Summary

Location
at UC Davis
Dates
study started
completion around
Principal Investigator
by Laura Kair, MD (ucdavis)
Headshot of Laura Kair
Laura Kair

Description

Summary

The central hypothesis guiding this project is that tailored breastfeeding support, that leverages easily accessible telemedicine technologies, can improve breastfeeding outcomes among late preterm dyads. The long-term goals of this project are to improve maternal and child health and reduce health disparities by designing and implementing evidence-based interventions to improve breastfeeding outcomes for this challenging patient population. This study seeks to identify lactation support practices that improve breastfeeding duration and to test the effect of telemedicine breastfeeding support on breastfeeding duration, among the nearly one in ten mothers who deliver late preterm (34-37 6/7 weeks), as this subpopulation of mothers faces the highest rates of premature breastfeeding cessation

Official Title

Telemedicine Breastfeeding Support Following Late Preterm Delivery: A Randomized Controlled Trial

Keywords

Breastfeeding, Telemedicine Support

Eligibility

You can join if…

  • maternal age 18-49 years
  • late preterm delivery (34-37 6/7 weeks)
  • enrollment up to 1 week postpartum
  • breastfeeding initiated
  • access to a smartphone, tablet, or laptop computer in their home

You CAN'T join if...

  • incarceration
  • inability to communicate in English
  • infant with medical condition compromising breastfeeding (e.g. cleft lip and/or palate).

Location

  • University of California-Davis
    Sacramento California 95817 United States

Lead Scientist at University of California Health

  • Laura Kair, MD (ucdavis)
    Associate Professor, Pediatrics, School of Medicine. Authored (or co-authored) 53 research publications

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Davis
Links
Learn more or sign up for the study here!
ID
NCT03901833
Study Type
Interventional
Participants
Expecting 56 study participants
Last Updated