Health

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 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:

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.

Description:

This article reports recent trends in influenza vaccination rates in Canada, provides data on predictors of vaccination for 2005, and examines longer-term effects of Ontario's universal influenza immunization program on vaccine uptake. The data are from the 1996/1997 National Population Health Survey and the 2000/2001, 2003 and 2005 Canadian Community Health Survey.

Description:

This article examines differences in birth outcomes by neighbourhood income and recent immigration for singleton live births in Toronto. The birth data were extracted from hospital discharge abstracts compiled by the Canadian Institute for Health Information.

Description:

This article compares levels of work stress - a factor that has been linked to poor physical and mental health and to occupational injury - among various types of health care providers. Associations between stress and selected job-related, socio-demographic and personal characteristics are also described. The data are from the 2003 Canadian Community Health Survey.

Description:

This article presents a profile of Canadians aged 60 or older who had sustained a hip fracture and were living in a household during the year after that fracture. The information is based on data from the 2003 Canadian Community Health Survey.

Description:

This publication presents a series of research articles based on cross-sectional data collected from Cycle 2.2 of the Canadian Community Health Survey, focusing on Nutrition. It also provides links to tables, other research articles and information about the survey.

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: Percentage of persons aged 15 years and over by level of sense of meaning and purpose, 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 frequency with which they have a hopeful outlook, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by frequency with which they have a hopeful outlook, 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 frequency with which they feel lonely, by gender, for Canada, regions and provinces.

Description: Percentage of persons aged 15 years and over by frequency with which they feel lonely, 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: Self-perceived general health of First Nations people living off reserve, Métis and Inuit by age group and gender, Canada, provinces and territories.

Description: Extreme heat has significant impacts on mortality. In Canada, past research has analyzed the degree to which non-accidental mortality increases during single extreme heat events; however, few studies have considered multiple causes of death and the impacts of extreme heat events on mortality over longer time periods. This study analyzes the impacts of extreme heat events on nonaccidental, cardiovascular, and respiratory deaths from 2000 to 2020 in 12 of the largest cities in Canada.

Description: Optimal oral health is an essential element of healthy aging. Oral health problems such as tooth loss, periodontal disease, and dry mouth accumulate throughout adult life and worsen with increasing age. Using data from the 2019/2020 Canadian Health Survey on Seniors, this study explores the link between dental insurance, income, and oral health care access among seniors (aged 65 and over) in Canada. It contributes to the understanding of oral health care among seniors before the implementation of the Canadian Dental Care Plan.

Description: This article examines trends in rates of employment and unemployment, as well as hourly wages and work hours, for the year 2023, and explores how disability intersects with age, sex, educational attainment, and racialized groups to influence labour market outcomes.

Description: The purpose of this document is to define the concept of peer groups, to give an overview of how they are created and to demonstrate their usefulness. This paper presents the 2023 classification of the peer groups.

Description: The Health Research Working Paper Series publishes: analytical work-in-progress; background documentation for specific research projects (e.g methodological papers); lengthy reports intended for specific clients, and; compendiums of data tables. Publication in this series does not preclude publication of specific aspects of the work in a peer-reviewed journal.

Description: This publication presents key highlights and results from the General Social Survey on the topics of caregiving and care receiving; social identity; giving, volunteering and participating; victimization; time use; and family.

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

Description: Using data from the 2022 Canadian Survey on Disability, this American Sign Language video examines disability characteristics among Canadians aged 15 years of age and older, as well as their employment experiences and information on income and poverty, and unmet needs for disability supports because of cost.

Description: This article is the first main release by Statistics Canada based on findings from the 2022 Canadian Survey on Disability (CSD). It is divided into three sections—demographics, employment, and income—and provides a general snapshot on persons with disabilities to inform on government priorities and community interest in the areas of disability prevalence, labour market participation, and income inequality. Where possible, the report will be compared with results from the 2017 CSD to provide insight into changes over the past five years.

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

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.