External Opportunities

The Ontario Caregiver Organization is frequently asked to connect researchers and other stakeholder organizations with caregivers. Where appropriate, we will share these invitations and connect interested members with relevant parties.

In the past, we have supported focus groups with the Ontario Ombudsman office, research initiatives with various academic institutions and research to practice initiatives with various health care providers. We will continue to share these opportunities and thank caregivers who have engaged and contributed in this way.

There are external opportunity for caregivers in French only. For these opportunities, please visit Perspectives Aidance Naturelle in French: https://www.perspectivesaidancenaturelle.ca/occasions-externes

The Ontario Caregiver Organization is frequently asked to connect researchers and other stakeholder organizations with caregivers. Where appropriate, we will share these invitations and connect interested members with relevant parties.

In the past, we have supported focus groups with the Ontario Ombudsman office, research initiatives with various academic institutions and research to practice initiatives with various health care providers. We will continue to share these opportunities and thank caregivers who have engaged and contributed in this way.

There are external opportunity for caregivers in French only. For these opportunities, please visit Perspectives Aidance Naturelle in French: https://www.perspectivesaidancenaturelle.ca/occasions-externes

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    Participants Needed for Study on Care Partner Involvement in Patient Safety!

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    The FI-COFFRE program is seeking individuals like you to become part of a growing community of patient partners in research.

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    Participants needed for research study on dementia

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    Exploring the Experiences of Caregivers from Minority Groups at the End-of-Life

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    Do you want to learn tips on how you can improve your nutrition?

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    Are you or someone you love living with dementia at home?

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    Racialized stroke survivors and family members/caregivers

    Your lived-experience expertise can help develop knowledge about the needs and goals of racialized people after a stroke, as well as the gaps in support and services available to them. Researchers at the University of Toronto are looking for people who are Black/African, South Asian, or Chinese to share their experiences in meetings and through photovoice. Participants will be compensated. See the flyers linked above or email Hardeep Singh for more information.

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    Frontotemporal Dementia and Related Disorders Online Survey

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    CLIENTS AND FAMILY CARE PARTNERS NEEDED FOR RESEARCH ON RESILIENCE IN HOME AND COMMUNITY CARE DURING COVID-19

    To participate in this study, please "Click" on the link below to access the letter of information and to provide consent for the interview.

    https://uwo.eu.qualtrics.com/jfe/form/SV_cXTSLHYIH6IU8FE

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    Patient and Family Advisory Council with the Bruyère Research Institute

    Patients and/or caregivers (unpaid caregivers) are needed to participate as members of a Patient and Family Advisory Council. This council will be an engaged as members of a research team working on a 3-year study that is focused on improving access to palliative home visits at the end-of-life.

    Ideal Participants:

    • Ontario-based individuals who have been designated as palliative by their healthcare team and either have or have not received home visits by a physician or nurse practitioner
    • Ontario-based caregivers to individuals in the prior group


    About the Study

    Home visits – a service delivered by physicians and nurse practitioners outside of formal homecare services – have known benefits for patients, including increasing satisfaction with care and quality of life, as well as reducing hospitalizations and in-hospital deaths. There has been no formal evaluation of Ontario-based policies designed to increase palliative home visits. We need to better understand factors that prevent or facilitate palliative providers’ willingness to provide home visits and the level of financial investment needed to increase physician and nurse practitioner provision of home visits for people near the end of life. A better understanding of strategies to increase access to palliative home visits and gauging political readiness for these strategies are critical to improving the dying experience of Canadians. Our findings will provide evidence and a business case for the Ontario government outlining how palliative home visits can be scaled up.

    About the Role

    We are looking for members to advise the team and help with research activities such as reviewing objectives, helping to prioritize work to align it with their lived experience, review results and provide interpretation, engage in knowledge translation, and ensure that policies informed by our research consider patients’ and caregivers’ perspectives and caregiving burden. Our Patient and Family Advisory Council currently has three members, and we are seeking to add an additional 1-3 members.

    Time commitment

    Participation in 1-hour virtual meetings approximately 4 times per year. Responsibilities will include review of study deliverables and manuscripts, if interested.

    Members will be compensated for their time at a rate of $25/hour, which is aligned with honorarium guidelines set out by the Strategy for Patient-Oriented Research (SPOR) Working Group.

    To express interest or if interested in learning more, contact: Madeline McCoy at mmccoy@bruyere.org