Core Stability, Postural Balance, and Flexibility in Healthy Women: A Comparative Study Between Pilates Practitioners and Sedentary Individuals (CSBF-P)

May 5, 2026 updated by: Wala Abbas Mohammed Taha, Istinye University
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.

Study Overview

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:

  1. Deep muscle stabilization measured via a Pressure Biofeedback Unit (PBU) in a prone position.
  2. Core endurance assessed using the McGill Core Endurance Battery (Flexor, Extensor, and Side Bridge tests).
  3. Dynamic postural balance evaluated through the Y-Balance Test (YBT) in anterior, posteromedial, and posterolateral directions.
  4. Static balance measured by the Single Leg Stance Test (SLST) with eyes open and closed.
  5. 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

Observational

Enrollment (Estimated)

55

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Zeytinburnu
      • Istanbul, Zeytinburnu, Turkey (Türkiye), 34010
        • Recruiting
        • Istinye University, Topkapi Campus
        • Contact:
          • WALA Abbas Mohammed TAHA PT. MSc student, PT Specialist,master's student
          • Phone Number: +966565787745 +905384112497
          • Email: 2433095066@stu.istinye.edu.tr
        • Contact:
        • Principal Investigator:
          • WALA TAHA, PT. MSc student
        • Principal Investigator:
          • Nalan Soydaş, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthy adult women from the general community and Pilates studios in Istanbul, Turkey.

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Pilates Group
Healthy women who have regularly practiced Pilates exercises for at least 5 months, with a minimum of two sessions per week.
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.

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)
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)
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)
Dynamic Postural Balance Y-Balance Test (YBT)
Time Frame: At the single assessment session (Day 1)
Assessed using the Y-Balance Test (YBT). The maximum reach distance in three directions (Anterior, Posteromedial, and Posterolateral) will be recorded in centimeters
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)
Lower Back and Hamstring Flexibility
Time Frame: At the single assessment session (Day 1)
ssessed using the Sit and Reach Test. The reach distance is measured in centimeters using a standard test box
At the single assessment session (Day 1)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: NALAN Soydaş, PhD, Istinye University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 13, 2026

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

March 13, 2027

Study Registration Dates

First Submitted

May 3, 2026

First Submitted That Met QC Criteria

May 5, 2026

First Posted (Actual)

May 11, 2026

Study Record Updates

Last Update Posted (Actual)

May 11, 2026

Last Update Submitted That Met QC Criteria

May 5, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared to ensure the privacy and confidentiality of the participants, as per the ethical approval guidelines of Istinye University. The aggregated results will be published as part of the Master's thesis and potential academic publications.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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