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Grant: Team Grant: Diabetes Mechanisms and Translational Solutions - LOI - General

Research Institute of the McGill University Health Centre

$10,000.00

Building CAPACIty for pediatric diabetes research and quality improvement across Canada.

EF 2020-21

Résumé
Diabetes is one of the most common chronic childhood disorders and affects close to 40,000 youth across Canada. Although there have been many advances in diabetes care since insulin was discovered 100 years ago, youth with diabetes continue to have a higher risk of other health problems, a lower quality of life, and a shorter life span than their peers without diabetes. This health gap is likely in part due to suboptimal access to and delivery of their diabetes care, which is worse in disadvantaged populations across Canada. Our project will develop strategies to address these gaps: The CAnadian PediAtric diabetes ConsortIum (CAPACIty) is a network of 15 childhood diabetes centers from across Canada, and their doctors and researchers who specialize in childhood diabetes. We are partnering with patients/families and health care professionals to jointly design and develop a Canada-wide childhood diabetes registry and research platform. The registry will enable us to improve diabetes care and health outcomes for Canadian youth through 1) comparison of diabetes care quality and outcomes between Canadian diabetes centers ("benchmarking"), 2) quality improvement initiatives, 3) patient-informed research initiatives across Canada, and 4) successful advocacy work. As a group we will regularly monitor, evaluate and discuss use of the registry and adapt our targets and strategies accordingly. We anticipate that the CAPACIty registry will not only lead to better health outcomes, but also serve as a powerful tool for governments and decision-makers to implement policy decisions that are driven by our data. For example, this could include coverage of diabetes technologies and other innovative care concepts, especially for the most disadvantaged among youth living with diabetes. Lastly, our patient advisory board will ensure better representation of youth with diabetes and their parents among provincial and national associations that advocate for people living with diabetes.
Programme
Team Grant: Diabetes Mechanisms and Translational Solutions - LOI - General
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
446657
Name
Von Oettingen Julia E
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Clinical
Prcname2
Team Grant: Diabetes Mechanisms and Translational Solutions - LOI
Projecttitle
Building CAPACIty for pediatric diabetes research and quality improvement across Canada.
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$10,000
Cihrequipment2
$0
Programname2
Team Grant: Diabetes Mechanisms and Translational Solutions - LOI - General
Keyworddelim
Benchmarking; Implementation Science; Models Of Care; Patient-Reported Outcomes; Pediatric Diabetes; Quality Improvement
Abstract
Diabetes is one of the most common chronic childhood disorders and affects close to 40,000 youth across Canada. Although there have been many advances in diabetes care since insulin was discovered 100 years ago, youth with diabetes continue to have a higher risk of other health problems, a lower quality of life, and a shorter life span than their peers without diabetes. This health gap is likely in part due to suboptimal access to and delivery of their diabetes care, which is worse in disadvantaged populations across Canada. Our project will develop strategies to address these gaps: The CAnadian PediAtric diabetes ConsortIum (CAPACIty) is a network of 15 childhood diabetes centers from across Canada, and their doctors and researchers who specialize in childhood diabetes. We are partnering with patients/families and health care professionals to jointly design and develop a Canada-wide childhood diabetes registry and research platform. The registry will enable us to improve diabetes care and health outcomes for Canadian youth through 1) comparison of diabetes care quality and outcomes between Canadian diabetes centers ("benchmarking"), 2) quality improvement initiatives, 3) patient-informed research initiatives across Canada, and 4) successful advocacy work. As a group we will regularly monitor, evaluate and discuss use of the registry and adapt our targets and strategies accordingly. We anticipate that the CAPACIty registry will not only lead to better health outcomes, but also serve as a powerful tool for governments and decision-makers to implement policy decisions that are driven by our data. For example, this could include coverage of diabetes technologies and other innovative care concepts, especially for the most disadvantaged among youth living with diabetes. Lastly, our patient advisory board will ensure better representation of youth with diabetes and their parents among provincial and national associations that advocate for people living with diabetes.
Competitiondate
202012
Approvedterm2
1 yr 0 mth
Pinamesdelim
Von Oettingen, Julia E; Amed, Shazhan
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $10,000~ $0~