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NCT Number: NCT07747259

Comparison of Core Stability, Body Awareness, Pelvic Health, Sleep, and Quality of Life in Physically Active Women With and Without Polyendocrine Metabolic Ovarian Syndrome

Aim of the study was to compare physically active women with and without Polyendocrine Metabolic Ovarian Syndrome (PMOS) in terms of core stability, body awareness, pelvic health, sleep, and quality of life, and to reveal the possible effects of the presence of PMOS on these parameters despite physical activity.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Observational

Primary location

About this study

The study plans to include female participants who have been regularly practicing Pilates at least twice a week for at least three months at a designated Pilates studio. Data on participants' socio-demographic characteristics, core stability, body awareness, pelvic floor function, sleep, and quality of life will be collected. This research study is designed as an observational and cross-sectional evaluation study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Being a woman aged 18-40 with a diagnosis of PMOS (n=25).
  • Being a healthy woman aged 18-40 (n=25).
  • Having practiced Pilates regularly for at least three months, at least twice a week.
  • Voluntarily agreeing to participate in the study.

Exclusion criteria

  • Being pregnant or in the first 6 months postpartum.
  • Being in menopause.
  • Having any other diagnosed gynecological pathology.
  • Having any significant physical limitations that would prevent the tests from being performed.
  • Having any diagnosed psychological disorder that would hinder communication.

Treatment and study plan

Primary outcomes

  1. Forearm Plank Test

    Time frame: Baseline

    The purpose of this test is to measure the core stability, or endurance, of the trunk muscles. Participants are asked to keep their body in a straight line against gravity with their forearms on the ground and their toes touching the ground, and to maintain their posture without changing position by contracting their abdominal muscles. The time (in seconds) spent in this position is measured and recorded with a stopwatch.

  2. Side Bridge Test

    Time frame: Baseline

    The participant lies on their side with their elbow and forearm placed on the ground at shoulder level. Legs and feet are placed on top of each other, forming a straight line. The individual lifts their hips off the ground against gravity, bringing their body into a side bridge position parallel to the ground. Both sides (right/left) are tested separately. The time (in seconds) spent in this position is measured and recorded with a stopwatch.

  3. Body Awareness Questionnaire (BAQ)

    Time frame: Baseline

    BAQ is an 18-item self-report scale designed to measure how attentive the participants are to normal, non-emotional internal bodily processes. It evaluates the sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions. Typically takes about 3 to 5 minutes. Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived condence and accuracy in monitoring the physical state over time.

  4. Pelvic Floor Distress Inventory-20 (PFDI-20)

    Time frame: Baseline

    This scale, which assesses pelvic floor-related symptoms and pelvic functionality, consists of three subscales: POPDI-6, CRADI-8, and UDI-6. The average of the responses for each subscale is calculated and multiplied by 25 to create a standard score on a scale of 0-100 for each subscale. The total PFDI-20 score is obtained by summing the scores of the three subscales and ranges from 0 to 300. Higher scores indicate more symptoms and discomfort.

  5. Pittsburgh Sleep Quality Index (PSQI)

    Time frame: Baseline

    This scale was developed to assess sleep quality and disturbances over a one-month period. The 18 items included in the scoring are grouped into 7 components. Some components are represented by a single item, while others are obtained by combining several items. Each item is rated on a scale of 0-3, and the scores of each component are added together to obtain a total score between 0-21. A higher total score indicates poor sleep quality, while a score above 5 generally indicates poor sleep quality.

  6. WHO - Quality of Life - Brief (WHOQOL-BREF)

    Time frame: Baseline

    The World Health Organization-developed quality of life assessment tool helps evaluate an individual's overall health status. It consists of 26 questions, each scored on a 5-point Likert scale from 1 (very poor) to 5 (very good). The scale covers four core areas of life: physical health, psychological health, social relationships, and environment. It also includes two additional items that assess an individual's overall quality of life and health satisfaction. Raw scores are converted into a total score on a scale of 0-100 using a formula. Higher scores indicate a higher perceived quality of life.

Study contacts

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

Ezgi Türkmen

CONTACT

[email protected]

0090 216 547 26 00

Sponsors and collaborators

Lead sponsor

Health Institutes of Turkey

Other Gov

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Aug 5, 2026
Registry last updated
Aug 6, 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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