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Pacifiers and Breastfeeding Among Mothers at Risk for Postpartum Depression

Breastfeeding Clinical Trial

Official title:
Effect of Hospital Pacifier Distribution on Breastfeeding Among Mothers at High Risk for Postpartum Depression

Clinical Trial Summary

We will enroll 40 mother-infant dyads in a randomized trial exploring the effect of distribution of pacifiers during the birth hospitalization to mothers at high risk for postpartum depression on pacifier use, infant feeding, and maternal stress.

Clinical Trial Description

This study is a pilot a randomized controlled trial to determine if pacifier distribution affects breastfeeding among mothers at high risk for postpartum depression. We will recruit 40 mothers of healthy singleton births in a U.S. hospital who are at high risk of postpartum depression and randomly assign them to receive a pacifier or not. We will ascertain pacifier use, maternal stress, and infant feeding behaviors with web-based surveys at 2, 4, 6, 12, 18, and 24 weeks. Mothers will also wear a wristband to detect maternal heart rate variability throughout the first 6 weeks as a marker of maternal stress. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03709004
Study type Interventional
Source University of California, Davis
Contact
Status Withdrawn
Phase N/A
Start date September 25, 2019
Completion date September 25, 2019
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