Archives du mot-clé Webinaire

Midi scientifique du 19 novembre 2025

Description: Le partenariat patient en recherche s’est imposé comme un levier essentiel pour une recherche plus inclusive, pertinente et ancrée dans les réalités vécues. En intégrant les savoirs expérientiels des patient(e)s, les équipes de recherche enrichissent leurs approches et renforcent l’impact de leurs travaux. Pour faire le point sur les avancées, les défis et les apprentissages issus de cette collaboration, nous vous invitons à vous joindre à une table ronde sur ce thème. Une patiente partenaire d’expérience et les membres de trois différentes équipes de recherche de la FMSS partageront leurs expériences concrètes et ouvriront le dialogue sur les meilleures pratiques à adopter pour l’avenir.

Public cible : personnes chercheuses et étudiantes, personnel de recherche, grand public. 

Présentateurs et présentatrices :  Anne-Marie Auger, coordonnatrice à la recherche, Chaire de recherche sur les dépendances comportementales Mathieu Bisson, agent de recherche, Chaire de recherche sur la mise en œuvre de soins intégrés pour les personnes avec des besoins complexes Marie-Eve Perron et Anaëlle Morin, candidates au doctorat, équipe de recherche sur les pratiques professionnelles en soins primaires optimales Marie-Dominique Poirier, patiente partenaire, Chaire de recherche sur la mise en œuvre de soins intégrés pour les personnes avec des besoins complexes, équipe de recherche sur les pratiques professionnelles en soins primaires optimales

Le comité organisateur:
Anne-Marie Auger, Chaire de recherche sur les dépendances comportementales de la Pre Magaly Brodeur Mathieu Bisson, Chaire de recherche sur la mise en œuvre de soins intégrés pour les personnes avec des besoins complexes de la Pre Catherine Hudon Mathieu Cook, Chaire de recherche sur la mise en œuvre de soins intégrés pour les personnes avec des besoins complexes de la Pre Catherine Hudon Marie-Eve Perron, Équipe de recherche sur les pratiques professionnelles optimales en soins primaires de la Pre Marie-Eve Poitras et Chaire de recherche du Canada sur les interventions de soutien à l’autogestion de maladies pour les patients et leurs proches aidants de la Pre Sylvie Lambert Stéphanie Tremblay-Lavoie, Laboratoire de recherche des Prs Isabelle Dufour et Yohann Moanahere Chiu Hanane Zabouche, étudiante de deuxième cycle au programme de recherche en sciences de la santé de l’Université de Sherbrooke supervisée par Pre Catherine Hudon et Pr Patrick Richard



Communautés noires et santé rénale : s’impliquer et avoir un impact sur les soins

À propos de cette séance :

Ce webinaire gratuit invite les membres des communautés noires vivant avec une maladie rénale — ainsi que leurs proches et leurs aidants — à explorer comment ils peuvent contribuer à transformer les soins rénaux au Canada en donnant leur avis et leurs conseils sur la recherche.

Objectifs d’apprentissage:

✅ Découvrez comment vous impliquer dans la recherche sur les maladies rénales
✅ Écoutez les partenaires patients noirs qui mènent déjà le changement
✅ Contribuez à bâtir un système de santé plus inclusif et équitable



Getting Oriented to the PEI Primary Care Roadmap – Where are we going?

Date et heure
24 sept. 2025 12:00 PM
Description
Panelists: Kelley Rayner, MSc -Assistant Deputy Minister, PEI Department of Health and Wellness -Senior healthcare executive focused on improving healthcare programs and services through program development and management -Work highlights include: establishing an Organized Stroke Care Model, the Queen Elizabeth Hospital Ambulatory Care Centre, overseeing the PEI Cancer Treatment Centre expansion and establishment of Provincial Cancer and Stroke Patient Navigator Programs
Lauren Kelly Weyman, MBA -Executive Director of Community Health and Pharmacy, PEI Department of Health and Wellness -Senior health care executive with over 15 years of experience working in both the public and private sectors with a focus on collaboration and relationship building -Work highlights include: National Pharmacare for PEI); Lead negotiator for PEI’s new Physician Services Agreement; Health PEI Medical Assistance in Dying Policy and Processes
Tim Edwards -Patient Partner, UPEI Health Research Network -Tim has had the privilege of working in helping professions his entire adult life and while also having a great deal of interaction with primary health care along the way. -In retirement, he is always looking to find ways of adding value to relationships and organizations.
Matthew Leyenaar, PhD -Health System Impact Scientist, UPEI Health Research Network -Research focus explores how health systems align service delivery with patient need -Prior experience as Provincial Coordinator, PEI EMS Board and Director, Emergency Health Services, PEI Department of Health and Wellness helping to modernize paramedic service delivery and practice regulations
When: September 24, 2025, at 1pm AT
Where: Online (Zoom)
Register: Meeting Registration – Zoom


Safe From the Start- Safe Care for Every Child (PFPSC)

Patients for Patient Safety Canada (https://www.patients4safety.ca) (PFPSC) is hosting a webinar about patient safety for all children – ‘Safe From the Start- Safe Care for Every Child’ on Sept. 17 connected to the World Health Organization’s celebration of World Patient Safety Day. PFPSC invites families and healthcare providers to this national webinar. The intent is for families to gain practical tools and insights to advocate effectively for their children’s healthcare and for healthcare providers to hear directly from families and experts about what matters most in pediatric safety.
When: September 17, 2025, from 12-1pm ET.
Register: You can register for the webinar here. 



BRIC NS Primary Care Learning Series Registration : September 2025

Date et heure
17 sept. 2025 11:00 AM
Description
Dr. Beth McDougall, PhD, will present:​ “Validation and Application of a Needs-Based Complexity Case-Mix System for Community-Based Primary Health Care Planning and Research » ​ Beth McDougall is a Senior Epidemiologist with Nova Scotia Health Performance and Analytics and has worked in health research for almost 20 years. She recently completed her PhD in Epidemiology and Applied Health Research at Dalhousie University under the supervision of Dr. George Kephart and is set to graduate in October 2025. She is passionate about health, with research interests spanning primary health care, mental health and addictions, health services research and clinical trials. She particularly enjoys contributing to projects that advance evidence-based decision-making in healthcare. In her spare time, Beth loves hiking and keeping up with her energetic 16-month-old and playful Labrador Retriever.


Série d’apprentissage francophone du CPCRC

La Série d’apprentissage francophone du CPCRC aura lieu le mercredi 15 octobre 2025 à 12 h (HE).

Cette session est organisée par le volet francophone du CPCRC, dirigé par Sharon Johnston Ontario), Mylaine Breton, Catherine Hudon et Catherine Lamoureux-Lamarche (Québec). Il s’agit de la première d’une nouvelle série qu’elles coordonneront afin de promouvoir la recherche et la collaboration en français au Canada et à l’international, en partenariat avec le Groupe francophone international en soins primaires. Ces sessions se dérouleront en français, avec des sous-titres anglais disponibles à travers Zoom.

La séance inaugurale est intitulée : Promouvoir la recherche francophone en soins primaires : réflexions tirées d’un forum international.

Panélistes:

Catherine Hudon, MD, Ph. D., CFPC, est professeure titulaire au Département de médecine de famille et médecine d’urgence de l’Université de Sherbrooke. Elle est titulaire de la Chaire de recherche du Canada sur la mise en œuvre de soins intégrés pour les personnes avec des besoins complexes.

Mylaine Breton, Ph. D., MBA, est professeure titulaire au Département des sciences de la santé communautaire de l’Université de Sherbrooke. Elle est titulaire de la Chaire de recherche du Canada en gouvernance clinique des services de première ligne.

Sharon Johnston, M.D., LLM, est professeure agrégée et chercheuse clinicienne au Département de médecine familiale de l’Université d’Ottawa et directrice scientifique et chercheuse à l’Institut du Savoir Montfort.

 

Voici le lien d’inscription zoom : https://us02web.zoom.us/meeting/register/Y1RncrMDRM2vsFYPfrfjhA



webinaire du Groupe Francophone de Soins Primaires (GFSP)

25 septembre 2025, 14h30-15h30 CET (Europe), 8h30-9h30 EST (Québec)

Lieu: Zoom

Titre: Le Centre Interdisciplinaire de Développement International en Santé de l’Université de Sherbrooke (CIDIS) : au cœur d’une approche interdisciplinaire et décoloniale en santé mondiale

Conférencier(ère)s: L’équipe du CIDIS

Discutant: Jean Macq, Université catholique de Louvain


Accessing Data through DASH

Are you a researcher seeking administrative health data from more than one province or territory in Canada? HDRN Canada’s Data Access Support Hub (DASH) offers coordinated services to researchers interested in accessing multi-regional datasets. Learn how DASH can help you navigate the data access process as well as the centralized services and tools available for researchers conducting research projects in more than one region, including:

  • the single data access request form for researchers to request data from multiple regions
  • support from experts at data centres across Canada
  • an inventory of all the datasets available via HDRN Canada and
  • an algorithm inventory to aid in analysis of the data.

