Primary health care utilization in the first year after arrival by refugee sponsorship model in Ontario, Canada: a population-based cohort study

#Abstract

#Background

Canada’s approach to refugee resettlement includes government sponsorship, a pioneering private sponsorship model and a third blended approach. Refugees are selected and supported differently in each approach including healthcare navigation.

Experiences and Needs of Young Black Canadian Mothers in Toronto: A Community-Based and Black-Centered Research

This report focuses on the experiences of young Black mothers in navigating the challenges of motherhood while facing systemic racism. TAIBU CHC and Researchers from Brock University draw on themes including maternal experiences of racism and gendered oppression, compounding stressors affecting Black mothers, and the impact of racism on early childhood growth and development. This research project is the first of its kind in Canada to explore this topic in a significant way.

Considerations for collecting data on race and Indigenous identity during health card renewal across Canadian jurisdictions

#Key Points

  • Canada’s health care systems do not routinely collect self-reported race and Indigenous identity data and often lack a standardized and consistent approach to data collection that would permit comparisons between organizations or jurisdictions.

“Can you hear me now?”: a qualitative exploration of communication quality in virtual primary care encounters for patients with intellectual and developmental disabilities

#Abstract

#Background

High quality communication is central to effective primary care. The COVID-19 pandemic led to a dramatic increase in virtual care but little is known about how this may affect communication quality.

2-pager: Virtual Care during COVID-19 Research Study

In 2020, the Alliance for Healthier Communities and its member centres embarked on a research study to explore the challenges and opportunities inherent in a shift towards virtual care. The study involved extracting EMR data from 36 CHCs, an organizational survey, as well as conducting phone interviews with 36 providers and 31 clients. This 2-page handout summarizes the main findings.

Sociodemographic Data Collection and Use in Ontario CHCs

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

Sociodemographic Data Toolkit

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

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