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

I

Izmir Katip Celebi University

Status

Enrolling

Conditions

Chronic Ankle Instability, CAI

Treatments

Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full description

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

Enrollment

38 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

38 participants in 2 patient groups

Conventional Treatment + Cervical and Oculomotor Exercises
Experimental group
Description:
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. The intervention will be conducted for 4 weeks, with 3 sessions per week. Participants will follow a home exercise program that includes ankle mobility, strengthening, balance, and oculomotor exercises on days when they do not attend the clinic.
Treatment:
Other: Exercise
Other: Exercise
Conventional Treatment
Active Comparator group
Description:
Participants in the control group will receive a conventional rehabilitation program consisting of mobility, strengthening, balance, and proprioceptive exercises targeting the ankle joint. The intervention will be conducted for 4 weeks, with 3 sessions per week. Participants will follow a home exercise program that includes ankle mobility, strengthening and balance exercises on days when they do not attend the clinic.
Treatment:
Other: Exercise
Other: Exercise

Trial contacts and locations

1

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Central trial contact

Simge N UNGAN, Phsiotherapist

Data sourced from clinicaltrials.gov

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