🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07578714
Recruiting Observational

Core Stability, Postural Balance, and Flexibility in Healthy Women: A Comparative Study Between Pilates Practitioners and Sedentary Individuals

NCT07578714 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-05-13
Last updated
2026-05-11

Condition(s) studied

Core StabilityPostural BalancePilates, Core StabilityPilatesHealthy Life Style

Study summary

This study aims to compare core muscle stability, postural balance, and flexibility between healthy women who regularly practice Pilates and those with a sedentary lifestyle. The researcher will evaluate if long-term Pilates practice (5 months or more) leads to significant improvements in physical performance compared to a lack of regular exercise. Assessment tools include the Pressure Biofeedback Unit (PBU) for core activation, the McGill battery for endurance, the Y-Balance test for dynamic stability, and the Sit-and-Reach test for flexibility.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Healthy female volunteers aged 20-45. 2. For the Pilates group: having practiced mat Pilates, reformer Pilates, or any equipment-based Pilates discipline for at least 6 months; attending regular 60-minute sessions at least twice a week with a certified instructor. 3. For the control group: having a sedentary lifestyle (weekly moderate physical activity time less than 150 minutes). 4. Objectively demonstrating sedentary status using the International Physical Activity Questionnaire (IPAQ); only participants in the "low physical activity" category will be included in the control group. 5. Having full cognitive ability to understand, follow, and execute all physical assessment instructions. 6. Willingness to voluntarily sign the informed consent form prior to the study. Exclusion Criteria: 1. History of any surgery involving the spine, pelvis, or lower extremities within the last 12 months prior to the study. 2. Currently pregnant or less than 6 months postpartum. 3. Diagnosed vestibular disorders or chronic clinical balance disorders. 4. History of neurological disease (MS, Parkinson's, etc.) or systemic metabolic disorder (diabetes, etc.). 5. Having a pain intensity greater than 2/10 on the visual analog scale (VAS) in the lower back or lower extremities. 6. Professional sports history or participation in other exercise programs exceeding 3 hours per week (excluding Pilates for the Pilates group). 7. Acute musculoskeletal injuries or acute illnesses that may affect energy levels on the day of evaluation. 8. Concurrent participation in other intensive core strengthening programs such as "advanced yoga" that may affect results.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istinye University, Topkapi Campus Istanbul Zeytinburnu Recruiting

More Istinye University trials in Turkey

Other trials for the same condition

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 NCT07578714 on ClinicalTrials.gov ↗ ← All trials in Turkey