Get Social Media and Risk-Reduction Training Using TodaysBaby Mobile Safe Sleep Program for Mothers of Healthy Newborns in the US
Led by University of Virginia · Updated on 2025-06-11
10000
Participants Needed
1
Research Sites
52 weeks
Total Duration
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 raceethnicity, 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 programs 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
Research Team
S
Sarah Roth, MPH
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This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
Factors
TodaysBaby low‑touch
TodaysBaby high‑touch
Standard of care
What it is
A low‑touch implementation of TodaysBaby combining text‑message educational videos and weekly safe sleep practice queries
Higher‑support ‘high touch’ hospital strategy for delivering TodaysBaby content
Current standard care without the TodaysBaby intervention
Role in trial
Tested intervention condition delivered during specific periods across hospitals
Original implementation style used for comparison periods
Control condition representing usual care without TodaysBaby
Primary purpose
To assess feasibility and effectiveness of delivering safe sleep education via text‑message videos and queries
To compare original higher‑support implementation strategy against low‑touch approach
To establish baseline adoption and equity outcomes under usual care
How it is delivered
Delivered via automated text‑message videos in first two months plus weekly text queries from home
Delivered via the original higher‑support hospital implementation method (unspecified more hands‑on support)
No TodaysBaby content is delivered
Evidence status
Trial ongoing; evidence on feasibility, equity, fidelity, effectiveness still being collected
Trial ongoing; comparative evidence pending
Trial ongoing; serves as baseline context without intervention
Important limitations
Effectiveness may vary by hospital engagement, digital access, language
Resource‑intensive implementation may be less scalable
Baseline care may lack structured education and reinforcement
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
Who Can Participate
FEMALE
Healthy Volunteers
Eligibility Criteria
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
You will not qualify if you...
Prenatal diagnosis expected to affect infant care practices incompatible with study goals, such as supine infant sleep positioning
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
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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Get Social Media and Risk-Reduction Training Using TodaysBaby Mobile Safe Sleep Program for Mothers of Healthy Newborns in the US
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Published Research Related To This Trial
Get Social Media and Risk-Reduction Training (GET SMART) to improve infant safe sleep practices through a mobile text message-delivered video safe sleep intervention for new parents: study protocol for a type 3 hybrid implementation-effectiveness cluster randomized trial in 20 US birth hospitals.