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NCT Number: NCT07578714

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

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.

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Key information

Age range

20 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Istinye University, Topkapi Campus

Istanbul, Zeytinburnu, 34010, Turkey (Türkiye)

Location status: Recruiting

Location contact

NALAN Soydaş. Assistant Professor,, PhD

CONTACT

[email protected]

+90 535 010 54 61

Nalan Soydaş, PhD

PRINCIPAL_INVESTIGATOR

WALA Abbas Mohammed TAHA PT. MSc student, PT Specialist,master's student

CONTACT

[email protected]

+905384112497 ext. +966565787745

WALA TAHA, PT. MSc student

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. 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.

  2. 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.

  3. 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

Secondary outcomes

  1. 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.

  2. 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

Study contacts

Contact information is provided by the study sponsor or research team.

WALA Abbas Mohammed TAHA, PT specialist

CONTACT

[email protected]

+905384112497 ext. +966565787745

Sponsors and collaborators

Lead sponsor

Istinye University

Other

Registry information

Acronym: CSBF-P

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 11, 2026
Registry last updated
May 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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