Effect of Mulligans Mobilization With Movement in Osteoarthritis Knee.
- Conditions
- Osteo Arthritis Knee
- 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
- 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.
- 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
- Primary Outcome Measures
Name Time Method Range of Motion 6 weeks Standard goniometer.
pain intensity 6 weeks Visual Analogue scale on 0 to10 cm
Western Ontario and McMaster universities osteoarthritis (WOMAC) index 6 weeks Western Ontario and McMaster universities osteoarthritis scale
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Rehabilitation center, Majmaah University
🇸🇦Al Majma'ah, Riyadh, Saudi Arabia
Rehabilitation center, Majmaah University🇸🇦Al Majma'ah, Riyadh, Saudi Arabia