Clinical trial Recruiting at 1 site Interventional Ages 18 to 35

Vestibo-ocular exercises added to balance training for chronic ankle instability

Official title: 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

Run by Bahçeşehir University · NCT07728526 · Data updated 2026-11-12

This study tests whether adding vestibulo-ocular reflex exercises to standard postural stabilization training helps people with chronic ankle instability.

Quick facts

Study typeInterventional
Ages18 Years to 35 Years
SexAll
Enrollment50 (estimated)
SponsorBahçeşehir University
Academic / other
Locations1 site (Istanbul)
StatusRecruiting
StartedJuly 22, 2026
Main results expectedJuly 22, 2027
Study endsJuly 22, 2027
Registry record updatedOctober 23, 2026
Trial IDNCT07728526 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are 18–35 years old with unilateral CAI, a history of recurrent sprains, and CAIT-T ≤ 24 or FAAM/FAAM-S scores below specified thresholds, plus demonstrable dorsiflexion differences.

Probably not a fit

Individuals without CAI or those already meeting high functional scores may not experience additional benefit from the added VOR exercises.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study investigates whether adding vestibulo-ocular reflex (VOR) exercises to a postural stabilization program improves balance and neuromuscular control in young adults with chronic ankle instability (CAI). Participants perform a structured training program that combines postural stabilization with VOR activities designed to challenge gaze stability during head movements, while also measuring cognitive load effects through dual-task scenarios. Outcomes focus on balance performance, ankle function, and possibly sensory reweighting between visual, vestibular, and somatosensory inputs. The study considers how neurocognitive factors such as attention and processing speed relate to functional ankle stability.

Why it matters

Potential benefit: If successful, participants may experience improved balance and reduced episodes of instability with a potentially more effective rehabilitation approach.

How similar studies have gone: Previous work suggests that sensorimotor training and sensory reweighting approaches can improve balance in CAI, but the additive value of VOR-specific exercises is still being explored.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Reset Fizyoterapi
    Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Mustafa Fatih Çetintaş, PT, PhD (c) — Bahçeşehir University
  • Study coordinator: Pelin Pisirici, PT, PhD
  • Email: pelin.pisirici@bau.edu.tr
  • Phone: 05055016076

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.