Health

Description: Differences in the number and proportion of employees with disabilities who were union members or covered by a union contract or collective agreement, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities who participated in workplace training, by province and territories (grouped), age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities who have difficulty changing jobs or advancing at present job, due to their condition, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities in terms of the reasons for not requesting their required accommodations, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities in terms of the reasons for experiencing difficulty in finding work, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities in terms of those who used and did not use the Internet for personal use from any location, during the past 12 months.

Description: Differences in the number and proportion of employees with disabilities in terms of their perceived qualification level for their current job, by age group and gender, Canada.

Description: Differences in the number and proportion of persons with disabilities who are not in the labour force, by main reason for not looking for work (grouped), aged 15 years and over, Canada.

Description: Differences in the number and proportion of persons with disabilities who are employed in part-time work by main reason (grouped) for working less than 30 hours a week and age group.

Description: Differences in the number and proportion of youth with disabilities who are not in employment, education, or training (NEET) by province or territory and gender.

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: This dashboard presents data that are relevant for monitoring mortality in Canada. The interactive visualization within the dashboard features insights on weekly death trends from the Canadian Vital Statistics - Death (CVSD) database.

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:

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.

Description:

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

Description:

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

Description:

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

Description:

We describe statistical disclosure control methods (SDC) developed for a public release Canadian Hospitals Injury Reporting and Prevention Program (CHIRPP) micro-data file. CHIRPP is a national injury surveillance database managed by the Public Health Agency of Canada (PHAC). After describing CHIRPP, the paper includes a brief overview of basic SDC concepts, as an introduction to the process for selecting and developing the appropriate SDC methods for CHIRPP given its specific challenges and requirements. We then summarize some key results. The paper concludes with a discussion of the implication of this work for the health information field and closing remarks with respect to the some methodological issues for consideration.

Description:

The process of public-use micro-data files creation involves a number of components. One of its key elements is RTI International's innovative MASSC methodology. However, there are other major components in this process such as treatment of non-core identifying variables and extreme outcomes for extra protection. The statistical disclosure limitation is designed to counter both inside and outside intrusion. The components of the process are accordingly designed.

Description:

In 1999, the first nationally representative survey of the mental health of children and young people aged 5-15 was carried out in Great Britain. A second survey was carried out in 2004. The aim of these surveys was threefold: to estimate the prevalence of mental disorders among young people, to look at their use of health, social and educational services, and to investigate risk factors associated with mental disorders. The achieved number of interviews was 10,500 and 8,000 respectively. Some key questions had to be addressed on a large number of methodological issues and the factors taken into account to reach decisions on all these issues are discussed.

Description:

In accordance with an effort to design a set of questions for the Current Population Survey (CPS) to measure disability, potential questions were drawn from existing surveys, cognitively and field tested. Based on an analysis of the test data, a set of seven questions was identified, cognitively tested, and placed in the February 2006 CPS for testing. Analysis of the data revealed a lower overall disability rate as measured in the CPS than in the field test, with lower positive response rates for each question. The data did not indicate that there was an adverse effect on the response rates.

Description:

On behalf of Statistics Canada, I would like to welcome you all, friends and colleagues, to Symposium 2006. This the 23rd International Symposium organized by Statistics Canada on survey methodology.

Description:

Now that we have come to the end of a day of workshops plus two very full days of sessions, I have the very pleasant task of offering a few closing remarks and, more importantly, of recognizing the efforts of those who have contributed to the success of this year's symposium. And it has clearly been a success.

Description:

General population health surveys often include small samples of smokers. Few longitudinal studies specific to smoking have been carried out. We discuss development of the Ontario Tobacco Survey (OTS) which combines a rolling longitudinal, and repeated cross-sectional components. The OTS began in July 2005 using random selection and data-collection by telephones. Every 6 months, new samples of smokers and non-smokers provide data on smoking behaviours and attitudes. Smokers enter a panel study and are followed for changes in smoking influences and behaviour. The design is proving to be cost effective in meeting sample requirements for multiple research objectives.

Description:

When Chiang's "standard" method is used, calculating life expectancy for (small) census agglomerations in Canada can produce estimates whose confidence intervals are too wide to be useful. However, we have been able to show that by combining small area estimation methods and simulation methods, we can obtain narrower confidence intervals.

Description:

Immigrants have health advantages over native-born Canadians, but those advantages are threatened by specific risk situations. This study explores cardiovascular health outcomes in districts of Montréal classified by the proportion of immigrants in the population, using a principal component analysis. The first three components are immigration, degree of socio-economic disadvantage and degree of economic disadvantage. The incidence of myocardial infarction is lower in districts with large immigrant populations than in districts dominated by native-born Canadians. Mortality rates are associated with the degree of socio-economic disadvantage, while revascularization is associated with the proportion of seniors in the population.

Description:

The classification and identification of locations where persons report to be more or less healthy or have more or less social capital, within a specific area such as a health region, is tremendously helpful for understanding place and health associations. The objective of the proposed study is to classify and map areas within the Zone 6 Health Region (Figure 1) of Nova Scotia (Halifax Regional Municipality and Annapolis Valley regions) according to health status (Dimension 1) and social capital (Dimension 2). We abstracted responses to questions about self-reported health status, mental health, and social capital from the master files of the Canadian Community Health Survey (Cycles 1.1, 1.2 and 2.1), National Population Health Survey (Cycle 5), and the General Social Survey (Cycles 13, 14, 17, and 18). Responses were geocoded using the Statistics Canada Postal Code Conversion File (PCCF+) and imported into a geographical information system (GIS) so that the postal code associated with the response will be assigned to a latitude and longitude within the Nova Scotia Zone 6 health region. Kernel density estimators and additional spatial interpolators were used to develop statistically-smoothed surfaces of the distribution of respondent values for each question. The smoothing process eliminates the possibility of revealing individual respondent location and confidential Statistics Canada sampling frame information. Using responses from similar questions across multiple surveys improves the likelihood of detecting heterogeneity among the responses within the health region area, as well as the accuracy of the smoothed map classification.

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: 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.