Postural Habits, Body Awareness, and Functional Performance Across BMI Categories in Women
Investigation of Postural Habits and Body Awareness in Relation to Functional Performance Across Body Mass Index Categories in Women
1 other identifier
observational
80
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 24, 2026
CompletedFirst Posted
Study publicly available on registry
March 30, 2026
CompletedStudy Start
First participant enrolled
April 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
March 30, 2026
March 1, 2026
3 months
March 24, 2026
March 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Postural Habits and Awareness Level (PHAS Score)
Postural habits and awareness will be assessed using the Posture Habits and Awareness Scale (PHAS), a validated self-reported questionnaire. The scale evaluates individuals' habitual postural behaviors and awareness during daily activities. Higher scores indicate better postural habits and greater awareness. The primary outcome will be the total PHAS score and its comparison across body mass index (BMI) categories, as well as its association with functional performance.
Baseline
Secondary Outcomes (7)
Body Awareness Level (BAQ Score)
Baseline
Functional Mobility (Timed Up and Go Test)
baseline
Lower Extremity Functional Strength (5 Times Sit-to-Stand Test)
Baseline
Composite Functional Performance Index
Baseline
Waist Circumference (Central Obesity Indicator)
Baseline
- +2 more secondary outcomes
Study Arms (4)
Normal Weight
Women aged 18-65 years with a body mass index (BMI) between 18.5 and 24.9 kg/m². Participants in this group represent the normal weight category and will be evaluated for postural habits, body awareness, and functional performance.
Overweight
Women aged 18-65 years with a BMI between 25.0 and 29.9 kg/m². This group includes participants classified as overweight and will undergo the same assessments as other groups
Obesity Class I
Women aged 18-65 years with a BMI between 30.0 and 34.9 kg/m². Participants in this group represent obesity class I and will be assessed for postural habits, body awareness, and functional performance.
Obesity Class II-III
Women aged 18-65 years with a BMI of 35.0 kg/m² or higher. This group includes participants with higher levels of obesity and will undergo the same evaluation protocol.
Interventions
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.
Eligibility Criteria
The study population will consist of women aged 18-65 years recruited from the general community. Participants will be categorized into four groups based on body mass index (BMI): normal weight, overweight, obesity class I, and obesity class II-III.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ondokuz Mayis University
Samsun, Samsun, 55270, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
March 24, 2026
First Posted
March 30, 2026
Study Start
April 30, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
March 30, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
The individual participant data will not be shared due to privacy concerns and restrictions in the informed consent provided by participants