Health

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 purpose of the Canadian Community Health Survey - Mental Health (CCHS - Mental Health) is to collect information about mental health status, access to and perceived need for formal and informal services and supports, functioning and disability, and covariates.

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

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Distribution of market, total and after-tax income by disability status for persons aged 16 years and over and persons aged 25 to 54, Canada and regions, annual.

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Income of individuals by disability status, age group, sex and income source, Canada, annual.

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Distribution of employment income of individuals by disability status, sex and work activity, Canada, annual.

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Poverty and low-income statistics by disability status, age group, sex and economic family type, Canada, annual.

Description: Number and percentage of persons by household food security status and economic family type, Canada and provinces.

Description: Number and percentage of persons by household food security status, age group, sex, visible minority group, Indigenous group and immigration status, Canada and provinces.

Description: Number and percentage of persons aged 16 years and over with unmet health care needs by sex (Canada and provinces) and age group (Canada only).

Description: Differences in the number and proportion of persons with and without disabilities, by age group and gender, Canada, provinces and territories.

Description: Differences in the number and proportion of persons with disabilities with either mild, moderate, severe, or very severe disabilities, by age group and gender, Canada, provinces and territories.

Description: Oral health is a crucial component of overall health, influencing both physical and mental well-being. Yet, despite the important role that access to and use of oral health care services play in maintaining optimal oral health, substantial disparities remain in access to oral health care services across population groups in Canada. Using data from the 2022 Canadian Community Health Survey, this study examines the association of dental insurance with oral health care access and use in Canada while accounting for income and sociodemographic factors. It contributes to a baseline of oral health care disparities before the implementation of the Canadian Dental Care Plan.

Description: Children’s oral health can affect functional capacities, psychological well-being, and social integration. Additionally, health behaviours established in childhood extend into adulthood and can influence oral health outcomes later in life. Using data from the 2019 Canadian Health Survey on Children and Youth, this study investigates the association between dental insurance, income, and dental care access for Canadian children and youth aged 1 to 17 years. It contributes to a baseline understanding of oral health care use before the implementation of the Canadian Dental Care Plan.

Description: This infographic provides estimates on health care workers' stress, alcohol consumption and positive health behaviours during the COVID-19 pandemic. Estimates are provided across three primary health care worker groups: nurses, physicians, and Personal Support Workers/Care Aides (PSWs/CAs).

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

Description: This infographic investigates sandwich caregiving in Canada in 2022, defined as providing care in the past 12 months to both children under 15 years old and care-dependent adults and youth over 15 years old with a long-term condition or disability. The infographic explores the prevalence of sandwich caregiving, the types of relationships involved, and the impacts of this type of caregiving.

Description: Using data from the 2022 Canadian Social Survey Wave 6 (Well-being and caregiving), this study explores unpaid caregiving in the past 12 months for care-dependent groups (children under 15 years old or adults and youth over 15 years old with a long-term condition or disability). This paper explores: Who are the unpaid caregivers, including "sandwich" caregivers? How much unpaid care is provided and to whom? What are the impacts of this unpaid caregiving on well-being, especially the gendered differences?

Description: Growing Up in Québec is a longitudinal population survey that began in the spring of 2021 at the Institut de la statistique du Québec. Among the children targeted by this longitudinal follow-up, some will experience developmental difficulties at some point in their lives. Those same children often have characteristics associated with higher sample attrition (low-income family, parents with a low level of education). This article describes the two main challenges we encountered when trying to ensure sufficient representativeness of these children, in both the overall results and the subpopulation analyses.

Description: Respondents to typical household surveys tend to significantly underreport their potential use of food aid distributed by associations. This underreporting is most likely related to the social stigma felt by people experiencing great financial difficulty. As a result, survey estimates of the number of recipients of that aid are much lower than the direct counts from the associations. Those counts tend to overestimate due to double counting. Through its adapted protocol, the Enquête Aide alimentaire (EAA) collected in late 2021 in France at a sample of sites of food aid distribution associations, controls the biases that affect the other sources and determines to what extent this aid is used.

Description: As the importance of subjective well-being to health continues to garner increasing attention from researchers and policy makers, community belonging has emerged as a potential population health target that has been linked to several self-rated measures of health and well-being in Canada. This study assessed novel area-level community belonging measures derived using small area estimation and examined associations with individual-level measures of community belonging and self-rated health.

