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Clinical Trials in Turkey / NCT07581535
Recruiting Not applicable

Effects of Cervical and Oculomotor Exercises on Functional Status, Balance, and Proprioception in Chronic Ankle Instability

NCT07581535 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-07
Last updated
2026-06-08

Condition(s) studied

Chronic Ankle Instability, CAI

Investigational drug(s) / intervention(s)

ExerciseExercise

Exercise: Participants in the experimental group will receive a conventional rehabilitation program including mobility, strengthening, balance, and proprioceptive exercises targeting the ankle joint. In addition, they will perform cervical stabilization and oculomotor exercises.

Exercise: Participants in the control group will receive a conventional rehabilitation program including mobility, strengthening, balance, and proprioceptive exercises targeting the ankle joint.

Study summary

Effects of Cervical and Oculomotor Exercises on Functional Status, Balance, and Proprioception in Chronic Ankle Instability

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with unilateral chronic ankle instability (CAI) in accordance with the International Ankle Consortium recommendations * A history of at least one significant lateral ankle sprain that occurred at least 12 months prior to participation, resulting in inflammatory symptoms such as pain and swelling and causing at least one day of interruption in physical activity * A history of "giving way" and/or recurrent ankle sprains and/or a feeling of instability in the affected ankle within the past 6 months * A Cumberland Ankle Instability Tool (CAIT) score of ≤ 25 Exclusion Criteria: * History of surgery or fracture in the lower extremities or spine * Acute musculoskeletal injury affecting other joints of the lower extremity within the past 3 months (e.g., sprains, fractures) that impaired joint integrity and function and caused at least one day of interruption in physical activity * History of injection in the affected ankle * History of ankle sprain in the affected extremity within the past 4 weeks * Presence of systemic musculoskeletal disorders, neurological disorders, vestibular disorders, or any other condition that may affect balance or sensory function * Previous participation in any rehabilitation program for the ankle or cervical region * History of head or neck trauma or diagnosed pathology within the past 12 months * History of neck pain greater than 3/10 in severity within the past 12 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Izmir Katip Celebi University Physiotherapy and Rehabilitation Department Izmir Çiğli Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07581535 on ClinicalTrials.gov ↗ ← All trials in Turkey