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Seed Funding Competition
Providing growth and development opportunities to the next generation of investigators in palliative care.
Download the 2024 competition Application Guide.

Providing growth and development opportunities to the next generation of investigators in palliative care.
This year we awarded four one-year-long grants of $20,000. Here are the abstracts from our winners.
Our recent research at the BC Centre for Palliative Care shows that there aren’t enough grief supports available for people experiencing homelessness after someone they care about dies. Additionally, there has been very little research conducted to understand this type of grief among people living within the context of homelessness. It is not possible to improve care for this vulnerable population if their experiences are not understood. In this research study we will interview people with lived experiences of both grief (from a death of someone they cared about) and homelessness. Our goal is to better understand their experiences and learn their perspectives on how they can be best supported moving forward. The findings of these studies will inform new policy development and service improvement efforts aiming to enhance the availability and access to quality grief supports tailored to the needs of people experiencing homelessness.
Family caregivers support older Canadians greatly and ensure dignity in their end-of-life days. Caregivers of individuals from racial, ethno-cultural, and linguistic minority groups often experience additional challenges and are less supported. Yet, little is known about their experiences. This study will explore the experiences and challenges of caregivers of individuals at the end-of-life who belong to racial, ethno-cultural, and/or linguistic minority groups.
Our aims are:
1) Document the experiences of spousal and child caregivers of individuals at the end-of-life, exploring nuances related to their minority status
2) Understand their experiences and perceptions of palliative care support and resources
3) Explore how caregiving experiences impact caregivers who are, or will soon be, care-recipients themselves in terms of decisions about their own care.
We will interview caregivers to collect in-depth information and interpret the findings with a health equity lens.
Conversations between clinicians and patients about goals of care become increasingly important when patients experience serious illness. The complexity of serious illness conversations multiplies dramatically when the patient is experiencing substance use disorders, mental health issues, homelessness or other challenges related to socio-economic factors (referred to as structural vulnerabilities). Currently, little is known about the preferences of structurally vulnerable patients while engaging in serious illness conversations. This is a major practice gap and an important area of palliative care research. Through one-on-one interviews, we will hear directly from patients about their experiences having these conversations. We will identify common themes and preferences for engaging in serious illness conversations. Ultimately, we hope to develop a best practice guide for clinicians and improve health care for patients experiencing structural vulnerabilities.
This project has been funded by a contribution from Health Canada, Health Care Policy and Strategies Program. The views expressed herein do not necessarily represent the views of Health Canada.
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