Optimizing Family Counseling for Anticipated Extremely Preterm Delivery

Recruiting N/A Interventional Study
Preterm Pregnancy Premature Birth
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 99
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
460 (estimated)
Sponsor
Boston Children's Hospital · Other
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About This Trial
Antenatal family counseling for anticipated extremely preterm deliveries remains ethically and practically challenging for maternal-fetal medicine specialists and neonatologists alike. The overall goal of this project is to improve antenatal counseling and counseling outcomes for families facing anticipated extremely preterm delivery through innovative, interdisciplinary simulation-based education…
Trial Locations
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Eligibility Criteria
1. Pregnant women and their partners Inclusion Criteria: * English-proficient adult pregnant woman admitted between 22 0/7-25 6/7 weeks' estimated gestation for anticipated extremely preterm delivery and her adult partner (if available) for whom an antenatal neonatal intensive care unit (NICU…
Contacts

Christy L Cummings, MD

617-355-2539

christy.cummings@childrens.harvard.edu

CONTACT

Vanessa J Young, RN, BA

617-355-8330

vanessa.young@childrens.harvard.edu

CONTACT