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LIFT: Telemedicine Breastfeeding Support

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03901833
Enrollment
56
Registered
2019-04-03
Start date
2019-07-24
Completion date
2024-03-29
Last updated
2024-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding

Brief 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

Interventions

BEHAVIORALTelemedicine Support

Telemedicine intervention

OTHERStandard of Care

Standard of Care

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
ExperienceOne month post-enrollmentMean score on a modified, 16-item Interactive Telehealth Satisfaction Scale \>48 (corresponding to better than neutral on a 5 point Likert scale, 16 questions).

Secondary

MeasureTime frameDescription
Time to cessationMonthly up to 12 monthsTime to breastfeeding cessation (assessed via monthly surveys as no to infant receiving any breast milk in last 24 hours)
Exclusive breastfeeding cessationMonthly up to 12 monthsTime to exclusive breastfeeding cessation (assessed via monthly surveys, defined by initiation of formula, water, juice, other liquids, or solid foods)
Breastfeeding at 3 months3 monthsProportion of infants breastfeeding at 3 months (assessed via 24 hour recall from infant's mother)
Exclusive breastfeeding3 monthsProportion of infants breastfeeding without supplementation with other food or liquids at 3 months (assessed via 24 hour recall from infant's mother)
Individual satisfaction questions1 month post enrollmentMean satisfaction on each Interactive Telehealth Satisfaction Scale question

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026