Effects of Mulligan Mobilization With Movement as Compared to Kaltenborn Joint Mobilization in the Management of Knee Osteoarthritis

NCT ID: NCT06444945

Last Updated: 2024-06-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-10

Study Completion Date

2024-12-30

Brief Summary

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This study is a randomised controlled trial and the purpose of this study is to determine the Effects of Mulligan mobilization with movement as compared to Kaltenborn joint mobilization in the management of knee osteoarthritis." To determine the effects of Mulligan MWM as compared to Kaltenborn joint mobilization in terms of pain, function, range of motion and gait in persons with knee osteoarthritis.

Detailed Description

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Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Parallel designed randomized control trial
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Mulligan MWM group

Group A receiving Mulligan MWM joint mobilization

Group Type EXPERIMENTAL

Heating pad

Intervention Type DEVICE

Heating pad will be used for heating purpose.

Transcutaneous electrical nerve stimulation(TENS)

Intervention Type DEVICE

TENS is used for symptomatic pain relief

Mulligan mobilization with movement (MWM)

Intervention Type PROCEDURE

It provides short term pain relief and to restore pain-free, functional movements by achieving full range at the joint

Resistance Training exercise

Intervention Type PROCEDURE

Resistance training increases muscle strength by making your muscles work against a weight or force.

Kaltenborn mobilization group

Group B receiving Kaltenborn Joint mobilization

Group Type EXPERIMENTAL

Heating pad

Intervention Type DEVICE

Heating pad will be used for heating purpose.

Transcutaneous electrical nerve stimulation(TENS)

Intervention Type DEVICE

TENS is used for symptomatic pain relief

Kaltenborn joint mobilization

Intervention Type PROCEDURE

The purpose of joint mobilization is to restore normal, painless joint function. In restricted joints, this involves the restoration of joint play to normalize the roll-gliding that is essential to active movement.

Resistance Training exercise

Intervention Type PROCEDURE

Resistance training increases muscle strength by making your muscles work against a weight or force.

Interventions

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Heating pad

Heating pad will be used for heating purpose.

Intervention Type DEVICE

Transcutaneous electrical nerve stimulation(TENS)

TENS is used for symptomatic pain relief

Intervention Type DEVICE

Mulligan mobilization with movement (MWM)

It provides short term pain relief and to restore pain-free, functional movements by achieving full range at the joint

Intervention Type PROCEDURE

Kaltenborn joint mobilization

The purpose of joint mobilization is to restore normal, painless joint function. In restricted joints, this involves the restoration of joint play to normalize the roll-gliding that is essential to active movement.

Intervention Type PROCEDURE

Resistance Training exercise

Resistance training increases muscle strength by making your muscles work against a weight or force.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Individuals aged 40-70 years (Osama et al, 2022)
* Having KOA history of no less than 3 months
* Knee pain less than 8/10 on numeric pain rating scale (NPRS).
* Radiological evidence of grade III or less on Kellgren classification
* Patients referred from rehab department

Exclusion Criteria

* Those with signs of serious pathology, such as malignancy, inflammatory disorder or infection.
* History of trauma or fractures in lower extremity.
* Signs of lumbar radiculopathy or myelopathy.
* History of knee surgery or replacement.
* Receiving intra-articular steroid therapy in the preceding two months.
Minimum Eligible Age

40 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Foundation University Islamabad

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Shanza Fatima, DPT

Role: PRINCIPAL_INVESTIGATOR

Foundation University Islamabad

Muhammad Osama, PHD*

Role: PRINCIPAL_INVESTIGATOR

Foundation University Islamabad

Locations

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Foundation University Islamabad

Islamabad, , Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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FUI/CTR/2024/13

Identifier Type: -

Identifier Source: org_study_id

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