Effect of Vestibular Rehabilitation on Trunk Kinetic and Kinematic Parameters in Patients With Multiple Sclerosis

November 22, 2022 updated by: Ahmed Magdy Alshimy, October 6 University
The Cawthorne Cooksey exercises and conventional program of physical therapy were administered.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

• The Cawthorne Cooksey exercises and conventional program of physical therapy were administered.

Study Type

Interventional

Enrollment (Actual)

30

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 Locations

  • Egypt
    • Giza
      • El-Sheikh Zayed City, Giza, Egypt, 1133
        • October 6 University

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

31 years to 51 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Aged 35-55 years.
  • Ambulatory without assistance.
  • Diagnosed with relapsing-remitting MS by a neurologist, with approximately five relapse attacks in the hemiparesis type with a muscular tone of 1 or 1+ depending on the MAS, or modified Ashworth scale.
  • All individuals were evaluated by a neurosurgeon to confirm central vertigo using test of Dix Hallpike.
  • Degree of MS-related disability based on the enlarged disability status scale, ranging from 2-2.5.

Exclusion Criteria:

  • People with musculoskeletal deformities.
  • People with inner ear abnormalities.
  • People with psychiatric disturbances or seizures.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group I
received conventional vestibular rehabilitation along with the Cawthorne Cooksey exercise protocol
Other: Cawthorne Cooksey exercise protocol
Cawthorne Cooksey exercise protocol
Other: conventional vestibular rehabilitation
conventional vestibular rehabilitation
Active Comparator: Group II
received conventional vestibular rehabilitation only
Other: conventional vestibular rehabilitation
conventional vestibular rehabilitation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Isokinetic dynamometer (average power)
Time Frame: 4 weeks
Assess trunk kinetic and kinematic parameters.
4 weeks
Isokinetic dynamometer (acceleration time)
Time Frame: 4 weeks
Assess trunk kinetic and kinematic parameters.
4 weeks
Isokinetic dynamometer (deceleration time)
Time Frame: 4 weeks
Assess trunk kinetic and kinematic parameters.
4 weeks

Collaborators and Investigators

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

Sponsor

October 6 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 (Actual)

May 6, 2022

Primary Completion (Actual)

August 10, 2022

Study Completion (Actual)

September 20, 2022

Study Registration Dates

First Submitted

November 13, 2022

First Submitted That Met QC Criteria

November 22, 2022

First Posted (Actual)

December 2, 2022

Study Record Updates

Last Update Posted (Actual)

December 2, 2022

Last Update Submitted That Met QC Criteria

November 22, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T.REC/012/003988

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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