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NCT Number: NCT07023458

The Effects of Hypoxic Burden on Executive Function (EF) in Preschool Children With Obstructive Sleep Apnea

The goal of this observational study is to study the effect of hypoxic burden on executive function in preschool children aged 2-6 years who have OSA.

The main question it aims to answer is Effect of hypoxic burden from OSA to executive function measured by BRIEF-P in preschool children..

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Key information

Age range

2 year–6 year

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

There is no comparison group in this study Participants will performed full night polysomnography, Denver and BRIEF-P test within 3 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 2-6 years old with OSA

Exclusion criteria

  • Underlying diseases : hypoventilation, neuromuscular diseases, etc.

Treatment and study plan

Brief-P

Diagnostic Test

Executive function test in preschool children with OSA

Primary outcomes

  1. Executive function from BRIEF-P test

    Time frame: 3 months

    T-scores at or below 59 are considered to be within the typical range

Study contacts

Contact information is provided by the study sponsor or research team.

Sarisa Thawongit, Pediatric sleep medicine

CONTACT

[email protected]

668-654-00288

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 17, 2025
Registry last updated
Jul 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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