ABOUT THE SPEAKERS:

Carrie-Anne Whyte is a Program Lead with HDRN Canada’s Data Access Support Hub (DASH). She is located at the Canadian Institute for Health Information (CIHI) in Ottawa, where she has worked for the last decade. Her areas of focus include analysis, methodology and health data. Prior to her career at CIHI and HDRN, Carrie-Anne held roles with the Public Health Agency of Canada and the Ottawa Hospital Research Institute. Carrie-Anne holds a Master of Public Health from McGill University.

Stefana Jovanovska is a Senior Research Project Manager on the Data and Analytic Services team at ICES. With a diverse professional background encompassing analytical chemistry, quality control and clinical research, she brings a wealth of expertise to her role. Stefana’s primary focus is supporting publicly funded research as well as multi-regional projects support in collaboration with HDRN Canada’s Data Access Support Hub (DASH) team.

PLEASE NOTE: This event will be recorded and posted on hdrn.ca. This webinar is presented in English.



CPCRN Learning Series: Making Wise Choices

Making Wise Choices: Community Engaged Data Governance lessons for Primary Care Research

25 June 2025 / 12 – 1 PM ET / Zoom

Session Description:
OKAKI is a Blackfoot word meaning Be Wise. OKAKI is also an Alberta based public health services and health informatics social enterprise that works with First Nations communities across Alberta. This session will explore lessons on healthcare data governance facilitating data sovereignty with Alberta First Nations communities, reflecting on principles of Ownership, Control, Access and Possession considering Blackfoot concepts of knowledge and decision making. The opportunity for
community-led primary health care implementation research will be discussed reflecting on OKAKI’s partnership with Alberta’s Network Environment for Indigenous Health Research, the Indigenous Primary Health Care and Policy Research (IPHCPR) Network.

Panelists:

Lindsay Crowshoe, MD
-Member of the Piikani First Nation
-Blackfoot Primary Care Physician and Researcher
-Associate Professor of Medicine and Assistant Dean Indigenous Health, University of Calgary, Cumming School of Medicine

Salim Samanani, MD
-Founder and Medical Director, OKAKI
-Adjunct Professor, School of Public Health, University of Alberta
-Adjunct Assistant Professor, Division of Medical Sciences, University of Victoria

Tyler White, MD
-Member of the Siksika First Nation
-Vice President of Indigenous Health, OKAKI
-Member, Board of Directors, OKAKI



Public Trust, Literacy & Health Data Foundations in Canada

It is critical for the public to have trust in governments and organizations that collect, protect, share and use health data. In this webinar, Julia Burt and Dr. Kim McGrail will provide an overview of a foundational paper developed by HDRN Canada, in collaboration with the Public Health Agency of Canada, on public trust and data literacy. This paper starts with principles outlined in the Pan-Canadian Health Data Charter, which puts people and populations at the centre of health data management. It then highlights the risks and benefits of data sharing and identifies other principles, all of which relate to public trust.

During the session, Julia and Dr. McGrail will highlight the engagement processes and methods used to develop the paper, and present its key findings, including the paper’s six recommendations for trustworthy data practices. These recommendations are intended to help different levels of government, health system organizations and others work together to earn trust in how health data are managed and used. They acknowledge that trust is earned based on what is done, how it is done, and how transparent and understandable government or organizational practices are.

About the Speakers

Julia Burt is HDRN Canada’s Public Engagement Operational Lead, working closely with the network’s Public Advisory Council to accelerate meaningful public engagement. She works with diverse members of the public on projects related to health data, including the co-creation of plain language about data, as well as exploring the public’s perception of acceptable uses and users of health data. Prior to her involvement with HDRN Canada, she was the Patient Engagement and Training and Capacity Lead with the Newfoundland and Labrador SPOR SUPPORT Unit.

Dr. Kim McGrail is a Professor in the School of Population and Public Health and Centre for Health Services Policy Research at the University of British Columbia. She is the Scientific Director of Population Data BC. Dr. McGrail’s research interests are quantitative policy evaluation and all aspects of population data science. She the 2009 -2010 Commonwealth Fund Harkness Associate in Health Care Policy and Practice, the 2016 recipient of the Cortlandt JG Mackenzie Prize for Excellence in Teaching, and the 2017 recipient of UBC’s Excellence in Clinical or Applied Research Award. She was part of the Expert Advisory Group for the pan-Canadian Health Data Strategy and is currently a member of the Global Partnership for AI as part of the Data Governance Working Group.