Screening of Postpartum Depression in Egyptian Women
Study Details
Study Description
Brief Summary
The goal of this cross-sectional study is to assess the Edinburgh Postnatal Depression Scale as screening tool for Postpartum Depression among women delivering at Egyptian tertiary health care system, University Hospital, regarding Prevalence and risk factors.
participants of this study with fill the Edinburgh Postnatal Depression Scale and their socio-demographic, obstetric and psychological data will be collected and analysed.
prevalence of postpartum depression in Egyptian women will be assessed as well as the associated risk factors
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Study Design
Outcome Measures
Primary Outcome Measures
- Number screening positive for possible postpartum depression by Arabic EPDS [2 weeks postpartum]
Number of participants screening positive for possible postpartum depression, defined as a score of 13 or higher on the validated Arabic version of the Edinburgh Postnatal Depression Scale (EPDS) Participants with a positive screen (EPDS score ≥13) will be referred for psychiatric consultation for diagnostic confirmation and treatment of postpartum depression
Secondary Outcome Measures
- Sociodemographic, clinical, and psychosocial predictors of postpartum depression risk [At 2 weeks postpartum]
Identification of sociodemographic, clinical, and psychosocial risk factors associated with screening positive for possible postpartum depression, as determined by bivariate and multivariate regression analyses of factors correlated with an Arabic EPDS score ≥13. Sociodemographic factors will include maternal age, education level, occupation, socioeconomic status, etc. Clinical factors will include obstetric history, delivery method, neonatal health status, etc. Psychosocial factors will include social support, stress levels, family dynamics, etc.
Eligibility Criteria
Criteria
Inclusion Criteria:
All patients who underwent vaginal/cesarean delivery and reported for follow and willing to participate in the study.
Exclusion Criteria:
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Patients who were unwilling to participate in the study.
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Patients who are having difficulties comprehending the questionnaire of the study.
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Women who were on psychiatric medication during pregnancy.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Faculty od Medicine, Department of Obstetrics and Gynecology. | Cairo | Cairo. | Egypt |
Sponsors and Collaborators
- Al-Azhar University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 520235