CClinicalTrials.gg
RecruitingNCT07230808Updated Jul 6, 2026

Digitally Delivered Child Obesity Prevention for Parents in Home Visiting Programs

An interventional study of digital intervention + home visiting curriculum and Home visiting curriculum in Childhood Obesity Prevention, sponsored by University of Florida. Recruiting at 1 site in United States. Open to participants aged 16 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by University of Florida · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started May 2026; still recruiting 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
16 Years to 65 Years
Sex
All
01

Study 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.

Read the detailed description

The first 1,000 days (conception to age 2) have been deemed a critical period for obesity prevention yet, effective, sustainable efforts are lacking. Current home visitation programs (HVP) targeting at-risk families for other child development related issues are a potential innovative opportunity for early childhood obesity prevention. The overall goal of the project is to reduce the prevalence of overweight and obesity in children under the age of 1 year thereby reducing obesity rates of older children and adults in the long term. Prior pilot work by members of the research team demonstrated feasibility of embedding an early childhood obesity prevention (ECHO) program in an existing home visitation program (HVP+) during an infant's first year of life.

Five obesity-associated behaviors (i.e., breastfeeding, introduction to solids, limiting juice, sleep routines, screen time) were emphasized through brief interactive lessons utilizing behavior change strategies and an ecological approach by providing linkages to community resources that support healthy behaviors. The pilot program was well received by families, mothers breastfed longer, infants had fewer nocturnal awakenings, were less likely to receive juice, and had a lower weight-for-length (WFL) z-score at 12 months. However, there is a critical need for alternative and innovative, consistent, and sustainable digital delivery methods especially during times when face-to-face home visits are not feasible. Qualitative interviews were conducted with home visitors (n=27) from Florida's (FL) Maternal, Infant Early Childhood Home Visitation (MIECHV) Program and revealed that they were highly receptive to using digital learning with at-risk families.

The specific aims of the proposed research are to a) Develop, refine, and conduct usability testing of early childhood obesity prevention digital learning modules with mothers participating in FL MIECHV; and b) Conduct a pilot RCT of a 12 month digitally-enhanced early childhood obesity prevention intervention (HVP+E), with 50 mother-infant pairs (25 HVP+E/25 standard HVP) participating in FL MIECHV to determine feasibility and acceptability of the HVP+E intervention and study recruitment, implementation and evaluation protocols; and obtain data on preliminary efficacy of the intervention on children's WFL z-scores (primary outcome), maternal feeding practices, child sleep and screen time (secondary outcomes).

Mother-infant dyads (n=50) enrolled in the Maternal, Infant Early Childhood Home Visitation (MIECHV) Program parentally or within one month of giving birth will be randomized to receive either the standard home visitation program (HVP) or the digitally delivered obesity prevention-enhanced home visitation program (HVP+E) for 1 year. HVP+E content will also be expanded to support mothers in engaging fathers and other family members in target behaviors. Mother-infant dyads will be assessed at study entry and at 4, 6 and 12 months. If efficacious, the intervention has potential for public health impact through early childhood obesity prevention in an underserved population, and dissemination through home visitation programs nationwide.

02

Conditions studied

  • Childhood Obesity Prevention

Browse trials for

Keywords

  • childhood obesity
  • home visiting
  • parents
  • infants
  • nutrition education
  • eHealth
  • digital intervention
03

In context

Pediatric Obesity

1,117 studies on the registry are indexed under Pediatric Obesity; 189 are open to participants now.

This study's planned enrollment of 50 is below the median of 103 across 862 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

University of Florida is the lead sponsor of 1,254 studies on the registry; 201 are open to participants now.

Of its 170 completed or terminated interventional studies of FDA-regulated products, 136 (80%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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 (\<2500 gms)
  • Mother has a significant maternal morbidity (e.g. cancer) or hospitalization for psychiatric disorder in past 6 months
  • Extended hospital stay for mom or infant > 5 days
  • Unable to speak and read English.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Digital intervention

    digitally delivered childhood obesity prevention intervention for parents

    Behavioral: digital intervention + home visiting curriculum

  • Active comparator
    standard home visiting curriculum

    standard home visiting program for parents

    Behavioral: Home visiting curriculum

Interventions

  • Behavioraldigital intervention + home visiting curriculum

    Digitally delivered childhood obesity prevention intervention for parents called THRIVES (Teaching Healthy Routines in Very Early Stages) will be provided to complement the standard home visiting curriculum. Parents will complete digital content containing videos, text and checkpoint questions with goal setting during the first year of their child's life over a 12 month period. Assessments will be collected at baseline, 4, 6 and 12 months.

  • BehavioralHome visiting curriculum

    Parents will receive a standard home visiting curriculum delivered in person for at least 1 year during the project timeframe and complete assessments at baseline, 4, 6 and 12 months.

06

What researchers measure

Primary outcomes

  1. Child Weight for Length

    Weight for Length (WFL) z-score. A z-score of 0 indicates a child is a the median for WFL. Scores above 0 indicate that a child has a higher WFL and may be at risk for overweight or obesity. Scores below 0 indicate that a child has a lower WFL and may be at risk for undernutrition.

