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Active, not recruiting Observational

Assessment of Intrinsic Risk Factors for Ankle Injuries in Ballet Dancers

NCT07199985 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-09-22
Last updated
2025-12-04

Condition(s) studied

Healthy

Study summary

This study aims to evaluate intrinsic risk factors (muscle strength, joint range of motion, static and dynamic balance) that may lead to ankle injuries in ballet dancers and to examine the relationship between these factors and ankle injuries experienced in the last 12 months. By comparing ballet dancers who have suffered injuries requiring physical therapy or forcing them to take a break from dancing for more than one week in the past year with uninjured ballet dancers and a control group, the findings aim to contribute scientifically to the development of individualized rehabilitation programs and the safe and effective planning of return-to-stage processes. Furthermore, it is believed that these data may support the reduction of time and financial losses among dancers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * For the Dancer Group: 1. Be 18 years of age or older 2. Be a professional or academic-level dancer who has been practicing classical ballet regularly (at least 3 days a week) for the past 3 years 3. Reside in the province of Izmir 4. Agree to participate voluntarily and have signed an informed consent form * For the Control Group: 1. Be 18 years of age or older 2. Have no prior dance experience 3. Not have participated in sports that place specific stress on the ankle area (such as ballet, artistic gymnastics, martial arts, soccer, etc.), even if engaging in regular physical activity 4. Reside in the province of İzmir 5. Agree to participate voluntarily and have signed an informed consent form Exclusion Criteria: 1. Having undergone surgery on the lower extremities within the last 6 months 2. Having a history of diagnosed chronic disease related to the nervous system, vestibular system, or musculoskeletal system (e.g., peripheral neuropathy, MS, rheumatoid arthritis, etc.) 3. Having a physical disability that prevents completion of isokinetic or balance tests 4. Pregnancy

Primary outcome measure(s)

  • Ankle muscle strength — baseline(single assessment session; Day 1)
    Isokinetic peak torque of the ankle muscles will be assessed using an isokinetic dynamometer (Isomed 2000). Plantar flexion / dorsiflexion (PF/DF): measured at 30°/s and 120°/s angular velocities, in both concentric and eccentric modes. Inversion / eversion (INV/EV): measured at 60°/s and 90°/s angular velocities, in both concentric and eccentric modes. Units: Newton-meters (Nm).
  • Dynamic Balance Ability — baseline(single assessment session; Day 1)
    Dynamic balance: Y-Balance Test (Lower Quarter). Reach distances in the anterior, posteromedial, and posterolateral directions will be normalized to leg length. A composite score will be calculated. Units: Reach distances (ANT, PM, PL): centimeters (cm) Composite score: percent of leg length (%) Directional asymmetries: centimeters (cm)
  • Range of Motion (ROM) of the Ankle and First Metatarsophalangeal (1st MTP) Joint — Baseline (single assessment session; Day 1)
    Active joint range of motion will be measured with a universal goniometer. Ankle: dorsiflexion, plantar flexion, inversion, eversion. 1st MTP joint: dorsiflexion, flexion Units: Degrees (°).
  • Static Balance Ability — baseline(single assessment session; Day 1)
    Static balance: Center of pressure (CoP) trace length, sway area, and mean CoP velocity will be recorded during 30-second quiet stance (feet hip-width apart) using a pedobarography system. Units: Millimeters (mm), square millimeters (mm²), millimeters per second (mm/s).

Trial sites (1)

FacilityCityRegionStatus
Ege University Faculty of Medicine, Department of Sports Medicine, Izmir Bornova
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 NCT07199985 on ClinicalTrials.gov ↗ ← All trials in Turkey