A Dementia Strategy for Canada: Together We Achieve - 2024 Annual Report

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Organization: Public Health Agency of Canada

Date published: November 2024

Cat.: HP22-1E-PDF

ISSN: 2562-7805

Pub.: 240543

Contents

Minister's message

This year's report marks five years since the release of the national dementia strategy and the funding investments to support implementation that resulted in the Dementia Strategic Fund and the Enhanced Dementia Surveillance Initiative at the Public Health Agency of Canada (PHAC). Other federal organizations are providing funding aligned with the strategy including for research and the health care system along with other targeted initiatives. The initiatives of non-governmental organizations along with provincial and territorial governments also contribute to continued progress on the strategy's implementation. Efforts across Canada are highlighted in this report as we review our progress in working together towards the aspirations of the strategy.

Dementia continues to impact many of those living in Canada either directly or through their families and other social circles. Recent public opinion research found that 49% of respondents feel that dementia is having a large impact in Canada. In 2021–2022, 6.3% of Canadians aged 65 and older were living with diagnosed dementia. Further, the number of people living with dementia is expected to increase with Canada's growing and aging population.

While the risk of dementia increases as we age, particularly among the oldest adults, it is important to remember that dementia is not an inevitable part of aging. In fact, the rate of newly diagnosed cases among Canadians aged 65 and over continues to decline from 1,545 new cases per 100,000 in 2011–2012 to 1,398 new cases per 100,000 in 2021–2022, taking into account the aging of the population over time. Research has indicated that 12 modifiable risk factors could explain 40% of dementia cases globally and recent studies suggest the same is true within Canada, as you will see within this year's report.

Given the evidence on dementia risk factors, it is a priority for the Government of Canada to continue to work with partners to share this information and encourage action to reduce risk. Rates for risk factors related to education, hypertension and smoking are moving in the right direction in Canada, as this report notes. However, there is more work to be done to reduce risk, as rates related to cholesterol, sleep, heavy alcohol drinking and stroke have remained stable, while rates of diabetes, obesity, physical inactivity and social isolation are increasing.

Since 2018, PHAC has funded more than 70 dementia projects across the country; a few are highlighted in this report. These projects aim to: increase awareness of dementia risk factors; promote dementia-inclusive communities including through stigma reduction; improve access to high-quality dementia guidance and online resources; improve the quality of life of people living with dementia and caregivers; and strengthen data on dementia. Together, these projects reached millions of Canadians this past year, creating innovative and tailored resources that help to reduce dementia risk and encourage communities to become more dementia-inclusive.

The 2024 report also highlights projects funded by other organizations that, for example, work to improve data on dementia caregivers, increase the social inclusion of people living with dementia, and help to manage the risks of people living with dementia going missing.

Research and innovation continues to be an essential pillar of Canada's national dementia strategy. Under the Canadian Institutes of Health Research's Brain Health and Cognitive Impairment in Aging (BHCIA) Research Initiative, 13 new funding opportunities have been launched. In addition, the Government of Canada is providing $80 million over four years starting in 2024 to the Brain Canada Foundation to advance brain research.

All of our investments in implementing the national dementia strategy take us one step closer to our vision of a Canada in which all people living with dementia and caregivers are valued and supported, quality of life is optimized, and dementia is prevented, well-understood and effectively treated. In closing, thank you once again to all those contributing to progress on the strategy.

Introduction

The 2024 Report to Parliament on the national dementia strategy continues to track key data points related to the strategy's objectives (see Figure 1 for an overview of the strategy). It notes some positive trends related to some dementia risk factors and efforts related to advancing therapies through research and innovation. It also flags areas where more work is needed in particular, including on reducing the rates of dementia risk factors such as diabetes, obesity, physical inactivity and social isolation.

This year's report highlights new results from projects funded through the Dementia Community Investment, the Dementia Strategic Fund and the Enhanced Dementia Surveillance Initiative at the Public Health Agency of Canada.Footnote 1 The report also shares information about projects funded through other federal government departments such as the Canadian Institutes of Health Research, Employment and Social Development Canada, Health Canada, and Indigenous Services Canada as well as projects led by non-governmental organizations. These projects demonstrate the collective action taking place across Canada to help advance the objectives of the national dementia strategy.

"Every person's experience with dementia is different. The social isolation experienced by many who live with dementia and by dementia caregivers can be detrimental to their physical and mental health. We can improve the inclusiveness of our communities by learning how to better interact with people living with dementia and by challenging our own assumptions about their abilities and potential for a good quality of life." – Theresa Tam, Chief Public Health Officer of Canada

Figure 1: Overview of Canada's dementia strategy
figure 1
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A Dementia Strategy for Canada: Together We Aspire

Vision: a Canada in which all people living with dementia and caregivers are valued and supported, quality of life is optimized, and dementia is prevented, well understood, and effectively treated.

Principles:

  • Quality of life
  • Diversity
  • Human rights
  • Evidence-informed
  • Results-focused
National objectives Areas of focus
Prevent dementia
  1. Advance research to identify and assess modifiable risk and protective factors
  2. Build the evidence base to inform and promote the adoption of effective interventions
  3. Expand awareness of modifiable risk and protective factors and effective interventions
  4. Support measures that increase the contribution of social and build environments to healthy living and adoption of healthy living behaviours
Advance therapies and find a cure
  1. Establish and review strategic dementia research priorities for Canada
  2. Increase dementia research
  3. Develop innovative and effective therapeutic approaches
  4. Engage people living with dementia and dementia caregivers in the development of therapies
  5. Increase adoption of research findings that support the strategy, including in clinical practice and through community supports
Improve the quality of life of people living with dementia and caregivers
  1. Eliminate stigma and promote measures that create supportive and safe dementia-inclusive communities
  2. Promote and enable early diagnosis to support planning and action that maximizes quality of life
  3. Address the importance of access to quality care, from diagnosis through end of life
  4. Build the capacity of care providers, including through improved access to and adoption of evidence-based and culturally appropriate guidelines for standards of care
  5. Improve support for family/friend caregivers, including through access to resources and supports

Pillars:

  • Collaboration
  • Research
  • Innovation
  • Surveillance and data
  • Information resources
  • Skilled workforce

Stigma can result from uninformed beliefs about dementia and incorrect assumptions about the capabilities of people living with dementia. It can be a barrier that removes opportunities for those living with dementia to participate in their communities, limits access to services and support, and reduces their quality of life. Stigma reduction is a key factor in enabling dementia-inclusive communities. The report shares notable results of public opinion research in 2023 on dementia-inclusive communities and stigma. It suggests that there is still more training and education needed to improve knowledge of how to positively interact with people living with dementia to help reduce stigma and make communities more inclusive.

This annual report shares information that was current as of June 2024.

Dementia is a term used to describe symptoms affecting brain function. It may be characterized by a decline in cognitive (thinking) abilities such as memory, planning, judgement, basic math skills, and awareness of person, place and time. Dementia can also affect language, mood and behaviour, and the ability to maintain activities of daily living. Dementia is not an inevitable part of aging.

Dementia is a chronic and progressive condition that may be caused by neurodegenerative diseases (affecting nerve cells in the brain), vascular diseases (affecting blood vessels like arteries and veins) or injuries. Types of dementia include vascular, Lewy body, frontotemporal, Alzheimer's disease and mixed (a combination of more than one type). In rare instances, dementia may be linked to infectious diseases, including Creutzfeldt-Jakob disease.

Tracking the state of dementia in Canada

Annual tracking of dementia data points helps gauge progress on the national dementia strategy's three national objectives to prevent dementia, advance therapies and find a cure, and improve the quality of life of people living with dementia and caregivers.Footnote 2 This year's data points show improvement in some trends related to all three objectives, while others have remained stable or worsened.

Objective: Prevent dementia

Data suggests the rate of newly diagnosed cases in Canada continues to decline and the level of some risk factors is also dropping. There was a decrease from 1,545 new cases in 2011–2012 to 1,398 new cases in 2021–2022 (per 100,000 Canadians aged 65 and older, age-standardized).Footnote 3 Footnote 4 To support a decline in new cases, efforts should continue to reduce key risk factorsFootnote 5 associated with developing dementia among Canadians.

The most recent data show a trend for some of these risk factors in the right direction with fewer Canadians with lower levels of education, smoking and being diagnosed with hypertension, while other risk factors (high-cholesterol, insufficient sleep, heavy alcohol drinking and experiencing a stroke) are relatively stable. The data also show an increase in diabetes, obesity, physical inactivity and social isolation, suggesting priorities for future efforts. See Table 1 for the list of potentially modifiable risk factors from the 2020 report of the Lancet Commission and Appendix C for further details on the level of risk factors in Canada, including a breakdown across provinces and territories.

Table 1: Increased risk associated with 12 potentially modifiable risk factors based on the 2020 report of the Lancet Commission
Risk factor Relative increased risk of developing dementia compared to someone without this risk factor
Early life (under 45 years old)
Lower levels of education 60%
Midlife (45 to 65 years old)
Hearing loss 90%
Traumatic brain injury 80%
Hypertension 60%
Obesity 60%
Alcohol use (over 21 units per week) 20%
Later life (over 65 years of age)
Depression 90%
Smoking 60%
Social isolation 60%
Diabetes 50%
Physical inactivity 40%
Air pollution 10%

Risk factors in Canada

Recent studies from the University of Western Ontario (UWO) and McMaster University have used data from the Canadian Longitudinal Study on Aging (CLSA)Footnote 6 to estimate the proportion of dementia cases that could be avoided in Canada by completely preventing a specific risk factor (a measure known as population attributable fraction—PAF), in either a specific life stage (UWO study) or among the population 45 and above (McMaster University study).Footnote 7 The risk factors examined in both studies are shown in Table 2.

Table 2: Population attributable fraction (PAF)Footnote 8 estimates by risk factor in different life stages
Life stage Risk factorFootnote 9 UWO PAF (%) 95% Confidence IntervalFootnote 10 (%) McMaster University PAF (%) 95% Confidence Interval (%)
Early life Less education 3.2 (1.9–4.3) 4.3 (2.0–6.9)
Midlife Hearing loss 6.5 (3.7–9.3) 3.3 (1.5–5.6)
Traumatic brain injury 4.4 (3.3–5.4) 4.8 (3.3–6.5)
Hypertension 6.2 (2.7–9.3) 6.0 (1.8–10.4)
Excessive alcohol consumption 0.9 (0.5–1.1) 0.4 (0.1–0.6)
Obesity 6.4 (4.1–7.7) 5.6 (3.4–8.0)
Later life Diabetes 2.5 (2.4–3.3) 3.5 (2.2–4.9)
Social isolation 0.4 (0.2–0.5) 4.7 (2.8–6.8)
Depression 4.0 (3.2–4.8) 7.7 (5.0–10.7)
Physical inactivity 10.2 (6.8–13.0) 11.6 (5.4–17.1)
Smoking 1.5 (0.6–2.4) 2.1 (0.6–4.0)
Sleep disturbance 3.0 (1.8–3.8) N/A N/A
Air pollution N/A N/A 0.8 (0.6–1.0)
Total All factors 49.2 (31.2–65.1) 43.4 (37.3–49.0)

The UWO study identified physical inactivity, hearing loss, and obesity as the top three risk factors contributing to dementia cases in their selected Canadian sample, while McMaster University's study identified physical inactivity, depression, and hypertension. UWO estimated that about half (49.2%) of dementia cases across Canada could be prevented or delayed by eliminating all 12 modifiable risk factors examined, while McMaster University calculated slightly under a half (43.3%). These results are similar to those of the 2020 report of the Lancet Commission on dementia. These findings shed light on risk factors to prioritize in Canada while confirming the importance of ongoing risk reduction efforts.

Health equity and risk factors in Canada

While a similar proportion of dementia cases can be prevented among both females and males according to the UWO study, certain risk factors were more common in one sex than the other. Hearing loss and excessive alcohol use were higher in males while physical inactivity and depression were more common in females. This suggests there would be benefits in tailoring interventions by sex.

Table 3: The five risk factors with the greatest difference in prevalence between high- and low-income groups
Risk Factor <$20,000 $20,000–<$50,000 $50,000–<$100,000 $100,000–<$150,000 >$150,000 Prevalence Ratio (lowest to highest income group)Footnote 11
Less education 47.3 32.6 13.3 7.2 3.4 13.9
Smoking 23.6 13.5 8.8 7.7 3.5 6.7
Depression 48.3 23.5 16.7 11.7 8.7 5.6
Hearing loss 26.1 25.8 15.5 8.4 6.0 4.4
Air pollution 37.8 27.4 17.9 12.6 12.0 3.2

McMaster University's study also found that the impact of risk factors in their selected Canadian sample increased as income decreased for nine of the twelve risk factors, suggesting that socioeconomic status meaningfully affects an individual's lifestyle and behavioural factors linked to developing dementia. For example, the 12 risk factors accounted for 58.7% of dementia cases among the lowest income group (less than $20,000 per year), compared to 31.8% for the highest income group (over $150,000 per year). Table 3 shows five risk factors that were notably more common in the low-income group than in the high-income group. This finding suggests a need for targeted initiatives to reduce differences in dementia risk across income groups.

Objective: Advance therapies and find a cure

Data points related to this objective are based on the Canadian Institutes of Health Research (CIHR)'s investments and activities related to dementia. Research and innovation is one of the cross-cutting pillars of the national dementia strategy. This pillar supports all three objectives, including advancing therapies and finding a cure. This investment includes investigator-initiated research (e.g., those funded through the CIHR Project Grant competitions), research in priority areas (e.g., the Brain Health and Cognitive Impairment in Aging (BHCIA) Research Initiative), and training and career support programs (e.g., fellowships).

A continued increase in investment in research in priority areas, along with training and career support has been observed over the last five years in dementia research. This represents an increase from approximately $42 million in 2019–2020 to approximately $52 million in 2022–2023. The number of CIHR supported unique nominated principal investigatorsFootnote 12 who conducted dementia research increased from 262 in 2019–2020 to 297 in 2022–2023. The number of CIHR supported grants and awards focused on dementia research increased from 306 in 2019–2020 to 331 in 2022–2023.

Objective: Improve the quality of life for people living with dementia and caregivers

Quality of life has many components. The data shows positive trends in some areas, including fewer people exhibiting withdrawal from activities of interest and/or reduced social interaction as well as depression, along with a decrease in caregiver distress.Footnote 13 However, the level of daily pain among people living with dementia in home care settings has remained stable.

The percentage of people living with dementia who exhibited withdrawal from activities of interest and/or reduced social interaction decreased from 19.1% in 2019–2020 to 17.7% in 2022–2023. Similarly, the percentage of people living with dementia who displayed a potential or actual problem with depression, based on a depression rating scale, also decreased from 24.8% in 2019–2020 to 23.9% in 2022–2023. However, the percentage of people living with dementia who experience daily painFootnote 14 stayed relatively stable from 34.6% in 2019–2020 to 34.0% in 2022–2023. The percentage of caregivers who provided care for people living with dementia who experienced distress decreased from 37.1% in 2019–2020 to 35.6% in 2022–2023.Footnote 15 Footnote 16

Research shows a difference in quality of life among social and economic groups.

A project by epidemiologists from the British Columbia Office of the Provincial Health Officer shows why it is important to think about inequalities in health when studying data and planning for dementia. They measured disability-adjusted life years (DALYs) due to dementia, which is the number of healthy years lost, either because of early death or disability linked to dementia in the population of British Columbia. Overall, they found that the rate of DALYs linked to dementia slightly increased in British Columbia between 2001–2002 and 2021–2022. However, the impact on health related to dementia wasn't the same across neighbourhoods with differing socioeconomic status (considering factors like income and education levels). The largest increase of DALYs occurred in neighbourhoods with the lowest socioeconomic status, compared to a slight reduction of DALYs in neighbourhoods with the highest socioeconomic status. This indicates a need to further explore links between dementia and broad socioeconomic factors.

Efforts across Canada supporting progress on the national dementia strategy

This chapter highlights a variety of efforts across the country supported by the Public Health Agency of Canada (PHAC), other federal organizations, provincial and territorial governments and non-governmental organizations. It shares newly-funded projects along with results from completed projects.

Results of dementia projects funded by the Public Health Agency of Canada

The PHAC plays a lead role in the implementation of the national dementia strategy. In this past year, this included the management and administration of multiple activities that contribute to increasing awareness about dementia, improving access to guidance, and conducting surveillance. These activities were funded through the PHAC's Dementia Community Investment (DCI), the Dementia Strategic Fund (DSF) and the Enhanced Dementia Surveillance Initiative (EDSI). PHAC also supports the operation of the Ministerial Advisory Board on Dementia, which provides guidance to the federal Minister of Health on dementia.

The DSF, which has funded 40 projects since 2019, has focused on increasing awareness about dementia, improving access to high-quality dementia guidance and enhancing online dementia information resources on provincial and territorial websites. The DCI funds community-based projects that seek to improve the wellbeing of people living with dementia and caregivers, and increase knowledge about dementia and its risk and protective factors. The DCI has funded 31 projects since 2018. This includes the Canadian Dementia Learning and Resource Network (CDLRN), which has recently published a playbook that showcases the work of DCI projects, their successes, and provides tools and resources for other organizations undertaking dementia-related projects.

The EDSI successfully broadened the scope of surveillance and addressed key data gaps to improve our understanding of dementia and its impact on the lives of Canadians. It also contributed to the surveillance and data pillar of Canada's national dementia strategy. Since 2019, the EDSI supported 15 projects, presented on the EDSI webpage, that have generated valuable evidence to guide public health interventions. The researchers involved in these projects have reported their results and findings in various formats, through peer-reviewed papers, technical reports, conferences, webinars, dashboards, and websites (including the EDSI webpage). To support this knowledge dissemination, PHAC is also developing a knowledge mobilization plan, working with its regional offices across the country.

The 2024 annual report highlights a few of PHAC's funded projects, including some with a focus on populations who are likely to be at higher risk of developing dementia or facing barriers to equitable care. Resources and results from these projects will be shared as final reports are received and examined. Information on the number of PHAC-funded projects within each province and territory can be found in Appendix A, and the total list of funded projects can be found in Appendix B.

Preventing dementia

Aligned with the national objective of the national dementia strategy to promote prevention, several projects have focused on increasing knowledge in Canada about risk factors linked to developing dementia and encouraging individuals to take steps to reduce their own risk.

Co-designed knowledge products to raise awareness about dementia prevention – Baycrest Academy for Research and Education

This dementia project has released eleven episodes of its Defy Dementia podcast, nine short videos, and ten infographics that raise awareness of modifiable risk factors such as loneliness and physical inactivity as well as protective factors such as having a brain-healthy diet and practicing cognitive engagement. The Defy Dementia team also partnered with the creators of Canuckle and Canoku to create a uniquely Canadian, educational and brain-healthy version of the logic puzzle sudoku: the Canoku Brain Health Edition. These resources have been co-designed through the participation of working groups with a diverse membership that includes older adults, those at risk of developing dementia and caregivers, and seek to highlight people with lived experience as positive role models. Defy Dementia was recently nominated for two Webby Awards in the category of Health, Wellness and Lifestyle podcast, where it was the only podcast in its category not based in the United States and one of only a small number of Canadian nominees overall. The Defy Dementia project successfully reached its wide-ranging target population through 76 knowledge products and 16 activities and events.

Project reach included:

Project results:

"I've done a lot of different little things [to reduce dementia risk]. I started learning a new language, I made conscious changes to my diet, I tried to take care of my health. I [had] already been doing yoga on and off, but I signed up after one of the podcasts to do it on a regular basis." – Ravi Venkatesh, Defy Dementia podcast guest

Expansion of the dementia risk reduction application Luci – Lucilab Inc.

The purpose of the Luci application is to improve knowledge and equip the public to adopt healthy lifestyles that foster cognitive health and thus reduce the risk of dementia. In particular, Luci provides guidance from an advisor who supports participants in meeting their personal goals regarding healthy eating, physical activity and intellectual stimulation.

Efforts to broaden the scope of Luci included:

Project reach included:

Project results by the end of the program, among the participants guided by an advisor:

« Participer au programme Luci a été une expérience très bénéfique pour moi. Dès le début, le simple fait de remplir le questionnaire m'a permis de m'interroger sur mes habitudes de vie, de faire le point sur ma situation. On se dit souvent « J'aimerais améliorer telle ou telle chose » mais on ne prend jamais le temps même d'y réfléchir. Le programme de 12 semaines avec le conseiller apporte ce surplus de motivation nécessaire pour arriver à mettre en place des habitudes de manière positive et durable. » ["Participating in the Luci program was a very beneficial experience for me. From the start, simply filling out the questionnaire made me look at my lifestyle and get an overview of my situation. We often tell ourselves 'I would like to improve this thing or that thing,' but we never take the time even to think about it. The 12-week program with the advisor provides the extra motivation needed to develop positive and lasting habits."] – Nicolas, British Columbia, a participant in the Luci guidance program

Direct health care costs for people living with dementia – Ottawa Hospital Research Institute

To improve our understanding of health care costs related to dementia and inform risk reduction efforts, researchers calculated the direct costs for people living with dementia in Ontario. Across the course of the condition, they found that direct health care costs are higher for people living with dementia compared to a similar group of people not living with dementia. That is, at every stage of the condition for someone living with dementia, another person with similar characteristics (considering factors like age, sex, income, comorbidities and care settings) was included in the comparison group.

The excess health care costs for people living with dementia compared to those without the condition in the year after meeting the dementia case definition and as the condition progresses (one year after meeting the case definition to one year before death) are about twice as high (see Figure 2). The direct cost is highest in the last year of life, with an excess cost of about $25,000 per person for females and $31,000 per person for males in those living with dementia. Excess costs are largely attributable to hospitalization and long-term care.

These cost estimates are being integrated into Statistic Canada's Population Health Microsimulation Model, which will be used to project the health care costs attributable to dementia until 2050. This integration may help improve understanding about the extent to which dementia risk reduction strategies (e.g., increased physical activity, smoking cessation, and alcohol reduction) could lessen future health care system costs of dementia.

Figure 2: Average annual health care spending per person for those living with dementia and for similar people without dementia, per condition phaseFootnote 17 and sex, Ontario, data from 2013–2014 to 2021–2022
figure 2
Text description
Condition phase Dollar Value (thousands)
Dementia (female) No dementia (female) Dementia (male) No dementia (male)
Pre-diagnosis phase 21 18 22 19
Diagnosis phase 32 13 34 14
Progression phase 30 14 29 15
End-of-life phase 92 66 109 77

Improving quality of life

A central focus of Canada's national dementia strategy is to expand the reach and impact of efforts to support the quality of life of those living with dementia and caregivers. These efforts work on a variety of aspects of quality of life, including improving experiences in the health care system as well as supporting our communities to be more inclusive of those living with dementia and caregivers.

Dementia-Inclusive Streets and Community Access, Participation, and Engagement (DemSCAPE) – Simon Fraser University

DemSCAPE, has focused on creating supportive neighbourhood environments where people living with dementia are able to remain engaged in their communities. Features of frequently visited areas of neighbourhoods affecting the mobility and social participation of people living with dementia have been identified through walk-along interviews of people living with dementia. Findings have been shared through a short documentary video; community-engagement workshops with city planners, engineers, and related decision-makers; peer-reviewed articles;Footnote 18 and an easy-to-use neighbourhood audit tool that assesses physical environmental barriers faced by people living with dementia. DemSCAPE, in partnership with Happy Cities, has also created Dementia-Inclusive Planning and Design Guidelines with more than 20 strategies and 69 actions to inform the physical planning and design of dementia-inclusive neighbourhoods. By engaging people living with dementia in the project, DemSCAPE created an opportunity for them to initiate change from the ground up by sharing their unique perspectives about their experiences with their neighbourhoods.

Project reach included:

Project results (among those surveyed after attending community engagement events):

"I really am thrilled to have been here today, and I will do whatever I can because we realize numbers [of people living with dementia] are growing in the area and we need to be aware and make it possible for us to live well together." – Maureen, community engagement event participant with lived experience

figure 3
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DemSCAPE
What influences the walking experience of older adults living with dementia in the community?

Physical Aspects

  • Physical environment facilitates or hinders outdoor walking experience
    • Features that enable access
    • Crossings
    • Terrain
    • Ambient conditions
    • Sidewalk width and clear space
    • Sidewalk condition and maintenance
    • Places to rest

Cognitive Aspects

  • Experiencing familiarity with and understanding neighbourhood environment
    • Taking familiar routes to destinations
    • Knowledge of neighbourhood layout
    • Identifying streets
    • Planning where to walk

Social Aspects

  • Positive social interaction and social support
    • Community members having dementia awareness and sensitivity
    • Social networks support walking
    • Direct and indirect support from others
    • Participating in advocacy and city planning

Psychological & Emotional Aspects

  • Supportive environments promote positive outdoor experiences
    • Environment provides stimulation
    • Valuing independence
    • Perceptions of safety

Temporal Aspects

  • The role of patterns, rhythms and personal histories
    • Changing walking patterns
    • Changes in the environment
    • Lifelong and historical connections to place
Artful Moments: Shared Learning – Art Gallery of Hamilton

Artful Moments: Shared Learning is an online learning website with an in-depth curriculum comprised of 6 modules, more than 300 mini lessons and 90 videos that provide guidance for staff at museums on how to develop engaging, meaningful and inclusive programming for people living with dementia. The curriculum is inspired by the gallery's longstanding programs for people with dementia and is based on the Artful Moments Model for Successful Engagement. By surveying staff at museums, galleries and other cultural organizations across Canada this dementia project also produced a report detailing the nature and scope of museum programming for people living with dementia in Canada. Artful Moments has increased confidence among museum staff in delivering programming to people living with dementia and has already led to new and expanding programs for people living with dementia in other museums in Canada. The project was recently awarded the Ontario Museum Association's Award of Excellence in Publications for this work.

Project reach included:

Project results:

"Our team didn't have any experience with this audience and we were worried that our exhibitions would not be relevant or accessible. The Artful Moments: Shared Learning website was an amazing resource – we learned about dementia and how to communicate and plan to suit this new audience. And we learned that the tours and activities we were already using in other programs would work really well when we knew what to do." – Museum Facilitator

"I saw that it was an art-related thing and I realized that it would be people like me there, so it was very non-threatening… These programs are important because you can be free to be yourself by the kind of ambience that's created." – Participant living with dementia

DREAM – Dementia Resources for Eating, Activity and Meaningful Inclusion – Moving, Eating, and Living Well – University of Waterloo

The University of Waterloo's DREAM project promoted the health and wellbeing of people living with dementia and caregivers by building community capacity through creating inclusive wellness services across Canada. The project team, including people living with dementia, caregivers, community organizations, and researchers from the University of Waterloo and University of Northern British Columbia, created and adapted physical activity and nutrition training resources. Service providers were trained using these adapted resources to work with people living with dementia and caregivers, facilitating health behaviours related to physical activity and healthy eating. In addition, an online toolkit was developed to support self-learning by the broader dementia community, including people living with dementia and caregivers. Intervention research assessed change in knowledge, attitudes, and practice among the service providers as well as people living with dementia and caregivers, including individuals from francophone and ethnocultural populations.

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Benefits of Dementia-Inclusive Physical Activity

This image is a drawing of a park, with several bushes, three trees, some flowers and the sun. On the left, there is an older man playing the guitar and an older woman dancing, holding her cane. In the middle, there are three older adults stretching. On the right, there are two adults running.

The text around the image reads (from left to right):

  • Feeling of mental well-being
  • Confidence
  • Sense of community
  • Maintenance of personal identity
  • Companionship
  • Peer and social support

Project reach included:

Project results:

"Oh, using it, it was very informative. And a lot of the stuff in it, I very much liked because it told me stuff I didn't know and it told me stuff I should be doing. That way, I was very impressed with it." – Person living with dementia

"And I got the feeling from him that it was a relief to find out some of these things. And the one thing that really came up was, when we were watching one video, and they were shooting bows. His comment was, 'I didn't know I could still do that. I guess I am allowed to.' And I said, 'Well, yes.'" – Caregiver

Building Capacity for Meaningful Participation by People Living with Dementia – University of British Columbia

This project adapted, implemented and evaluated an asset-based community development approach to create meaningful opportunities for people living with dementia and caregivers to remain active and connected in their communities through art, social, fitness and volunteer activities. This project was built on existing partnerships with community groups and focused on two communities in British Columbia and Ontario. The next phase of the project will include the creation of an action guide for use by new communities.

Project reach included:

Project results:

"When I was diagnosed, I worried I wouldn't be productive anymore. But I'm doing something everyday to improve people's lives around me. That feels good." – Person living with dementia, peer support group leader

Dementia in long-term care and home care settings – Canadian Institute for Health Information

To help inform service provision and policy planning, and in turn, improve quality of life of people living with dementia, the Canadian Institute for Health Information sought to gain a better understanding of health care trajectories using data from British Columbia, Alberta, Ontario, and Newfoundland and Labrador. A cohort was followed for five years after their first medical record of dementia in 2017–2018 using assessments in home and long-term care settings.

Main findings from this project indicated the following trends:

Disease and mortality trajectory among Canadians living with dementia – British Columbia, Ontario, Prince Edward Island and Quebec

Many of those who live with dementia are also living with other chronic conditions, known as comorbidities. The presence of comorbidities can impact the quality of life of people living with dementia. For example, they may have symptoms from these other conditions that require management, which can create additional challenges for their dementia care. To understand the frequency of comorbidities among people living with dementia, a multi-provincial project using health administrative databases was led out of ICES (a research institute with a community of data and clinical experts) in Ontario, with the support of other provincial organizations in British Columbia, Prince Edward Island, and Quebec.

Researchers found that, across all four provinces, the proportion of older adults living with dementia (aged 65 years and older) with five or more comorbidities was more than double the proportion in individuals without dementia (over 50% compared to around 25%). Researchers also found that the most common comorbidities for people living with dementia in these provinces were cardiovascular diseases (e.g., hypertension, ischemic heart disease, stroke), diabetes, and age-related conditions (e.g., osteoarthritis and osteoporosis). These comorbidities were often present before meeting the dementia case definition, while traumatic brain injury and chronic obstructive pulmonary disease were equally likely to occur before and after meeting the dementia case definition.

Navigating Dementia NB piloted a patient navigation program in New Brunswick for individuals living with dementia and caregivers, funded through the Healthy Seniors Pilot Project and led by the University of New Brunswick and Horizon Health Network. Between July 2022 and July 2023, four anglophone and two francophone patient navigators worked out of primary care clinics and health centres throughout the province.

Engaging 287 individuals (the program worked with people living with dementia and caregivers, either offering services to both parties at the same time or offering services to either the caregiver or the person living with dementia), the program aimed to enhance knowledge of, and access to, health and social services related to dementia care. The most common reasons for contacting navigators during the project included connecting with social services, receiving informational resources on dementia and advance care planning, and accessing community resources and home health care services.

Survey data from 56 caregiver respondents revealed that 84% were generally satisfied with the patient navigator. Additionally, 75% reported greater knowledge of health and/or social services, and 74% reported increased access to such resources as a result of using this navigation service. Findings from interviews with caregivers suggest the following considerations for future efforts:

  • the navigation program would be most helpful if it starts early in the care process, preferably immediately after a dementia diagnosis; and,
  • the need to address systemic barriers to accessing health and social services, such as ineligibility or co-pay requirements.

Recognizing the potential impact of the program, the Navigating Dementia NB project team is engaging in discussions with government partners to explore scaling up the program with the intention to implement and evaluate a province-wide patient navigation system tailored to meet the needs of people with dementia and caregivers.

Focusing on populations that are likely to be at higher risk of developing dementia and/or to face barriers to equitable care

The national dementia strategy emphasizes the importance of considering the needs of those belonging to populations who may have a higher risk of developing dementia and/or face barriers to equitable care, and several projects have included a focus on these populations. Two examples are highlighted below.

Dementia Guidance Online Resource Hub for Chinese Communities in Canada – Yee Hong Centre for Geriatric Care

This project developed a dementia guidance resource hub for Chinese-speaking individuals in communities across Canada to improve access to, and encourage adoption of, high-quality dementia guidance. This user-friendly hub provides a one-stop source of credible, evidence-based dementia information in English, Traditional Chinese, and Simplified Chinese, facilitating better understanding and access to culturally appropriate dementia resources and support. The content includes 28 dementia care guidance web pages featuring articles, e-books, videos, infographics, and presentations that share various supports and services, tutorials for culturally relevant physical activities, resources to improve quality of life, and online courses and workshops about dementia.

Project reach included:

Project results:

"When we build ramps for wheelchair access, we are benefitting anyone that has a mobility challenge. This hub is like an information ramp for Chinese-speaking Canadians to access dementia care resources and support. It will benefit all patients and family members that need similar information." – Wendy Wu, a user of the website and a caregiver

A National Indigenous Dementia Surveillance Initiative – McMaster University

Guided by partners at the Anishinabek Nation and Za-Geh-Do-Win Information Clearing House, a team of researchers from McMaster University and University of Saskatchewan created and released a series of online training videos to help facilitate the uptake of the Canadian Indigenous Cognitive Assessment (CICA). The CICA is a culturally informed dementia screening tool developed with Anishinaabe communities on Manitoulin Island, Ontario. McMaster University has facilitated four CICA training sessions, reaching more than 150 health care providers who serve First Nations health organizations in Ontario. The ultimate goal of this project was to contribute to enhanced Indigenous dementia surveillance through training and implementation of the CICA training platform and by enhancing data collection to increase monitoring for dementia.

An article on the results of the Homelessness Counts: Exploring Dementia in People Experiencing Homelessness project (showcased in the 2023 report) has now been published in The Lancet Public Health journal.

National public education campaign on dementia

The Public Health Agency of Canada (PHAC)'s 2023–2024 national public education campaign on dementia included a variety of efforts to reach Canadians such as digital advertising, outreach activities including articles provided to media organizations to use, and a risk reduction digital poster shared with Indigenous audiences across Canada.

Digital advertising

The digital advertising aspect of the campaign focused on confronting stigma and reducing the risk of developing dementia. Traffic to the Government of Canada dementia web pages increased by over seven-fold during the campaign period compared to the five-month period before the campaign, for a total of 479,500 visits from September 18, 2023 to March 31, 2024.

Two new video testimonials from Canadians living with dementia were a feature of the stigma campaign which ran from September 18 to October 29, 2023. These videos were shown 1.1 million times, and users clicked on the video links a total of 3,000 times, directing them to Canada.ca/dementia for more information.

Advertising on risk reduction ran from October 30, 2023 to March 31, 2024. This phase of the campaign built on the success of past tactics while adding a new television feature on Canadian Broadcasting Corporation (CBC)'s Family Feud and Société Radio-Canada (SRC)'s Au Suivant game shows. Skill-testing questions on ways to reduce the risk of developing dementia were integrated into the game show format, a new approach to public education for PHAC. Other advertising tactics included two videos on dementia risk factors (physical inactivity and high blood pressure), interactive quizzes, search engine marketing, digital banners, out of home ads in pharmacies, clinics, casual dining and transit stations, and social media ads focused on social isolation. Digital ads were shown 62.5 million times and users clicked on the ads a total of 409,300 times.

Figure 3: PHAC's campaign on confronting stigma – testimonial videos

Egale delivered a national bilingual awareness campaign to promote the acceptance and understanding of people living with dementia who are also members of Two-Spirit, lesbian, gay, bisexual, transgender, queer, intersex, and additional sexually and gender diverse (2SLGBTQI+) communities. Among 2SLGBTQI+ people who have experienced trauma due to lifelong stigma and/or violence, there may be an increased risk of cognitive decline. During Alzheimer's Awareness Month in January 2024, Egale launched the Help Us Remain campaign to urge Canadians to take a closer look at a community facing a hidden battle. This campaign used billboards, bus shelter ads, social media content, a short film, and audio stories to raise awareness of the need for tailored, inclusive health care support to preserve the identities and dignity of 2SLGBTQI+ people living with dementia. Over 4.1 million individuals were reached by this campaign. The short film was awarded three golds and one silver at the 2024 Clio Health Awards, which recognizes creative marketing, advertising and communications in the fields of physical health, mental health and social wellbeing.

Dementia resources toolkit

The dementia toolkit brings together awareness resources developed since 2019 in both a clickable PDF document and an accessible web-based version. Resources are presented by topic (overview, risk reduction, stigma and dementia-inclusive communities) and media type (web links, images, videos, social media posts) in both English and French. These resources can be used by all Canadians to further share key messages on risk reduction and encourage dementia-inclusive communities.

Figure 4: Dementia resources – toolkit
figure 4
Text description

This photo is a screenshot of a page in the Dementia Awareness Resources Toolkit.

There are four tabs at the top of the page: overview, risk reduction, confronting stigma, and dementia-inclusive communities. The one selected is dementia-inclusive communities.

Under those tabs, there are three sub-tabs: web links, videos, and social media. The one selected is social media.

Under the sub-tabs, there are seven screenshots of social media posts. There are four social media posts titled "dementia-inclusive communities" and three social media posts titled "be patient".

Under the social media posts, the page reads: for more information, visit Canada.ca/dementia.

New resources for media use

The two 30-second stigma reduction videos mentioned above and five articles focused on reducing stigma and promoting dementia-inclusive communities were made available from January to June 2024 to local and national media outlets to publish. These articles and videos had a reach of over 17.5 million.

Risk reduction poster for Indigenous audiences

In March 2024, an email and poster about dementia risk reduction was developed and distributed to Indigenous audiences through an email network of approximately 21,000 subscribers reaching Indigenous communities across the country. Indigenous peoples have been identified as having a higher risk of developing dementia along with facing barriers to equitable care.

Figure 5: Reducing risk – Indigenous communities poster
figure 5
Text description

A poster with drawings of three individuals going on a walk: a younger woman, an older woman and a middle-aged man. The man is taking a photo of all of them next to some trees and rocks. The sky is blue with a few clouds.

The text reads:

4 ways to help reduce your risk of dementia

  • Focus on healthy foods
    • Eat healthy foods daily to help reduce high blood pressure and avoid diabetes. Both conditions may increase the risk of dementia.
    • Choose fruits, vegetables, whole grains, and traditional nourishing foods as often as possible.
  • Be active
    • Exercise improves blood flow, which can help keep your brain healthy.
    • Walk, dance, garden, hike or bike – find your favourite activities and do them regularly.
  • Stay connected with community
    • Spending time with others may reduce the risk of developing dementia.
    • Sharing stories, enjoying meals together, and attend community gatherings.
  • Learn something new
    • Learning is good for your brain – and even better when you do it with others.
    • Learn something new – like a new language, a new type of exercise or a new hobby.

For more information on reducing the risk of dementia visit canada.ca/dementia

Latest dementia projects

The Public Health Agency of Canada has funded six new Dementia Community Investment projects and two new projects through the Dementia Strategic Fund since the 2023 Report to Parliament. Projects will advance efforts aimed at improving the quality of life for both Canadians living with dementia and caregivers and improve online dementia resources and guidance.

Some examples include:

Investments by other government departments and non-governmental organizations

Implementing the national dementia strategy relies on the work of a wide range of organizations from across Canada, including other federal government departments, provincial and territorial governments, academic institutions, non-governmental organizations. Here are some examples of other initiatives across Canada that are helping to implement the strategy's objectives to prevent dementia and improve quality of life.

Investing in research and innovation on brain health in aging

One of the objectives of the national dementia strategy is to advance therapies and find a cure. The strategy also has several cross-cutting pillars that support all three of its objectives. One of these pillars is research and innovation which is essential to supporting implementation of the strategy and moving closer to its aspirations.

Canadian Institutes of Health Research

Through the Canadian Institutes of Health Research (CIHR), the Government of Canada continues to support critical research to contribute to all three objectives of the national dementia strategy.

CIHR's Brain Health and Cognitive Impairment in Aging (BHCIA) Research Initiative, led by the CIHR Institute of Aging, supports research and knowledge mobilization, as well as training and capacity building on topics ranging from the healthy aging brain to cognitive impairment and care for those living with dementia and the wellbeing of caregivers. CIHR has leveraged partnership funding for the BHCIA Research Initiative, doubling the federal Budget 2022 investment of $20 million over five years to over $40 million.Footnote 22 As of March 2024, CIHR has launched 13 new funding opportunities under the BHCIA Research Initiative in alignment with the strategy.

Figure 6: CIHR Brain Health and Cognitive Impairment in Aging (BHCIA) Research Initiative
figure 6
Text description
CIHR Brain Health and Cognitive Impairment in Aging (BHCIA) Research Initiative
CIHR funding and CIHR Institute of Aging Strategic Programs Canadian Consortium on Neurodegenerative in Aging (CCNA) Dementia Research and Innovation Funders Alliance
Research on: Risk Reduction, Care & Support and Caregivers Training and Capacity Building Accelerate progress in research on age-related neurodegenerative diseases, including Alzheimer disease, vascular dementia, frontotemporal dementia, and Lewy body dementia. Established in 2014. Bring together key stakeholders in the brain health and dementia funding ecosystem in Canada. Through this alliance, we will leverage and amplify dementia research, identify the scope of current activities and identify research gaps and needs.
Knowledge Mobilization Hub
Impact: Innovation and Implementation Impact: Synergy between researchers Impact: Collaboration with funding partners
Knowledge creation

Through the BHCIA Research Initiative, the Government of Canada funds research that advances knowledge of the brain as it ages to help identify and reduce the risks that can result in cognitive impairment in aging.

Since 2023, CIHR, in partnership with the Azrieli Foundation and its Canadian Centre for Caregiving Excellence, has been supporting 13 projects (for a total investment of $8.7 million) through the BHCIA Mechanisms in Brain Aging and Dementia funding opportunity to advance understanding of the protective factors involved in cognitive health, risk reduction, and mitigating the changes occurring in the onset of cognitive impairment. Some examples of the funded research projects include:

Knowledge mobilization

In 2023, CIHR launched funding opportunities under the BHCIA Research Initiative to promote the mobilization and uptake of evidence. For example, CIHR invested over $1.5 million over one year in 16 projects as part of the BHCIA Knowledge Synthesis and Mobilization Grants funding opportunity. These projects are summarizing the knowledge base on cognitive impairment, identifying areas of research strengths and gaps, and promoting knowledge sharing to increase the usefulness and uptake of findings.

To further the knowledge mobilization efforts, CIHR launched a call in 2023 to support the creation of a Canadian BHCIA Knowledge Mobilization (KM) Hub for dementia research in Canada. The BHCIA KM Hub will serve as a national, centralized research resource for researchers, knowledge users, including people with lived and living experience of dementia and their care partners (i.e., family, friends, caregivers and care providers), and will foster collaboration among the cognitive impairment in aging and dementia community. The successful applicant team is expected to be announced in late 2024.

The Canadian Consortium on Neurodegeneration in Aging (CCNA) is a national program for dementia research and a key component of the BHCIA Research Initiative. The CCNA was established in 2014 to promote collaboration and foster synergies between researchers. The CCNA was funded for a second phase in 2019 for five years, with $31.6 million in federal funding and an additional $14.4 million from partners. As part of CCNA's third phase (2024–2029), in March 2024, CIHR announced an investment of $20.6 million in a CCNA Operations Centre to optimize the capacity of the CCNA to support the neurodegenerative disease research community. Some recent CCNA highlights include:

  • In 2023, a team led by Manuel Montero-Odasso from the University of Western Ontario published results of the first CCNA randomized clinical trial, revealing that a combination of physical exercise, cognitive training and vitamin D supplementation can significantly improve cognitive function in older adults with mild cognitive impairment. These results have the potential to reshape cognitive care for the aging population by opening the pathway for non-pharmacological inventions.
  • A team of CCNA researchers led by Ziv Gan-Or from McGill University published the world's first genome-wide association study on rapid eye movement sleep behaviour disorder. The genes identified in this study can be used as targets for therapeutic development aiming to prevent the progression to dementia and Parkinson's disease in individuals with this disorder, also referred to as RBD.
Research training and capacity building

CIHR is investing in initiatives to train and mentor the next generation of dementia researchers in Canada, providing a solid foundation for the future. These include, among others, the CIHR Research Excellence, Diversity, and Independence Early Career (REDI) Transition Award, CIHR postdoctoral fellowships and the Health System Impact Fellowship program. Further, CIHR is funding three projects within the Future Leaders in Canadian Brain Research program led by the Brain Canada Foundation and three projects within the Alzheimer Society Research Program led by the Alzheimer Society of Canada.

For example, through REDI grants, CIHR supports early career health researchers from specific underrepresented groups. This includes Myuri Ruthirakuhan, a postdoctoral researcher at Sunnybrook Research Institute. She aims to improve how we predict dementia and will design trials that lower dementia risk by using personalized biological (e.g., biomarkers from blood tests) and clinical characteristics (e.g., diabetes, hypertension).

One of the cross-cutting components of the BHCIA Research Initiative is to strengthen research partnerships. In November 2023, the Minister of Health announced the Dementia Research and Innovation Funders Alliance (the Alliance) led by the CIHR Institute of Aging with its partners to foster collaboration between funders and other partners in research and innovation across Canada. The launch event brought together more than 50 participants from 22 organizations including the Alzheimer Society of Canada, the Brain Canada Foundation, the Centre for Aging + Brain Health Innovation, Healthcare Excellence Canada, and the Public Health Agency of Canada, as well as people living with dementia and caregivers. The Alliance will support and enable the implementation of the research and innovation pillar of Canada's national dementia strategy. Its objectives include providing a forum for research and innovation funders to work together and encouraging them to align their dementia research investment strategies across Canada.

Investments in the Centre for Aging + Brain Health Innovation

The Centre for Aging + Brain Health Innovation (CABHI), supported by an initial investment of $44 million from the Public Health Agency of Canada (PHAC) (2015–2021) and a subsequent $30 million (2022–2025), accelerates innovations that enhance the health and wellbeing of older adults living with and at-risk for dementia and caregivers.

CABHI has supported more than 510 projects, including over 400 unique innovative solutions. It fosters collaboration to develop the most promising innovations emerging from older adult care settings, academia, industry, and entrepreneurial ventures. CABHI's multifaceted approach involves co-designing innovation through Leap—a community of older adults, caregivers, innovators, and policymakers—to ensure solutions are informed by the diverse lived experience of target users and are adapted to meet their needs.

Some of the innovative solutions that have received support from CABHI include:

Gaining a better understanding of dementia in Canada

Dementia-inclusiveness and stigma

This past year, the Public Health Agency of Canada (PHAC) continued to invest in public opinion research whose results inform efforts in support of the national dementia strategy's implementation.Footnote 23 The focus of two recent projects was on reducing stigma and enabling dementia-inclusive communities in Canada. Some key results are shared below.

General perceptions of people living with dementia

Through a public opinion research study (2023) for PHAC, respondents were asked about their perceptions of the views of people in Canada related to dementia.Footnote 24 These questions included whether: people generally have negative assumptions about those living with dementia; they see them as able to communicate their ideas and wishes to others; they need others to make decisions for them; they need around-the-clock assistance with activities of daily living; and they need supervision due to dangerous behaviour. They were also asked how knowledgeable, respectful and supportive their communities appear to be regarding people living with dementia.

Results from this survey can be broken into demographic groups. For example, women were more likely (64%) than men (54%) to agree that people living with dementia usually are viewed as needing around-the-clock assistance with daily living. This belief was also higher among those aged 18 to 24 (68%), while those aged 65 and older (50%) were the least likely age group to agree. Further differences between ethnic and cultural minority groups can be seen in Figure 7.

Unpaid caregivers were more likely to agree (33%) that people in their community are knowledgeable, respectful, and supportive of people living with dementia, compared to 27% of Canadians overall. Men were more likely than women to share this view as well.

Figure 7: Societal perceptions of dementia (percentage of respondents that believe society generally agrees with the statements below), by self-identified ethnicity
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Text description
Self-identified ethnicity People living with dementia are usually viewed as able to communicate their ideas and wishes to others People have negative assumptions about the abilities of people living with dementia People living with dementia usually are viewed as needing around-the-clock assistance with daily living People in my community are knowledgeable, respectful and supportive of people living with dementia
Canada overall 24% 83% 59% 28%
British 22% 88% 64% 29%
Southeast Asian 21% 83% 69% 29%
Latin American 21% 81% 62% 25%
Indigenous 29% 74% 55% 23%
American 13% 82% 68% 26%
African 19% 69% 49% 30%
French 28% 80% 45% 24%
Other Western European 22% 87% 64% 27%
Scandinavian 18% 89% 68% 28%
Eastern European 20% 83% 68% 25%
Southern European 20% 88% 60% 20%
Arabic 10% 78% 63% 19%
South Asian 35% 81% 64% 29%

Individual perceptions of quality of life

People living with dementia, particularly those who live in dementia-inclusive communities and who have access to tailored supports, can sometimes continue activities they enjoy for years following a diagnosis. However, public opinion research suggests that some Canadians are less likely than others to believe that this is possible (see Figures 8 and 9). Respondents who identified as British and other Western European (German, Dutch) were more likely to agree, whereas those identifying as African and Latin American were least likely to agree.Footnote 25 There are also some notable differences across groups on views regarding the quality of life experienced by people living with dementia. Those identifying as Arabic and French Canadian are most likely to believe that people living with dementia experience a poor quality of life, while those identifying as Indigenous, other Western European and African were least likely to believe this.

Figure 8: Percentage of respondents who agree that people living with dementia are often able to continue activities that they enjoy, by self-identified ethnicity
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Text description
Self-identified ethnicity Percentage of respondents who agree that people living with dementia are often able to continue activities that they enjoy
Overall Canadians 69%
British 79%
Other Western European 78%
American 73%
Eastern European 71%
Scandinavian 70%
Southern European 69%
Indigenous 65%
French 61%
Southeast Asian 60%
Arabic 60%
South Asian 59%
African 53%
Latin American 49%
Figure 9: Percentage of respondents that believe the people living with dementia have a moderate to poor quality of life, by self-identified ethnicity (3–5 on a scale of 1–5)
figure 9
Text description
Self-identified ethnicity Percentage of respondents that believe the people living with dementia have a moderate to poor quality of life
Overall Canadians 84%
French 87%
British 85%
Arabic 85%
Southern European 84%
Southeast Asian 84%
South Asian 84%
Indigenous 83%
Latin American 82%
Scandinavian 82%
Other Western European 82%
Eastern European 82%
American 81%
African 79%

Having experience as an unpaid caregiver appears to positively influence perceptions of the abilities of people living with dementia. For example, many unpaid caregivers (74%) agreed that people living with dementia can continue activities they enjoy compared to all other respondents (69%). Similarly, 78% of unpaid caregivers agreed that people living with dementia can sometimes continue living in their own homes for years following diagnosis compared to 68% of those who are not unpaid caregivers.

Whether views about dementia are changing

More than half of respondents (59%) reported no changes in their views towards dementia in the past five years, while over a quarter of respondents (26%) indicated that they have a more positive view, and 10% indicated that they have a more negative view. The views of those aged 25 to 44 (21%) were the least likely to have improved while those aged 65 and older (33%) were more likely than respondents generally (26%) to say their views had become more positive. Those identifying as South Asian and Latin American were also more likely than others to report a more positive view (see Figure 10).

For respondents who reported a change in their views, the main reasons provided were knowing or caring for someone living with dementia (46%), and having more knowledge about dementia through general information from sources other than the media and care providers (25%) (see Figure 11). Those aged 65 and older were more likely to indicate that their own personal aging process or worry about developing dementia themselves (14%) and information shared through media (8%) were reasons for changing their views, compared to 9% and 6% of overall respondents. Those aged 18 to 24 were more likely to indicate that their views changed due to information they received from paid care providers (21% compared to 6% of overall respondents).

Figure 10: Percentage of respondents reporting a more positive view of dementia over the last five years, by self-identified ethnicity
figure 10
Text description
Self-identified ethnicity Percentage of respondents reporting a more positive view of dementia over the last five years
Canada overall 26%
Latin American 33%
South Asian 30%
Scandinavian 28%
British 28%
African 26%
American 26%
Other Western European 25%
French 23%
Eastern European 22%
Southeast Asian 22%
Indigenous 20%
Southern European 19%
Arabic 15%
Figure 11: Main reasons for Canadians reporting a more positive view of dementia over the past five years, by self-identified ethnicity
figure 11
Text description
Self-identified ethnicity Knowing or caring for someone with dementia General information from sources other than the media and care providers/more is known about it I am now worried about getting dementia/I am aging
Canada overall 46% 25% 9%
British 46% 26% 10%
Southeast Asian 33% 24% 11%
Indigenous 37% 32% 6%
American 42% 35% 5%
African 37% 33% 3%
French 44% 28% 10%
Other Western European 44% 27% 11%
Scandinavian 50% 22% 14%
Eastern European 49% 22% 10%
Southern European 54% 27% 9%
South Asian 48% 25% 4%

Familiarity with dementia-inclusive communities

Creating dementia-inclusive communities across Canada is an important part of advancing the national dementia strategy's objective of improving quality of life for people living with dementia and dementia caregivers. A dementia-inclusive community is one where people living with dementia are welcomed, supported and valued and where the care they receive is culturally safe and culturally appropriate. Dementia-inclusive communities help to enable independence and reduce barriers such as stigma that can discourage or prevent people living with dementia from being active and engaged in their communities and their favourite activities.

In 2023, the Public Health Agency of Canada commissioned public opinion research to explore attitudes, knowledge, and experiences related to dementia-inclusive communities across Canada.Footnote 26 To better understand differences between groups, this research included a focus on unpaid caregivers, individuals working in sectors more likely to interact with people living with dementia, those who identify as Two-Spirit, lesbian, gay, bisexual, transgender, queer, intersex and additional sexually and gender diverse (2SLGBTQI+), and members of some ethnic and cultural minority communities.

When asked if they had heard of the concept of "dementia-inclusive communities," 75% of survey respondents had not. The highest level of awareness within Canada was people living in British Columbia (27%) and the lowest people living in Quebec (8%). Further, English-speaking respondents (21%) were significantly more likely to have heard of dementia-inclusive communities than French speakers (7%), suggesting a greater need for awareness raising among francophones.

Whether dementia-inclusive communities are a priority

After being provided a definition of dementia-inclusive communities during the survey, 53% of respondents indicated that having their communities become more dementia-inclusive was either a high or very high priority (see Figure 12). Within this group, women (58%) were nine percentage points more likely than men (49%) to say so, and respondents living in Quebec (59%), the Territories (59%), and Atlantic Canada (58%) were slightly more likely to agree.

For many of these respondents, improving the quality of life for older people (25%) and preparing for the needs of Canada's aging population (23%) were key reasons for stating such communities should be a high priority. Among those who felt making their community more dementia-inclusive was lower than a moderate priority (7%), the most common explanation was that other concerns were more important, and/or that it was not needed (26%).

Figure 12: Priority ranking for having their community become more dementia-inclusive
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Text description
Priority ranking for having their community become more dementia-inclusive Percentage
Don't know/No response 9%
1 - Not at all a priority 2%
2 5%
3 - Moderate priority 30%
4 29%
5 - Very high priority 24%

Knowledge and availability regarding elements of dementia-inclusive communities

Most of the survey respondents (81%) did not know if their community had a guide or plan to be more dementia-inclusive and 63% did not know what types of measures or activities a dementia-inclusive community might provide. When asked to select from a list of which measures their community had in place that contribute to it being more dementia-inclusive respondents most often mentioned:

Easy to recognize public washrooms were selected the least often (24%). Respondents living in Atlantic Canada (27%), Manitoba/Saskatchewan (24%) and rural or remote communities (29%) most often indicated that their community had none of the listed dementia-inclusive measures in place, compared to 16% of respondents generally.

Regarding measures designed specifically to welcome and include people living with dementia, community centre activities (37%), peer support groups (22%), and cultural activities such as participating in dance sessions and visiting museums (21%) were most commonly identified by respondents as available in their communities. However, 40% of all respondents did not know whether any dementia-inclusive activities were provided in their community. This knowledge gap was highest among people living in Quebec (50%) and lowest among people living in the Territories (14%) where respondents were more likely to say their communities offered all the dementia-inclusive activities they were asked about.

Encouraging healthy aging in the community

Just over a third (36%) of respondents said their communities were either good or very good at supporting healthy aging, including making it possible for older adults to remain engaged in community life. This rating was slightly higher among people living in British Columbia (41%) and the Territories (44%). At 50%, those identifying as South Asian are the most likely ethnic or cultural minority group to rate their community good or very good at supporting healthy aging, and 43% of those identifying as Black felt the same. The most common reason (37%) for giving their community a good rating as a place that supports healthy aging was the availability of community activities (senior centres, support programs, and social activities). Conversely, a lack of resources and supports (51%) was the most common reason for a negative rating among the 17% of respondents who gave their communities a poor or very poor score.

Working and volunteering with people living with dementia

Those who interact with people living with dementia as part of their work are important contributors to a dementia-inclusive community. Just over one quarter (26%) of respondents work(ed) or volunteer(ed) over the past ten years in a sector where they interact(ed) with someone living with dementia, however, only half of respondents said their organization provided training on how to do so.Footnote 27 Of those, 18 to 34 year olds were the most likely age group to have done so (35%), while also most likely across all age groups to say they are not knowledgeable about dementia. This finding suggests that younger individuals are a key audience for dementia-inclusive training in relevant work and volunteer settings (see Figure 13).

Figure 13: Percentage of respondents working in a sector where they may need (or may have needed) to interact with people living with dementia and percentage of respondents who report that they are not knowledgeable about dementia, by age
figure 13
Text description
Age Have been in a role (work or volunteer) where they have interacted or may need to interact with people living with dementia Consider themselves not knowledgeable about dementia
18-34 35% 32%
35-54 26% 30%
55-64 22% 24%
65+ 23% 20%

Compared to all respondents (15%), those who identified as Black were more likely than any other ethnic or cultural group to report that they work or have worked in a role where they are likely to interact with a person living with dementia (24%). Among those identifying as Black, 15% reported currently doing so for work compared to 6% of all respondents. The most common work sector for interaction with a person living with dementia was health care (57%), followed by retail and food services (16%), and recreation/fitness/community and religious organizations (14%). Interactions within the retail sector were more common among those identifying as South Asian (25% compared to 10% of total respondents) as well as in food services (19% compared to 8%).

Training to support dementia-inclusive communities

Providing inclusive services to people living with dementia often requires learning new skills and approaches that may differ from typical interactions with the general public. Roughly half of respondents who either currently or formerly work(ed) or volunteer(ed) in a role where they interact(ed) with people living with dementia said their organization provided training on how to do so. Where training was offered, 68% said they personally received that training and women (73%) were more likely to have done so than men (62%). This training most often focused on general knowledge about dementia such as signs or symptoms, communication and interaction tips and/or how to assist someone who appears confused or lost. Almost a third (30%) of those with experience interacting with people living with dementia at work either disagreed or strongly disagreed that their organization does or did enough to provide this type of training for staff and volunteers.

Comfort interacting with people living with dementia

The level of comfort when interacting with people living with dementia can influence the inclusiveness of a community. Public opinion research suggests there has been a small decline in the number of Canadians who feel at least moderately comfortable (3 to 5 on a five-point scale) interacting with people living with dementia as of 2023 compared to 2020 (down to 80% from 84%). However, this research also revealed that these levels of comfort were higher in 2023 among respondents who were unpaid caregivers (91%), identify as South Asian (85%), Black (84%), or women (83%). Women were also more likely to say they would be very comfortable (5 on a five-point scale) interacting with someone living with dementia (22%) compared to men (17%).Footnote 28

There are recommended tips to ensure supportive interactions with people living with dementia; however, knowledge of those tips appears to vary widely in Canada. Survey results suggest that many are unaware of how best to communicate with people living with dementia in a supportive way. Almost half of respondents incorrectly identified "physical contact like handshakes" (46%) and "provide plenty of information" (40%) as recommended tips. As well, 17% of respondents incorrectly thought that avoiding non-verbal encouragement is recommended. This tendency to incorrectly identify recommended tips was higher among unpaid caregivers, suggesting a particular need to reach this group with information about supportive communication.

Recommendations for how best to interact with people living with dementia:

  • sit or stand at the same level and make eye contact
  • respect physical space
  • speak directly to the person living with dementia and not their caregiver
  • stand directly in front of them, do not approach from behind

Communication tips:

  • use shorter sentences with one point each
  • find a quiet place to talk and lower the volume around you
  • avoid correcting the person
  • try drawing pictures or pointing to objects
  • pay attention to non-verbal cues—such as body language, facial expressions, hand gestures and posture

Conclusion

We thank all those who contributed information in this year's report, including those who participated in the Public Health Agency of Canada (PHAC)'s public opinion research studies. Further details on the results of the public opinion research conducted on behalf of PHAC can be accessed through Library and Archives Canada.

We also thank the many individuals and organizations across Canada working to support Canada's national dementia strategy and its vision of a Canada in which all people living with dementia and caregivers are valued and supported, quality of life is optimized, and dementia is prevented, well-understood and effectively treated.

If you would like to receive communications about the national dementia strategy and funding opportunities or provide information about relevant dementia-related activities, please contact the PHAC Dementia Policy Secretariat.

Appendices

Appendix A: Map of dementia projects distributed across the country

Figure 1: Map of the Public Health Agency of Canada (PHAC) investments
figure map
Text description

Map of Canada with dots that represent dementia project sites in each province and territory for projects funded by the Public Health Agency of Canada (number of sites is in table 1 below).

Table 1: Overview of provincial/territorial locations of PHAC investments
  Total projects funded National projects Provincial projects Number of project sites
DSF 40* 17 21 81
DCI 31 5 26 111
EDSI 15 5 10 33
Total 86 27 57 225
  NL PEI NS NB QC ON MB SK AB BC YT NWT NU
DSF 2 1 5 6 4 14 2 13 18 12 4 0 0
DCI 1 1 4 6 14 33 13 4 5 16 0 8 0
EDSI 1 1 2 2 6 8 2 2 3 5 1 0 0
Total 4 3 11 14 24 55 17 19 26 33 5 8 0
*This includes two grants to the World Health Organization for global efforts

Appendix B: Projects funded through the Dementia Strategic Fund, the Dementia Community Investment and the Enhanced Dementia Surveillance Initiative

Note: Projects marked with an asterisk (*) indicate that they are national in scope

Dementia Strategic Fund (DSF) projects

Awareness Raising Initiatives
Dementia Guidelines and Best Practices Initiative
Provincial/Territorial Online Dementia Information Resources
Projects with the World Health Organization

Dementia Community Investment (DCI) projects

Emerging Stream—Projects are based on some evidence; funding is used to develop, implement and evaluate the intervention.
Advanced Stream—Projects that have strong evidence of effectiveness; funding is used to support scale up and expansion of reach to new populations/jurisdictions/sectors.
Knowledge Hub

Enhanced Dementia Surveillance Initiative (EDSI) projects

Appendix C: Trends in risk factors across Canada

Dementia risk and protective factors among Canadians

Table 1: Percentage of Canadians with modifiable dementia risk/protective factors over time
Dementia risk or protective factor Percentage (%) of Canadians with factor (Year 1) Percentage (%) of Canadians with factor (Year 2) TrendFootnote 29 Footnote 30 SourceFootnote 31 Footnote 32 Footnote 33
% of population (aged 20+) that reports having less than a high school educationFootnote 34 Footnote 35 12.2 (2016) 8.2 (2022) BetterFootnote 36 Canadian Community Health Survey (CCHS), 2016 (CCDI); Custom tabulations by BELD/CSAR, 2022
% of population (aged 20+) with diagnosed hypertension (high blood pressure) 23.7 (2016–2017) 22.4 (2021–2022)Footnote 37 Better Canadian Chronic Disease Surveillance System (CCDSS), 2016–2017; 2021–2022
% of population (aged 12+) that reports being current smokers (daily or occasional) 16.9 (2016) 11.6 (2022) BetterFootnote 38 CCHS, 2016; 2022
% of population (aged 18–79) with elevated blood cholesterol 18.4 (2014–2015) 14.0 (2018–2019) No statistically significant change Canadian Health Measures Survey (CHMS), 2014–2015; 2018–2019
% of population (aged 12+) that reports heavy drinkingFootnote 39 19.0 (2016) 19.7 (2022) No statistically significant changeFootnote 40 CCHS, 2016; 2022
% of population (aged 18–79) that reports obtaining the recommended amount of daily sleepFootnote 41 61.8 (2009–2011) 64.9 (2014–2015) No statistically significant change CHMS, 2009–2011; Canadian Chronic Disease Indicators (CCDI) 2014–2015
% of population (aged 20+) with diagnosed stroke 2.6 (2016–2017) 2.6 (2021–2022)Footnote 42 No statistically significant change CCDSS, 2016–2017; 2021–2022
% of population (aged 20+) with diagnosed diabetes 10.2 (2016–2017) 10.6 (2021–2022)Footnote 43 Worse CCDSS, 2016–2017; 2021–2022
% of adults (aged 18+) that are living with obesity (self-reported, adjusted BMI)Footnote 44 26.5 (2016) 30.0 (2022) WorseFootnote 45 CCHS, 2016; 2022
% of population (aged 18+) who report accumulating at least 150 minutes of moderate-to-vigorous physical activity each week, in bouts of 10 minutes or moreFootnote 46 Footnote 47 58.5 (2016) 53.9 (2021)  Worse CCHS, 2016; 2021
% of population (aged 12+) that reports a "very strong" or "somewhat strong" sense of belonging to their local community (social isolation is a dementia risk factor)Footnote 48 68.8 (2016) 64.5 (2022) WorseFootnote 49 CCHS, 2016; 2022

Dementia risk and protective factors across Canada

Table 2a: Dementia risk factors across CanadaFootnote 50 Footnote 51 Footnote 52
Dementia risk factor Source Footnote 53 Footnote 54 Footnote 55 National AB BC MB NB NFL NWT NS NU ON PEI QC SK YK
% of population (aged 20+) with diagnosed diabetes CCDSS (2021–2022) 10.6 10.3 10.4 12.5 N/A 11.8 N/A 10.4 9.1 11.6 9.8 8.6 N/A 9.1
% of population (aged 12+) that reports heavy drinkingFootnote 56 CCHS (2022) 19.7 20.7 18.9 21.4 21.3 25.0 N/A 21.5 N/A 18.1 23.6 21.4 19.9 N/A
% of population (aged 20+) that reports having less than a high school educationFootnote 57 Footnote 58 CCHS (2022) 8.2 8.0 6.2 10.1 11.4 12.6 N/A 7.8 N/A 6.7 10.3Footnote 59 10.9 9.1 N/A
% of population (aged 20+) with diagnosed hypertension (high blood pressure) CCDSS (2021–2022) 22.4 24.4 21.8 28.3 N/A 29.3 N/A 24.8 23.1 23.0 23.3 19.1 N/A 21.7
% of population (aged 18+) that are living with obesity (self-reported, adjusted BMI)Footnote 60 CCHS (2022) 30.0 31.1 25.5 33.7 43.2 41.9 N/A 35.9 N/A 29.7 36.4 28.6 38.4 N/A
% of population (aged 12+) that reports being current smokers (daily or occasional) CCHS (2022) 11.6 11.4 8.9 11.7 13.2 16.3 N/A 15.1 N/A 10.8 15.5 13.2 14.9 N/A
% of population (aged 20+) with diagnosed stroke CCDSS (2021–2022) 2.6 2.4 2.6 3.0 N/A 2.1 N/A 1.8 3.6 2.7 3.0 2.4 N/A 2.1
Table 2b: Dementia protective factors across CanadaFootnote 61
Dementia protective factor Source Footnote 62 Footnote 63 National AB BC MB NB NFL NWT NS NU ON PEI QC SK YK
% of population (aged 18+) that report accumulating at least 150 minutes of moderate-to-vigorous physical activity each week, in bouts of 10 minutes or moreFootnote 64 Footnote 65 CCHS (2021) 53.9 58.0 62.4 52.8 50.6 50.3 N/A 55.4 N/A 51.5 51.3 51.7 52.2 N/A
% of population (aged 12+) that reports a "very strong" or "somewhat strong" sense of belonging to their local community (social isolation is a dementia risk factor)Footnote 66 CCHS (2022) 64.5 64.7 65.3 67.9 69.9 74.5 N/A 69.0 N/A 65.4 68.4 59.6 70.2 N/A

Endnotes

Footnote 1

Please note that some of the websites this report links to may not have content in both English and French.

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Footnote 2

A caregiver is defined as a person who provides care and support to a person living with dementia, and who is not a paid care provider. A caregiver is likely to be a relative, close friend, neighbour or volunteer. Support provided by a caregiver may include assisting with the activities of daily living and helping with advance care planning.

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Footnote 3

Please note that many Canadian Chronic Disease Surveillance System (CCDSS) measures were influenced by the COVID-19 pandemic in 2021–2022, which should be considered when interpreting data for that year. Further, New Brunswick, Northwest Territories and Saskatchewan data were not available for 2021–2022.

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Footnote 4

Public Health Agency of Canada. Canadian Chronic Disease Surveillance System (CCDSS), Data Tool 20002022, 2024 Edition. Government of Canada. 2024. Available from: https://health-infobase.canada.ca/ccdss/data-tool/Index

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Footnote 5

In 2020, the medical journal the Lancet reported that 12 potentially modifiable risk factors account for approximately 40% of dementia cases worldwide, each at different life stages. This report (https://www.sciencedirect.com/science/article/pii/S0140673620303676?via%3Dihub) and other related research findings help to provide insight into how Canadians may be able to reduce their risk of developing dementia at all stages of life. For example, the World Health Organization released guidelines (https://www.who.int/publications/i/item/9789241550543) in 2019 that includes additional risk factors.

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Footnote 6

Canadian Longitudinal Study on Aging (CLSA) data is collected from a longitudinal cohort, and there are some considerations when generalizing to the general population. For more information on the methods and limitations, see the following publications: McMaster University (https://link.springer.com/article/10.17269/s41997-024-00920-7) and the University of Western Ontario (https://link.springer.com/article/10.14283/jpad.2024.105). These studies used different study populations, implementation of life course stages and methodologies. As such, the study cohorts used in this research are not entirely representative of the Canadian ethno-cultural landscape. Lastly, the population attributable fractions were weighted to account for overlap between risk factors.

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Footnote 7

University of Western Ontario (UWO) used the following age groups: early life analyses was performed on those aged 45 years and older; midlife analyses were performed on 45 to 64 years; and later life analyses were performed on those aged 65 years and older. McMaster University used the all ages (45 years and older) for all analyses.

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Footnote 8

This is an approach used to estimate the proportion of dementia cases that could be avoided by completely preventing a specific risk factor, in either the specific life stage (UWO study) or in the 45 years and older population (McMaster University study).

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Footnote 9

McMaster University's study (in line with the 2020 report of the Lancet Commission on Dementia (https://www.thelancet.com/article/S0140-6736(20)30367-6/fulltext)) also explored air pollution as a potentially modifiable risk factor. The University of Western Ontario's study did not include air pollution, but instead examined sleep disturbances as an emerging risk factor.

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Footnote 10

A confidence interval (CI) is a statistical measurement of the precision of an estimate, with narrow CIs indicating greater precision than those that are wider. The 95% CI shows an estimated range of values that is likely to include the true value 19 times out of 20.

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Footnote 11

The ratio is calculated by dividing the prevalence among individuals in the lowest income group by the prevalence among individuals in the highest income group. A prevalence ratio greater than one indicates that individuals in the lowest income group have a higher prevalence compared to those in the highest income group.

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Footnote 12

The nominated principal investigator (NPI) is the grantee, or awardee, of a Canadian Institutes of Health Research (CIHR) funding application. The grantee is responsible for leading the intellectual direction of the proposed activities as well as coordinating the financial and administrative aspects of the grant.

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Footnote 13

Caregivers who are distressed are defined as primary caregivers who express feelings of distress, anger or depression and/or any caregiver who is unable to continue in their caring activities.

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Footnote 14

Experiencing daily pain includes severe and not severe.

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Footnote 15

Chi-square tests were applied. Significance level set at 0.05, indicating whether any changes in trends are statistically significant.

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Footnote 16

Parts of these materials are based on data and information provided by the Canadian Institute for Health Information (CIHI). However, the analyses, conclusions, opinions and statements expressed herein are those of the author and not necessarily those of CIHI. This data was drawn from the Resident Assessment Instrument—Home Care©—Home Care Reporting System, fiscal year 2022–2023. It is representative of people living with dementia receiving home care in British Columbia (all regions except Northern Health), the Yukon, Alberta (except the Calgary Zone), and Newfoundland and Labrador.

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Footnote 17

Canadian Institute for Health Information. Understanding health care trajectories of people living with dementia. Canadian Institute for Health Information. 2024. Available from: https://www.cihi.ca/en/understanding-health-care-trajectories-of-people-living-with-dementia

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Footnote 18

Peer-reviewed articles can be found in the International Journal of Qualitative Methods (https://journals.sagepub.com/doi/10.1177/16094069231157350) and Journal of Medical Internet Research Research Protocols (https://www.researchprotocols.org/2024/1/e50548); conference proceedings were published in Innovation in Aging (https://academic.oup.com/innovateage/article/7/Supplement_1/224/7488157?login=false).

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Footnote 19

This total includes web hits and views on the DemSCAPE website (14,214), event clicks, downloads, and shares (28,445), those who viewed journal articles (1,701), newsletter subscribers (18), YouTube video views (788), social media follows (1,360), and impressions on LinkedIn (28,009).

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Footnote 20

Other steps included: Supporting initiatives like this one, keeping oneself physically and cognitively active, participating in events that create awareness about dementia, writing letters to city council asking for more funding, continuing to attend dementia-related courses and discussions, and supporting knowledge translation and mobilization of dementia-inclusive community research.

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Footnote 21

Benefits to caring for individuals living with dementia in their communities include familiarity of settings, culturally appropriate care, the ability to speak in one's own language, continuity in families and friends, and the maintenance of Elders' roles in the community (National Collaborating Centre for Aboriginal Health, 2018).

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Footnote 22

This amount represents exclusively the investment allocated through pillar one of the Brain Health and Cogntive Impairment in Aging (BHCIA) Research Initiative, as shown in figure 6, namely, CIHR Institute of Aging Strategic Programs. It does not include the funding for the Canadian Consortium on Neurodegeneration in Aging (CCNA) or the Dementia Research and Innovation Funders Alliance, represented by the second and third pillar respectively in figure 6.

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Footnote 23

All public opinion reports are published online on the Library and Archives Canada site.

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Footnote 24

Nanos Reseach for the Public Health Agency of Canada. Stigma Related to Dementia in Canada: Final Report. Government of Canada. 2023. Available from: https://epe.bac-lac.gc.ca/100/200/301/pwgsc-tpsgc/por-ef/public_health_agency_canada/2023/103-22-e/index.html

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Footnote 25

Respondents were asking the following question: Other than Canadian, to which ethnic or cultural groups do you consider yourself to belong?

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Footnote 26

Earnscliffe Strategy Group for the Public Health Agency of Canada. Understanding Canadians' Attitudes and Knowledge to Promote Safe and Supportive Dementia-Inclusive Communities: Final Report. Public Health Agency of Canada. 2023. Available from: https://epe.bac-lac.gc.ca/100/200/301/pwgsc-tpsgc/por-ef/public_health_agency_canada/2023/133-22-e/index.html

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Footnote 27

Earnscliffe, Strategy Group for the Public Health Agency of Canada. Understanding Canadians' Attitudes and Knowledge to Promote Safe and Supportive Dementia-Inclusive Communities: Final Report. Public Health Agency of Canada. 2023. Available from: https://epe.bac-lac.gc.ca/100/200/301/pwgsc-tpsgc/por-ef/public_health_agency_canada/2023/133-22-e/index.html

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Footnote 28

Earnscliffe, Strategy Group for the Public Health Agency of Canada. Understanding Canadians' Attitudes and Knowledge to Promote Safe and Supportive Dementia-Inclusive Communities: Final Report. Public Health Agency of Canada. 2023. Available from: https://epe.bac-lac.gc.ca/100/200/301/pwgsc-tpsgc/por-ef/public_health_agency_canada/2023/133-22-e/index.html

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Footnote 29

For Canadian Community Health Survey (CCHS) data: Significant differences for these indicators are based on 95% confidence intervals (i.e., "better" or "worse" if confidence intervals between two points do not overlap AND "no significant change" is confidence intervals overlap between two data points). Note that data interpretation of significant differences based on confidence intervals is a conservative approach. The current table includes an estimate using the latest data available (e.g., 2022 CCHS for alcohol heavy drinking, education, smoking, and community belonging). Please note that the CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

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Footnote 30

For CCDSS data: Trend analyses were calculated using the Joinpoint software, which tests the statistical significance of the trend over different time periods (P ≤.05). A statistically increasing trend was labelled as "worse" and on the contrary, a statistically decreasing trend was labelled as "better." If the trend was not statistically significant (P >.05), it was reported as "no significant change."

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Footnote 31

Statistics Canada. Table 13-10-0096-01 Health characteristics, annual estimates. Government of Canada. 2023. Available from: https://doi.org/10.25318/1310009601-eng

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Footnote 32

Public Health Agency of Canada. Canadian Chronic Disease Surveillance System (CCDSS), Data Tool 20002019, 2021 Edition. Government of Canada. 2023. Available from: https://health-infobase.canada.ca/ccdss/data-tool/Index

Return to footnote 32 referrer

Footnote 33

Custom tabulations by PHAC for education indicator using CCHS 2022.

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Footnote 34

All data from the CCHS and Canadian Health Measures Survey (CHMS) are representative of Canada, excluding the territories. There are other exclusions in the CCHS that limit its generalizability: "Persons living on reserves and other Aboriginal settlements in the provinces; full-time members of the Canadian Forces; the institutionalized population, children aged 12 to 17 that are living in foster care, and people living in the Quebec health regions of Région du Nunavik and Région des Terres-Cries-de-la-Baie-James."

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Footnote 35

All rates are age-standardized to the 2011 Canadian population.

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Footnote 36

The CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

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Footnote 37

Many CCDSS measures were influenced by the COVID-19 pandemic in 2020–2021 and 2021–2022. As the data should be interpreted with caution, the trend analysis did not include these two years.

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Footnote 38

The CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

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Footnote 39

Heavy alcohol drinking is defined as binge drinking (i.e., five or more drinks for males and four or more drinks for females, on a single occasion) at least once a month in the past year.

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Footnote 40

The CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

Return to footnote 40 referrer

Footnote 41

All rates are age-standardized to the Canadian population. All data from the CCHS and CHMS are representative of Canada, excluding the territories.

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Footnote 42

Many CCDSS measures were influenced by the COVID-19 pandemic in 2020–2021 and 2021–2022. As the data should be interpreted with caution, the trend analysis did not include these two years.

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Footnote 43

Many CCDSS measures were influenced by the COVID-19 pandemic in 2020–2021 and 2021–2022. As the data should be interpreted with caution, the trend analysis did not include these two years.

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Footnote 44

Obesity among adults is defined as a body mass index (BMI) ≥ 30.0 kg/m2. This indicator is based on self-reported weight and height. BMI calculations are adjusted to respondent bias to more closely approximate measured values. Excludes pregnant women and persons less than 3 feet tall or greater than 6 feet 11 inches.

Return to footnote 44 referrer

Footnote 45

The CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

Return to footnote 45 referrer

Footnote 46

This physical activity measure uses self-reported data from the CCHS. Self-reported estimates of physical activity, which report perceived time, are often significantly higher than device-based measures, which measure actual movement. Self-report and device-measured data provide complementary information about different aspects of physical activity but should not be used interchangeably.

Return to footnote 46 referrer

Footnote 47

Numbers come from Statistics Canada—crude rates: Although in surveillance we continue recommending using measured data from the CHMS (also note that the physical activity recommendations within the Canadian 24-Hour Movement Guidelines changed in 2020 to "without bouts"), we recognize that self-reported data (currently only available "with bouts") as presented in this indicator is still useful to examine trends in particular before and during the COVID-19 pandemic.

Return to footnote 47 referrer

Footnote 48

Sense of belonging to a local community illustrates the social attachment of individuals with communities. Social isolation tends to be detrimental to health, while social engagement and attachments are associated with positive health outcomes (both physical and mental).

Return to footnote 48 referrer

Footnote 49

The CCHS underwent a second major redesign in 2022. The redesign centred on a change in data collection mode. As a result, caution should be used when comparing data between 2022 and previous cycles.

Return to footnote 49 referrer

Footnote 50

For Tables 2a and 2b, provincial and territorial differences observed with the CCDSS should be interpreted with caution. Although differences are statistically significant, methodological differences may explain the patterns observed in addition to actual differences in the health status of the populations. For instance, differences in detection and treatment practices, as well as differences in data coding, remuneration models and shadow billing practices likely play a role in the patterns observed.

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Footnote 51

Provincial and territorial data for blood cholesterol and daily sleep are not available.

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Footnote 52

Territorial estimates based on the 2021 CCHS are unavailable. Data are only representative in the territories after two years of data collection. The latest estimates for territories come from the 2019–2020 CCHS (https://www150.statcan.gc.ca/t1/tbl1/en/tv.action?pid=1310011301). The next territorial estimates will come from the 2021–2022 CCHS.

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Footnote 53

Statistics Canada. Table 13-10-0096-01 Health characteristics, annual estimates. Government of Canada. 2023. Available from: https://doi.org/10.25318/1310009601-eng

Return to footnote 53 referrer

Footnote 54

Public Health Agency of Canada. Canadian Chronic Disease Surveillance System (CCDSS), Data Tool 20002022, 2024 Edition. Government of Canada. 2024. Available from: https://health-infobase.canada.ca/ccdss/data-tool/Index

Return to footnote 54 referrer

Footnote 55

Custom tabulations by the Public Health Agency of Canada (PHAC) for education indicator using the 2022 CCHS.

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Footnote 56

Heavy alcohol drinking is defined as binge drinking (i.e., five or more drinks for males and four or more drinks for females, on a single occasion) at least once a month in the past year.

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Footnote 57

All data from the CCHS and CHMS are representative of Canada, excluding the territories. There are other exclusions in the CCHS that limit its generalizability: "Persons living on reserves and other Aboriginal settlements in the provinces; full-time members of the Canadian Forces; the institutionalized population, children aged 12 to 17 that are living in foster care, and people living in the Quebec health regions of Région du Nunavik and Région des Terres-Cries-de-la-Baie-James."

Return to footnote 57 referrer

Footnote 58

All rates are age-standardized to the 2011 Canadian population.

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Footnote 59

Estimate should be interpreted with caution due to high variability.

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Footnote 60

Obesity among adults is defined as a body mass index (BMI) ≥ 30.0 kg/m2. This indicator is based on self-reported weight and height. BMI calculations are adjusted to respondent bias to more closely approximate measured values. Pregnant women excluded.

Return to footnote 60 referrer

Footnote 61

Territorial estimates based on the 2021 CCHS are unavailable. Data are only representative in the territories after two years of data collection. The latest estimates for territories come from the 2019–2020 CCHS (https://www150.statcan.gc.ca/t1/tbl1/en/tv.action?pid=1310011301). The next territorial estimates will come from the 2021–2022 CCHS.

Return to footnote 61 referrer

Footnote 62

Statistics Canada. Table 13-10-0096-01 Health characteristics, annual estimates. Government of Canada. 2023. Available from: https://doi.org/10.25318/1310009601-eng

Return to footnote 62 referrer

Footnote 63

Public Health Agency of Canada. Canadian Chronic Disease Surveillance System (CCDSS), Data Tool 20002019, 2021 Edition. Government of Canada. 2023. Available from: https://health-infobase.canada.ca/ccdss/data-tool/Index

Return to footnote 63 referrer

Footnote 64

This physical activity measure uses self-reported data from the CCHS. Self-reported estimates of physical activity, which report perceived time, are often significantly higher than device-based measures, which measure actual movement. Self-report and device-measured data provide complementary information about different aspects of physical activity but should not be used interchangeably.

Return to footnote 64 referrer

Footnote 65

Numbers come from Statistics Canada—crude rates: Although in surveillance we continue recommending using measured data from CHMS (also note that the physical activity recommendations within the Canadian 24-H Movement Guidelines changed in 2020 to "without bouts"), we recognize that self-reported data (currently only available "with bouts") as presented in this indicator is still useful to examine trends in particular before and during the COVID-19 pandemic.

Return to footnote 65 referrer

Footnote 66

Sense of belonging to a local community illustrates the social attachment of individuals with communities. Social isolation tends to be detrimental to health, while social engagement and attachments are associated with positive health outcomes (both physical and mental).

Return to footnote 66 referrer

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