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Lactation Achievement With Texts at Home

LATcH: Lactation Achievement With Texts at Home

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04108533
Acronym
LATcH
Enrollment
124
Registered
2019-09-30
Start date
2020-01-06
Completion date
2021-03-30
Last updated
2021-09-02

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

Conditions

Breastfeeding, Breastfeeding, Exclusive, Postpartum Depression

Brief summary

The objective of this study is to determine if text-based breastfeeding support improves breastfeeding initiation, exclusivity, and duration when compared to usual postpartum care. All women without a contraindication to breastfeeding and access to a mobile phone with unlimited text messaging capability who deliver a healthy term neonate will be eligible for inclusion. Consented women will be randomized to either text-based breastfeeding support using the Way to Health platform or usual care.

Detailed description

Breastfeeding is a public health priority. The CDC and WHO, among other professional organizations, have issued the following recommendations with respect to breastmilk. Infants should be exclusively breastfed through the first 6 months of life and continue to receive breastmilk through at least the first year of life. Many women, however, are not meeting these benchmarks even among those who desire to do so. Approximately one quarter of infants are exclusively breastfed at 6 months and a little over 1/3 are still receiving breastmilk at the time of their 1st birthday.1 What looking at these numbers alone miss is the number of women who attempt to breastfeed and do not continue to do so. 83% of women attempt breastfeeding indicating that there is a significant drop off that occurs between delivery and 6 and 12 months of life. While the risk factors for this are vast, lack of education poor socioeconomic status and poor social support are important contributors to breastfeeding problems. Both professional and informal support through family or friends have a significant impact on breastfeeding outcomes. Not all patients, however, have the resources needed to obtain professional support or the family experience necessary to meet their breastfeeding goals. Digital support in other medical specialties have shown success in health outcomes. Multiple international studies have also demonstrated the benefits of text-messaging on breastfeeding rates including improved rates and duration of exclusivity. Thus far, none of these studies have been performed in the United States. Therefore, the aim of this study is to determine if text-based breastfeeding support improves breastfeeding initiation, duration, and exclusivity when compared to usual postpartum care. All women without a contraindication to breastfeeding and access to a mobile phone with unlimited text messaging capability will be approached in the 34-36 week of pregnancy. All consented women will be enrolled in a run-in period in which they receive weekly text messages with factual information about breastfeeding. A response is required to one or more of these texts in order to be eligible for randomization at delivery. Upon delivery of a healthy term neonate, women who responded in the run-in period will be randomized to either text-based breastfeeding support using the Way to Health platform or usual care.

Interventions

Text-based breastfeeding support as described in arm/group descriptions

Sponsors

University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \>18 years of age * English-speaking * Own a cellular phone with unlimited text-messaging * Singleton gestation consented at 34-36 weeks of pregnancy * Willing and able to sign consent form

Exclusion criteria

* Contraindication to breastfeeding * Delivery of infant requiring ICN admission * Physician discretion that patient will be unable to comply with the protocol

Design outcomes

Primary

MeasureTime frameDescription
Exclusivity6 weeks postpartumExclusive breastfeeding

Secondary

MeasureTime frameDescription
Any Breastfeeding6 weeks postpartumAny reported breastfeeding
Duration6 weeks postpartumDuration of breastfeeding
Formula6 weeks postpartumRate of formula use
Compliance6 weeks postpartumCompliance with postpartum visit
Mood2 and 6 weeks postpartumMood assessment using PHQ-2

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026