COVID-19, Dyspareunia, Postpartum Period
Conditions
Keywords
Postpartum Period, Dyspareunia, COVID-19
Brief summary
The aim of this study is to identify women with postpartum sexual dysfunction and dyspareunia risk in the early period and to use the treatment and care services they need effectively. Our secondary aim is to reveal the difference in sexual life in the postpartum period between healthy pregnant women and pregnant women diagnosed with COVID-19.
Interventions
None listed
Sponsors
Kanuni Sultan Suleyman Training and Research Hospital
Study design
Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Pregnant Patient with COVID-19
Exclusion criteria
* Those with known sexual dysfunction disorder
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of pregnant women diagnosed with COVID-19 using Carol Postpartum Sexual Function and Dyspareunia Scale | 3 months | In the study planned to be carried out, it is aimed to identify women at risk of postpartum sexual dysfunction and dyspareunia early and benefit from the treatment and care services they need effectively. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of pregnant women diagnosed with COVID-19 using Carol Postpartum Sexual Function and Dyspareunia Scale | 3 Months | To reveal the difference in sexual life in postpartum period between healthy pregnant women and pregnant women diagnosed with COVID-19. |
Countries
Turkey (Türkiye)
Outcome results
None listed