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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05577403
Other study ID # Shahnaz Hasan
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 5, 2022
Est. completion date November 14, 2023

Study information

Verified date November 2023
Source Majmaah University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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 information / eligibility

Status Completed
Enrollment 60
Est. completion date November 14, 2023
Est. primary completion date November 10, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 65 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Behavioral:
Mulligan's mobilization with movement MWM added isometric strength training
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.

Locations

Country Name City State
Saudi Arabia Rehabilitation center, Majmaah University Al Majma'ah Riyadh

Sponsors (2)

Lead Sponsor Collaborator
Majmaah University King Saud University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain intensity Visual Analogue scale on 0 to10 cm 6 weeks
Primary Range of Motion Standard goniometer. 6 weeks
Primary Western Ontario and McMaster universities osteoarthritis (WOMAC) index Western Ontario and McMaster universities osteoarthritis scale 6 weeks
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