The Effects of Vestibular Exercise and Cervical Stabilization Exercise Training on Balance and Gait in MS Patients

Sponsor
Sanko University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05409599
Collaborator
(none)
36
1
3
11
3.3

Study Details

Study Description

Brief Summary

The population of this research consists of individuals between the ages of 18-65 with MS disease. MS patients to be included in the study will be directed by the Neurology outpatient clinic of Sanko University Hospital. All volunteers who agreed to participate in this randomized controlled pretest-posttest design study and met the sample criteria will be included in the study.Individuals who agree to participate will be divided into three groups by simple random method and closed envelope method. Vestibular exercise training group will be formed as Group 1 and Cervical stabilization exercise training group as Group 2, control group, and Group 3 as control group.Functional reach test, tandem stand test, 25 step walking test scale form, Multiple Sclerosis Quality of Life Scale form ( MSQOL-54),Fatigue Impact Scale,Beck depression inventory, MS walking scale (msys-12), dizziness disability inventory, four step square test, timed sit and stand test

, 2 minutes walking test be performed before and after treatment,

Condition or Disease Intervention/Treatment Phase
  • Other: Exercises
N/A

Detailed Description

Group 1: Vestibular exercise training will be given in addition to conventional treatment (including TENS, electrical stimulation and normal joint range of motion exercises) for 12 weeks. Cawthorne-Cooksey Exercises will be given as a treatment protocol for vestibular exercise training.

Group 2 :Cervical stabilization exercise training will be given in addition to conventional treatment (including Tens, electrical stimulation and normal range of motion exercises) for 12 weeks. Cervical stabilization training improves the sense of cervical proprioception as well as strength and endurance, thereby reducing joint position sense error. Cervical stabilization exercises and training, consisting of 3 stages with increasing difficulty level, will be applied.

Group3: Classical balance exercise training will be given to the control group in addition to conventional treatment (including Tens, electrical stimulation and normal range of motion exercises) for 12 weeks. These exercises were selected among the exercises routinely used in balance rehabilitation in the literature and clinic.

Balance exercise program: walking on tiptoe and heel, walking straight and diagonally on the line, standing on a balance board, supine/prone rolling on the rehabilitation ball, pelvis control in the sagittal and frontal planes on the rehabilitation ball, prone balance on the rehabilitation ball, walking on mats of different softness , was created from side walking exercises.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparison of the Effects of Vestibular Exercise and Cervical Stabilization Exercise Training on Balance and Gait in Multiple Sclerosis Patients
Actual Study Start Date :
Oct 1, 2021
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Cawthorne-Cooksey Exercises

Cawthorne-Cooksey Exercises applied to 1st group for 3 days/week for 12 weeks

Other: Exercises
Exercises

Active Comparator: cervical stabilization Exercises

cervical stabilization Exercises applied to 1st group for 3 days/week for 12 weeks

Other: Exercises
Exercises

Active Comparator: classical balance Exercises

classical balance Exercises applied to 1st group for 3 days/week for 12 weeks

Other: Exercises
Exercises

Outcome Measures

Primary Outcome Measures

  1. Balance [12 weeks]

    functional reach test

  2. Gait speed [12 weeks]

    25-step walking test

  3. Dizziness [12 weeks]

    dizziness disability inventory

  4. Balance [12 weeks]

    tandem stance test

  5. Balance [12 weeks]

    4 square step test

  6. Endurance [12 weeks]

    2-minute walk test

  7. Balance and coordination [12 weeks]

    timed sit and stand test

  8. Postural swing [12 weeks]

    GYKO

  9. Walkiing difficulty [12 Weeks]

    Multiple Sclerosis Walking Scale-12 (MSYS-12)

Secondary Outcome Measures

  1. Fatigue [12 weeks]

    fatigue impact scale

  2. Depression [12 weeks]

    beck depression inventory

  3. MSQ54 İnventory [12 weeks]

    quality of life

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • be diagnosed with MS

  • Not having received physiotherapy-oriented treatment in the last 1 year

  • not have had an attack in the last 1 month and not be in the attack period

Exclusion Criteria:
  • having systemic diseases such as hypertension, heart disease, diabetes mellitus, hyperlipidemia, malignancy

  • individuals whose ambulation is not independent

  • Those who have undergone any surgery in the last 6 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sanko University Gaziantep Şehitkamil Turkey 27500

Sponsors and Collaborators

  • Sanko University

Investigators

  • Study Director: hakan Polat, Sanko University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hakan Polat, Director, Sanko University
ClinicalTrials.gov Identifier:
NCT05409599
Other Study ID Numbers:
  • HakanP
First Posted:
Jun 8, 2022
Last Update Posted:
Jun 8, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hakan Polat, Director, Sanko University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 8, 2022