RecruitingNCT07367022

Portable Sleep Monitors in Children With Autism Spectrum Disorder

The Accuracy of Portable Sleep Monitoring for Children With Autism Spectrum Disorder


Sponsor

Lena Xiao

Enrollment

20 participants

Start Date

Aug 12, 2025

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 6 YearsMax Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Portable sleep monitor (Nox T3s) for people with autism spectrum disorder (asd) and obstructive sleep apnea (osa). The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPortable sleep monitor (Nox T3s)

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


Locations(1)

British Columbia Children's Hospital

Vancouver, British Columbia, Canada

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NCT07367022


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