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Completed NON-SBIR/STTR RPGS NIH (US)

Positive Airway Pressure For The Treatment Of The Obstructive Sleep Apnea Syndrome In Children With Down Syndrome

$639.4K USD

Funder NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Recipient Organization University of Miami School of Medicine
Country United States
Start Date Sep 01, 2023
End Date Aug 31, 2025
Duration 730 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10912150
Grant Description

Abstract Individuals with Down syndrome (DS) are predisposed to OSAS due to craniofacial features (midface hypoplasia, glossoptosis) and studies have shown that the prevalence of OSAS in this population is markedly increased compared to that of typically developing children. Adenotonsillectomy (AT) is considered first-line

treatment for childhood OSAS. However, OSAS resolves in only a portion of children with DS after AT. In fact, many children with DS are referred for positive airway pressure (PAP) therapy initiation due to persistent OSAS after AT, and PAP appears to be an important feature of the experience of living with DS. PAP has been

shown to be highly effective at treating OSAS and improve OSAS-associated neurobehavioral symptoms, such as quality of life, behavior, mood, daytime sleepiness and school performance. However, PAP as a treatment for OSAS has not been well-studied in children with DS. Therefore, we propose to leverage the HEalthy SLeeP

for Children with Down Syndrome (HELP-DS, U01HL125295-S1 and U01HL123507-S1) infrastructure and conduct in two HELP-DS sites (Philadelphia and Cincinnati) plus the University of Miami, a randomized controlled trial to test a 6-month intensive behavioral intervention (INT) to improve PAP adherence vs standard

clinical care (CON). Participants with DS and OSAS, aged 6-17.9-years, referred to PAP initiation for the treatment of OSAS will be included. They will undergo standardized evaluations of quality of life, behavior, attention, and family-relevant outcomes, PAP adherence, and health care utilization at baseline, 6, and 12

months. This rigorous design and comprehensive study will resolve existing uncertainties on initial management approaches for children with DS and OSAS treated with PAP by addressing critical issues: a) determine the efficacy of INT vs CON in promoting PAP adherence, b) elucidate which factors mediate or

moderate adherence to PAP in children with DS and OSAS, c) determine the effect of PAP use on neurobehavioral and family-relevant outcomes, and quality of life.

All Grantees

University of Miami School of Medicine

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