Lactation Achievement With Texts at Home

Breastfeeding Clinical Trial

— LATcH  

Official title:

LATcH: Lactation Achievement With Texts at Home

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04108533
• Other study ID #: 833824
• Status: Completed
• Phase: N/A
• Start date: January 6, 2020
• Est. completion date: March 30, 2021

Study information

• Verified date: August 2021
• Source: University of Pennsylvania
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 124
• Est. completion date: March 30, 2021
• Est. primary completion date: January 20, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Breastfeeding
• Breastfeeding, Exclusive
• Depression, Postpartum
• Postpartum Depression

Intervention

Behavioral:
• Text-Based Support
Text-based breastfeeding support as described in arm/group descriptions

Locations

Country	Name	City	State
United States	Hospital of the University Of Pennsylvania	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Exclusivity	Exclusive breastfeeding	6 weeks postpartum
Secondary	Any Breastfeeding	Any reported breastfeeding	6 weeks postpartum
Secondary	Duration	Duration of breastfeeding	6 weeks postpartum
Secondary	Formula	Rate of formula use	6 weeks postpartum
Secondary	Compliance	Compliance with postpartum visit	6 weeks postpartum
Secondary	Mood	Mood assessment using PHQ-2	2 and 6 weeks postpartum