About this trial
The purpose of this study is to evaluate maternal mental health during antenatal and postnatal periods after Ultrasonography diagnosis of fetal anomalies.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Pregnant women with confirmed pregnancy with viable fetus (whether singleton or multiple)
Fetal anomaly should be diagnosed with ultrasonography (whether minor or major) after 12 weeks of gestational age
Disqualifiers
None
Trial population
Pregnant women receiving obstetric care at our tertiary perinatal care
Trial design
Cohort
Prospective
Treatments tested in this trial
Questionnaire and Physical Exam
Other interventionDiagnosis of Anxiety using the state-trait anxiety inventory scale (STAI). Depression using Edinburgh Postnatal Depression Scale (EPDS) * Coping using the Brief Coping Scale * Socioeconomic using the Socioeconomic Scale of Egypt * Personality using the short-form Eysenck Personality Questionnaire-Revised (EPQ-R) * Behaviour using Impact of Erect Scale (IES-22)
Treatment groups
Trial outcomes
Primary outcomes
Difference in anxiety scores between the study groups
using the state-trait anxiety inventory scale (STAI).
Secondary outcomes
Difference in Depression scores between the study groups
Depression using Edinburgh Postnatal Depression Scale (EPDS)
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: