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Evaluation of Maternal Mental Health Following Ultrasonography Detection of Fetal Congenital Anomalies

A

Assiut University

Status

Not yet enrolling

Conditions

Mental Disorder

Treatments

Other: Questionnaire and Physical Exam

Study type

Observational

Funder types

Other

Identifiers

NCT06594952
Maternal psychology on anomaly

Details and patient eligibility

About

The purpose of this study is to evaluate maternal mental health during antenatal and postnatal periods after Ultrasonography diagnosis of fetal anomalies.

Full description

Fetal congenital anomalies are responsible for a great deal of abortions in desired pregnancies . In clinical practice, prenatal screening programs in 1st and 2nd trimester target both chromosomal and structural abnormalities. These congenital anomalies are classified as minor and major anomalies than may lead to death or stillbirth . Half of all anomalies are detectable during weeks 18-22 of pregnancy. Due to the advances occurring in Ultrasonography and screening paradigms, the rate of diagnosed anomalies is increasing dramatically which in turn leading to psychological distress in the pregnant mother. Receiving a diagnosis of fetal anomaly is a highly stressful and potentially traumatic event that can elicit immediate feelings of grief, loss, anger, depression, and anxiety. However, the foreknowledge of a fetal anomaly during pregnancy may enable the mother to prepare mentally resulting in reduced maternal stress after delivery. The American College of Medical Genetics recommends underscoring the importance of psychological assessment and substantive communication with parents facing a prenatal diagnosis of fetal anomaly. Despite the accessibility of establishing the significant symptoms of maternal psychological distress, the evidence on the definite nature of this distress in consideration to other life stressors and an accurate the prediction of women vulnerability in the critical period have not been clear yet due to many methodological issues. Identification of women at highest risk for poor adaptation to the diagnosis may allow for targeted psychological support services for those most vulnerable.

Enrollment

120 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • Women with history of psychiatric disorders.

Trial design

120 participants in 3 patient groups

minor anomalies group
Description:
pregnant women with minor fetal structural anomaly detected by ultrasound.
Treatment:
Other: Questionnaire and Physical Exam
major anomalies group
Description:
pregnant women with major fetal structural anomaly detected by ultrasound
Treatment:
Other: Questionnaire and Physical Exam
Control Group
Description:
Pregnant women with normal ultrasound.
Treatment:
Other: Questionnaire and Physical Exam

Trial contacts and locations

0

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Central trial contact

Ahmed Abbas Professor, MD

Data sourced from clinicaltrials.gov

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