Ressources
It takes 17 years to turn 14% of original research into an outcome that can benefit patient care? This is why knowledge translation planning and implementation matters. Access the knowledge translation Information Sheet for an overvoew of KT and it's signficance in health research.
This info shee…
Resources developed by the Can-Solve CKD Network to facilitate meaningful patient-oriented research.
As a patient partner on a health research team, you may ask yourself, ‘What can I contribute’? The answer is, more than you may think! Everyone brings transferable skills to the table that are usually broader than any given role within a team. They relate more to leadership, communication, critical…
This toolkit is designed for individuals who are designing, developing and undertaking research. The resources you create with these tools can also be used to inform your peers and other healthcare professionals on the progress of your research.
The toolkit will help you construct information that…
This session describes the concept of gender-affirming public health and positions 2SLGBTQI+ health equity as a public health priority. An overview of literature related to the roots of health inequities and key priority issues experienced by 2SLGBTQI+ people is shared. Opportunities for and exampl…
As territory acknowledgements become more common place, and are often prescribed and pre-scripted, they run the risk of becoming a token gesture rather than a meaningful practice. This guide will answer some common questions around why and how to acknowledge traditional First Nations territories in…
The Public and Patient Engagement Lunchtime Learning series introduces participants to the principles of public and patient engagement in health research. Participants will learn how to build meaningful partnerships between researchers and people with lived experience to inform decision-making and …
In the United States, the Latinx community, especially those that are undocumented, face significant barriers in healthcare. In this conversation, we will establish a foundational understanding of the Hispanic culture, values, and beliefs and discuss the ethical paradox Latinx people face when it c…
The online tutorial CORE-2022 (Course on Research Ethics) is an introduction to the TCPS for the research community. It focuses on the TCPS ethics guidance that is applicable to all research involving human participants, regardless of discipline or methodology.
Through this toolkit, Clinical Trials Ontario aims to help its community in their efforts to improve clinical trial participants’ experiences. The goal is to help clinical trial participants feel informed and valued. In briefly reviewing the literature, the topic areas highlighted in the toolkit ar…
The CHILD-BRIGHT Network Patient-Oriented Research Toolkit provides practical guidance for child health researchers on meaningfully engaging partners with lived and living experience (PWLEs)* throughout the research cycle. By bringing together best practices in POR, offering clear explanations and …
When it comes to data analysis and the interpretation of findings, patient-partners are less frequently engaged in the process.
In this session, the CHILD-BRIGHT Network adopts a co-learning approach and explore how to promote authentic patient participation in this area. Participants explore sev…
In this session hosted by CHILD-BRIGHT Network, they provide an overview of a select number of resources aimed at developing capacity in patient-oriented research and outline the benefits & drawbacks of each.
Equity, diversity, and inclusion (EDI) are foundational to effective, impactful and sustainable health research. EDI considerations ensure that:
This webinar is intended for a broad audience with an interest in ethics and patient engagement in health research including patient partners, researchers, Research Ethics Board members, health care professionals, decision-makers and trainees.
The webinar was hosted by the NL Support Unit.
