About this trial
The goal of this observational retrospective cohort study is to examine the association between mode of delivery and early postpartum depressive symptoms in adult women who delivered at Massachusetts General Hospital. Specifically, the study evaluates whether the urgency of cesarean delivery (elective versus emergency) is associated with differences in Edinburgh Postnatal Depression Scale (EPDS) scores at 6-8 weeks postpartum, compared with elective cesarean delivery and vaginal delivery. The EPDS is a validated 10-item self-report questionnaire with scores ranging from 0 to 30, where higher scores indicate more severe depressive symptoms.
The primary questions are whether EPDS scores differ among women undergoing emergency cesarean delivery, elective cesarean delivery, and vaginal delivery, and whether perioperative and obstetric factors are associated with postpartum depressive symptoms.
This study involves retrospective analysis of de-identified electronic health record data. Participants will not undergo any study-specific interventions.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
adult patients (≥18 years old) who underwent cesarean delivery or vaginal delivery
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Edinburgh Postnatal Depression Scale (EPDS) scores, a 10-item self-reported screening tool for postpartum depression (range: 0-30, with higher scores indicating more severe depressive symptoms)
Secondary outcomes
Prevalence of postpartum depression
Prevalence of postpartum depression (EPDS ≥ threshold) across delivery groups.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Jingping Wang, MD, Ph.D.
Lead sponsor
Massachusetts General Hospital
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: