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NCT Number: NCT06520696

MILC: A Comprehensive Mobile Application That Addresses the Breastfeeding Challenges of Low-income Hispanic Mothers

The innovative platform MILC is designed to provide an integrated and comprehensive professional and social support network with personalized breastfeeding (BF) education to target exclusive breastfeeding (EBF) and any BF behaviors in low-income Hispanic women. Formative research conducted for the development of MILC and results from pilot testing will help guide the completion of the development and testing of this prototype that specifically caters to Hispanic women. In the long term, MILC has the potential to increase the rates of EBF and any BF up to 12 months.

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Key information

Age range

18 year–44 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

UCONN Health, Farmington, Connecticut, United States

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About this study

Breastfeeding (BF) is positively associated with health benefits for infants. It reduces an infant's risks for various conditions such as respiratory tract infections, non-specific gastroenteritis, diarrhea, asthma, and sudden infant death syndrome (SIDS).

Despite high breastfeeding (BF) initiation of approximately 80% among the Hispanic population in the United States (US), less than 25% of infants were exclusively breastfed (EBF) through 6 months, further perpetuating ethnic disparities in chronic diseases such as diabetes, obesity, and hypertension. Hispanic women are more likely to supplement feeding with formula, than non-Hispanic or African American (AA) mothers. Research has reported that barriers such as insufficient BF education, lack of BF technical support (i.e. latching issues, sore nipples), returning to work, easy access to free or discounted formula milk from Women Infants and Children (WIC), lack of social support, perceived inconvenience, cultural belief that both formula and breastmilk (los-dos) is best for the babies, perception that the infant is not satiated, and embarrassment associated with breastfeeding result in premature weaning off BF among low-income Hispanic mothers. Therefore, increasing the duration of EBF and continuous BF among low-income Hispanic women would require an innovative and comprehensive approach that addresses the diverse range of barriers listed above.

The investigators hypothesize that MILC will show significantly higher percentages of BF mothers in the intervention group at each time (1 month, 3 months, and 6 months) point compared with the control group. In the short term, MILC will be shown to be usable and acceptable by Hispanic BF mothers to receive BF support, education, and guidance from primary care providers (PCP) and certified lactation consultants/international board certified lactation consultants (CLC/IBCLC). In the long term, the impact of MILC will increase the rates of EBF for up to 6 months along with increasing rates of any BF up to 12 months.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for focus groups:

  • Mothers who successfully exclusively breastfed for up to 6 months, at least one child OR mothers who attempted EBF but were unsuccessful at breastfeeding, in the past 3 years
  • Self-identify as Hispanic
  • Be WIC-eligible
  • Voluntarily consent
  • Speak English

Inclusion criteria

for Randomized Control Trial (RCT):

  • In their late third trimester (approximately 4 weeks from delivery)
  • Can initiate BF immediately
  • Self-identify as Hispanic
  • Be WIC-eligible
  • Voluntarily consent
  • Not have psychiatric hospitalization within the last 3 months
  • Not have current or suicidal thoughts or past attempts
  • Own a smartphone device
  • Speak English

Exclusion criteria

for focus groups and Randomized Control Trial (RCT):

  • Participants who are under the age of 18 or over 44
  • Women experiencing a fetal demise or infant death
  • Women who report the following conditions also will be excluded:
  • Human immunodeficiency virus (HIV)
  • Taking antiretroviral medication or chemotherapy agents
  • Untreated, active tuberculosis
  • T-Cell lymphotropic virus type I or type II
  • Illicit drug use
  • Receiving radiation therapy
  • Exposed to anthrax
  • Undergone breast surgery
  • Known exposure to environmental toxins
  • Active hepatitis B and C
  • Prescription drug use incompatible with lactation

Treatment and study plan

MILC application

Behavioral

Eligible Hispanic participants in their third trimester will be recruited for the study. Intervention group will receive standard WIC services plus the MILC application. Standard WIC support includes on-site lactation consultation, bilingual peer counseling, weekly peer support meetings, free breast pump, and enhanced food package for BF mothers. If a participant has trouble with breastfeeding, she will be referred to a home-visiting breastfeeding peer counselor in the area. Participants will be asked to participate in the periodic follow-up assessments at 1, 3 and 6 months along with demonstrating breastfeeding via MILC app. Participants will send in 1 BF video per month using the MILC app to verify continued BF and fill out monthly self-report to verify EBF. Participants in the incentive group will receive escalating monthly points as incentives for every additional month of continued BF and EBF.

