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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-40
SponsorHealth Institutes of Turkey

About this trial

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.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

50 Participants
are grouped into 2 trial groups

Sponsors and collaborators