- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04838886
The Effect of Telerehabilitation Based Pilates Training in Multiple Sclerosis Patients
The Effect of Telerehabilitation Based Pilates Training on Physical Performance and Quality of Life in Multiple Sclerosis Patients
Multiple Sclerosis (MS) is a chronic inflammatory disease of the central nervous system characterized by myelin, oligodendrocyte, and axon damage. MS usually begins with attacks due to demyelination of axons in the brain, optic nerve, and spinal cord; over time it develops into a neurodegenerative disease associated with neurotrophic support deficiency and neuronal loss. In MS, various loss of strength, balance, fatigue, cognitive and gait disturbances arise in the central nervous system due to sensory and/or motor neuron degeneration. These disorders affect the quality of life by limiting the individual's activities and participation in their daily lives. Therefore, it is important to treat these disorders in the treatment of MS.
There are various pharmacological treatments and invasive procedures for the management of MS symptoms and one of the most commonly used treatment options is rehabilitation. Clinically-based exercise and rehabilitation are some of the most beneficial rehabilitation strategies in people with MS (PwMS). Clinically-based exercise and rehabilitation have been shown to stabilize or improve many physical symptoms of MS including loss of strength, balance dysfunction, impaired mobility, and fatigue. These benefits have led many practitioners to consider physical exercise as a nonpharmaceutical disease-modifying treatment. However, due to various factors such as mobility disorders, fatigue, and related problems, geographic location, time constraints, transportation difficulties, health insurance coverage, and financial burden, clinical-based exercise may be problematic in some pwMS. To overcome these challenges, approaches to rehabilitation have been developed such as telerehabilitation. The telerehabilitation system provides benefits such as continuity in patient education and rehabilitation, showing progress in rehabilitation, making changes in the treatment program, and saving individuals time and financial expenses. It is also an innovative and potential alternative to face-to-face interventions for treating disease-related disorders in pwMS. In literature, there are many studies examining the effectiveness of telerehabilitation in pwMS. According to these studies, ıt has been shown that telerehabilitation, with its technical facilities, had the potential to make clinical interventions widely accessible and effective for MS, however, telerehabilitation-based interventions could not replace traditional interventions but could perfectly complement. It has been found that telerehabilitation improved balance and postural control in MS patients and had no side effects. However, it was emphasized that the evidence levels of the studies were insufficient for methodological reasons. It has been determined additional studies are needed to investigate examining the effect on walking.
Another clinical-based exercise method is Pilates. Pilates is a "core" stability-based exercise method that includes endurance, flexibility, movement, posture, and respiratory control. Studies have shown that Pilates training can improve balance, mobility, and muscle strength, fatigue in pwMS due to its structure consisting of balance and strengthening exercises. When the literature is reviewed in terms of Telerehabilitation based on Pilates in pwMS, it is seen that there are only two studies. In both studies, pwMS were given 20 minutes of yoga, 20 minutes of Pilates, and 20 minutes of dual-task exercise. However, these studies were in the project phase and the results are still not reported. On the other hand, in both studies, Pilates is given as combined training.
As a result, telerehabilitation is an alternative method to MS treatment. In addition, while there are many clinical-based Pilates studies in the literature, telerehabilitation-based Pilates studies are insufficient. Telerehabilitation-based Pilates training studies are needed. Therefore, the investigators planned this study to investigate the effect of telerehabilitation-based pilates training on physical performance and quality of life in pwMS.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is planned as a randomized control trial. Patients will be randomly divided into two groups as intervention and control. The intervention group will be received telerehabilitation-based pilates training three times a week for six weeks. Telerehabilitation-based pilates will be provided via videoconferencing.
The first session will be the introduction session, patients will be informed about basic principles of Pilates and it will be included teaching inward movement of the lower abdominal wall and supine exercises of segmental movements involving trunk muscle recruitment to maintain a neutral posture. Afterward the session, a typical session will be included supine, side-lying, quadruped exercise, sitting on the exercise ball, and standing exercises. Exercises will be included thoracic extension, general abdominal strengthening, core stabilization exercises for the deep abdominal muscles. The difficulty of these exercises will be gradually increased and focused on keeping neutral positions of the spine in different gravity orientations. The control group will be a wait-list group without any additional specific treatment. All assessments will be done before and after the 6-week intervention program or waiting period. The demographic characteristics of the participants initially will be taken and the Expanded Disability Status Scale score of those of MS will be recorded. Primary outcomes are balance, gait, core endurance and power, and muscle strength; secondary outcomes are physical activity, fatigue, and quality of life
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey
- Gazi University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18-65 years of age
- Voluntarily participate in research to accept
- Having a diagnosis of "Multiple Sclerosis" by a specialist physician
- Relapse free in the last 3 mounts
- An Expanded Disability Status Scale (EDSS) score less than or equal to 4
Exclusion Criteria:
- Any cardiovascular, orthopedic, visual, hearing, and perception problems that may affect the results of the research.
Study Plan
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: Exercise group
The intervention group will be received telerehabilitation-based pilates training three times a week for 6 weeks.
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The group that will receive telerehabilitation-based pilates training via telerehabilitation
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No Intervention: Waitlist
The control group will be a wait-list group without any additional specific treatment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic Balance- Baseline
Time Frame: Assessment will be conducted before the intervention
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Berg Balance Scale.
It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function.
(0 = worst,56 = best)
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Assessment will be conducted before the intervention
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Dynamic Balance-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Berg Balance Scale.
It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function.
(0 = worst,56 = best)
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Assessment will be conducted immediately after the intervention.
