Comparison of Core Stability, Body Awareness, Pelvic Health, Sleep, and Quality of Life in Physically Active Women With and Without Polyendocrine Metabolic Ovarian Syndrome
5 de agosto de 2026 actualizado por: Ezgi Türkmen, Health Institutes of Turkey
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.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Descripción detallada
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.
Tipo de estudio
De observación
Inscripción (Estimado)
50
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Ezgi Türkmen
- Número de teléfono: 0090 216 547 26 00
- Correo electrónico: turkmnezgi@gmail.com
Ubicaciones de estudio
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Istanbul, Turquía (Türkiye)
- Reclutamiento
- Haliç Üniversitesi
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Contacto:
- Ayşenur Çetinkaya
- Número de teléfono: 0090 212 924 24 44
- Correo electrónico: aysenurcetinkaya@halic.edu.tr
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
No
Método de muestreo
Muestra no probabilística
Población de estudio
Participants with Polyendocrine Metabolic Ovarian Syndrome & Healthy Adults
Descripción
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.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
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Group I
Paricipants with Polyendocrine Metabolic Ovarian Syndrome
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Group II
Healthy Adult Participants
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Forearm Plank Test
Periodo de tiempo: Baseline
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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.
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Baseline
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Side Bridge Test
Periodo de tiempo: Baseline
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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.
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Baseline
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Body Awareness Questionnaire (BAQ)
Periodo de tiempo: Baseline
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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.
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Baseline
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Pelvic Floor Distress Inventory-20 (PFDI-20)
Periodo de tiempo: Baseline
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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.
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Baseline
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Pittsburgh Sleep Quality Index (PSQI)
Periodo de tiempo: Baseline
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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.
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Baseline
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WHO - Quality of Life - Brief (WHOQOL-BREF)
Periodo de tiempo: Baseline
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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.
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Baseline
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
5 de agosto de 2026
Finalización primaria (Estimado)
1 de septiembre de 2026
Finalización del estudio (Estimado)
1 de septiembre de 2026
Fechas de registro del estudio
Enviado por primera vez
27 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
30 de julio de 2026
Publicado por primera vez (Actual)
5 de agosto de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
6 de agosto de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
5 de agosto de 2026
Última verificación
1 de agosto de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- ETurkmen0426
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .