Stories from the field: Inclusive Care
How can we combat inequity and offer more inclusive care? Patient-physician and patient-nurse pairs discuss these issues in this webinar.
Cultural Safety in Indigenous Health Research Context: a report of recommendations drawn from an unprecedented round-table discussion
To define and identify the best ways of conducting culturally safe indigenous health research, placing the voices and knowledge of indigenous people and their allies at the heart of the process. This is the challenge that several partners have set themselves. To achieve this, they organized an unprecedented round table with people representing 10 of the 11 nations present on Quebec territory.
Training: Evaluating Patient Engagement in Research
Upon the completion of this training, you will know the main steps that are required to evaluate a partnership with the patients and the public in research. You will also understand why it is interesting to evaluate it.
Online training on patient engagement in continuous quality improvement
How can you effectively integrate patient partners into a continuous quality improvement process? Find out in this asynchronous training course.
Microsite on patient partnership in research: interactive tour, resources and testimonials
What can you expect as a patient or citizen when you become a research partner? This microsite explains!
Decision Aid for Colorectal Cancer Screening
The use of the colorectal cancer screening decision aid helps to enhance the screening experience and personalize the care trajectory.
PADA: a Collaborative Digital Platform for Authors of Healthcare Decision Aids
Would you like to develop an interactive decision aid with low design costs? PADA is for you.
The Community of Practice evaluation questionnaire (CoPeval)
CoPeval aims to evaluate and improve communities of practice in partnership with their members, for example on an annual basis (formative evaluation). The two constructs evaluated are the processes and the effects of the Communities of Practice.
Module 201 – Patient partnership in research: the first steps
This training aims to initiate organizational transformation through the implementation of patient partnership.
Module 101 – Basis of patient partnership
Become familiar with the basics of patient partnership.
A framework for evaluating patient and public engagement in research
This national tool can be used to plan and evaluate the patient and public engagement process before, during and at the end of a research project.
Training on the life-course with illness approach
What is the life-course with illness approach, and how can it be used as a methodological tool for co-construction?
An infographic summarizes how to activate Québec’s learning healthcare system
75 people co-constructed an action plan with the aim of inspiring decision-makers and all members of the health and social services network to do things differently and, ultimately, make the Québec healthcare system a learning one.
Research grant applications: Sensitive Approach to Equity, Diversity, and Inclusion (EDI) in Research
The Equity, Diversity and Inclusion (EDI) and Sex and Gender-Based Analysis (SBGA) mandates adopted in recent years by academic bodies require research teams to meet criteria when submitting grant applications. Following this premise, this document aims to accompany research teams in an approach sensitive to EDI-G and SBGA.
Roadmap for partnering with patients, families, and caregivers in a Learning Health System
The purpose of this tool is to explain the roles of users and their families in a LHS and to describe how these people can, individually and collectively, contribute to its many dimensions.