Health-related Quality of Life of Women with Polycystic Ovary Syndrome At Sohag University Hospital
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorSohag University
About this trial
It is well-established that PCOS women suffer from anxiety, depression, and markedly reduced QoL ,but There has not yet been a nationally representative study to evaluate the PCOS health related Qol and factors affecting it among women in Egypt. So here we try to cover this gap in this study that will be designed to record the QOL of women with PCOS and factors affecting it.
This study aims to assess the health related quality of life of polycystic ovary syndrome and determine factors affecting the HRQOL
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
• Female cases between 18 and 45.
Females diagnosed with PCOS per Rotterdam criteria , the most commonly accepted and used for PCOS, a diagnosis is confirmed if any two of the three features (hyperandrogenism, oligomenorrhea or anovulation, and polycystic ovaries) are present in a woman of reproductive age
Disqualifiers
• Females below 18 years old.
Females above 45 years old.
Patients having major life event or problem also affecting quality of life.
Trial population
women with PCOS visiting Gynecology and clinical nutrition outpatient clinics at Sohag university hospital during the period of 6 months.
Trial design
Design model
Case-only
Time perspective
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
352 Participants
are grouped into 1 trial groupGroup A: Women with Polycystic ovary syndrome
Trial outcomes
Primary outcomes
1
health related quality of life of women with PCOS
The quality of life of the participants will be studied using Polycystic Ovary Syndrome Questionnaire (PCOSQ), which consists of 26 questions and 5 domains ,including emotions (eight questions), body hair (five questions), weight (five questions), infertility (four questions), and menstrual problems (four questions)
Time frame
2 months after answering the polycystic ovary syndrome questionnaireSecondary outcomes
1
Factors affecting health related quality of life of women with PCOS
by medical chart developed by the investigator and the supervisors that will include Socio-demographic data of the women with PCOS, medical history and body measurements.
Time frame
2 months after collecting data from the medical chartSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: