Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant
Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph
Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant
Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph
Funding Agency: Social Sciences and Humanities Research Council of Canada Insight Development Grant
Principal Investigator: Dr. Julia Gruson-Wood, Postdoctoral Fellow, Department of Family Relations & Applied Nutrition, University of Guelph
The Alliance and our partners at the Canadian Institute for Health Information (CIHI) have developed an interactive Data Quality Assessment Tool for Community Health Centres who have agreed to share their EMR data with CIHI. With this tool, participating CHCs can review the completeness and accuracy of their organization’s clinical and sociodemographic data for primary health care clients.
The Clinician Change Virtual Care Toolkit shares information and resources of virtual care in practice to support clinicians with the tools they need to provide safe, high quality virtual care.
This toolkit contains:
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.
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.
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.
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.
This toolkit consists of guidance for healthcare providers as well as an informative patient handout to support access to Paxlovid, a COVID-19 antiviral treatment.