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All (2,334) (2,310 to 2,320 of 2,334 results)

  • Surveys and statistical programs – Documentation: 5113
    Description: The survey collects expenditure data on health research and development activities by therapeutic class in the Canadian business enterprise sector.

  • Surveys and statistical programs – Documentation: 5125
    Description: The Canadian Coroner and Medical Examiner Database (CCMED), by storing information on deaths reported to Coroners and Medical Examiners (C/MES), will facilitate the identification and characterization of emerging and known safety hazards with the aim of contributing to a decrease in preventable deaths among Canadians.

  • Surveys and statistical programs – Documentation: 5138
    Description: The general purpose of the survey is to measure Canadians' experiences with health care, specifically, experiences with various types of doctors and clinics, access to different types of health care including emergency room and prescription medication use. Special attention was given to respondents diagnosed with certain chronic conditions in terms of their general experiences and their participation in managing their own health care.

  • Surveys and statistical programs – Documentation: 5144
    Description: The Longitudinal and International Study of Adults collects information from people across Canada about their jobs, education, health and family. The study is also interested in how changes in these areas have affected people's lives. This survey aims to help improve education, employment, training and social services in Canada.

  • Surveys and statistical programs – Documentation: 5146
    Description: The purpose of the Canadian Community Health Survey - Healthy Aging is to collect new information about the factors, influences and processes that contribute to healthy aging. The survey focuses on the health of Canadians aged 45 and over.

  • Surveys and statistical programs – Documentation: 5152
    Description: Statistics Canada is conducting a test of new survey modules on mental health stigma and discrimination. In addition to the new modules, the test questionnaire includes Canadian Community Health Survey modules on general health, health status, income and sociodemographic characteristics.

  • Surveys and statistical programs – Documentation: 5160
    Description: The purpose of the Survey on Living with Chronic Diseases in Canada (SLCDC) is to provide information on the impact of chronic disease on individuals, as well as how people with chronic disease manage their health condition.

  • Surveys and statistical programs – Documentation: 5172
    Description: This is a national longitudinal survey that collects information on the transition from military to civilian life, general health and well-being, chronic conditions, labour force participation and other related information. An important goal of the survey is to understand the transition period from military to civilian life and health outcomes in Canadian Veterans.

  • Surveys and statistical programs – Documentation: 5182
    Description: The purpose of the Survey on Living with Neurological Conditions in Canada is to collect new information about Canadians' experiences with chronic neurological conditions. The survey will report on various factors that impact on health for individuals living with these conditions, their families and caregivers.

  • Surveys and statistical programs – Documentation: 5184
    Description: This pilot survey asks both smokers and non-smokers about their past and present smoking habits, their attitudes towards smoking, and other related issues.
Data (896)

Data (896) (20 to 30 of 896 results)

Analysis (1,311)

Analysis (1,311) (0 to 10 of 1,311 results)

  • Stats in brief: 11-001-X202002820365
    Description: Release published in The Daily – Statistics Canada’s official release bulletin
    Release date: 2020-01-28

  • Stats in brief: 11-627-M2020002
    Description:

    The 2018 General Social Survey on Caregiving and Care Receiving collects information on Canadians who provide care to family and friends with a long-term health condition, disability or problems related to aging. The survey also covers individuals who receive this care and about the challenges both groups face. This infographic provides an overview of selected key findings for care receivers in Canada in 2018.

    Release date: 2020-01-22

  • Articles and reports: 82-003-X202000100001
    Description:

    This study uses the 1996 and 2011 Canadian Census Health and Environment Cohorts (CanCHECs), with a five-year mortality follow-up, to estimate the life expectancy (LE) of the household population. It also incorporates information from two national health surveys to estimate health-adjusted life expectancy (HALE). The objectives of this study are to examine LE, HALE and disparities in LE and HALE in the 1996 and 2011 cohorts at ages 25 and 65 for men and women, according to highest level of educational attainment and household income quintile; to examine these disparities according to the combination of education and income in the 2011 cohort; and to examine how education- and income-related disparities in LE and HALE changed over time.

    Release date: 2020-01-15

  • Articles and reports: 82-003-X202000100002
    Description:

    Using data from the Canadian Cancer Registry, this study examines thyroid cancer (TC) incidence from 1992 to 2016. It presents sex-specific incidence estimates according to age, histology and province for the most recent five-year period (2012 to 2016), and examines changes in rates over the entire period. These findings are supplemented with similar information on TC mortality and five-year net survival.

    Release date: 2020-01-15

  • Stats in brief: 11-001-X202001522784
    Description: Release published in The Daily – Statistics Canada’s official release bulletin
    Release date: 2020-01-15

  • Stats in brief: 11-627-M2020004
    Description:

    This infographic examines life expectancy and health expectancy of the Canadian population at age 25 or older by education and income.

    Release date: 2020-01-15

  • Journals and periodicals: 82-003-X
    Geography: Canada
    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 2.768 for 2018 and a five-year impact factor of 2.905. All articles are indexed in PubMed. Our online catalogue is free and receives more than 500,000 visits per year. External submissions are welcome.

    Release date: 2020-01-15

  • Articles and reports: 75-006-X202000100001
    Description:

    Many Canadians are providing care or help to someone with a long-term health condition, a physical or mental disability, or problems related to aging. Support given to caregivers may help alleviate potential economic and health-related implications of caregiving. This study uses the 2018 General Social Survey - Caregiving and Care Receiving (Cycle 32) to examine the types of support provided to caregivers. It also examines the relationship between unmet support needs and some indicators of well-being.

    Release date: 2020-01-08

  • Stats in brief: 11-001-X202000821983
    Description: Release published in The Daily – Statistics Canada’s official release bulletin
    Release date: 2020-01-08

  • Stats in brief: 11-627-M2020001
    Description:

    The 2018 General Social Survey on Caregiving and Care Receiving collects information on Canadians who provide care to family and friends with a long-term health condition, disability or problems related to aging. The survey also covers individuals who receive this care and about the challenges both groups face.

    This infographic provides an overview of selected key findings for caregivers in Canada in 2018.

    Release date: 2020-01-08
Reference (103)

Reference (103) (20 to 30 of 103 results)

  • Surveys and statistical programs – Documentation: 82-225-X20070109650
    Description:

    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.

    Release date: 2007-06-21

  • Surveys and statistical programs – Documentation: 82-225-X20060099202
    Description:

    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.

    Release date: 2006-07-07

  • Surveys and statistical programs – Documentation: 82-225-X20060099203
    Description:

    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.

    Release date: 2006-07-07

  • Surveys and statistical programs – Documentation: 82-225-X20060099204
    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.

    Release date: 2006-07-07

  • Surveys and statistical programs – Documentation: 82-225-X20060099205
    Description:

    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.

    Release date: 2006-07-07

  • Surveys and statistical programs – Documentation: 82-225-X20060099206
    Description:

    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.

    Release date: 2006-07-07

  • Surveys and statistical programs – Documentation: 82-619-M2006003
    Description:

    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.

    Release date: 2006-04-04

  • Surveys and statistical programs – Documentation: 84-548-X
    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.

    Release date: 2005-11-23

  • Surveys and statistical programs – Documentation: 82-619-M2005002
    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.

    Release date: 2005-09-30

  • Surveys and statistical programs – Documentation: 82-619-M2005001
    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.

    Release date: 2005-08-16

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