (in the case of bilateral involvement, the more symptomatic knee was included), and pain in and around the knee.
Exclusion Criteria
  • Patient will be excluded, if they had any deformity of the knee, hip, or back, had any central or peripheral nervous system involvement.
  • They had received steroids or intra-articular injection within the previous three months, uncooperative patients.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental GroupMulligan's mobilization with movement MWM added isometric strength trainingMulligan's mobilization with movement added isometric strength training will be given 3 days a week for six weeks.
Control GroupMulligan's mobilization with movement MWM added isometric strength trainingMobilization-added isometric strength training will be given 3 days a week for six weeks.
Primary Outcome Measures
NameTimeMethod
pain intensity6 weeks

Visual Analogue scale on 0 to10 cm

Range of Motion6 weeks

Standard goniometer.

Western Ontario and McMaster universities osteoarthritis (WOMAC) index6 weeks

Western Ontario and McMaster universities osteoarthritis scale

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Rehabilitation center, Majmaah University

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Al Majma'ah, Riyadh, Saudi Arabia

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