- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07331350
Exercise Balance Program for Fall Prevention in Multiple Sclerosis
Effects of an Otago-Based Exercise and Game-Inspired Balance Training Program on Balance, Mobility, and Fall-Related Outcomes in Individuals With Multiple Sclerosis: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Falls are a common and clinically significant problem in individuals with multiple sclerosis (MS), primarily associated with impairments in balance, mobility, muscle strength, sensory function, and neuromuscular coordination. Exercise-based interventions focusing on balance, strengthening, functional mobility, and fall-prevention education constitute a core component of physiotherapeutic fall-prevention strategies; however, the optimal structure, intensity, and clinical implementation of such programs for individuals with MS remain under investigation.
This randomized controlled trial investigated the effects of a 6-week combined Otago-based and game-inspired balance-training program on static balance, functional mobility, fear of falling, and perceived walking ability in individuals with MS. A total of 30 adults with a confirmed diagnosis of MS were randomly allocated to either an intervention group or an active control group using a parallel-group design.
Both groups received fall-prevention counselling and performed home-based Otago-related exercises three times per week. The active control group followed the home-based Otago-related exercise program supported by instructional video material, without supervised sessions or additional task-oriented balance-training activities. The intervention group, in addition to performing the same home-based Otago-related exercises, participated in one supervised physiotherapy session per week. During these supervised sessions, participants performed progressively challenging colored-circle and Twister-inspired task-oriented balance exercises designed to challenge static and dynamic postural control, enhance neuromuscular coordination, promote visuomotor integration, improve reaction speed, and support adaptability to changing motor demands.
Outcome assessments were conducted at baseline and immediately after completion of the 6-week intervention period. Static balance was assessed using the FICSIT-4, functional mobility was evaluated with the Timed Up and Go test, fear of falling was measured using the Falls Efficacy Scale-International (FES-I), and perceived walking ability was assessed using the 12-item Multiple Sclerosis Walking Scale (MSWS-12).
This study was designed to contribute to a better understanding of exercise-based fall-prevention strategies for individuals with MS and to inform the development of targeted rehabilitation programs aimed at improving balance and mobility in this population.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Thessaloniki, Greece
- International Hellenic University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Confirmed diagnosis of multiple sclerosis according to the 2010 McDonald criteria.
- Age between 18 and 65 years.
- Ability to ambulate independently with or without an assistive device.
- Ability to understand and follow exercise instructions.
- Written informed consent prior to participation.
Exclusion Criteria:
- Presence of other neurological, musculoskeletal, or medical conditions that could significantly affect balance or mobility.
- Acute relapse of multiple sclerosis at the time of enrollment.
- Participation in another structured balance or fall-prevention program during the study period.
Study Plan
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 |
|---|---|
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Experimental: Combined Otago-Based and Game-Inspired Balance Training
Participants in the intervention group received fall-prevention counselling and performed home-based Otago-related exercises three times per week for 6 weeks.
In addition, they attended one supervised physiotherapy session per week, during which they performed colored-circle and Twister-inspired task-oriented balance exercises.
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This intervention combined home-based Otago-related exercises with supervised task-oriented balance training.
The home-based component included selected balance and lower-limb strengthening exercises performed three times per week.
The supervised component was delivered once weekly and included exercises with colored floor markers, postural tasks linked to color cues, and Twister-inspired stepping activities.
These tasks were used to challenge postural control, coordination, visuomotor responses, and movement adaptability.
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Active Comparator: Home-Based Otago-Related Exercises and Fall-Prevention Counselling
This intervention consisted of selected Otago-related balance and lower-limb strengthening exercises performed at home three times per week for 6 weeks.
Participants also received fall-prevention counselling and instructional material for home practice.
No supervised colored-marker or Twister-inspired balance tasks were included.
|
This intervention consisted of selected Otago-related balance and lower-limb strengthening exercises performed at home three times per week for 6 weeks.
Participants also received fall-prevention counselling and instructional material for home practice.
No supervised colored-marker or Twister-inspired balance tasks were included.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Balance Performance (FICSIT-4)
Time Frame: Baseline and immediately after completion of the 6-week intervention
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Static balance was assessed using the FICSIT-4.
Participants attempted to maintain progressively challenging standing positions, including feet together, semi-tandem stance, tandem stance, and single-leg stance, for up to 10 seconds each.
The outcome was recorded as a total score, with higher values indicating better static balance.
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Baseline and immediately after completion of the 6-week intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Functional Mobility (Timed Up and Go Test)
Time Frame: Baseline and immediately after completion of the 6-week intervention
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Functional mobility was assessed using the Timed Up and Go (TUG) test.
Participants were instructed to stand up from a standard chair, walk a distance of 3 meters, turn around, walk back to the chair, and sit down at a comfortable and safe pace.
The time required to complete the task was recorded in seconds.
Shorter completion times indicated better functional mobility.
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Baseline and immediately after completion of the 6-week intervention
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Fear of Falling (Falls Efficacy Scale-International)
Time Frame: Baseline and immediately after completion of the 6-week intervention
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Fear of falling was assessed using the Falls Efficacy Scale-International (FES-I), a validated self-reported questionnaire consisting of 16 items that assess concern about falling during a range of daily activities.
Each item was scored on a 4-point Likert scale, with total scores ranging from 16 to 64.
Higher scores indicated greater concern about falling.
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Baseline and immediately after completion of the 6-week intervention
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Walking Limitations (12-item Multiple Sclerosis Walking Scale)
Time Frame: Baseline and immediately after completion of the 6-week intervention
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Perceived walking limitations were assessed using the 12-item Multiple Sclerosis Walking Scale (MSWS-12), a disease-specific, self-reported questionnaire that evaluates the impact of multiple sclerosis on walking ability.
Items were scored on a Likert scale and transformed to a total score ranging from 0 to 100, with higher scores indicating greater walking impairment.
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Baseline and immediately after completion of the 6-week intervention
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Collaborators and Investigators
Investigators
- Principal Investigator: Dimitrios Lytras, PhD, International Hellenic University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- EC-1/2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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