Digitally Delivered Child Obesity Prevention for Parents in Home Visiting Programs

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16-65
SponsorUniversity of Florida

About this trial

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

Qualifiers

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

Disqualifiers

Child has a major malformation

Child admitted to the NICU

Child considered small for gestation age (SGA) and/or have a low birth weight (<2500 gms)

Mother has a significant maternal morbidity (e.g. cancer) or hospitalization for psychiatric disorder in past 6 months

Trial design

Treatments tested in this trial

  • digital intervention + home visiting curriculum
  • Home visiting curriculum

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

University of Florida

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator