Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06462339
Other study ID # MS-Cognition-Onlinepilates
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 6, 2024
Est. completion date September 1, 2024

Study information

Verified date June 2024
Source Gazi University
Contact Kader Eldemir, PT, MSc.
Phone +90452226 52 00
Email fztkader2015@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Multiple sclerosis (MS) is a chronic, inflammatory, degenerative disease of the central nervous system, causing demyelination and axonal damage. MS typically begins with attacks resulting from demyelination of axons, eventually evolving into a neurodegenerative disease associated with neurotrophic support deficiency and neuronal loss. Depending on the location and degeneration, various neurological disorders and symptoms such as walking and balance problems, fatigue, sensory loss, and cognitive impairments are observed in MS patients. Cognitive impairments in MS are associated with lesion count, localization, axonal loss, and brain atrophy, affecting approximately 50-60% of patients. Patients exhibit impairments in verbal fluency, visual-spatial memory, processing speed, executive functions, and episodic memory. Cognitive impairments also lead to a decrease in dual-task performance, referred to as the ability to perform two tasks simultaneously, in MS patients. Cognitive problems and impaired dual-task performance negatively impact various aspects of daily life, including social participation and employment status, thus reducing their quality of life. Clinical-based exercise interventions are frequently utilized and effective in improving cognitive functions and dual-task performance in MS. Pilates is a commonly used exercise modality in clinical practice. Pilates is a core stability-based exercise method involving endurance, flexibility, movement, posture, and respiratory control. Previous studies have indicated that clinical Pilates improves cognitive functions. On the other hand, telerehabilitation approaches, the use of which has increased rapidly due to technological developments in recent times, enable the delivery of rehabilitation services to patients in distant places by using communication technologies. For this purpose, it is highly valuable to implement Pilates, which consists of core stability exercise content, through telerehabilitation. While there are studies on clinical-based Pilates interventions, no study has investigated the efficacy of one-on-one online Pilates exercises on cognitive functions and dual-task performance in an online platform. Therefore, this study aims to investigate the effects of online Pilates on cognitive functions and dual-task performance in patients with MS.


Description:

This study is a randomized controlled study. The patients will be randomly divided into two groups exercise and control. Pilates exercises consisting of 3 days a week for 6 weeks will be given to the exercise group. 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. As the outcome measures, cognitive functions and dual-task performance will be evaluated.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date September 1, 2024
Est. primary completion date August 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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: 0-5 Exclusion Criteria: - Any cardiovascular, orthopedic, visual, hearing, and perception problems that may affect the results of the research - Having a cardiovascular, pulmonary or hormonal disorder that would prevent exercise - Having an accompanying neurological disorder other than MS

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Experimental: Intervention Group
The group that will receive pilates training via telerehabilitation

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Gazi University

References & Publications (2)

Abasiyanik Z, Ertekin O, Kahraman T, Yigit P, Ozakbas S. The effects of Clinical Pilates training on walking, balance, fall risk, respiratory, and cognitive functions in persons with multiple sclerosis: A randomized controlled trial. Explore (NY). 2020 Jan-Feb;16(1):12-20. doi: 10.1016/j.explore.2019.07.010. Epub 2019 Jul 17. — View Citation

