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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 6
Maximum Age: 18
Healthy Volunteers: f
View:

• Children between 6 to 18 years of age, AND;

• Children diagnosed with autism spectrum disorder, AND;

• Children who will be undergoing a polysomnogram (PSG) for the first time, AND;

• Caregiver willing to complete questionnaires about child's sleep and behavior

Locations
Other Locations
Canada
British Columbia Children's Hospital
RECRUITING
Vancouver
Contact Information
Primary
Lena J Xiao, MD MSc
lena.xiao@cw.bc.ca
604-875-2345
Backup
Macyn LY Leung, MSc
macyn.leung@bcchr.ca
604-875-2345
Time Frame
Start Date: 2025-08-12
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 20
Treatments
Children with ASD testing a portable sleep monitor
Children aged 6-18 years old with autism spectrum disorder concurrently testing a portable sleep monitor (Nox T3s) during their first clinical polysomnogram. Children and their caregivers may also complete a qualitative interview about sleep testing preferences after their sleep test.
Sponsors
Leads: Lena Xiao

This content was sourced from clinicaltrials.gov