Clinical trial Recruiting at 1 site Interventional Ages 21 and up Women only

Using technology and peer support to help parents prevent early childhood dental issues

Official title: Technology-enabled Anticipatory Guidance and Peer Support in Empowering Parents to Prevent Early Childhood Caries: A Randomized Controlled Trial

Run by National University of Singapore · NCT06558955 · Data updated 2026-11-12

This study is testing if a new program that uses technology and support from other parents can help moms and dads prevent dental problems in their young kids better than regular education.

Quick facts

Study typeInterventional
Ages21 Years and up
SexWomen only
Enrollment600 (estimated)
SponsorNational University of Singapore
Academic / other
Locations1 site (Singapore)
StatusRecruiting
StartedJune 15, 2024
Main results expectedDecember 31, 2027
Study endsSeptember 1, 2028
Registry record updatedAugust 19, 2024
Trial IDNCT06558955 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are mothers who are expecting or have infants under 3 months old, have internet access, and can communicate in English.

Probably not a fit

Patients whose children have serious medical conditions affecting oral health or who plan to emigrate within three years may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study tests the effectiveness of a technology-enabled approach combined with peer support to empower parents in preventing early childhood caries (ECC). It is designed as a randomized controlled trial with two groups: one receiving conventional oral health education and the other receiving the innovative intervention. Up to 600 mother-child pairs will participate, with the intervention group attending four online sessions tailored to their child's developmental milestones. Outcomes will be measured through questionnaires, food diaries, and dental examinations to assess the impact on parental efficacy, childcare practices, and the incidence of ECC.

Why it matters

Potential benefit: If successful, this approach could significantly reduce the incidence of early childhood caries and improve oral health practices among parents.

How similar studies have gone: Other studies have shown promise with technology-enabled health interventions, suggesting potential success for this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Mother is currently expecting or has an infant below 3 months of age
* Biological mother of the child
* Mother with internet access and a mobile device
* Mother can communicate in English
* Mother aged 21 years and above

Exclusion Criteria:

* Child with disqualifying medical condition (e.g., tube feeding, severe neuromuscular disability) that would limit oral dietary intake, at-home oral hygiene practices, or receipt of dental examinations
* Child with serious congenital syndrome that is expected to adversely affect the development of primary teeth
* Family plans to emigrate within 3 years

Where it's running

  • National University Hospital
    Singapore, Singapore
    Recruiting

Study contacts

  • Principal investigator: Xiaoli Gao, PhD — National University of Singapore
  • Study coordinator: Xiaoli Gao, PhD
  • Email: dengx@nus.edu.sg
  • Phone: (65) 6772 4990

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.