Actively Recruiting
OSA-18 in Children With Mild Obstructive Sleep Apnea: Can it be a Helpful Decision Making Tool?
Led by Connecticut Children's Medical Center · Updated on 2025-04-08
130
Participants Needed
1
Research Sites
243 weeks
Total Duration
On this page
Sponsors
C
Connecticut Children's Medical Center
Lead Sponsor
R
ResMed Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The concept is a novel research idea that incorporates the potential impact of patient quality of life (QOL) on decision-making for treatment of mild obstructive sleep apnea (OSA). Our hypothesis is that in children with mild OSA there is significant conflict with parental decision-making; in the absence of significant sleep apnea, there is limited research regarding comparative efficacy of various treatment options. The impact of a QOL questionnaire can be a significant deciding factor and may help guide management decisions in such situations.
CONDITIONS
Official Title
OSA-18 in Children With Mild Obstructive Sleep Apnea: Can it be a Helpful Decision Making Tool?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parent or caregiver of a child diagnosed with mild obstructive sleep apnea defined by a polysomnography apnea-hypopnea index (AHI) score between 1 and 5
- Parent or caregiver of a child aged between 3 and 12 years
- Parent or caregiver of a child diagnosed with tonsillar hypertrophy grade 2 or higher
You will not qualify if you...
- Parent or caregiver of a child diagnosed with a syndromic or known neurological condition
- Parent or caregiver of a child with more than two medical cardiac or respiratory conditions
- Parent or caregiver of a child who has previously had a tonsillectomy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Connecticut Children's Medical Center
Hartford, Connecticut, United States, 06106
Actively Recruiting
Research Team
N
Nancy Grover, MD
CONTACT
C
Cameron King, MA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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