Health

Description:

This article summarizes the background, history and rationale for the Canadian Health Measures Survey, and provides an overview of the objectives, methods and analysis plans.

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This overview describes the sampling strategy used to meet the collection and estimation requirements of the Canadian Health Measures Survey.

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This article describes how the Canadian Health Measures Survey has addressed the ethical, legal and social issues (ELSI) arising from the survey. The development of appropriate procedures and the rationale behind them are discussed in detail for some specific ELSI.

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This article describes some of the logistical and operational requirement and procedures employed to perform the clinic component of the Canadian Health Measures Survey.

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This article summarizes the design, methods and results emerging from the Canadian Health Measures Survey pre-test, which took place from October through December 2004 in Calgary, Alberta.

Description: Since 2000, Statistics Canada has produced a themed report on population health in its "How Healthy are Canadians?" series. This publication, which is released on an occasional basis, is released free of charge to subscribers of Health Reports, a quarterly peer-reviewed journal.

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The Participation and Activity Limitation Survey (PALS) is Canada's national survey that gathers information about adults and children whose daily activities are limited by a physical, mental, or other health-related condition or problem.

This report presents some basic information about the survey and an overview of the methodological and content changes between the 2001 and 2006 PALS. The major difference involves a change in coverage resulting from the inclusion of a number of aboriginal communities, the addition of the three territories, and the modification to the definition of collective dwellings.

Description:

The Participation and Activity Limitation Survey (PALS) is Canada's national survey that gathers information about adults and children whose daily activities are limited by a physical, mental, or other health-related condition or problem.

This paper is the first in a series of PALS data releases. It contains initial survey results on the number of persons with disabilities, disability rates as well as the type and severity of disability, by age and sex, for Canada, provinces and territories.

Description:

The Participation and Activity Limitation Survey (PALS) is Canada's national survey that gathers information about adults and children whose daily activities are limited by a physical, mental, or other health-related condition or problem.

This document presents data tables associated to the first report "The 2006 Participation and Activity Limitation Survey: A Profile of Disability in Canada".

Description:

The Maternity Experiences Survey (MES) is the first Canadian survey devoted to pregnancy, labour, birth and postpartum experiences. It is a core project of the Canadian Perinatal Surveillance System of the Public Health Agency of Canada who sponsored this survey.

Description:

Optional content to the Canadian Community Health Survey was negotiated by some provinces or territories and for some health regions. The data from that content provide information on the following variables: self esteem, mastery, alcohol dependence, sedentary activities, changes made to improve health, decision latitude at work, home care utilization, social support, influenza immunization, bicycle-helmet use, condom use, tobacco alternatives, smoking cessation aids, physical check-up, eye examination, dental visits, breast examinations and breast self-examinations, blood pressure check, suicidal thoughts and attempts, distress, moods, and spirituality.

Related tables to the Canadian Community Health Survey provide information on the following variables: unmet health-care needs, prostate-specific antigen and former smokers.

Description:

The 2001 Participation and Activity Limitation Survey (PALS) is a post-censal survey of adults and children whose everyday activities are limited because of a condition or health problem. A sample of those persons who answered 'Yes' to the 2001 Census disability filter questions were included in the PALS survey population. Approximately 35,000 adults and 8,000 children living in private and some collective households in the 10 provinces were selected to participate in the survey. The data were collected after the 2001 Census, in the fall of 2001.

These tables contain data on the number of adults and children with disabilities, disability rates, as well as the type and severity of disability, by age and sex, for Canada and the provinces.

Description: Body mass index (BMI), Canadian standard, by age group and sex, household population aged 20 to 64 excluding pregnant women, territories.

Description: Body mass index (BMI), International standard, by age group and sex, household population aged 20 to 64 excluding pregnant women, territories.

Description:

The National Population Health Survey (NPHS) used the Labour Force Survey sampling frame to draw the initial sample of approximately 20,000 households starting in 1994 and for the sample top-up this third cycle. The survey is conducted every two years. The sample collection is distributed over four quarterly periods followed by a follow-up period and the whole process takes a year. In each household, some limited health information is collected from all household members and one person in each household is randomly selected for a more in-depth interview.

The survey is designed to collect information on the health of the Canadian population and related socio-demographic information. The first cycle of data collection began in 1994, and continues every second year thereafter. The survey is designed to produce both cross-sectional and longitudinal estimates. The questionnaires includes content related to health status, use of health services, determinants of health, a health index, chronic conditions and activity restrictions. The use of health services is probed through visits to health care providers, both traditional and non-traditional, and the use of drugs and other mediciations. Health determinants include smoking, alcohol use and physical activity. A special focus content for this cycle includes family medical history with questions about certain chronic conditions among immediate family members and when they were acquired. As well, a section on self care has also been included this cycle. The socio-demographic information includes age, sex, education, ethnicity, household income and labour force status.

Description:

The National Population Health Survey (NPHS) program is designed to collect information related to the health of the Canadian population. The first cycle of data collection began in 1994. The institutional component includes long-term residents (expected to stay longer than six months) in health care facilities with four or more beds in Canada with the principal exclusion of the Yukon and the Northwest Teritories. The document has been produced to facilitate the manipulation of the 1996-1997 microdata file containing survey results. The main variables include: demography, health status, chronic conditions, restriction of activity, socio-demographic, and others.

Description:

Information in this microdata file refers to survey data collected in September - November, 1994 for persons 15 years of age and older in Canada's ten provinces. The survey's main data objectives were to measure the prevalence and patterns of alcohol and other drug use, to assess harm and other consequences of drug use and to evaluate trends in recent patterns of use. Canada's Alcohol and Other Drugs Survey (CADS) also updates and expands upon data collected in the first survey, the National Alcohol and Other Drugs Survey (NADS), conducted in 1989.

Description:

This compendium of vital statistics includes summary data on births, deaths, marriages and divorces. The introduction covers the data sources, data quality, and methods pertaining to each event, and includes a glossary defining the terms used. The first chapter is a brief overview of vital statistics for 1996. Subsequent chapters treat marriage, divorce, birth, fetal and infant mortality, total mortality, causes of death, vital statistics by census division, and international comparisons. Most charts and tables show Canada data for 1986 though 1996, while the charts and tables for causes of death show Canada data for 1979 through1996. Data for the provinces and territories are usually shown for 1995 and 1996. Appendices include population denominator data, age-standardized mortality rate (ASMR) calculation methods, and leading causes of death methodology.

Description:

Statistics in the tables of Section B are in two divisions. Series Bl-81 contain data on vital statistics and series B82-543 on health. Data on social welfare, formerly contained in this section, are presented separately in Section C.

Description:

Cycle 11 collected data from persons 15 years and older and concentrated on help given or received during temporary difficult times or out of necessity due to long-term health or physical limitations in daily activities either inside or outside the household. The target population of the General Social Survey consisted of all individuals aged 15 and over living in a private household in one of the ten provinces.

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

Description: This infographic features the highlights of the Canadian Survey on Disability, 2022.

Description: This video features the highlights of the Canadian Survey on Disability, 2022, using American Sign Language (ASL).

Description: The Health of Canadians infographic aims to provide a snapshot into the population health of Canadians by highlighting health data from the annual report. It includes key statistics on population health such as health outcomes (e.g., chronic conditions), health behaviours (e.g., smoking and alcohol consumption) and access to health care.

Description: This report presents a conceptual framework of Canada’s care economy. This framework is based on a review of Canadian and international research on the topic as well as consultations with key stakeholders and experts. The report summarizes relevant research on the care economy, delineates the scope and boundaries for the Canadian context, and proposes key definitions of paid and unpaid care work.

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

Description: At the onset of the COVID-19 pandemic, there was an overrepresentation of males in COVID-19 deaths worldwide, with Canada reporting more female COVID-19 deaths. This study examines the overrepresentation of female COVID-19 deaths in Canada, with an immigration lens. This study also evaluates whether there is a sex difference in COVID-19 deaths by immigrant status in Canada and, if so, for which age groups and in which provinces or census metropolitan areas (CMAs).

Description: On average, 45% of Canadian adults meet the recommended 150 minutes per week of moderate-to-vigorous physical activity. Using six combined cycles of the Canadian Health Measures Survey (2007 to 2019), this study examines how the percentage of Canadian males and females aged 18 to 79 years meeting the physical activity recommendation differs across socio-demographic, family arrangement and health factors. The purpose of this paper is to determine how sex, age and family arrangement intersect with known risk factors for physical inactivity to identify groups within the Canadian population most at risk of not meeting the physical activity recommendation.

Description: This study examines the relationship between income and food insecurity, looking at families most at risk, as well as the possible role of assets and debts in food insecurity.

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

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.

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.

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.

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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.

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.

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.