Comparison of Mulligan Mobilization Technique and Mckenzie Exercises Among Patient With Sacroilliac Joint Dysfunction

June 1, 2022 updated by: Muhammad Naveed Babur, Superior University
Comparison of Mulligan Mobilization Technique and Mckenzie Exercises Among Patient with Sacroilliac Joint Dysfunction

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

To determine comparison of mulligan mobilization technique and McKenzie exercises in patient with sacroiliac joint dysfunction.

Study Type

Interventional

Enrollment (Anticipated)

58

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Pakistan
      • Lahore, Pakistan
        • Social Security hospital Manga road Raiwind.,Chaudary Muhammad Akram research and teaching hospital.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age between 18 to 65.(29)
  • Both male and female and Pain in low back. (17)
  • Pain in sacroiliac joint (PSIS) with or without radiating to buttocks.(30)
  • With acute/subacute pain within 4-12 weeks of onset and at least three of four clinical tests positive.(14)

Exclusion Criteria:

  • Midline pain in back, Lumber stenosis, Lumber radiculopathy, Spondylolisthesis, Disc related pain, Pregnant females with SIJD(29),Any lower limb pathology or hip fracture, Rheumatoid arthritis(17)
  • History of any orthopedic surgery, and conditions such as ankylosing spondylitis.(14)
  • Spinal leminectomy
  • Arthodesis

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: HEALTH_SERVICES_RESEARCH
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Mulligan Mobilization
Using the Technique of Mulligan Mobilization
Diagnostic test: Mulligan Mobilization
Using the Technique of Mulligan Mobilization
EXPERIMENTAL: Mckenzie Exercises
Using Mckenzie Exercises
Diagnostic test: Mckenzie Exercises
Using Mckenzie Exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mulligan Mobilization Technique
Time Frame: 6 Month
29 Participents with Mobilization applied by a therapist and an active physiological movement to end range applied by the patient. Mulligan mobilization with 10 repetitions; 3 sets. Oswestry disability questionnaire with visual analog scale (0 for minimum and 10 for Maximum pain)
6 Month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mckenzie Exercises
Time Frame: 6 Months
29 Participents with intervention technique Lie down on your stomach. Prop yourself up on your forearms with your shoulders above your elbows, Hold for 2 to 3 minutes, Lower your upper body. Repeat up to eight times a day. Modified Oswestry disability questionnaire with visual analog scale(0 for minimum and 10 for Maximum pain)
6 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Superior University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

June 1, 2022

Primary Completion (ANTICIPATED)

August 1, 2022

Study Completion (ANTICIPATED)

November 1, 2022

Study Registration Dates

First Submitted

May 10, 2022

First Submitted That Met QC Criteria

June 1, 2022

First Posted (ACTUAL)

June 3, 2022

Study Record Updates

Last Update Posted (ACTUAL)

June 3, 2022

Last Update Submitted That Met QC Criteria

June 1, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DPT/Batch-Fall17/515

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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