Actively Recruiting

Phase Not Applicable
FEMALE
Healthy Volunteers
ID06618586

Get Social Media and Risk-Reduction Training (GET SMART)

Led by University of Virginia · Updated on 2025-06-11

10000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Virginia

Lead Sponsor

W

Washington University School of Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the TodaysBaby mobile safe sleep intervention program in U.S. hospitals to understand its reach, fairness in access based on income and race/ethnicity, ease of use, acceptance, long-term use, accuracy in delivery, and overall effectiveness. The study focuses on reducing infant death and sudden infant death by promoting safe sleep practices. This research is sponsored by the University of Virginia and does not involve medication or invasive treatments. The study randomly assigns hospitals to one of three groups during two six-month intervention periods. One group receives a low-touch approach where mothers find TodaysBaby through ads and sign up themselves using a QR code. Another group receives a high-touch approach where hospital staff assist mothers in signing up and watching videos in a one-on-one setting. A third group serves as a control and receives standard postpartum care without the TodaysBaby intervention. The TodaysBaby program sends educational videos and text message questions about infant sleep practices during the first two months after birth. Mothers participate by enrolling in TodaysBaby within seven days after birth, completing surveys about infant care, and responding to text messages over several months. Researchers measure how many mothers sign up, the fairness of access, and how well the program is delivered and used. They also assess the program’s impact on safe sleep behaviors up to 180 days after birth. The study includes ongoing feedback about feasibility, acceptability, sustainability, and cost. Participation lasts through the intervention periods with ongoing data collection and follow-up.

CONDITIONS

Brief Title

Get Social Media and Risk-Reduction Training

Who Can Participate

FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must speak English or Spanish
  • Must live in the United States
  • Must have given birth to a healthy, term infant (37 weeks or greater) and be discharged within 7 days of birth
  • Must plan to care for infant and live in the same household as infant after birth
  • Must enroll in the TodaysBaby program by the time their infant is 7 days of age
Not Eligible

You will not qualify if you...

  • Prenatal diagnosis expected to affect infant care practices incompatible with study goals, such as supine infant sleep positioning

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) to confirm eligibility and enroll in the study

Intervention Period

Duration - Up to 6 months depending on hospital assignment

Participants receive the TodaysBaby program, which includes text message-delivered educational videos and text queries about safe sleep practices during the first 2 months after birth.

1 to 2 text message questions weekly and access to a web portal; sign up during the first week after birth

Follow-up Assessments

Duration - Up to 1 year after enrollment

Participants complete surveys and qualitative assessments on feasibility, acceptability, sustainability, fidelity, effectiveness, and program cost up to 1 year after enrollment.

Surveys and assessments conducted remotely at various timepoints between 60 and 180 days after birth and within 1 year after enrollment

Trial Site Locations

Total: 1 location

1

Boston University

Boston, Massachusetts, United States, 02118

Actively Recruiting

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Research Team

S

Sarah Roth, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

3

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Frequently Asked Questions

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