Description: Canada is experiencing rapid population aging, which has a wide range of implications, including an increased need for health care services. However, very few studies have examined use of specialized health care services (e.g., visits to medical specialists, non-emergency tests, and surgeries) among older Canadians. Using data from the 2019/2020 Canadian Health Survey on Seniors, this study examines the prevalence of specialized health care service use and evaluates the association of predisposing factors, enabling resources, and need-related factors with specialized health care service use in the past 12 months among Canadians aged 65 or older.

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The User Guide to Record Linkage Feedback Reports C1 and C2 is intended for the users of the reports. The reports were developed to facilitate the exchange of information and decisions between the Canadian Cancer Registry and the Provincial and Territorial Cancer Registries.

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The User Guide to Record Linkage Feedback Reports C1 and C2 is intended for the users of the reports. The reports were developed to facilitate the exchange of information and decisions between the Canadian Cancer Registry and the Provincial and Territorial Cancer Registries.

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The user guide to Death Clearance Feedback Reports is intended for users of the feedback reports. The feedback reports were developed to facilitate the exchange of information and decisions between the Canadian Cancer Registry and the Provincial and Territorial Cancer Registries.

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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.

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The Death Clearance Overview document describes the Death Clearance module of the Canadian Cancer Registry, its structure, its function and its role in the operation of the national cancer registry. Inputs and outputs are listed and briefly described, as well as the different steps constituting the Death Clearance process.

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The Guidelines for Abstracting and Determining Death Certificate Only Cases are intended for use by all provincial and territorial cancer registries during their Death Clearance Process. The guidelines should be used when performing a comparison between the Death Certificate Notification and the cancer registry database.

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This document examines the functional limitations, physical, emotional and social, related to the musculoskeletal conditions having the largest impact on the health of Canadians. These functional limitations are described and classified using the Classification and Measurement System of Functional Health (CLAMES).

These descriptions and classifications are the first step in a new approach to measuring the health of Canadians that examines what factors are adversely affecting population health and how to address them. This document also provides health professionals, advocacy groups, and individual Canadians with an overview of how living with certain musculoskeletal conditions affects day-to-day functioning.

Description:

This report describes the design, methodology, and results of the first study undertaken by Statistics Canada to measure the impact on Canadian cause of death trends of a new revision of the World Health Organization's International Classification of Diseases (ICD).

Using 1999 Canadian mortality data, Statistics Canada carried out a comparability, or "bridge-coding", study by dual-coding deaths to both the Ninth and Tenth Revisions of the International Classification of Diseases (ICD-9 and ICD-10). The preliminary results of this exercise were used to generate comparability ratios; these ratios measure the net effect of the new revision, with ratios above 1.00 indicating a net increase in deaths classified to a cause of death, and ratios below 1.00 indicating a net decrease.

The comparability ratios derived from dual-coding medical certificates of cause of death presented in this report estimate the size and direction of the disruption to cause of death trends due to the implementation of ICD-10. Researchers and analysts using Canadian mortality data should use these summary measures to calculate comparability-modified death counts and mortality rates to bridge the gap between ICD-9 and ICD-10.

Description:

This document examines the functional limitations-physical, emotional and social-related to the most common types of diabetes and the conditions that result from the disease. These functional limitations are described and classified using the Classification and Measurement System of Functional Health (CLAMES).

These descriptions and classifications are the first step in a new approach to measuring the health of Canadians that examines what factors are adversely affecting population health and how to address them. This document also provides health professionals, advocacy groups, and individual Canadians with an overview of how living with diabetes affects day-to-day functioning.

Description:

This document examines the functional limitations - physical, emotional and social -experienced by patients at the time of diagnosis of cancer and as they undergo various treatments, remission, and palliative and terminal care. These functional limitations are described and classified using the Classification and Measurement System of Functional Health (CLAMES).

These descriptions and classifications are the first step in a new approach to measuring the health of Canadians that examines what factors are adversely affecting population health and how to address them. This document also provides health professionals, advocacy groups, and individual Canadians with an overview of how living with cancer affects day-to-day functioning.