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Recruiting NCT07176767

NCT07176767 The IPAD Cohort Study: Insomnia and Positive Airway Pressure Adherence in Children and Adolescents

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Clinical Trial Summary
NCT ID NCT07176767
Status Recruiting
Phase —
Sponsor Lena Xiao
Condition Sleep Apnea, Obstructive
Study Type OBSERVATIONAL
Enrollment 82 participants
Start Date 2025-06-12
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 8 Years
Max Age 18 Years
Study Type OBSERVATIONAL
Interventions
Positive airway pressure therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 82 participants in total. It began in 2025-06-12 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Positive Airway Pressure (PAP) is a treatment used to help people with sleep-disordered breathing, particularly those with obstructive sleep apnea (OSA). The device delivers pressurized air through a mask to keep the airways open during sleep, improving breathing and preventing interruptions in sleep. Studying how insomnia affects PAP adherence in children can help improve future treatments. However, no long-term studies have looked at this in children. Based on previous research, the investigators plan to conduct a study across multiple centers focusing on children with OSA starting PAP therapy. The study will explore how insomnia affects PAP adherence and how race and ethnicity play a role.

Eligibility Criteria

Inclusion Criteria: 1. Children aged 8-18 years old 2. Obstructive apnea-hypopnea index ≥ 5/hour on baseline diagnostic polysomnogram (PSG) 3. Newly prescribed PAP therapy Exclusion Criteria: 1\) Developmental disability precluding ability to answer questionnaires

Contact & Investigator

Central Contact

Lena J Xiao, MD MSc

✉ lena.xiao@cw.bc.ca

📞 6048752345

Principal Investigator

Lena J Xiao, MD, MSc

PRINCIPAL INVESTIGATOR

Provincial Health Services Authority British Columbia

Frequently Asked Questions

Who can join the NCT07176767 clinical trial?

This trial is open to participants of all sexes, aged 8 Years or older, up to 18 Years, studying Sleep Apnea, Obstructive. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07176767 currently recruiting?

Yes, NCT07176767 is actively recruiting participants. Contact the research team at lena.xiao@cw.bc.ca for enrollment information.

Where is the NCT07176767 trial being conducted?

This trial is being conducted at Vancouver, Canada.

Who is sponsoring the NCT07176767 clinical trial?

NCT07176767 is sponsored by Lena Xiao. The principal investigator is Lena J Xiao, MD, MSc at Provincial Health Services Authority British Columbia. The trial plans to enroll 82 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology