Comparing Bipedal and Unipedal Exercises for Chronic Ankle Instability

Is this trial a fit for you?

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

What this trial studies

This study investigates the effectiveness of bipedal versus unipedal exercises in patients with chronic ankle instability (CAI). Participants diagnosed with CAI will be divided into two groups, one receiving early bipedal exercises and the other receiving late bipedal exercises. The aim is to assess improvements in proprioception, strength, and overall ankle stability through targeted therapeutic exercises. The study will include voluntary participants who meet specific inclusion criteria and will exclude those with certain pre-existing conditions.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* The documented unilateral ankle instability confirmed through clinical examinations (drawer test, talar tilt test) and MRI in cases requiring differential diagnosis.
* A history of an initial ankle sprain occurring at least 6 months ago.
* The presence of a recurrent sense of giving way that started at least 6 months ago and has been intermittently persistent.

Exclusion Criteria:

* Presence of a history of previous surgery in the lower extremity.
* Identification of organic and non-organic lesions such as cartilage injuries, periarticular tendon tears, and impingement syndromes.
* The existence of a fracture accompanying instability in the foot-ankle.
* Presence of congenital deformities in the foot-ankle.
* Diagnosis of talus osteochondral lesion.
* Diagnosis of ankle arthritis.
* Presence of medial ligament lesion.
* Existence of peripheral neuropathy.
* Presence of additional rheumatological diseases.
* Regular moderate-level exercise for at least 3 days a week in the last 6 months.

Where it's running

• Acibadem Mehmet Ali Aydinlar University
  Istanbul, Turkey (Türkiye) Recruiting

Study contacts

• Principal investigator: Ayşenur Erekdağ, MSc — Bezmialem Vakif University
• Study coordinator: Ayşenur Erekdağ, MSc
• Email: aysenurerekdag@gmail.com
• Phone: 05548959013

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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.