The objective of this program is to foster the development of relationships between researchers and patients as well as other knowledge users for the purpose of co-producing B-H research and/or mobilizing research evidence. In line with BHI commitments to IDEAS (Inclusion, Diversity, Equity, Accessibility and Social Justice), the program aims to expand the diversity of voices meaningfully engaged, co-leading and benefiting from B-H research to include Indigenous people and underrepresented groups including racialized individuals; African, Caribbean, and Black individuals; persons with disabilities; women; and individuals from 2SLGBTQIA+ communities.
BHI defines patients as individuals with lived experiences with a health issue, informal caregivers (including family and friends) and/or individuals that are at risk of, or otherwise, affected by brain-heart conditions. Knowledge users are people, including representatives of communities and organizations who are likely to use research results to make informed decisions, or anybody who may benefit or be otherwise affected by research results. This can include, but is not limited to Indigenous leaders and communities, patients, health professionals, community-based organizations, health charities, health system leaders, policy-makers, and private sector organizations.
Within the Research Relationship Ignition Program, funding can be used to:
- Enable researchers, patient partners and other knowledge users to conduct activities that support the identification of brain-heart issues and research priorities and/or plan a co-produced research project. Activities could include, for example, meetings of potential teams, consultations with partners and groups under-represented in research or public engagement activities.
- Advance pilot projects using a research co-production approach with patient partners and other knowledge users to assess viability of the project and the partnership.
- Support knowledge mobilization activities such as co-development of knowledge mobilization products, tools or events that support knowledge exchange with groups such as patients, health professionals, community organizations or policy-makers.
- Support Indigenous-, patient-, or community-led groups to advance knowledge of brain-heart conditions and promote patient and community co-creation, leadership and benefit in research and dissemination.