Health

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.

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.

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.

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.

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.

Description: The purpose of the Childhood National Immunization Coverage Survey is to collect information on national immunization coverage for childhood vaccines.

Description: This survey collects data on the prevalence of several neurological conditions in long-term care facilities.

Description: The objectives of the BCPCHC Survey are: - To provide more information on how people manage their chronic conditions; - To identify barriers to care for those living with chronic conditions including economic and travel related barriers; - To identify barriers to self-management of chronic conditions.

Description: The health effects reported by individuals living in communities in close proximity to noise sources such as traffic, airports, railways and wind turbine installations are not fully understood due to limited scientific research in this area. The CNHS was developed to address this gap by investigating the prevalence of health effects or health indicators among a sample of Canadians exposed to these noise sources using both self-reported and objective health measures.

Description: This survey collects data on non-acute health care facilities that provide medical or professional nursing supervision or some higher level of care to residents.

Description: The public use microdata file (PUMF) from the Canadian Community Health Survey (CCHS) provides data for health regions and combinations of health regions across Canada. Over the two year period, data are based on interviews with approximately 130,000 respondents aged 12 or older, residing in households in all provinces and territories.

The files include information on a wide range of topics, including: physical activity, height and weight, smoking, exposure to second hand smoke, alcohol consumption, general health, chronic health conditions, injuries, and use of health care services. It also provides information on the socio-demographic, income and labour force characteristics of the population.

Description: Differences in the number and proportions of persons with disabilities who experienced one or more barriers to accessibility, by the type of disability, age group and gender, Canada.

Description: Differences in the number and proportions of persons with disabilities who experienced one or more barriers to accessibility, by the severity of the disability, age group and gender, Canada.

Description: Differences in the number and proportions of persons with disabilities who experienced a barrier to accessibility, Canada, provinces and territories.

Description: This dashboard allows users to examine data on barriers to accessibility experienced by persons with disabilities. These are barriers encountered in different aspects of daily living including those found in public spaces; communicating in different situations; using the Internet and barriers related to behaviours, misconceptions or assumptions by others. The data can be organized by province, gender and other characteristics such as age group. This dashboard is based on the 2022 Canadian Survey on Disability.

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: Number and percentage of persons by household food security status and economic family type, Canada and provinces.

Description:

The National Health and Nutrition Examination Surveys (NHANES) is one of a series of health-related programs sponsored by the United States National Center for Health Statistics. A unique feature of NHANES is the administration of a complete medical examination for each respondent in the sample. To standardize administration, these examinations are carried out in mobile examination centers (MECs). The examination includes physical measurements, tests such as eye and dental examinations, and the collection of blood and urine specimens for laboratory testing. NHANES is an ongoing annual health survey of the noninstitutionalized civilian population of the United States. The major analytic goals of NHANES include estimating the number and percentage of persons in the U.S. population and in designated subgroups with selected diseases and risk factors. The sample design for NHANES needs to create a balance between the requirements for efficient annual and multiyear samples and the flexibility that allows changes in key design parameters to make the survey more responsive to the needs of the research and health policy communities. This paper discusses the challenges involved in designing and implementing a sample selection process that satisfies the goals of NHANES.

Description:

In the last two decades, considerable international effort has been put into the development of summary measures of population health that integrate information of mortality and non-fatal health outcomes and international policy interest in such indicators is increasing. There are two main classes of summary measures of population health: health gaps and health expectancies. The Disability-Adjusted Life Year (DALY) is the best known health gap measure and quantifies the gap between a population's actual health and a normative health goal, defined in terms of a global standard life table specifying the healthy years of life lost due to a death at any given age.

This paper gives an overview of the Global Burden of Disease (GBD) conceptual framework, the relationship of the DALY to other measures of population health, and the GBD analytical approach, with particular attention to issues in (1) dealing with biased and missing data, (2) dealing with uncertainty and (3) specific technical issues in ensuring cross-population comparability. The latter include dealing with variations in quality and completeness of cause of death information, explicit use of a comprehensive framework and internal consistency checks for improving comparability of estimates of incidence, prevalence and mortality for causes, the assessment of disability weights, and techniques for improving the comparability of the assessment of the disease burden attributable to risk factors.

Description:

During the last three decades, there has been general acceptance of an approach to describing health states of individuals in terms of multiple domains of health, and in developing self-report instruments that seek information on each of these domains. A health state is thus a multi-dimensional attribute of an individual that reflects his or her levels on the various components or domains of health. Thus, a health state differs from pathology, risk factors or etiology, and from health service encounters or interventions.

How to describe health states, is a central challenge in undertaking the measurement of health. The relationship of health states to other aspects of health such as future non-fatal health outcomes or risk of mortality need to be examined. The way people report their own health varies consistently with factors such as education, sex, age, or other cultural factors. Various people use different response category cut-points across cultures or population sub-groups, and this 'response shift' implies that self-report categorical data are not comparable across individuals. The responses cannot be directly used to measure health without adjustment.

In recognition of this the WHO World Health Surveys (WHS), used a set of questions across a core set of domains to measure health states and employed vignettes to detect and correct for biases in self-report in order to adjust for response category cut-point shifts. This paper will describe the instrument used in the WHS and the methods used to provide cross population comparable data. It will present results from the WHS demonstrating the existence of systematic reporting biases, the ability of respondents to rate vignettes and their use to adjust for biases in order to make data more comparable. Future strategies to address these problems will be discussed.

Description:

In this presentation, Mr. Murray discusses the notion of functional health status and proposes an agenda for developing comparable methods of measuring this concept.

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: 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.