RECRUITING

OSA-18 in Children With Mild Obstructive Sleep Apnea: Can it be a Helpful Decision Making Tool?

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

OSA-18 in Children With Mild Obstructive Sleep Apnea: Can it be a Helpful Decision Making Tool?

Quick Facts

Study Start:2021-06-02
Study Completion:2024-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05911646

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:3 Years to 12 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Parent/caregiver of child with an initial diagnosis mild obstructive sleep apnea defined as polysomnography AHI score between 1 and 5
  2. * Parent/caregiver of child between 3 and 12 years of age
  3. * Parent/caregiver of child who has been diagnosed with tonsillar hypertrophy grade 2 or higher
  1. * Parent/caregiver of child diagnosed with a syndromic or known neurologic condition and/or multiple (more than two) medical cardiac or respiratory medical conditions
  2. * Parent/caregiver of child who has previously underwent tonsillectomy

Contacts and Locations

Study Contact

Nancy Grover, MD
CONTACT
860- 545- 9650
ngrover@connecticutchildrens.org
Cameron King, MA
CONTACT
8608375595
CKing02@connecticutchildrens.org

Principal Investigator

Nancy Grover, MD
PRINCIPAL_INVESTIGATOR
Connecticut Children's Medical Center

Study Locations (Sites)

Connecticut Children's Medical Center
Hartford, Connecticut, 06106
United States

Collaborators and Investigators

Sponsor: Connecticut Children's Medical Center

  • Nancy Grover, MD, PRINCIPAL_INVESTIGATOR, Connecticut Children's Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-06-02
Study Completion Date2024-12-30

Study Record Updates

Study Start Date2021-06-02
Study Completion Date2024-12-30

Terms related to this study

Keywords Provided by Researchers

  • Mild Obstructive Sleep Apnea

Additional Relevant MeSH Terms

  • Apnea, Obstructive Sleep
  • Obstructive Sleep Apnea