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NCT05982236Completed

The Psychological and Social Impact of PCOS

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

The aim of the study is to assess the association between the quality of life of patients with PCOS and various factors (age, BMI, socio-professional category, delay in diagnostic of PCOS, infertility, hyperandrogenism, parity, history of anxiety and depression, cycles disorders). This study will be proposed to patients known to have PCOS, during a follow-up consultation or a visit to a day hospital in the Gynaecology Department and/or a consultation in the Reproductive Medicine Department. No-objection forms will be collected at the same time. A link will be sent by e-mail to the patient to access the online questionnaire on the WEPI software and complete it after the consultation. Responses to the questionnaire will be collected progressively and stored in a secure RedCAP file.

Status (registry)
Completed
Study type
Observational
Enrollment
100 (actual)
First submitted
31 Jul 2023
Start date
4 Jul 2023
Primary completion date
26 Dec 2023
Lead sponsor
University Hospital, Lille
NCT number
NCT05982236

What you commit to

  • Study type: Observational
  • Participants enrolled: 100
  • From 4 Jul 2023 to the primary completion date, 26 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patient with no health insurance cover
  • Difficulties understanding or speaking French
  • Computer (tablet/smartphone) and internet connection required.
  • Refusal to take part in research
  • Under court protection (guardianship/curatorship/privation of liberty)

Who the study is looking for

  • Female sex
  • Adult patient (aged 18 or over)
  • Able to read and write in French
  • diagnosed at a previous consultation as having PCOS according to the Rotterdam criteria (at least 2 out of 3 criteria from:
    • Clinical signs of hyperandrogenism (hirsutism, acne, androgenic alopecia) and/or biochemical signs of hyperandrogenism (total testosterone \> 0.39 ng/mL and/or androstenedione \> 1.75 ng/mL)
    • Ovulation disorders (infertility, oligomenorrhoea or amenorrhoea or cycle length either \<21 days or \>35 days),
    • Polymicrocystic ovaries on ultrasound (either 19 or more follicles measuring 2-9 mm in diameter and/or increased ovarian volume (\>10 cm3) and/or increased ovarian area (\> 5.5 cm²) without presence of cyst or dominant follicle.)
  • Informed consent

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Lille hôpital Jeanne de Flandre
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.