Eye-Brain-Balance link: could VOR exercises sharpen Athletes' reactions and cut injury fear?
NCT ID NCT07760233
First seen Aug 12, 2026 · Last updated Aug 18, 2026 · Updated 3 times
Summary
This trial tests whether adding vestibulo-ocular reflex (VOR) exercises—which train the eye-movement system that keeps vision stable during head motion—to standard balance training improves reaction time and reduces fear of re-injury in amateur athletes with chronic ankle instability. Participants will receive either balance training alone or balance training plus VOR exercises. The study measures changes in visuo-motor reaction performance and psychological barriers like kinesiophobia, aiming to see if this combined approach offers a more complete rehabilitation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Vestibulo-ocular reflex (VOR) exercises added to postural stabilization training
- What this could lead to
- If effective, this combined training approach could offer a better rehabilitation strategy for athletes with chronic ankle instability, improving reaction time and reducing fear of re-injury.
- What could go wrong
- This is a small, early-stage trial, and the added benefit of VOR exercises over standard balance training is unproven. Results may not apply to all athletes or levels of competition.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 56 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 35 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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. Exclusion Criteria: * 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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Reset Fizyoterapi
RECRUITINGIstanbul, Turkey, 34728, Turkey (Türkiye)
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