RECRUITING

Get Social Media and Risk-Reduction Training

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study examines the implementation of the TodaysBaby™ mobile safe sleep intervention program in US hospitals. The main aims of this study are to examine: 1) differences in program penetration and the equity of penetration according to income and race/ethnicity; 2) differences in feasibility, acceptability, sustainability and fidelity top the intervention; and 3) the effectiveness of the intervention.

Official Title

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

Quick Facts

Study Start:2025-05-01
Study Completion:2028-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06618586

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must speak English or Spanish
  2. * Must live in the United States
  3. * Must have given birth to a healthy, term infants (37 weeks or greater) and be discharged within 7 days of birth
  4. * Must plan to care for infant and live in the same household as infant after birth
  5. * Must enroll in the TodaysBaby program by the time their infant is 7 days of age
  1. * A prenatal diagnosis expected to have impact on infant care practices not compatible with study goals, such as supine infant sleep positioning.

Contacts and Locations

Study Contact

Sarah Roth, MPH
CONTACT
(617)206-6198
saroth@bu.edu

Principal Investigator

Rachel Y Moon, MD
PRINCIPAL_INVESTIGATOR
University of Virginia School of Medicine

Study Locations (Sites)

Boston University
Boston, Massachusetts, 02118
United States

Collaborators and Investigators

Sponsor: University of Virginia

  • Rachel Y Moon, MD, PRINCIPAL_INVESTIGATOR, University of Virginia School of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-01
Study Completion Date2028-06-01

Study Record Updates

Study Start Date2025-05-01
Study Completion Date2028-06-01

Terms related to this study

Keywords Provided by Researchers

  • Safe Sleep
  • Mobile Messaging

Additional Relevant MeSH Terms

  • Infant Death
  • Sudden Infant Death