The Effects of Vestibulo-Ocular Reflex Exercises Added to Postural Stabilization Training in Chronic Ankle Instability
Effects of Vestibulo-Ocular Reflex Exercises Added to Postural Stabilization Training on Dynamic Balance, Functional Instability and Neurocognitive Performance in Amateur Athletes With Chronic Ankle Instability
1 other identifier
interventional
56
1 country
1
Brief Summary
Chronic ankle instability (CAI) is a common condition after lateral ankle sprain. CAI is characterized by mechanical and/or functional instability, or recurrent episodes of "giving way," persisting for at least 12 months after the initial injury, and is associated with limitations in activity and participation. In amateur athletes, CAI may be overlooked or undertreated, although sport-specific activities require rapid integration of visual, vestibular, somatosensory, and cognitive information. Postural stabilization training is commonly used to improve balance and neuromuscular control in individuals with CAI. However, individuals with CAI may show increased reliance on visual information and altered visual-vestibular sensory reweighting during postural control tasks. The vestibulo-ocular reflex (VOR) contributes to gaze stability and visual clarity during head movements and may also be related to neurocognitive processes such as attention and processing speed. This study is designed as a randomized controlled, prospective, parallel-group, pretest-posttest design trial to investigate whether VOR exercises added to postural stabilization training improve dynamic balance, functional instability, and neurocognitive performance in amateur athletes with CAI.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 22, 2026
CompletedStudy Start
First participant enrolled
July 22, 2026
CompletedFirst Posted
Study publicly available on registry
July 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 22, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 22, 2027
September 29, 2026
September 1, 2026
1 year
July 22, 2026
September 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Y Balance Test
The Y-Balance Test will be used to assess dynamic postural control. Participants will perform the test barefoot, standing on the test limb with hands on the hips, and will reach in the anterior, posteromedial, and posterolateral directions with the free limb. Invalid trials, including loss of balance, movement of the stance foot, or removal of the hands from the hips, will be repeated. Reach distances will be recorded in centimeters, normalized to limb length, and a composite score will be calculated.
baseline, 6 weeks after baseline, and 10-week after baseline
Secondary Outcomes (8)
Cumberland Ankle Instability Tool
baseline, 6 weeks after baseline, and 10-week after baseline
Single-Leg Stance + Number / Word Sequence Task
baseline, 6 weeks after baseline, and 10-week after baseline
Side Hop Test + Pinhole Glasses
baseline, 6 weeks after baseline, and 10-week after baseline
Figure-of-Eight Hop Test + Backward Counting Task
baseline, 6 weeks after baseline, and 10-week after baseline
Stroop Test
baseline, 6 weeks after baseline, and 10-week after baseline
- +3 more secondary outcomes
Study Arms (2)
Postural Stabilization Training Group
ACTIVE COMPARATORParticipants in this group will receive ankle joint mobilization followed by a structured postural stabilization training program. The program will include single-leg stance progression, hop stabilization tasks, and number-sequence hop tasks. Exercises will be progressed according to the participant's ability to complete each task without errors. Ankle joint mobilization will include talocrural anteroposterior mobilization and distal fibular mobilization with movement, applied before the exercise session for approximately 5 minutes.
Vestibulo-Ocular Reflex Exercise in addition to Postural Stabilization Training Group
EXPERIMENTALParticipants in this group will receive the same ankle joint mobilization and postural stabilization training program as the Postural Stabilization Training Group. In addition, vestibulo-ocular reflex (VOR) exercises involving fixation on a visual target during head movements will be implemented. VOR exercises will be structured to progressively increase postural demands and will include sitting, standing, walking, and single-leg stance positions.
Interventions
Participants in this group will receive ankle joint mobilization followed by a structured postural stabilization training program. The program will include single-leg stance progression, hop stabilization tasks, and number-sequence hop tasks. Exercises will be progressed according to the participant's ability to complete each task without errors. Ankle joint mobilization will include talocrural anteroposterior mobilization and distal fibular mobilization with movement, applied before the exercise session for approximately 5 minutes. The total session will last approximately 45 minutes and will be performed 3 times per week for 6 weeks.
Participants in this group will receive the same ankle joint mobilization and postural stabilization training program as the Postural Stabilization Training Group. In addition, vestibulo-ocular reflex (VOR) exercises involving fixation on a visual target during head movements will be implemented. VOR exercises will be structured to progressively increase postural demands and will include sitting, standing, walking, and single-leg stance positions. The total session will last approximately 45 minutes and will be performed 3 times per week for 6 weeks.
Eligibility Criteria
You may qualify if:
- Being between 18 and 35 years of age.
- Being classified as a Tier 2 athlete according to the McKay et al. Participant Classification Framework (trained/developmental level).
- Having a history of at least one lateral ankle sprain (LAS) occurring at least 12 months before enrollment, resulting in swelling, pain, and functional impairment, and followed by persistent instability.
- Having the most recent ankle sprain at least 3 months before study enrollment.
- Having a history of recurrent ankle sprains or episodes of "giving way."
- Having a diagnosis of unilateral chronic ankle instability (CAI).
- Having a Cumberland Ankle Instability Tool - Turkish Version (CAIT-T) score of ≤24.
- Having a Foot and Ankle Ability Measure (FAAM) score of \<90%.
- Having a Foot and Ankle Ability Measure Sports subscale (FAAM-S) score of \<80%.
- A side-to-side difference of ≥2.5 cm in Weight-Bearing Lunge Test distance, with the affected side demonstrating less dorsiflexion than the unaffected side.
You may not qualify if:
- History of acute lateral ankle sprain within the last 3 months.
- History of lower extremity surgery.
- History of acute injury to other musculoskeletal structures of the lower extremity joints within the last 3 months that affected joint integrity and function and caused interruption of desired physical activity for at least one day.
- History of balance or vestibular disorders, including cerebellar, vestibular, cochlear, or inner ear dysfunction.
- Visual problems that may affect the administration or interpretation of the Dynamic Visual Acuity Test, including a history of amblyopia, diplopia, or significant visual loss.
- Persistent symptoms related to a previous concussion or traumatic brain injury.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Reset Fizyoterapi
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mustafa Fatih Çetintaş, PT, PhD (c)
Bahçeşehir University
- STUDY CHAIR
Pelin Pisirici, PT, PhD
Bahçeşehir University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Professor
Study Record Dates
First Submitted
July 22, 2026
First Posted
July 27, 2026
Study Start
July 22, 2026
Primary Completion (Estimated)
July 22, 2027
Study Completion (Estimated)
July 22, 2027
Last Updated
September 29, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share