Myra Drolet, auteur sur Unité soutien SSA Québec

An Indigenous Patient Circle is launched in Quebec

The Indigenous Patient Circle of Quebec is an independent and self-determined community whose purpose is to provide a safe space for its members to share and to guide the implementation of the Unité de soutien SSA Québec's Indigenous Health Program.

Patient and Public Engagement Toolkit

The objective of this joint effort was to co-create a common toolbox by identifying and adapting existing engagement tools in order to support a wider adoption of patient partnership practices in research and beyond.

ENGAGE: participatory methods and visual and auditory tools to get vulnerable populations involved in research

How can you get vulnerable people and those with low literacy levels involved in health research? How can you reduce barriers between university researchers and members of the community? Co-built by community-based organizations and members of the Canadian and international research communities, ENGAGE is a bilingual website offering participatory methods, as well as visual and auditory tools.

Écosanté: enhancing knowledge, competencies and collaboration opportunities related to health economics

Objective Écosanté aims to enhance knowledge, competencies and collaboration opportunities related to health economics, in particular health economic assessment. Team The project is led by a group of health economics experts. A Quebec-wide effort, the project includes researchers from each of the four RUISSSs. It is co-managed by Maude Laberge, assistant professor in the operations […]

Accès RECHERCHE

ACCÈS RECHERCHE is a platform for accessing research facilitation services, developed in partnership with Réseau-1 Québec, to provide research capacity to frontline clinical settings, as well as advisory services to researchers on methodology, clinical realities, writing protocols, recruitment, dissemination, letters of support and cost estimates.

CoPaQ: Measuring health care costs for patients

Tool to measure health care costs for patients. In addition to distinguishing between direct and indirect costs, CoPaQ differentiates between costs for patients and their family members.

Rapid and Rigorous TransCultural Adaptation (RR-TCA) methods

Structured approach for the translation and transcultural adaptation of various questionnaires. High potential for use in Indigenous health care.

CLARET

Transparency- and consent-driven ethical framework designed to share research data.

TorSaDE

Toolbox to query a cohort of the population on care trajectories and a research community including researchers from the four RUISSSs.

PARS3

Learning platform designed to link the queries of care and research teams with information systems specific to each data custodian. It allows data to be transmitted securely to other secure third-party systems through which the requesting unit can access it.

Canada-wide survey of patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs)

As part of a project to document the use of PROMs and PREMS in Canada, the ISOQOL Canada-PRO special interest group is launching a survey of anyone who has used patient-reported outcome measures and/or patient-reported experience measures (PROMs, PREMs) in their field in Canada.

A new name and a new website!

A new name and a new website! Unité de Soutien SRAP du Québec has become the Unité de soutien SSA Québec, placing the learning health system (LHS) at the centre of its mandate.

The Quebec team leading the international PaRIS-OECD survey publishes a recommendations report

The Unit helped fund the PaRIS-OECD Quebec survey.

The Unité de soutien SSA Québec helps to develop a new decision aid for lung cancer screening in Quebec

Under the leadership of Dr. Hervé Zomahoun and Dr. France Légaré, our team was able to rally family physicians, pneumologists, nurses, respiratory therapists, researchers, public servants, members of the public, decision-makers and other key people around a consensus, which led to the drafting of guidelines to be used in the creation of a decision aid to help people who are eligible for lung cancer screening make an informed choice about whether or not to undergo screening.