The Psychological and Social Impact of PCOS

University Hospital, Lille100 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Polycystic Ovary Syndrome

Interventions

QuestionnaireOTHER

Questionnaire on WEPI software (secure data), with link sent by e-mail to patients included in the study, including PCOSQOL, HADS, FACT G7 et ASEX scores.

Medical Language ↔ Plain English

Inclusion Criteria: * 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 Exclusion Criteria: * 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)

Outcomes

Primary Outcomes

Assessment to the The Polycystic Ovary Syndrome Quality of Life scale questionnaire score

according to predefined factors (age, BMI, socio-professional category, delay in diagnosis of Polycystic Ovary Syndrome, infertility, hyperandrogenism, parity, history of anxiety and depression, cycle disorders). Mininum score: 35, maximum score: 245, A higher score means best result

Time frame: Day of inclusion

Secondary Outcomes

Assessment of the Hospital Anxiety and Depression Scale (HADS) questionnaire score according to predefined factors

minimun: 0 maximum: 42. A higher score means worse result

Time frame: Day of inclusion

Assessment of the functional Assessment of Cancer Therapy-General (FACT G7) score according to predefined factors

minimun: 0 maximum: 28 A higher score means worse result

Time frame: Day of inclusion

Assessment of the Arizona Sexual Experience Scale (ASEX) score according to predefined factors

minimun: 0 maximum: 30. A higher score means better result

Time frame: Day of inclusion

The Psychological and Social Impact of PCOS

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts