Resources
The PORLET measures how closely a project aligns with the definition of patient-oriented research as described by the CIHR Strategy for
Patient-Oriented Research.1-3 It assists grant review committees in evaluating patient-oriented research proposals, explains patient-oriented research to individua…
The Indigenous Research Level of Engagement Tool (IRLET) measures the degree to which a given project meets
patient-oriented research criteria in the context of Indigenous communities. The criteria evaluated in this tool include
Partnership (Indigenous Stakeholders), Knowledge into Practice, Streng…
The goal of the SCPOR Patient-Oriented Research Escape Room is to share the concept of patient-oriented research with individuals interested in health research. It is increasingly important for health disciplines to work together to offer optimal patient care, especially in complex situations. Sim…
PxP stands for ‘For Patients, By Patients’
PxP is entirely led by an international team of experienced patient and public partners. Their mission is to bring resources, mentorship and community to other patient partners in any kind of health research, no matter their experiences as a patient partn…
This guide is intended as an orientation tool for researchers whose objective is to strengthen the health system and improve populations health through partnerships with users, patients, lived experience experts, or community-based members or organizations, known as community partners (PFD Partners…
This guide was developed through a collaboration between the Public and Patient Engagement Collaborative (PPEC) and the Public Engagement in Health Policy (PEHP) Project at McMaster University.
Resources and tools were identified through a comprehensive search conducted between June and July 2022 …
Les patients et les partenaires publics jouent un rôle important dans la conception et la conduite de la recherche et sont de plus en plus impliqués dans le processus de publication, y compris en tant que co-auteurs. Cette vidéo présente le processus de publication aux patients et partenaires publi…
Patient and public partners play important roles in the design and conduct of research, and are increasingly more involved in the publication process, including as co-authors. This video introduces the publication process to patient and public partners who are currently or planning to become public…
This glossary provides simple definitions for words and acronyms commonly used in health research, as well as a few of terms that are specific to the MSSU and the Maritimes.
Many of these definitions were adapted from glossaries created by the Canadian Institutes of Health Research (CIHR), INVOLVE…
Le Present document présente les definitions des principaux concepts fondateurs du partenariat patient en santé et services sociaux. Cette terminologie est le fruit du travail des patients et des professionnels (éducateurs et chercheurs)de l’Université de Montréal, principalement regroupés au Centr…
A website created to demystify research and provides resources such as video tutorials, a glossary of research terms, and a guide for reading research articles. The website is organised into the following sections:
Each year, researchers publish millions of new scientific articles. Given the large amount of information, it is hard to find out what is already known about any given health topic.
It is important to look at existing evidence before starting a new research project, or when considering a new polic…
As a PFD partner involved in research, you will often hear the terms "systematic review" and "scoping review."This resource provides an introduction of both types of reviews
This flowchart was designed to guide individuals preparing data request proposals as well as grant and trainee support applications to ensure they have adequately addressed sex and gender considerations in their submission.
This document is for anyone applying for a grant, making a data request proposal or completing our trainee support application. This resource:
