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Portable Sleep Monitors in Children With Autism Spectrum Disorder

NCT07367022 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2026-01-26

No results posted yet for this study

Summary

The goal of this study is to evaluate the ability of a portable sleep monitor to detect obstructive sleep apnea in children with autism spectrum disorder (ASD). The main study objectives are to:

1. Evaluate the correlation between the obstructive apnea-hypopnea index (OAHI) on a portable sleep monitor and an in-laboratory polysomnogram (PSG);
2. Determine the sensitivity and specificity of a portable sleep monitor to diagnose obstructive sleep apnea (OSA);
3. Evaluate patient and family preferences for sleep testing.

Conditions

  • Autism Spectrum Disorder (ASD)
  • Obstructive Sleep Apnea (OSA)

Interventions

DEVICE

Portable sleep monitor (Nox T3s)

Participants will test the Nox T3s portable sleep monitor concurrently during their in-hospital clinical polysomnogram.

Sponsors & Collaborators

  • Lena Xiao

    lead OTHER

Eligibility

Min Age
6 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-12
Primary Completion
2026-12-31
Completion
2026-12-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07367022 on ClinicalTrials.gov