- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07494500
Vestibular Training on Community Ambulation and Fall Risk in Stroke
March 20, 2026 updated by: Yea-Ru Yang, National Yang Ming Chiao Tung University
Effects of Vestibular Training on Community Ambulation and Fall Risk in Individuals With Chronic Stroke
Nearly half of individuals with stroke experience limitations in community ambulation, and 35.7% of community-dwelling stroke survivors experienced falls while walking, indicating that falls are common during routine daily activities in community settings.
Sensory reweighting refers to the ability to appropriately prioritize and integrate sensory inputs to maintain postural stability.
Stroke survivors often demonstrate impaired sensory reweighting, characterized by excessive reliance on visual and proprioceptive cues and insufficient integration of vestibular information.
This deficit adversely affects postural control and subsequently compromises gait performance and fall risk .In addition, many individuals with stroke exhibit reduced gaze stability during walking and turning, suggesting potential impairments in the vestibulo-ocular reflex (VOR), a key mechanism for maintaining stable vision during head movement.
Insufficient gaze stability has been associated with gait disturbances; therefore, deficits in sensory reweighting and VOR function may contrib-ute to limited community ambulation and increased fall risk.
Although previous studies have primarily focused on general balance training, few have directly targeted vestibular input.
Thus, the effectiveness of vestibular-specific training for improving community ambulation and reducing fall risk in chronic stroke remains unclear.
This study aims to investigate the effects of vestibular training on community ambulation and fall risk in individuals with chronic stroke.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
40
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 Contact
- Name: Yea-Ru Yang, PhD
- Phone Number: +886228267279
- Email: yryang@nycu.edu.tw
Study Locations
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Taipei, Taiwan, 112
- Department of Physical Therapy and Assistive Technology, National Yang Ming Chiao Tung University
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Contact:
- Yea-Ru Yang, PhD
- Phone Number: +886-2-2826-7279
- Email: yryang@nycu.edu.tw
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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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Diagnosis of First-occurrenced stroke
- ≥ 6 months after stroke
- Ability to walk at least 400 meters with or without the use of a walking assistive device
- Mini-Mental State Examination score ≥ 24
- Age between 18 and 80 years
Exclusion Criteria:
- Other neurological or musculoskeletal conditions affected postural stability
- Presence of dizziness or vertigo
- Presence of conditions affecting cervical blood flow or limiting cervical range of motion
- Visual impairment
- Unstable cardiac status or uncontrolled hypertension
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 |
|---|---|
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Experimental: Vestibular training group
The intervention is a 40-minute session and 3 sessions/week, totaling 4 weeks.
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Gaze stabilization exercises and balance training under visual and head-movement challenges to stimulate vestibular input and maintain balance.
Other Names:
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Active Comparator: Conventional physical therapy Group
The intervention is a 40-minute session and 3 sessions/week, totaling 4 weeks.
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Strength, posture, gait, and functional training.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Walking Ability Questionnaire
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Walking Ability Questionnaire to evaluate community ambulation ability.
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Baseline, 4 weeks after training, and 4-week follow-up
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Community Walking Speed
Time Frame: Baseline, post-intervention, 4 weeks after training, and 4-week follow-up
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Using a timer to measure average walking speed in the community
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Baseline, post-intervention, 4 weeks after training, and 4-week follow-up
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Taiwan Chinese version of the Falls Efficacy Scale
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Taiwan Chinese version Falls Efficacy Scale to evaluate fall risk
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Baseline, 4 weeks after training, and 4-week follow-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gait performance
Time Frame: Baseline, post-intervention, 4 weeks after training, and 4-week follow-up
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Using GAITRite system to measure the gait spatiotemporal parameters
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Baseline, post-intervention, 4 weeks after training, and 4-week follow-up
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Activities-specific Balance Confidence Scale
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Activities-specific Balance Confidence Scale to evaluate individual's balance confidence in performing daily activities
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Baseline, 4 weeks after training, and 4-week follow-up
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Functional Gait Assessment
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Functional gait assessment to evaluate walking performance
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Baseline, 4 weeks after training, and 4-week follow-up
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Six-minute Walk Test
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Six-minute Walk Test to evaluate walking endurance
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Baseline, 4 weeks after training, and 4-week follow-up
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Mini-Balance Evaluation Systems Test
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Mini-Balance Evaluation Systems Test to evaluate balance performanc
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Baseline, 4 weeks after training, and 4-week follow-up
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Tinetti Performance-Oriented Mobility Assessment
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Baseline, 4 weeks after training, and 4-week follow-up
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Modified Clinical Test of Sensory Integration and Balance
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Biodex system to evaluate sensory reweighting ability
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Baseline, 4 weeks after training, and 4-week follow-up
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Dynamic Visual Acuity Test
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Dynamic Visual Acuity Test to evaluate vestibulo-ocular reflex function
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Baseline, 4 weeks after training, and 4-week follow-up
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Stroke Impact Scale
Time Frame: Baseline, 4 weeks after training, and 4-week follow-up
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Using Stroke Impact Scale to evaluate quality of life
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Baseline, 4 weeks after training, and 4-week follow-up
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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 (Estimated)
April 1, 2026
Primary Completion (Estimated)
July 31, 2028
Study Completion (Estimated)
July 31, 2028
Study Registration Dates
First Submitted
March 20, 2026
First Submitted That Met QC Criteria
March 20, 2026
First Posted (Actual)
March 27, 2026
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 20, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NYCU114245AF2
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.
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