Usual Care

Behavioral

Participants in the control group will receive care as usual with standard breastfeeding services from the WIC program and will be asked to participate in the periodic follow-up assessments at 1, 3 and 6 months. Participants in the control group can receive financial compensation for the completion of assessments. This is necessary to maximize retention and adherence to the monthly assessment schedule, provide comparable remuneration as the incentive group, and minimize demoralization of control group participants following treatment assignment. All participants are informed of the differential group procedures during the randomization consent process. In addition to the follow-up assessment, control group will also complete a monthly self-report on BF status (both for EBF and "any BF"). For attention control purposes in this group, participants will be referred to a mobile app for tracking the baby's milestones called Baby Connect.

Primary outcomes

  1. Exclusive breastfeeding

    Time frame: 1 month, 3 months and 6 months

    Investigators will assess if participants are breastfeeding exclusively (EBF)through monthly self-reported information. Investigators will record information on EBF at 1 month, 3 months and 6 months among women in the intervention arm.

  2. Any breastfeeding rate(EBF)

    Time frame: 1 month, 3 months and 6 months

    Investigators will assess if participants are continuous breastfeeding through monthly breastfeeding videos uploaded in the system. Investigators will report information on any breastfeeding at 1 month, 3 months and 6 months.

Secondary outcomes

  1. Infant weight (Medical outcomes)

    Time frame: Baseline, 1 month, 3 months and 6 months

    Infant's weight using medical report collected at 1 month, 3 month and 6 months

  2. Emergency department visit (Medical outcomes)

    Time frame: Baseline, 1 month, 3 months and 6 months

    Number of emergency department visited for infant will be collected at 1 month, 3 month and 6 months

Other outcomes

  1. Latching

    Time frame: Baseline, 1 month, 3 months and 6 months

    It will be assessed using LATCH breastfeeding assessment scale. LATCH stands for latch, audible swallowing, type of nipple, comfort and hold. Each component is scored from 0-2. A LATCH score of 0-3 is regarded as poor, 4-7 as moderate, and 8-10 as good.

  2. BF history & attitudes questionnaire

    Time frame: Baseline, 1 month, 3 months and 6 months

    New survey based on constructs that potentially moderate BF

  3. Self-Efficacy Scale

    Time frame: Baseline, 1 month, 3 months and 6 months

    It will be assessed using the BF Self-Efficacy Scale Short Form (BSES-SF). The BSES-SF is a 14-item self-administered instrument derived from the original 33-item BSES that measures breastfeeding confidence. Total scores range from 14 to 70, with higher scores reflecting more significant levels of breastfeeding self-efficacy.

  4. Iowa Infant Feeding Attitude

    Time frame: Baseline, 1 month, 3 months and 6 months

    It will be collected using the Iowa infant feeding attitudes scale (IIFAS). The scale is composed of 17 items for assessing attitude towards BF. The total IIFAS score can range from 17 to 85 with higher scores reflecting positive attitude towards breastfeeding

  5. Acculturation

    Time frame: Baseline, 1 month, 3 months and 6 months

    It will be assessed by using the Acculturation Rating Scale for Mexican Americans II. The scale contains 48 items to which participants respond on a 5-point Likert scale ranging from "Not at all" to "Extremely often or almost always," with higher scores indicating greater cultural orientation.

  6. Postnatal depression

    Time frame: Baseline, 1 month, 3 months and 6 months

    It will be assessed using Edinburgh Postnatal depression Scale (EPDS). The EPDS has a maximum score of 30; a score of 10 or more may indicate possible depression of varying severity.

  7. Usability

    Time frame: Month 6 postpartum

    System Usability Scale (SUS)survey will be used to assess usability of the MILC app. A SUS score above 68 would be considered above average and anything below 68 is below average.

  8. Acceptance and Adoption

    Time frame: Month 6 postpartum

    Technology Acceptance Model (TAM) will be used to assess acceptance of MILC app

Study contacts

Contact information is provided by the study sponsor or research team.

Katie Chang, MS

CONTACT

[email protected]

(703) 662-5858 x143

Tony Ma, MS

CONTACT

[email protected]

(703) 919-3234

Sponsors and collaborators

Lead sponsor

Benten Technologies, Inc.

Industry

Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)
  • RTI International
  • Temple University
  • UConn Health

Registry information

Official study title

Multi-modal Intervention for Lactation Care (MILC)

Acronym: MILC

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 25, 2024
Registry last updated
Jul 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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