- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04252053
The Effects of Pilates-Based Core Stabilization Training in Multiple Sclerosis
January 6, 2021 updated by: Feray Güngör, Istanbul University - Cerrahpasa (IUC)
The Effects of Pilates-Based Core Stabilization Training on Isokinetic Knee Strength and Postural Sway in People With Multiple Sclerosis
Multiple Sclerosis (MS) is a chronic, autoimmune and neurodegenerative disease characterized by inflammation and progressive demyelination of the central nervous system.
It is characterized by muscle weakness, balance and coordination disorder, which is more common in the lower extremities and trunk muscles.
Over time, these symptoms decrease the individual's level of physical activity, mobility and quality of life, leading to further deterioration of the disorder.
One of the most important problems that cause these problems in individuals with MS is reduced core stabilization.
Decrease in core stabilization affects the quality of limb movements as well as trunk stability when considering the kinetic chain in the body.
Pilates-based core stabilization training (PBCST) are a controlled exercise form used to improve the stabilization of trunk muscles.
There are no studies on the effect of this training on lower extremity isokinetic muscle strength in individuals with MS.
The aim of this study is to determine the effect of PBCST on lower extremity muscle strength, postural sway and kinetic chain in individuals with MS.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study was planned as randomized controlled.
Individuals included in the study wiil randomly allocate to the group receiving the supervised PBCST and the home exercise group.
While the supervised exercise group receives PBCST for 2 days and 8 weeks in the clinic, the home exercise group will perform the same exercises at home for the same time as the brochures prepared for them.
The exercise program will show progression at 2-week intervals.
A session will be held for both groups to teach the basic principles of pilates and will not be counted in the 8-week program.
At the beginning and end of treatment, individuals will be evaluated for isokinetic muscle strength, balance and postural sway, fatigue level, quality of life and functional capacity parameters.
PBCST is thought to reduce postural sways and increase lower extremity muscle strength by increasing core stability with the effect of kinetic chain and increased stabilization.
Study Type
Interventional
Enrollment (Actual)
50
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
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Istanbul, Turkey, 34147
- Istanbul University-Cerrahpasa
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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
16 years to 61 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being diagnosed with MS according to McDonald's criteria
- Disability level less than 6 according to EDSS (Expanded Disability Status Scale) score
- No attacks during the last 3 months
- Being an ambulatory
- Volunteering to participate in the study
Exclusion Criteria:
- Having orthopedic, neurological, psychological, etc. diseases that accompany MS and may affect treatment outcomes
- Doing regular sports
- Being involved in another physiotherapy and rehabilitation program related to MS
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Supervised Pilates-Based Core Stability Training Group
In order to detect the effects of pilates-based core stabilization training (PBCST) on isokinetic knee strength and postural sways, individuals with MS will receive pilates-based core stabilization training for 8 weeks and 2 days a week.
One educational session will perform to teach basic principles of pilates based training.
Individuals in this group will receive treatment at the clinic by physiotherapist supervision.
All sessions will be individualized (not group training).
|
Pilates-based core stabilization training (PBCST) is a controlled form of exercise provided improvement in stabilization of abdominal and back muscles.
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Active Comparator: Home exercise group
The home exercise group will perform the same PBCST exercises at home during the same period (8 weeks, 2 days a week) as the brochures prepared for them.
Individuals in this group will receive one educational session which includes basic principles of pilates and one session which includes two-week exercise program.
Participants will be invited to the clinic every two weeks to ensure the progression of the exercises and the exercise program will be updated.
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Home exercises which include pilates based core stabilization training will be structured for the people with MS according to their physical condition and will perform at home by them.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Isokinetic strength
Time Frame: 8 weeks
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Concentric isokinetic muscle strength of the knee flexor and extensor muscles will be evaluated at angular velocities of 30,60 and 90°/s.
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8 weeks
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Postural sways
Time Frame: 8 weeks
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Postural sways will be evaluated with biodex balance system in different condition such as open eyes on firm and foam surface, closed eyes on firm and foam surface, tandem stance on firm and foam surface,
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8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Core strength
Time Frame: 8 weeks
|
Core strength will be evaluated within the scope of core assessment.
Curl-Up and Modified Push-Up test will be used for the evaluation of core strength.
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8 weeks
|
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Core endurance
Time Frame: 8 weeks
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Core endurance will be evaluated within the scope of core assessment.
Trunk Flexor Endurance Test, Trunk Extensor Endurance Test, Trunk Lateral Endurance Test and Plank Test will be used in the evaluation of core endurance.
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8 weeks
|
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Balance
Time Frame: 8 weeks
|
Berg Balance Scale (BBS) will be used to evaluate balance.
BBS is a test developed for functional evaluation of balance in adults.
BBS consists of 14 general equilibrium activities that change the orientation of the body center of gravity relative to the support surface and the ability to maintain the static position during the reduction of the support surface.
The highest score is 56.
The decrease in the score indicates poorer balance.
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8 weeks
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Mobility
Time Frame: 8 weeks
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Two-minute walk test (2-MWT) will be used to evaluate the mobility of the people with MS. 2-MWT is a measure of self-paced walking ability and functional capacity.
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8 weeks
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Fatigue
Time Frame: 8 weeks
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Fatigue Severity Scale (FSS) will be used to evaluate fatigue levels.
This scale evaluates the severity of fatigue with 9 questions.
Each question scores between 1 (I do not agree) and 7 (fully agree).
The FSS score is the average value of nine sections.
A high score indicates increased fatigue severity.
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8 weeks
|
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Quality of life
Time Frame: 8 weeks
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Multiple Sclerosis Quality of Life -54 (MSQOL-54) will be used to evaluate the effectiveness of the treatment on quality of life.
The MSQOL-54 is a multidimensional health-related quality of life measure that combines both generic and MS-specific items into a single instrument.
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8 weeks
|
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Fall risk
Time Frame: 8 weeks
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Timed Up and Go (TUG) will be used.
TUG is a test used to determine fall risk and measure the progress of balance, sit to stand and walking.
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8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
February 6, 2020
Primary Completion (Actual)
January 3, 2021
Study Completion (Actual)
January 3, 2021
Study Registration Dates
First Submitted
January 27, 2020
First Submitted That Met QC Criteria
January 31, 2020
First Posted (Actual)
February 5, 2020
Study Record Updates
Last Update Posted (Actual)
January 7, 2021
Last Update Submitted That Met QC Criteria
January 6, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 59491012-604.01.02-
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.
Clinical Trials on Multiple Sclerosis
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BiogenCompletedMultiple Sclerosis | Relapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple Sclerosis | Multiple Sclerosis, Primary Progressive | Multiple Sclerosis, Remittent ProgressiveJapan
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-
BiogenElan PharmaceuticalsCompletedRelapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple SclerosisUnited States
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