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Static Balance- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Biodex Balance System
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Assessment will be conducted before the intervention.
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Static Balance- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Biodex Balance System
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Assessment will be conducted immediately after the intervention.
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An individual's confidence in performing activities- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Activities-specific Balance Confidence Scale.
Items are rated on a 0% to 100% whole number rating scale.
(0 = worst,100 = best)
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Assessment will be conducted before the intervention.
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An individual's confidence in performing activities- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Activities-specific Balance Confidence Scale.
Items are rated on a 0% to 100% whole number rating scale.
(0 = worst,100 = best)
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Assessment will be conducted immediately after the intervention.
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Exercise capacity- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Six minute walk test
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Assessment will be conducted before the intervention.
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Exercise capacity- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Six minute walk test
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Assessment will be conducted immediately after the intervention.
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Gait parameters- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Wearable system (G-Walk)
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Assessment will be conducted before the intervention.
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Gait parameters- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Wearable system (G-Walk)
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Assessment will be conducted immediately after the intervention.
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Functional mobility- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Timed up go test
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Assessment will be conducted before the intervention.
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Functional mobility- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Timed up go test
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Assessment will be conducted immediately after the intervention.
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Core endurance- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Mcgill core endurance tests
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Assessment will be conducted before the intervention.
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Core endurance- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Mcgill core endurance tests
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Assessment will be conducted immediately after the intervention.
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Core strength- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Mcgill core strength tests
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Assessment will be conducted before the intervention.
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Core strength-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Mcgill core strength tests
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Assessment will be conducted immediately after the intervention.
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Muscle Strength outcomes- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Hand dynamometer (Baseline®, White Plains, New York, US)
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Assessment will be conducted before the intervention.
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Muscle Strength outcomes- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Hand dynamometer (Baseline®, White Plains, New York, US)
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Assessment will be conducted immediately after the intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical activity level- Baseline
Time Frame: Assessment will be conducted before the intervention.
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international physical activity questionnaire (IPAQ).
IPAQ assesses physical activity undertaken across a comprehensive set of domains including leisure time, domestic and gardening (yard) activities, work-related and transport-related activity.
The items were structured to provide separate scores on walking; moderate-intensity; and vigorous-intensity activity as well as a combined total score to describe overall level of activity.
Computation of the total score requires summation of the duration (in minutes) and frequency (days) of walking, moderate-intensity and vigorous-intensity activity.
(0 Metabolic equivalents (MET) minutes/week= worst, >3000 MET minutes/week= best)
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Assessment will be conducted before the intervention.
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Physical activity level- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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international physical activity questionnaire (IPAQ).
IPAQ assesses physical activity undertaken across a comprehensive set of domains including leisure time, domestic and gardening (yard) activities, work-related and transport-related activity.
The items were structured to provide separate scores on walking; moderate-intensity; and vigorous-intensity activity as well as a combined total score to describe overall level of activity.
Computation of the total score requires summation of the duration (in minutes) and frequency (days) of walking, moderate-intensity and vigorous-intensity activity.
(0 Metabolic equivalents (MET) minutes/week= worst, >3000 MET minutes/week= best)
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Assessment will be conducted immediately after the intervention.
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Fatigue severity- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Fatigue severity scale, A self-report scale is a 9-item scale which measures the severity of fatigue.
Answers are scored on a seven point scale where 1 = strongly disagree and 7 = strongly agree.
This means the minimum score possible is nine and the highest is 63 (9 = best, 63 = worst)
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Assessment will be conducted before the intervention.
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Fatigue severity- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Fatigue severity scale, A self-report scale is a 9-item scale which measures the severity of fatigue.
Answers are scored on a seven point scale where 1 = strongly disagree and 7 = strongly agree.
This means the minimum score possible is nine and the highest is 63 (9 = best, 63 = worst)
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Assessment will be conducted immediately after the intervention.
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Impact of fatigue on activities- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Fatigue impact scale.
The FIS was developed to assess the symptom of fatigue as part of an underlying chronic disease or condition.
Consisting of 40 items, the instrument evaluates the effect of fatigue on three domains of daily life: cognitive functioning, physical functioning, and psychosocial functioning.
Answers are scored on a four point scale where 0 = no problem and 4 = extreme problem.
(0 = best, 160 = worst)
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Assessment will be conducted before the intervention.
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Impact of fatigue on activities- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Fatigue impact scale.
The FIS was developed to assess the symptom of fatigue as part of an underlying chronic disease or condition.
Consisting of 40 items, the instrument evaluates the effect of fatigue on three domains of daily life: cognitive functioning, physical functioning, and psychosocial functioning.
Answers are scored on a four point scale where 0 = no problem and 4 = extreme problem.
(0 = best, 160 = worst)
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Assessment will be conducted immediately after the intervention.
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Health related quality of life- Baseline
Time Frame: Assessment will be conducted before the intervention.
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Multiple Sclerosis Quality of Life (MSQOL)-54 scale..
There is no single overall score for the MSQOL-54.
Two summary scores -physical health and mental health- can be derived from a weighted combination of scale scores.
(0=worst, 100=best)
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Assessment will be conducted before the intervention.
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Health related quality of life- Post intervention- Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
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Multiple Sclerosis Quality of Life (MSQOL)-54 scale..
There is no single overall score for the MSQOL-54.
Two summary scores -physical health and mental health- can be derived from a weighted combination of scale scores.
(0=worst, 100=best)
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Assessment will be conducted immediately after the intervention.
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Kader Eldemir, PT, MSc., Research Assistant
- Study Director: Arzu Güçlü-Gündüz, PT, PhD, Professor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Gazi 2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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