Methods:
Participants:In our study, a total of 291 patients were included who applied for routine antenatal control or gynecologic complaints. They had no clinical symptoms of Covid-19 and had no suspicion of disease. 174 of the participants were pregnant, and 117 were non-pregnant patients. The study was designed as cross sectional study and data was obtained from both qualitative and quantitative methods between 05 May (after the start of restrictions) and 31 May (the date restrictions eased) during the Covid-19 outbreak.
Participants are exluded if they: had a history of psychiatric disorders, could not read or write in Turkish, did not agree to participate in the study, had Covid-19 symptoms and Covid-19 PCR positivity.
The study protocol was approved by the institutional ethical review board.