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Clinical Trials/NCT05577403
NCT05577403CompletedNot Applicable

Effect of Mulligan's Mobilization With Movement Added With Isometric Exercises on Muscle Strength Pain and Disability Associated With Knee Osteoarthritis: A Randomized Controlled Study

Majmaah University2 sites in 1 country50 target enrollmentStarted: November 5, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
2
Primary Endpoint
Range of Motion

Study Overview

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

The protocol was submitted to and approved by the Rehabilitation Research Chair, King Saud University Research Ethics Committee (RRC-2021-17)

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

Experimental Group

Experimental

Mulligan's mobilization with movement added isometric strength training will be given 3 days a week for six weeks.

Intervention: Mulligan's mobilization with movement MWM added isometric strength training (Behavioral)

Control Group

Active Comparator

Mobilization-added isometric strength training will be given 3 days a week for six weeks.

Intervention: Mulligan's mobilization with movement MWM added isometric strength training (Behavioral)

Outcomes

Primary Outcomes

Range of Motion

Time Frame: 6 weeks

Standard goniometer.

pain intensity

Time Frame: 6 weeks

Visual Analogue scale on 0 to10 cm

Western Ontario and McMaster universities osteoarthritis (WOMAC) index

Time Frame: 6 weeks

Western Ontario and McMaster universities osteoarthritis scale

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shahnaz Hasan, PhD

Associate Professor

Majmaah University

Study Sites (2)

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