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.
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.
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.
Working in partnership in health and social services: a team testifies to its success
A literacy facilitator, a literacy patient-partner and a researcher share their inspiring stories of partnership, equity, diversity and inclusion.
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.
Inclusive Practices in Participatory or Partnership-based Research with socially excluded persons
This guide addresses how research teams can work in partnership with people who are socially excluded.
PREMs and PROMs Toolkit: Patient-reported outcome and experience measures
Although most professional or patient organizations claim to incorporate the concept of Patient-Reported Outcome Measures (PROMs) or Patient-Reported Experience Measures (PREMs), how the information is collected is not necessarily adequate. To be compliant, PROMs and PREMs must be measured using scientifically validated tools and must be completed by patients. Let's see together the definition of PROMs and PREMs and what characterizes them.
eSRAP: Collaborative monitoring system of trends in patient-oriented research
eSRAP is a collaborative monitoring system to monitor and share the latest literature on patient-oriented research.
PROMIS® is the tool of choice for patient-oriented research worldwide
We supported the first steps in implementing the PROMIS® system, in English and in French, to improve patient-oriented research and care.
Understanding research: a website to demystify the basic concepts of research
The Understanding Research site aims to demystify the basic concepts of research. Videos, glossary and guide are available.
Snapshot of the use of Teleconsultations
Supported by the Unité de soutien SSA Québec, Mylaine Breton, a researcher at the Université de Sherbrooke, and her team have drawn up a portrait of the level of implementation of teleconsultations in the COVID-19 context and their advantages and disadvantages compared to in-person medical visits. Read the results of an environmental scan on the use of teleconsultations in the front line and its conclusions.
18 videos to help you do participatory research
Our Capacity Building team was able to put its expertise to good use, particularly by providing advice on techno-pedagogy.