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Clinical Trials in Turkey / NCT07500389
Starting soon Observational

Postural Habits, Body Awareness, and Functional Performance Across BMI Categories in Women

NCT07500389 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-30
Last updated
2026-04-07

Condition(s) studied

Obesity & OverweightBody Mass IndexPostural ControlBody AwarenessFunctional Performance

Investigational drug(s) / intervention(s)

Observational Assessment

Observational Assessment: Participants will undergo a comprehensive observational assessment including anthropometric measurements, self-reported questionnaires, and performance-based functional tests. Body mass index and waist circumference will be measured to classify participants into BMI categories. Postural habits and awareness will be evaluated using the Posture Habits and Awareness Scale (PHAS), and body awareness will be assessed the Body Awareness Questionnaire (BAQ). Functional performance will be measured using the Timed Up and Go (TUG) test and the Five Times Sit-to-Stand (5×STS) test. No therapeutic or experimental intervention will be applied.

Study summary

This cross-sectional study aims to investigate the relationship between postural habits and body awareness with functional performance across different body mass index (BMI) categories in women. Participants will be categorized into four groups based on BMI (normal weight, overweight, obesity class I, and obesity class II-III). Postural habits and awareness, body awareness, and functional performance will be assessed using validated questionnaires and performance-based tests. The study also aims to explore the potential contribution of central adiposity (waist circumference) and psychological factors to these relationships. Findings are expected to provide a more comprehensive understanding of the biomechanical and perceptual factors associated with obesity.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Female individuals aged 18-65 years * Classified into BMI categories (normal weight, overweight, obesity class I, obesity class II-III) * No obesity-related medical or surgical treatment in the last 6 months * Able to understand instructions and complete questionnaires Exclusion Criteria: * Neurological disorders affecting mobility (e.g., stroke, Parkinson's disease, multiple sclerosis, peripheral neuropathy) * Rheumatologic or inflammatory diseases (e.g., rheumatoid arthritis, ankylosing spondylitis) * Severe orthopedic conditions limiting mobility (e.g., advanced osteoarthritis) * Major surgery within the last 12 months affecting mobility or physical performance * Pregnancy * Acute musculoskeletal injury within the last 4 weeks

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ondokuz Mayis University Samsun Samsun

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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 NCT07500389 on ClinicalTrials.gov ↗ ← All trials in Turkey