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LIFT: Telemedicine Breastfeeding Support

University of California (UC) Davis logo

University of California (UC) Davis

Status

Completed

Conditions

Breastfeeding

Treatments

Other: Standard of Care
Behavioral: Telemedicine Support

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03901833
1382496

Details and patient eligibility

About

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

Enrollment

56 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

56 participants in 2 patient groups, including a placebo group

Telemedicine Support
Experimental group
Description:
Weekly telemedicine breastfeeding support visits for four weeks, delivered via telemedicine
Treatment:
Behavioral: Telemedicine Support
Control
Placebo Comparator group
Description:
Standard of care
Treatment:
Other: Standard of Care

Trial contacts and locations

1

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Central trial contact

Hadley Sauers-Ford, MPH; Iesha Miller, MA

Data sourced from clinicaltrials.gov

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