Ozkul C, Guclu-Gunduz A, Eldemir K, Apaydin Y, Yazici G, Irkec C. Combined exercise training improves cognitive functions in multiple sclerosis patients with cognitive impairment: A single-blinded randomized controlled trial. Mult Scler Relat Disord. 2020 Oct;45:102419. doi: 10.1016/j.msard.2020.102419. Epub 2020 Jul 23. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mini-Mental test-Baseline Mini Mental Test (MMT) consists of eleven items grouped under five main headings: orientation, recording memory, attention and calculation, recall and language, and is evaluated out of a total score of 30. Accordingly, getting 24 points and above is considered normal. Assessment will be conducted before the intervention
Primary Mini-Mental test-Post intervention Mini Mental Test (MMT) consists of eleven items grouped under five main headings: orientation, recording memory, attention and calculation, recall and language, and is evaluated out of a total score of 30. Accordingly, getting 24 points and above is considered normal. Assessment will be conducted immediately after the intervention
Primary Montreal Cognitive Assessment-Baseline The Montreal Cognitive Assessment (MoCA) was developed as a rapid screening test for mild cognitive impairment. MoCA evaluates different cognitive functions. These; attention and concentration, executive functions, memory, language, visual structuring skills, abstract thinking, calculation and orientation. The highest total score that can be obtained from the test is 30. Higher scores mean a better outcome. Assessment will be conducted before the intervention
Primary Montreal Cognitive Assessment-Post intervention The Montreal Cognitive Assessment (MoCA) was developed as a rapid screening test for mild cognitive impairment. MoCA evaluates different cognitive functions. These; attention and concentration, executive functions, memory, language, visual structuring skills, abstract thinking, calculation and orientation. The highest total score that can be obtained from the test is 30. Higher scores mean a better outcome. Assessment will be conducted immediately after the intervention
Primary Trail Making Test-Baseline Trail Making Test (TMT) is used to evaluate individuals' executive functions, task-sequence switching ability, attention, visual scanning speed, visual-motor perception, planning, organization, abstract thinking and reaction limitation. The test consists of 2 parts: A and B. In part A, the individual is asked to combine numbers from 1 to 25 and the completion time is recorded. In part B, the individual completes the sequence corresponding to a number and a letter respectively, and the completion time is recorded. Assessment will be conducted before the intervention
Primary Trail Making Test-Post intervention Trail Making Test (TMT) is used to evaluate individuals' executive functions, task-sequence switching ability, attention, visual scanning speed, visual-motor perception, planning, organization, abstract thinking and reaction limitation. The test consists of 2 parts: A and B. In part A, the individual is asked to combine numbers from 1 to 25 and the completion time is recorded. In part B, the individual completes the sequence corresponding to a number and a letter respectively, and the completion time is recorded. Assessment will be conducted immediately after the intervention
Primary Stroop Test-Baseline Stroop Test, one of the neuropsychological tests, is used to evaluate selective attention, information processing speed and cognitive flexibility. The test consists of three parts. The first section contains words written in black (e.g. 'blue'), the second section contains colors, and the last section contains words written in different colors (e.g. the word blue written in red ink). The participant is expected to fulfill the tasks in these three sections respectively. While keeping time for each part, the participant must read the words correctly at first, say the colors in the next part, and say the color in which the word is written in the last part. In the test, reading time, number of errors made and number of spontaneous corrections are recorded. Assessment will be conducted before the intervention
Primary Stroop Test-Post intervention Stroop Test, one of the neuropsychological tests, is used to evaluate selective attention, information processing speed and cognitive flexibility. The test consists of three parts. The first section contains words written in black (e.g. 'blue'), the second section contains colors, and the last section contains words written in different colors (e.g. the word blue written in red ink). The participant is expected to fulfill the tasks in these three sections respectively. While keeping time for each part, the participant must read the words correctly at first, say the colors in the next part, and say the color in which the word is written in the last part. In the test, reading time, number of errors made and number of spontaneous corrections are recorded. Assessment will be conducted immediately after the intervention
Primary Functional mobility-baseline Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again. Assessment will be conducted before the intervention
Primary Dual task performance in functional mobility, Cognitive additional task (arithmetic)-baseline Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again.
Cognitive additional task (arithmetic): Individuals will be asked to perform tasks by counting backward from 3 to 3 from 100.
Assessment will be conducted before the intervention
Primary Dual task performance in functional mobility, Cognitive additional task (verbal)-baseline Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again.
Cognitive additional task (verbal): Individuals will be asked to fulfill their duties by producing name.
Assessment will be conducted before the intervention
