Health

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: 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: The Joint Canada/United States Survey of Health (JCUSH) will collect information from both Canadian and U.S. residents, about their health, their use of health care and their functional limitations.

Description: The Canadian Community Health Survey - Nutrition is a national health survey that collected information from Canadians about their eating habits and use of nutritional supplements, as well as other health factors.

Description: This survey collected new statistical information to measure the size and scope of the natural health product activities in Canada. National estimates of products manufactured, imported and sold in Canada were produced by product class, based on active ingredients used.

Description: The principal survey objective was to create a comprehensive national source of objective information about the prices faced by persons with disabilities, their families, and health and social service organizations.

Description: The Canadian Health Measures Survey (CHMS) aims to collect important health information through a household interview and direct physical measures at a mobile examination centre (MEC), sometimes referred to as a mobile clinic.

Description: The National Survey of the Work and Health of Nurses (NSWHN) focuses on the work and health of nurses in Canada.

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:

The National Population Health Survey (NPHS) is designed to enhance the understanding of the processes affecting health. The survey collects cross-sectional as well as longitudinal data. In 1994/95 the survey interviewed a panel of 17,276 individuals, then returned to interview them a second time in 1996/97. The response rate for these individuals was 96% in 1996/97. Data collection from the panel will continue for up to two decades. For cross-sectional purposes, data were collected for a total of 81,000 household residents in all provinces (except people on Indian reserves or on Canadian Forces bases) in 1996/97.

This overview illustrates the variety of information available by presenting data on perceived health, chronic conditions, injuries, repetitive strains, depression, smoking, alcohol consumption, physical activity, consultations with medical professionals, use of medications and use of alternative medicine.

Description:

The statistical tables in the first part of this document relate to the numbers and rates of live births and stillbirths of at least twenty weeks gestation; total, general and age specific fertility rates; live births by age of mother and order of live birth; male and female birth weights by age of mother and gestation period at the time of birth; and live births by census division and counties in the province(s).

In the second part of this document, the statistical tables, for Canada, the ten provinces and the two territories, relate to the numbers and rates of deaths by marital status, age and sex; infant, neonatal, postnatal and perinatal deaths; maternal deaths; and stillbirths of at least twenty weeks gestation at the time of birth.

Description:

The special ten year anniversary edition of Canadian cancer statistics 1997 represents a collaborative effort between Statistics Canada, the National Cancer Institute of Canada, Health Canada, the Canadian Cancer Society, and provincial/territorial cancer registries. This 71 page monograph contains estimates of cancer incidence and mortality for 1997, historical (actual and estimated) data from 1969 to 1997, and selected indicators on the burden of cancer. Estimates were produced by modelling actual cancer incidence and mortality data by province for selected cancer sites. The special topic this year is a comparison of the burden of cancer in Canada in 1997 to that reported in the first edition in 1987.

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

Description: This infographic presents information on pedestrian fatalities collected from the Canadian Coroner and Medical Examiner Database (CCMED). This infographic illustrates demographic profile of the deceased such as sex and age. The product also summarizes information on select circumstances surrounding pedestrian fatalities.

Description: The COVID-19 pandemic had a detrimental impact on the physical activity and screen time of youth, in particular among girls. Using The Canadian Community Health Survey, the purpose of this study is to give an update on the screen time and physical activity habits of Canadian youth in 2021 by providing a comparison with values previously reported before and during the first year of the pandemic. This study takes a focused look at how the physical activity and screen time of boys and girls were affected differently.

Description: Canadian and international research have shown that the COVID-19 pandemic led to changes in health behaviours, including participation in physical activity and screen time. Using The Canadian Community Health Survey, the purpose of this study is to compare screen time and physical activity before and during the 2020 and 2021 pandemic years among Canadian adults and older adults.

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

Description: Using combined data from the Canadian Community Health Survey (CCHS) from 2017 to 2020, this study examines various indicators of access to primary health care providers (referred to as regular health care providers in the CCHS) and usual places of care among First Nations people living off reserve, Métis and Inuit. These indicators are explored by various socio-demographic characteristics, including sex, age, income, region, and remoteness.

Description: Using data from the Survey on Accessible Print Material (SAPM), this American Sign Language video examines access to alternate format material among Canadians who had difficulties with print material.

Description: Using data from the Survey on Accessible Print Materials (SAPM), this factsheet examines the experiences of persons who have difficulties with print materials. It provides information on the usage of assistive aids, devices and technologies for a difficulty with print material. As well as information on the usage of alternate formats, how these formats are accessed and barriers encountered in obtaining them.

Description: Using data from the 2022 Mental Health and Access to Care Survey, this article provides updated prevalence estimates for some of the most common mental disorders, including mood, anxiety, and substance use disorders. These results are compared to those from the previous 2012 and 2002 Canadian Community Health Survey – Mental Health cycles. This article also describes some key aspects of mental health care services in Canada.

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.

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 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.

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.

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.