Social Media and Risk Reduction Teaching-Enhanced Reach

NCT04387552 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2126

Last updated 2026-04-17

No results posted yet for this study

Summary

This study aims to improve adherence to American Academy of Pediatrics safe sleep (SS) recommendations and improve rates of initiation and duration of partial and exclusive breastfeeding (BF) through direct education of mothers using Mobile Health (mHealth) technologies (ex. text messaging).

Conditions

  • Breastfeeding
  • SUID
  • SIDS

Interventions

BEHAVIORAL

Prenatal Safe Sleep Mobile Health (mHealth) Messaging

Participants will receive prenatal Safe Sleep mHealth messaging starting at 34 weeks gestation until birth of their baby.

BEHAVIORAL

Prenatal Breastfeeding Mobile Health (mHealth) Messaging

Participants will receive prenatal Breastfeeding mHealth messaging starting at 34 weeks gestation until birth of their baby.

BEHAVIORAL

Postnatal Safe Sleep Mobile Health (mHealth) Messaging

Upon birth of baby, participants will begin receiving postnatal Safe Sleep mHealth messaging for a two month period.

BEHAVIORAL

Postnatal Breastfeeding Mobile Health (mHealth) Messaging

Upon birth of baby, participants will begin receiving postnatal Breastfeeding mHealth messaging for a two month period.

Sponsors & Collaborators

  • University of Virginia

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • Boston Medical Center

    collaborator OTHER
  • University of Kentucky

    collaborator OTHER
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH
  • Boston University

    lead OTHER

Principal Investigators

  • Michael J Corwin, MD · Boston University School of Public Health, Dept of Pediatrics, BUSM

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
14 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-20
Primary Completion
2025-06-07
Completion
2025-06-07

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04387552 on ClinicalTrials.gov