- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07578714
Core Stability, Postural Balance, and Flexibility in Healthy Women: A Comparative Study Between Pilates Practitioners and Sedentary Individuals (CSBF-P)
Study Overview
Status
Detailed Description
This cross-sectional comparative study involves 55 healthy female participants divided into two groups: a Pilates group (minimum 5 months of practice, twice weekly) and a sedentary control group (less than 150 minutes of physical activity per week). To ensure objectivity and high-quality data, an "Assessor Blinding" protocol will be implemented, where the investigator performing physical measurements remains unaware of the participants' group allocation.
Primary outcomes include:
- Deep muscle stabilization measured via a Pressure Biofeedback Unit (PBU) in a prone position.
- Core endurance assessed using the McGill Core Endurance Battery (Flexor, Extensor, and Side Bridge tests).
- Dynamic postural balance evaluated through the Y-Balance Test (YBT) in anterior, posteromedial, and posterolateral directions.
- Static balance measured by the Single Leg Stance Test (SLST) with eyes open and closed.
- Hamstring and lower back flexibility assessed by the Sit and Reach Test. Statistical analysis will be performed using IBM SPSS version 26.0 to compare the outcomes between the two groups.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: WALA Abbas Mohammed TAHA, PT specialist
- Phone Number: +966565787745 +905384112497
- Email: 2433095066@stu.istinye.edu.tr
Study Locations
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Zeytinburnu
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Istanbul, Zeytinburnu, Turkey (Türkiye), 34010
- Recruiting
- Istinye University, Topkapi Campus
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Contact:
- WALA Abbas Mohammed TAHA PT. MSc student, PT Specialist,master's student
- Phone Number: +966565787745 +905384112497
- Email: 2433095066@stu.istinye.edu.tr
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Contact:
- NALAN Soydaş. Assistant Professor,, PhD
- Phone Number: +90 535 010 54 61
- Email: nalan.engin@istinye.edu.tr
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Principal Investigator:
- WALA TAHA, PT. MSc student
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Principal Investigator:
- Nalan Soydaş, PhD
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy female volunteers aged 20-45.
- 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.
- For the control group: having a sedentary lifestyle (weekly moderate physical activity time less than 150 minutes).
- 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.
- Having full cognitive ability to understand, follow, and execute all physical assessment instructions.
- Willingness to voluntarily sign the informed consent form prior to the study.
Exclusion Criteria:
- History of any surgery involving the spine, pelvis, or lower extremities within the last 12 months prior to the study.
- Currently pregnant or less than 6 months postpartum.
- Diagnosed vestibular disorders or chronic clinical balance disorders.
- History of neurological disease (MS, Parkinson's, etc.) or systemic metabolic disorder (diabetes, etc.).
- Having a pain intensity greater than 2/10 on the visual analog scale (VAS) in the lower back or lower extremities.
- Professional sports history or participation in other exercise programs exceeding 3 hours per week (excluding Pilates for the Pilates group).
- Acute musculoskeletal injuries or acute illnesses that may affect energy levels on the day of evaluation.
- Concurrent participation in other intensive core strengthening programs such as "advanced yoga" that may affect results.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Pilates Group
Healthy women who have regularly practiced Pilates exercises for at least 5 months, with a minimum of two sessions per week.
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Sedentary Group
Healthy women with a sedentary lifestyle, defined as having less than 150 minutes of physical activity per week and no regular exercise routine in the past 3 months.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deep Muscle Stabilization Pressure Biofeedback Device - PBU
Time Frame: At the single assessment session (Day 1)
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Measurement of the transversus abdominis muscle activation using a Pressure Biofeedback Unit (PBU).isolation is confirmed by a drop in pressure of 4-10 mmHg from a 70 mmHg baseline, sustained for 10 seconds in prone position.
|
At the single assessment session (Day 1)
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|
Core Muscle Endurance
Time Frame: At the single assessment session (Day 1)
|
Measured using the McGill Core Endurance Battery, including the Trunk Flexor, Trunk Extensor, and Side Bridge tests.
Results are recorded as the duration (in seconds) the position is maintained.
|
At the single assessment session (Day 1)
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Dynamic Postural Balance Y-Balance Test (YBT)
Time Frame: At the single assessment session (Day 1)
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Assessed using the Y-Balance Test (YBT).
The maximum reach distance in three directions (Anterior, Posteromedial, and Posterolateral) will be recorded in centimeters
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At the single assessment session (Day 1)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Static Postural Balance Test or Single Leg Standing Test (SLST)
Time Frame: At the single assessment session (Day 1)
|
The participant should stand on their dominant leg with their hands on their hips. Conditions: The test is performed under two conditions: Eyes open and eyes closed. Measurement: The time it takes to maintain this balance without putting the foot down or moving it is measured in seconds. |
At the single assessment session (Day 1)
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Lower Back and Hamstring Flexibility
Time Frame: At the single assessment session (Day 1)
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ssessed using the Sit and Reach Test.
The reach distance is measured in centimeters using a standard test box
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At the single assessment session (Day 1)
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: NALAN Soydaş, PhD, Istinye University
Publications and helpful links
General Publications
- Alshehre Y, Alkhathami K, Brizzolara K, Weber M, Wang-Price S. Reliability and Validity of the Y-balance Test in Young Adults with Chronic Low Back Pain. Int J Sports Phys Ther. 2021 Jun 1;16(3):628-635. doi: 10.26603/001c.23430.
- Fallahasady E, Rahmanloo N, Seidi F, Rajabi R, Bayattork M. The relationship between core muscle endurance and functional movement screen scores in females with lumbar hyperlordosis: a cross-sectional study. BMC Sports Sci Med Rehabil. 2022 Oct 13;14(1):182. doi: 10.1186/s13102-022-00567-2.
- De Blaiser C, Roosen P, Willems T, De Bleecker C, Vermeulen S, Danneels L, De Ridder R. The role of core stability in the development of non-contact acute lower extremity injuries in an athletic population: A prospective study. Phys Ther Sport. 2021 Jan;47:165-172. doi: 10.1016/j.ptsp.2020.11.035. Epub 2020 Nov 30.
- Wells C, Kolt GS, Bialocerkowski A. Defining Pilates exercise: a systematic review. Complement Ther Med. 2012 Aug;20(4):253-62. doi: 10.1016/j.ctim.2012.02.005. Epub 2012 Mar 13.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2026/53
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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