Clinical trial Recruiting at 1 site Observational Ages 8 to 13

Early screening for sleep-disordered breathing in kids at the dentist

Official title: Early Dental Risk Screening for Pediatric Sleep-Disordered Breathing

Run by University of North Carolina, Chapel Hill · NCT07581938 · Data updated 2026-11-12

This study tests whether a simple kid-friendly questionnaire can flag risk for sleep-disordered breathing in children aged 8–13 when checked during a dental visit.

More Obstructive Sleep Apnea (OSA) trials

Quick facts

Study typeObservational
Ages8 Years to 13 Years
SexAll
Enrollment60 (estimated)
SponsorUniversity of North Carolina, Chapel Hill
Academic / other
Locations1 site (Chapel Hill, North Carolina)
StatusRecruiting
StartedJune 2, 2026
Main results expectedMay 2027
Study endsMay 2027
Registry record updatedSeptember 23, 2026
Trial IDNCT07581938 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are children aged 8–13 without prior sleep-disordered breathing diagnosis, not having craniofacial conditions, and able to use a smartphone app for the wearable device.

Probably not a fit

Children with existing sleep-disordered breathing, prior adenotonsillectomy, or ongoing orthodontic treatment may not benefit from this screening approach.

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

What this trial studies

This is a prospective, cross-sectional observational study conducted at a pediatric dentistry clinic to see if the Pediatric Sleep Questionnaire can reliably screen for sleep-disordered breathing in children. Participants are 8–13 years old and are categorized as low- or high-risk based on PSQ scores, then compared using wearables that track sleep parameters and additional assessments from psychosocial questionnaires and craniofacial measurements. No intervention is given; the study purely observes and correlates screening results with objective sleep data collected over up to three weeks. The goal is to assess feasibility and accuracy of adding SDB screening to routine pediatric dental care.

Why it matters

Potential benefit: If successful, dental visits could help identify kids at risk for sleep-disordered breathing earlier, enabling timely follow-up with medical care.

How similar studies have gone: Previous work shows the PSQ can help flag SDB risk in pediatric populations, but applying it within a dental setting with wearable sleep data is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Ages 8-13 years old
* American Society of Anesthesiologists Class I or II
* Ability to read and understand the English or Spanish language
* Ability to assent, with parent/legal guardian able to provide informed consent
* Access to a smartphone capable of supporting the wearable monitoring application

Exclusion Criteria:

* Diagnosis of a craniofacial syndrome or condition known to significantly alter craniofacial morphology
* Prior diagnosis of sleep disordered breathing and/or obstructive sleep apnea
* History of adenotonsillectomy
* Prior or current orthodontic treatment
* Prior orthognathic surgery

Where it's running

  • UNC Adams School of Dentistry
    Chapel Hill, North Carolina, United States
    Recruiting

Study contacts

  • Principal investigator: Parker Norman, DMD, ML — University of North Carolina Adam's School of Dentistry
  • Study coordinator: Parker Norman, DMD, ML
  • Email: parkern@ad.unc.edu
  • Phone: 919-537-3956

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.