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Recruiting
NCT07230808
Digitally Delivered Child Obesity Prevention for Parents in Home Visiting Programs
Conditions: Childhood Obesity Prevention
Sex: All
Ages: 16 Years – 65 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 50
Sponsor: University of Florida
Location: University of Florida Gainesville Florida
Summary
The goal of this clinical trial is to determine feasibility and acceptability of a digitally-based obesity prevention intervention for mothers of infants participating in a home visitation program.
The main questions it aims to answer are:
* What impact does the digitally based obesity prevention intervention for parents have on children's weight?
* What impact does the digitally based obesity prevention intervention have on mothers' feeding practices, child sleep, and child screen time? Researchers will compare the digital intervention to home visiting standard curriculum to see if the intervention results in larger improvements.
Participants will view several digital modules including videos on feeding, activity and family topics over the course of 1 year. They will complete questionnaires at the beginning of the study and again at 4, 6 and 12 months and their child will be weighed and measured at each time point.
Eligibility Criteria
Inclusion Criteria:
* Enrolled in or eligible for home visiting program
* Ages 16 years or older
* Speaks and reads English
* Has no chronic health condition affecting growth or development
* Has a singleton birth \> 37 weeks gestation.
Exclusion Criteria:
* Child has a major malformation
* Child admitted to the NICU
* Child considered small for gestation age (SGA) and/or have a low birth weight (\ 5 days
* Unable to speak and read English.
Source: ClinicalTrials.gov (NCT07230808). StuddyBuddy aggregates publicly available trial information.