Actively Recruiting
Effects of Cervical and Oculomotor Exercises Added to Conventional Treatment on Ankle Functional Status, Balance, and Proprioception in Individuals With Chronic Ankle Instability: A Randomized Controlled Trial
Led by Izmir Katip Celebi University · Updated on 2026-06-08
38
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
I
Izmir Katip Celebi University
Lead Sponsor
I
Izmir Bakircay University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate the effects of adding cervical stabilization and eye movement exercises to a standard rehabilitation program for individuals with chronic ankle instability (CAI). The study compares how these combined exercises impact ankle function, balance, and body awareness, addressing ongoing issues like recurrent ankle sprains and instability in affected individuals. The trial is a randomized controlled study evaluating these exercise approaches over a set period. Participants are randomly assigned to either an experimental group receiving conventional rehabilitation plus cervical and oculomotor exercises or a control group receiving only the conventional rehabilitation program. Both groups participate in therapy sessions three times a week for four weeks, with additional home exercises on non-clinic days. The conventional program includes ankle mobility, strengthening, balance, and proprioceptive exercises, while the experimental group adds cervical stabilization and eye movement exercises. Throughout the study, participants undergo assessments at the start and after four weeks, including balance tests like the Y-Balance Test, functional ability measures such as the Foot and Ankle Ability Measure, and proprioception evaluations. Secondary measures include joint position error tests, computerized balance assessments, hop tests, and pain evaluations. These outcomes help researchers understand the effects of adding cervical and oculomotor exercises to standard care. The total participation time is four weeks, with close monitoring of functional changes and balance improvements.
CONDITIONS
Brief Title
Effects of Cervical and Oculomotor Exercises on Functional Status, Balance, and Proprioception in Chronic Ankle Instability
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with unilateral chronic ankle instability according to International Ankle Consortium recommendations
- History of at least one significant lateral ankle sprain at least 12 months before participation with pain, swelling, and interruption of physical activity
- History of "giving way", recurrent ankle sprains, or feeling of instability in the affected ankle within the past 6 months
- Cumberland Ankle Instability Tool (CAIT) score of 25 or less
- Age between 18 and 45 years
You will not qualify if you...
- History of surgery or fracture in lower limbs or spine
- Acute musculoskeletal injury affecting other lower extremity joints within the past 3 months causing activity interruption
- History of injection in the affected ankle
- Ankle sprain in the affected extremity within the past 4 weeks
- Systemic musculoskeletal, neurological, vestibular disorders, or other conditions affecting balance or sensory function
- Previous rehabilitation program for 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 out of 10 severity within the past 12 months
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants receive a 4-week rehabilitation program. The experimental group performs conventional ankle mobility, strengthening, balance, and proprioceptive exercises plus cervical stabilization and oculomotor exercises. The control group performs conventional ankle exercises only. Sessions occur 3 times per week in the clinic, with home exercises on non-clinic days.
3 in-person sessions per week plus home exercises on other days
Trial Site Locations
Total: 1 location
1
Izmir Katip Celebi University Physiotherapy and Rehabilitation Department
Izmir, Çiğli, Turkey (Türkiye), 35650
Actively Recruiting
Research Team
S
Simge N UNGAN, Phsiotherapist
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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