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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07747259
Enrollment
50
Registered
2026-08-05
Start date
2026-08-05
Completion date
2026-09-01
Last updated
2026-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polyendocrine Metabolic Ovarian Syndrome

Keywords

Ovarian Syndrome

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Health Institutes of Turkey
Lead SponsorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Forearm Plank TestBaselineThe 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.
Side Bridge TestBaselineThe 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.
Body Awareness Questionnaire (BAQ)BaselineBAQ 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.
Pelvic Floor Distress Inventory-20 (PFDI-20)BaselineThis 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.
Pittsburgh Sleep Quality Index (PSQI)BaselineThis 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.
WHO - Quality of Life - Brief (WHOQOL-BREF)BaselineThe 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.

Countries

Turkey (Türkiye)

Contacts

CONTACTEzgi Türkmen
turkmnezgi@gmail.com0090 216 547 26 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 7, 2026