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NCT06457750Not yet recruiting

Anthropometric Outcomes of a Mobile Health Intervention for Eating Behaviour and Lifestyle in Infancy

Anthropometric and Body Composition Outcomes of a Mobile Health Intervention to Improve Eating Behaviours and Lifestyle Habits During Infancy

Source: ClinicalTrials.gov · Last updated 5 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Lifestyle, activity, and feeding behaviours during early childhood set the foundation for subsequent lifelong metabolic health as an adult. The investigators have developed a digital tool, called Feeding, Lifestyle, Activity Goals (FLAGs) to assess lifestyle and feeding behaviours of young infants, simultaneously providing guidance and tailored advice for parents on ideal practices specific to their children. The investigators aim to assess its usability, acceptability, and feasibility , before proceeding to determine efficacy of the FLAGs intervention through conducting a randomized controlled trial, enrolling 440 infants from KK Women's and Children's Hospital. Half of them will receive standard routine infant care, whereas the other half will additionally receive the digital FLAGs assessment and advisory tool, complete with mobile nudges. The follow-up period will be over 12 months, with the main outcomes being i) indicators of good feeding and lifestyle behaviour at 12 months old, and ii) physical growth trends, body fat proportions. Demonstrating the benefits of using FLAGs will underscore the importance of integrating this digitalized tool into the screening and evaluation of well children, with the potential to be upscaled and adopted across hospitals, primary care, and community-based health programmes.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
440 (estimated)
First submitted
30 May 2024
Start date
Nov 2025
Primary completion date
Dec 2026
Lead sponsor
KK Women's and Children's Hospital
Diseases
Obesity
NCT number
NCT06457750

What you commit to

  • Study type: Interventional
  • Planned participants: 440
  • From Nov 2025 to the primary completion date, Dec 2026
  • 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.

Age

  • Women less than 21 years old

Other

  • Unable to understand English
  • Not planning to reside in Singapore until baby is at least 1 year old
  • Premature birth of baby (defined as below 37 weeks' gestation)
  • Birth of a baby with congenital abnormalities, physical or neurodevelopmental disabilities

Who the study is looking for

  • Women
  • 34-36 weeks' pregnant, or 3 days post-delivery.
  • Pre-pregnancy BMI of at least 23 kg/m\^2, and/or with the diagnosis of gestational diabetes mellitus or type 2 diabetes mellitus.

Sex: All · 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
KK Women's and Children's Hospital
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status

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