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NCT06319807Completed

GrowWell - Responsive Bottle Feeding

Using Digital Health Technologies to Prevent Obesity Among Infants of Parents Receiving Nutrition Assistance Benefits.

Source: ClinicalTrials.gov · Last updated 30 Sept 2025

Brief summary (registry, in English)

The overall goal of this research is use digital health to augment the clinical encounter with Women, Infants, and Children (WIC) clinicians and prevent rapid infant weight gain among children living in low-income households. Intervening on weight gain during infancy offers an opportunity to influence lifelong obesity risk. Using personalized motivational messages and targeted skills-training resources, the intervention will support parents and caregivers in adopting responsive feeding strategies. Knowledge gained from this project will be used to develop a future, larger grant submission focused on developing healthy feeding and eating habits among mother-infant dyads.

Status (registry)
Completed
Study type
Interventional
Enrollment
69 (actual)
First submitted
13 Mar 2024
Start date
28 Oct 2024
Primary completion date
18 Aug 2025
Lead sponsor
Wake Forest University Health Sciences
Diseases
Obesity
NCT number
NCT06319807

What you commit to

  • Study type: Interventional
  • Participants enrolled: 69
  • From 28 Oct 2024 to the primary completion date, 18 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • any medical or congenital condition that would interfere with infant feeding or growth (ie, Down syndrome or cleft lip or palate)

Other

  • participating in in a different research study that, in the opinion of the investigator, would conflict or would otherwise be too problematic if the subject were to participate in this study
  • planning to leave North Carolina in the next 6 months
  • subjects who do not have the capacity to give legally effective consent

Who the study is looking for

  • Aged ≥18 years
  • as a smartphone and an email address
  • willing to send and receive daily text messages
  • can read and write in English
  • child is \<=6 weeks

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Wake Forest University Health Sciences
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.