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Completed

NCT Number: NCT05577403

Effect of Mulligans Mobilization With Movement in Osteoarthritis Knee.

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

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Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rehabilitation center, Majmaah University

Al Majma'ah, Riyadh Region, 15341, Saudi Arabia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Mulligan's mobilization with movement MWM added isometric strength training

Behavioral

Mulligan's mobilization with movement added isometric exercise:

the participants in the experimental group will receive a Mulligan's mobilization with movement added isometric exercise.

Treatment will be given for the period of three weeks, for five days a week in both groups.

Data will be collected before intervention and after 2nd & 4th week of intervention.

Other names: Sham MWM added isometric strength training

Primary outcomes

  1. pain intensity

    Time frame: 6 weeks

    Visual Analogue scale on 0 to10 cm

  2. Range of Motion

    Time frame: 6 weeks

    Standard goniometer.

  3. Western Ontario and McMaster universities osteoarthritis (WOMAC) index

    Time frame: 6 weeks

    Western Ontario and McMaster universities osteoarthritis scale

Sponsors and collaborators

Lead sponsor

Majmaah University

Other

Collaborators

  • King Saud University

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 13, 2022
Registry last updated
Sep 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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