Primary functional mobility-post intervention Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again. Assessment will be conducted immediately after the intervention
Primary Dual task performance in functional mobility, Cognitive additional task (arithmetic)-post intervention Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again.
Cognitive additional task (arithmetic): Individuals will be asked to perform tasks by counting backward from 3 to 3 from 100.
Assessment will be conducted immediately after the intervention
Primary Dual task performance in functional mobility, Cognitive additional task (verbal)-post intervention Timed up and go test measures the time taken in seconds to arise from a standard chair, walk 3 m, turn through 180 degrees, walk back, and sit down again.
Cognitive additional task (verbal): Individuals will be asked to fulfill their duties by producing name.
Assessment will be conducted immediately after the intervention
Primary balance-baseline The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability. Assessment will be conducted before the intervention
Primary balance, Cognitive additional task (arithmetic)-baseline The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability.
Cognitive additional task (arithmetic)
Assessment will be conducted before the intervention
Primary Dual task performance in balance, Cognitive additional task (verbal)-baseline The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability.
Cognitive additional task (verbal)
Assessment will be conducted before the intervention
Primary Dual task performance in balance,Cognitive additional task (arithmetic)-post intervention The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability.
Cognitive additional task (arithmetic)
Assessment will be conducted immediately after the intervention
Primary balance-post intervention The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability. Assessment will be conducted immediately after the intervention
Primary Dual task performance in balance,Cognitive additional task (arithmetic) -post intervention The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability.
Cognitive additional task (arithmetic)
Assessment will be conducted immediately after the intervention
Primary Dual task performance in balance,Cognitive additional task (verbal) -post intervention The posturography (Biodex Balance System-BioSwayTM) will be used to assess postural stability.
Cognitive additional task (verbal)
Assessment will be conducted immediately after the intervention
Primary gait-baseline Wearable system (G-Walk) will be used to assess gait parameters. Assessment will be conducted before the intervention
Primary Dual task performance in gait, Cognitive additional task (arithmetic)-baseline Wearable system (G-Walk) will be used to assess gait parameters. Cognitive additional task (arithmetic) Assessment will be conducted before the intervention
Primary Dual task performance in gait, Cognitive additional task (verbal)-baseline Wearable system (G-Walk) will be used to assess gait parameters. Cognitive additional task (verbal) Assessment will be conducted before the intervention
Primary gait-post intervention Wearable system (G-Walk) will be used to assess gait parameters. Assessment will be conducted immediately after the intervention
Primary Dual task performance in gait, Cognitive additional task (arithmetic)-post intervention Wearable system (G-Walk) will be used to assess gait parameters. Cognitive additional task (arithmetic) Assessment will be conducted immediately after the intervention
Primary Dual task performance in gait, Cognitive additional task (verbal)-post intervention Wearable system (G-Walk) will be used to assess gait parameters. Cognitive additional task (verbal) Assessment will be conducted immediately after the intervention
See also
  Status Clinical Trial Phase
Completed NCT05528666 - Risk Perception in Multiple Sclerosis
Completed NCT03608527 - Adaptive Plasticity Following Rehabilitation in Multiple Sclerosis N/A
Recruiting NCT05532943 - Evaluate the Safety and Efficacy of Allogeneic Umbilical Cord Mesenchymal Stem Cells in Patients With Multiple Sclerosis Phase 1/Phase 2
Completed NCT02486640 - Evaluation of Potential Predictors of Adherence by Investigating a Representative Cohort of Multiple Sclerosis (MS) Patients in Germany Treated With Betaferon
Completed NCT01324232 - Safety and Efficacy of AVP-923 in the Treatment of Central Neuropathic Pain in Multiple Sclerosis Phase 2
Completed NCT04546698 - 5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis
Active, not recruiting NCT04380220 - Coagulation/Complement Activation and Cerebral Hypoperfusion in Relapsing-remitting Multiple Sclerosis
Completed NCT02835677 - Integrating Caregiver Support Into MS Care N/A
Completed NCT03686826 - Feasibility and Reliability of Multimodal Evoked Potentials
Recruiting NCT05964829 - Impact of the Cionic Neural Sleeve on Mobility in Multiple Sclerosis N/A
Withdrawn NCT06021561 - Orofacial Pain in Multiple Sclerosis
Completed NCT03653585 - Cortical Lesions in Patients With Multiple Sclerosis
Recruiting NCT04798651 - Pathogenicity of B and CD4 T Cell Subsets in Multiple Sclerosis N/A
Active, not recruiting NCT05054140 - Study to Evaluate Efficacy, Safety, and Tolerability of IMU-838 in Patients With Progressive Multiple Sclerosis Phase 2
Completed NCT05447143 - Effect of Home Exercise Program on Various Parameters in Patients With Multiple Sclerosis N/A
Recruiting NCT06195644 - Effect of Galvanic Vestibular Stimulation on Cortical Excitability and Hand Dexterity in Multiple Sclerosis Patients Phase 1
Completed NCT04147052 - iSLEEPms: An Internet-Delivered Intervention for Sleep Disturbance in Multiple Sclerosis N/A
Completed NCT03594357 - Cognitive Functions in Patients With Multiple Sclerosis
Completed NCT03591809 - Combined Exercise Training in Patients With Multiple Sclerosis N/A
Completed NCT03269175 - BENEFIT 15 Long-term Follow-up Study of the BENEFIT and BENEFIT Follow-up Studies Phase 4