Grant: Project Grant
Research Institute of the McGill University Health Centre
$921,826.00
Enhanced Multi-modal, Patient-Centred treatment Option Pathway for Women Experiencing Sleep-Disordered Breathing in PRegnancy (EMPOWER-SDB): A Type 1 Hybrid Effectiveness-Implementation Trial
EF 2025-26
Résumé
Sleep disordered breathing (SDB), a condition where breathing repeatedly stops or becomes shallow during sleep, affects up to half of pregnant individuals, especially later in pregnancy and among those with medical complications. The standard treatment is continuous positive airway pressure (CPAP), which is medically effective, yet many pregnant patients struggle to use it consistently. In our prior study, nearly half had low adherence-even though those who used CPAP showed meaningful metabolic benefits. This highlights the need for treatment options that fit patient comfort and preferences.
Mandibular advancement splints (MAS), a mouthguard like device that holds the jaw forward, are an established alternative for SDB and are often easier to tolerate. However, in pregnancy MAS is rarely used, largely due to limited awareness of its value as an adjunct to CPAP and challenges obtaining MAS quickly within the short pregnancy timeline.
Our qualitative work showed that pregnant individuals strongly preferred having access to both CPAP and MAS, allowing them to switch between therapies based on nightly comfort, symptoms, and changes across pregnancy.
This study will test whether offering both CPAP and MAS-letting patients choose their nightly treatment-improves overall treatment success compared with CPAP alone. We will enroll 350 participants across three Canadian centres.
We will examine treatment effectiveness, usage patterns, patient satisfaction, feasibility of offering dual therapy in real world clinics, and potential associations with maternal and fetal health.
This research aims to provide an evidence based, scalable, patient centred model of care that improves comfort, adherence, and ultimately pregnancy health outcomes.
Programme
Project Grant
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
566050
Name
Pamidi Sushmita
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Clinical
Prcname2
Health Services Evaluation & Interventions Research 5
Projecttitle
Enhanced Multi-modal, Patient-Centred treatment Option Pathway for Women Experiencing Sleep-Disordered Breathing in PRegnancy (EMPOWER-SDB): A Type 1 Hybrid Effectiveness-Implementation Trial
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$921,826
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Adherence; Cpap; Efficacy; Implementation Outcomes; Mandibular Advancement Splint; Pregnancy; Pregnancy Complications; Sleep-Disordered Breathing
Abstract
Sleep disordered breathing (SDB), a condition where breathing repeatedly stops or becomes shallow during sleep, affects up to half of pregnant individuals, especially later in pregnancy and among those with medical complications. The standard treatment is continuous positive airway pressure (CPAP), which is medically effective, yet many pregnant patients struggle to use it consistently. In our prior study, nearly half had low adherence-even though those who used CPAP showed meaningful metabolic benefits. This highlights the need for treatment options that fit patient comfort and preferences.
Mandibular advancement splints (MAS), a mouthguard like device that holds the jaw forward, are an established alternative for SDB and are often easier to tolerate. However, in pregnancy MAS is rarely used, largely due to limited awareness of its value as an adjunct to CPAP and challenges obtaining MAS quickly within the short pregnancy timeline.
Our qualitative work showed that pregnant individuals strongly preferred having access to both CPAP and MAS, allowing them to switch between therapies based on nightly comfort, symptoms, and changes across pregnancy.
This study will test whether offering both CPAP and MAS-letting patients choose their nightly treatment-improves overall treatment success compared with CPAP alone. We will enroll 350 participants across three Canadian centres.
We will examine treatment effectiveness, usage patterns, patient satisfaction, feasibility of offering dual therapy in real world clinics, and potential associations with maternal and fetal health.
This research aims to provide an evidence based, scalable, patient centred model of care that improves comfort, adherence, and ultimately pregnancy health outcomes.
Competitiondate
202603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Pamidi, Sushmita; Almeida, Fernanda R; Fontaine, Guillaume; Huynh, Nelly
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $921,826~ $0~