    Time frame: 0, 4, 6, 12 months

Secondary outcomes

  1. Structure and Control in Parent Feeding Questionnaire (SCFQ)

    The SCFQ contains questions related to structure and controlling parental feeding practices. The validated questionnaire has two subscales: 1) Structure (meal routines, feeding environment, etc.) and 2) Control (pressure to eat, restriction, etc.). Responses are captured on a 5-point Likert scale with 1 indicating "never" and 5 indicating "always." Higher scores indicate greater structure or control while lower scores indicate lower structure or control.

    Time frame: 0, 4, 6, 12 months

  2. Baby's Basic Needs Questionnaire (BBNQ)

    Feeding to soothe practices will be captured using the BBNQ which assesses infant's feeding history and extent to which mothers use feeding to soothe their infants. Responses are captured on a 5-point Likert scale (1=Never; 5=Always). Higher scores indicate more frequent use of feeding to soothe while lower scores indicate less use of feeding to soothe.

    Time frame: 0, 4, 6, and 12 months

  3. Feeding behaviors of parents (breastfeeding, timing of juice and solid food introduction)

    Questions were adapted from the Beverage Intake Questionnaire, Preschool Version (BEVQ-PS), an instrument designed to assess the frequency of preschool children's intake of beverages, including 100% fruit juice. In the BEVQ-PS, parents report how often their child consumes specific beverages using responses options ranging from "Never" to "3 or more times per day." Higher responses indicate more frequent intake and lower responses indicate less frequent intake. Other measures were adapted from the National Survey of Children's Health (NSCH) questionnaire, which includes standardized items assessing infant feeding practices. Parents report the age at which their child was first given food other than breastmilk or formula or juice, using response options as follows: \<1 month, 2-3 months, 4-5 months, 6-8 months, 9-11 months, or 12 months or older. Responses will be compared to current solid food and juice guidance.

    Time frame: 0, 4, 6 and 12 months

  4. Parental obesity prevention knowledge, attitudes, and behaviors

    Checkpoint questions associated with digital intervention module topics will administered after parents complete the digital modules. These items evaluate parents' knowledge, attitudes, and intentions related to obesity-prevention behaviors, including feeding, sleep, screen time, and soothing practices. The questions are not part of a validated scale; responses are summarized descriptively based on accuracy of answers and qualitatively.

    Time frame: From date of randomization until date of completion of the digital modules, assessed up to 1 year.

  5. Dietary Screener Questionnaire

    The 26-item Dietary Screener Questionnaire (DSQ) will be used to assess the frequency of consumption in the past month of selected foods and drinks. The DSQ captures intakes of fruits and vegetables, dairy/calcium, added sugars, whole grains/fiber, red meat, and processed meat. The DSQ can be interviewer-administered on paper or the web. Each of the 26 items on the screener was selected because of its relationship to one or more dietary factors of interest in dietary guidance.The scoring algorithms convert screener responses to estimates of dietary intake for fruits and vegetables (cup equivalents), dairy (cup equivalents), added sugars (tsp), whole grains (ounce equivalents), fiber (g), and calcium (mg). Responses to the red meat and processed meat questions may be used as qualitative indicators of intake frequency.

    Time frame: 0, 4, 6 and 12 months

  6. Activity and Screen time

    Parent and Child activity and screen time questions are adapted from a combination of project developed items and from the Infant Feeding Practices Study II (IFPS-II) and the National Survey of Children's Health (NSCH). The questionnaires are not operationalized on a validated scale; responses are summarized descriptively.

    Time frame: 0, 4, 6 and 12 months

  7. Brief Infant Sleep Questionnaire

    Infant sleep duration and awakenings are measured using the Brief Infant Sleep Questionnaire (BISQ). The BISQ does not equate to an overall score with minimum or maximum values. Individual sleep parameters are reported descriptively

    Time frame: 0, 4, 6 and 12 months

  8. Family Social Support Questionnaire

    The Multidimensional Scale of Perceived Social Support (MSPSS), a 12-item validated measure, will be used to assess social support of the parent and is scored from 1 to 7. Subscale and total mean scores also range from 1 to 7, with higher scores indicating greater perceived social support and lower scores indicating less perceived social support. Results are summarized using mean scores.

    Time frame: 0, 4, 6 and 12 months

  9. Perceived Stress Scale

    The Perceived Stress Scale (PSS), a validated 10-item measure of perceived stress over the past month, will be used to assess stress of the parent. Each item is scored from 0 to 4, with a total score ranging from 0 to 40. Higher scores indicate greater perceived stress, and lower scores indicate lower perceived stress.

    Time frame: 0, 4, 6 and 12 months

07

Study locations

1 of 1 sites recruiting
  • University of Florida
    Gainesville, Florida 32608, United States
    • Amy Mobley · Contact · amy.mobley@ufl.edu · 352-294-1813
    • Amy Mobley, PhD · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07230808
Lead sponsor
University of Florida
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Sponsor
First posted
Nov 17, 2025
Start date
May 21, 2026
Primary completion
Aug 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Jul 6, 2026

Study contacts

Amy Mobley, PhD, RD
Contact
amy.mobley@ufl.edu
352-294-1813
Alyssa Watkins, MPH
Contact
alyssaberger94@ufl.edu
Amy Mobley, PhD, RD
principal investigator · University of Florida

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion