Health

Description: The two primary objectives of the General Social Survey (GSS) are: to gather data on social trends in order to monitor changes in the living conditions and well being of Canadians over time; and to provide information on specific social policy issues of current or emerging interest. The core content on health covered short and long term disability, well-being, height and weight, health problems, smoking alcohol use, physical activity, sleep and use of health care services.

Description: The main objective of the Youth Smoking Survey (YSS) is to provide current information on the smoking behaviour of students in grades 5 to 9 (in Quebec primary school grades 5 and 6 and secondary school grades 1 to 3), and to measure changes that occurred since the last time the survey was conducted. Additionally, the survey collects basic data on alcohol and drug use by students in grades 7 to 9 (in Quebec secondary 1 to 3). Results of the Youth Smoking Survey will help with the evaluation of anti-smoking and anti-drug use programs, as well as with the development of new programs.

Description: The data will be used by Health Canada, the Health Promotion Directorate as well as Researchers for alcohol and other drug use in Canada. Information will be used to inform the decision making and program planning efforts of policy makers, practitioners and researchers.

Description: The main purpose of this survey is to collect data to monitor cigarette smoking in Canada and attempt to measure the effect of cigarette price reductions on smoking behaviour.

Description: The results from this survey will be used to develop new programs to educate and inform the public, and to determine the need for new services.

Description: The main objective of the survey is to provide continual and reliable data on tobacco, alcohol and drug use and related issues, with the primary focus on 15 to 24 year olds.

Description: The two primary objectives of the General Social Survey (GSS) are: to gather data on social trends in order to monitor changes in the living conditions and well being of Canadians over time; and to provide information on specific social policy issues of current or emerging interest. The purpose of this survey is to provide a snapshot of the lives of caregivers and care receivers in today's Canada.

Description: The objective of the survey was to provide information on the experiences of respondents in using some selected health care services. The survey focused on two main topics: waiting for specialized services for a new illness or condition and access to basic health care.

Description: The NPHS Health Institutions Component survey data support national level estimates only.

Description: The National Population Health Survey (NPHS) collects information related to the health of the Canadian population and related socio-demographic information.

Description: The public use microdata file (PUMF) from the Canadian Health Survey on Seniors (CHSS) provides data at the provincial level. Over the two-year period, data were collected from approximately 42,000 respondents aged 65 or older, residing in households in all provinces.

The file includes information on a wide range of topics, including oral health, care receiving, community service use, access to health care services, vaccines, smoking, alcohol consumption, general health, chronic health conditions and provides information on the socio-demographic characteristics of the population.

Note: The Canadian Health Survey on Seniors (CHSS) is a supplement to the Canadian Community Health Survey (CCHS) - Annual component.

Description: The public use microdata file (PUMF) from the Canadian Community Health Survey (CCHS) provides data for health regions and combinations of health regions across Canada. Over the two year period, data are based on interviews with approximately 130,000 respondents aged 12 or older, residing in households in all provinces and territories.

The files include information on a wide range of topics, including: physical activity, height and weight, smoking, exposure to second hand smoke, alcohol consumption, general health, chronic health conditions, injuries, and use of health care services. It also provides information on the socio-demographic, income and labour force characteristics of the population.

Description: This dashboard allows users to examine data on barriers to accessibility experienced by persons with disabilities. These are barriers encountered in different aspects of daily living including those found in public spaces; communicating in different situations; using the Internet and barriers related to behaviours, misconceptions or assumptions by others. The data can be organized by province, gender and other characteristics such as age group. This dashboard is based on the 2022 Canadian Survey on Disability.

Description: Differences in the number and proportions of persons with disabilities who experienced one or more barriers to accessibility, by the type of disability, age group and gender, Canada.

Description: Differences in the number and proportions of persons with disabilities who experienced one or more barriers to accessibility, by the severity of the disability, age group and gender, Canada.

Description: Differences in the number and proportions of persons with disabilities who experienced a barrier to accessibility, Canada, provinces and territories.

Description: This dashboard provides an interactive view of eight indicators from the Quality of Life Framework for Canada: Life satisfaction, sense of meaning and purpose, future outlook, loneliness, someone to count on, sense of belonging to local community, perceived mental health, and perceived health. The data can be organized by province, gender and other characteristics such as age group. This dashboard is based on quarterly data from the Canadian Social Survey.

Description: Percentage of persons aged 15 years and over by level of life satisfaction, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by level of life satisfaction, by gender and other selected sociodemographic characteristics: age group; immigrant status; visible minority group; Indigenous identity; persons with a disability, difficulty or long-term condition; LGBTQ2+ people; highest certificate, diploma or degree; main activity; and urban and rural areas.

Description: Percentage of persons aged 15 years and over by level of sense of meaning and purpose, by gender, for Canada, regions and provinces.

Description: This infographic details the prevalence of vitamin D inadequacy among the Canadian population aged 3 to 79 by focusing on risk factors as well as behaviours that can reduce the likelihood of low vitamin D.

Description: Individuals who are nearing death report a preference to be cared for and to die outside of hospital. The reasons for this preference are complex and multifactorial. This study examined differences in the use of end-of-life acute care and the location of death among residents with dementia in rural long-term care homes, compared with those in urban long-term care homes, in Ontario, Canada.

Description: Mental health disparity is associated with diverse characteristics, such as gender, socioeconomic status, Indigenous identity, immigrant status, race, disability, and sexual orientation. However, intersectional studies on women’s mental health have been rare, particularly during the COVID-19 pandemic period. To fill this research gap, this study examines women’s and girls’ self-reported mental health before and during the COVID-19 pandemic using seven characteristics, including Indigenous identity, immigrant status, racialized background, LGB+ sexual orientation, disability, and socioeconomic status (low income and unemployment).

Description:

Health Reports, published by the Health Analysis Division of Statistics Canada, is a peer-reviewed journal of population health and health services research. It is designed for a broad audience that includes health professionals, researchers, policymakers, and the general public. The journal publishes articles of wide interest that contain original and timely analyses of national or provincial/territorial surveys or administrative databases. New articles are published electronically each month.

Health Reports had an impact factor of 5.0 for 2022 and a five-year impact factor of 5.6. All articles are indexed in PubMed. Our online catalogue is free and receives more than 700,000 visits per year. External submissions are welcome.

Description: This article provides insights into the rates of COVID-19 mortality among First Nations peoples and Métis living in private dwellings and the social determinants of COVID-19 mortality among these populations using data from the 2016 Canadian Census Health and Environment Cohorts linked to the Canadian Vital Statistics – Death Database from 2016 to 2021.

Description: Release published in The Daily – Statistics Canada’s official release bulletin

Description: Release published in The Daily – Statistics Canada’s official release bulletin

Description: Using data from the 2022 Canadian Survey on Disability (CSD), this factsheet examines the experiences of 2SLGBTQ+ persons with disabilities. It provides information on various sociodemographic and disability characteristics, such as age, disability type, severity of disability, and employment. It also includes comparisons to the non-2SLGBTQ+ persons with disabilities population by age group.

Description: The Canadian Survey on Disability (CSD) is a national survey of Canadians aged 15 and over whose everyday activities are limited because of a long-term condition or health-related problem.

Description: This study presents an updated sociodemographic profile of children aged 0 to 14 years with affirmative responses largely based on parent reports to the questions on the 2021 Census long-form questionnaire about difficulties with activities of daily living.

Description:

Introductory video for the survey provided to respondents at the household and posted on the Canadian Health Measures Survey Respondent relations (Statcan) website.

Description:

The Canadian Survey on Disability (CSD) is a national survey of Canadians aged 15 and over whose everyday activities are limited because of a long-term condition or health-related problem.

The 2012 CSD Concepts and Methods Guide is designed to assist data users by providing relevant information on survey content and concepts, sampling design, collection methods, data processing, data quality and product availability. Chapter 1 of this guide provides an overview of the 2012 CSD by introducing the survey's background and objectives. Chapter 2 explains the key concepts and definitions and introduces the indicators measured by the CSD questionnaire modules. Chapters 3 to 6 cover important aspects of survey methodology, from sampling design to data collection and processing. Chapters 7 and 8 cover issues of data quality, including the approaches used to minimize and correct errors throughout all stages of the survey. Users are cautioned against making comparisons with data from previous Participation and Activity Limitations Surveys. Chapter 9 outlines the survey products that are available to the public, including data tables, a fact sheet and reference material. Appendices provide more detail on survey indicators as well as a glossary of terms.

Description:

Mental illnesses largely involve alterations in mood, thinking, and behaviour, as well as other domains of mental functioning, and affect almost all Canadians in some way, either directly or indirectly. They routinely cause significant impairments in emotional functioning, which may lead to social or physical limitations. In some cases, such as in agoraphobia, individuals cannot even leave their homes due to intense anxiety; depression can cause an individual to lose all interest in life. This document describes the mental illnesses that have the greatest impact on Canadians in terms of prevalence or severity of disability, and how they affect the health status of Canadians.

Description:

This report presents the results of the 3rd Consensus Conference on Health Indicators that was convened in March 2009, including information that was presented at the conference, a summary of the consultation process leading up to the event, and the priority health areas deemed most important for future indicator development work.

The conference marked the 10th anniversary of the Health Indicators project, a collaboration between Statistics Canada and Canadian Institute for Health Information (CIHI). The goal of the project is to provide health regions, health care providers and the public in general with reliable and comparable data on the health of Canadians and to assist stakeholders and decision makers in the use and interpretation of the indicator data.

Description:

Since 2007/2008, Statistics Canada has centred analysis of data holdings related to health as well as our program of dissemination of health research within the new Health Information and Research Division (HIRD).

The new division has launched a comprehensive approach to analytical planning including environmental scanning and consultation; establishment of strategic multi-year priorities for health research at Statistics Canada; a process of project selection and review that ensures that analytical effort addresses our priorities; metrics to measure our adherence to priorities and the impact of our analytical effort; and communication and dissemination of analytical plans.

This multi-year analytical plan identifies the key high-level priority areas for Statistics Canada's investment in health research for 2008/2009 to 2010/2011, and serves as a blueprint for subsequent operational research planning.

Description:

This special methodological paper will help readers understand and assess reports that rank the health status or health system performance of a country, province or jurisdiction. The report outlines the components and processes that underlie health rankings, explores why such rankings can be difficult to interpret and includes a plain-language checklist to use as a critical evaluative resource when reading health-ranking reports.

Description:

This report highlights the latest developments and rationale behind recent cycles of the General Social Survey (GSS). Starting with an overview of the GSS mandate and historic cycle topics, we then focus on two recent cycles related to families in Canada: Family Transitions (2006) and Family, Social Support and Retirement (2007). Finally, we give a summary of what is to come in the 2008 GSS on Social Networks, and describe a special project to mark 'Twenty Years of GSS'.

The survey collects data over a twelve month period from the population living in private households in the 10 provinces. For all cycles except Cycles 16 and 21, the population aged 15 and older has been sampled. Cycles 16 and 21 sampled persons aged 45 and older.

Cycle 20 (GSS 2006) is the fourth cycle of the GSS to collect data on families (the first three cycles on the family were in 1990, 1995 and 2001). Cycle 20 covers much the same content as previous cycles on families with some sections revised and expanded. The data enable analysts to measure conjugal and fertility history (chronology of marriages, common-law unions, and children), family origins, children's home leaving, fertility intentions, child custody as well as work history and other socioeconomic characteristics. Questions on financial support agreements or arrangements (for children and the ex-spouse or ex-partner) for separated and divorced families have been modified. Also, sections on social networks, well-being and housing characteristics have been added.

Description:

The Record Linkage Overview describes the process used in annual internal record linkage of the Canadian Cancer Registry. The steps include: preparation; pre-processing; record linkage; post-processing; analysis and resolution; resolution entry; and, resolution processing.

Description:

The compendium of Canadian Cancer Registry procedures manuals set out the rules for reporting cancer data to the CCR for all provincial and territorial cancer registries.

Description:

The Record Linkage Overview describes the process used in annual internal record linkage of the Canadian Cancer Registry. The steps include: preparation; pre-processing; record linkage; post-processing; analysis and resolution; resolution entry; and, resolution processing.