Actively Recruiting

Age: 6Years - 18Years
All Genders
NCT07367022

Portable Sleep Monitors in Children With Autism Spectrum Disorder

Led by Lena Xiao · Updated on 2026-01-26

20

Participants Needed

1

Research Sites

72 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

Portable Sleep Monitors in Children With Autism Spectrum Disorder

Who Can Participate

Age: 6Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children between 6 to 18 years of age
  • Diagnosed with autism spectrum disorder
  • Undergoing a polysomnogram (PSG) for the first time
  • Caregiver willing to complete questionnaires about child's sleep and behavior
Not Eligible

You will not qualify if you...

  • Currently using respiratory therapy
  • Previously completed a polysomnogram (PSG)
  • Caregiver unwilling to complete questionnaires about child's sleep and behavior

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

British Columbia Children's Hospital

Vancouver, British Columbia, Canada, V6H 3N1

Actively Recruiting

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Research Team

L

Lena J Xiao, MD MSc

CONTACT

M

Macyn LY Leung, MSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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