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Curated

Eurobarometer 64.3: Foreign Languages, Biotechnology, Organized Crime, and Health Items, November-December 2005 (ICPSR 4590)

Released/updated on: 2010-06-23
Geographic coverage: Cyprus, Portugal, Global, Malta, Greece, Netherlands, Sweden, Austria, Latvia, Luxembourg, Ireland, Poland, Slovenia, Slovakia, France, Bulgaria, Lithuania, Croatia, Romania, Hungary, Europe, United Kingdom, Spain, Czech Republic, Turkey, Belgium, Finland, Denmark, Italy, Germany, Estonia
Time period: 2005-11-05--2005-12-07
This round of Eurobarometer surveys diverged from the standard Eurobarometer measures and queried respondents on (1) foreign languages, (2) biotechnology, (3) organized crime and corruption, (4) health consciousness, (5) smoking, (6) AIDS prevention, (7) medical errors, and (8) consumer rights. For the first topic, foreign languages, respondents were asked to identify their native language, and first, second, and third foreign languages spoken, including proficiency and frequency of use. In addition, respondents were asked to identify the main reasons to learn a new language, methods used in learning, and barriers preventing learning. Respondents' opinions were sought regarding the best age to start learning a first and second new language, language support, and whether there should be a common language used throughout the European Union (EU). For the second topic, respondents were asked about their understanding of biotechnology, including gene therapy, pharmacogenetics, genetically modified foods and plants, nanotechnology, stem cell research, and its application in industry. Respondents' opinions were sought regarding the use of these techniques, governing safety and regulatory processes, new technology development, and integration of biotechnology into society. Respondents were also queried about their knowledge of science and politics and discussion of these matters with others, their opinions regarding entity involvement, including the EU, in utilizing or advancing biotechnology, and their personal political involvement in this area. For the third topic, organized crime and corruption, respondents were asked to identify the degree of national corruption, sources where corruption exists, a regulatory force in reducing it, and any personal involvement with corruption, in addition to providing an opinion about whether information sharing or policy development may reduce corruption. For the fourth topic, health consciousness, respondents were asked about their current state of health, breastfeeding, dieting, views on eating, foods consumed, changes in eating or drinking patterns and associated reasons for these changes, ease of and barriers to eating healthily, and exercise. Respondents were asked about their knowledge of sports and physical activity, and their opinion about obesity among adults and children. For the fifth topic, smoking, respondents were asked about their smoking habits and use with other substances, sensitivity to smoke, knowledge about second-hand smoke, exposure to tobacco cessation campaigns, and the likelihood of quitting. In addition, respondents were asked to provide an opinion about smoking bans in public places and the consumption of alcohol and tobacco among pregnant women. For the sixth topic, AIDS prevention, respondents were asked about their knowledge of AIDS transmission, changes in personal behaviors influenced by AIDS, and their opinions regarding current national measures in managing the AIDS pandemic and the potential coordination with the EU. For the seventh topic, medical errors, respondents were asked about their awareness of incidents of medical errors in their country, the significance of those errors, personal experience of a medical error, the likelihood of avoiding an error, and their degree of concern about suffering a medical error. For the eighth and final topic covered by this survey, consumer rights, those respondents living in Poland were asked about where and how often they saw or heard information about consumer rights, how frequently the media talked about consumer rights, and who in the media was the source of this information. Respondents were also asked whether they had heard a particular message and to define the meaning of that message, to evaluate Poland's consumer rights in comparison to other EU countries, and to assess the effectiveness of the justice system in protecting consumer rights. In addition, respondents were queried about their knowledge of consumer rights in certain situations, which organizations they would trust to provide correct advice and information about consumer rights, and whether they would refer others to a specific organization that deals with consumer rights, Federacja Konsumentow. Demographic and other background information includes respondent's age, gender, height, and weight, nationality, origin of birth (personal and parental), religious affiliation and involvement, marital status, left-to-right political self-placement, occupation, age when stopped full-time education, household composition, use of a fixed or a mobile telephone, size of locality, region of residence, and language of interview.
Curated

Human Mortality Database (ICPSR 138)

Released/updated on: 2006-06-19
Geographic coverage: United States, Wales, England, Iceland, Global, Russia, Netherlands, Sweden, Austria, Latvia, Slovakia, France, Bulgaria, Lithuania, Hungary, Japan, Switzerland, Spain, New Zealand, Canada, Czech Republic, Belgium, Norway, Finland, Denmark, Italy, Australia, Germany
The Human Mortality Database (HMD) was created to provide detailed mortality and population data to researchers, students, journalists, policy analysts, and others interested in the history of human longevity. The project began as an outgrowth of earlier projects in the Department of Demography at the University of California, Berkeley, USA, and at the Max Planck Institute for Demographic Research in Rostock, Germany. It is the work of two teams of researchers in the USA and Germany. The main goal of the database is to document the longevity revolution of the modern era and to facilitate research into its causes and consequences. At present, the database contains detailed data for a collection of 26 countries. The countries involved are Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, the total and civilian populations of England and Wales, Finland, France, Germany, West Germany, East Germany, Hungary, Iceland, Italy, Japan, Latvia, Lithunia, Netherlands, the Maori and Non-Maori populations of New Zealand, Norway, Russia, Slovakia, Spain, Sweden, Switzerland, and the United States.
Curated

Integrated Public Use Microdata Series: North Atlantic Population Project (ICPSR 35985)

Released/updated on: 2015-06-18
Geographic coverage: Canada, Sweden, Great Britain, United States, Norway, Ireland, Egypt, Denmark, Mexico, Germany, Iceland, Albania
The North Atlantic Population Project (NAPP), which was created by research teams in the United States, the United Kingdom, Canada, Iceland, Norway, and Sweden, is a massive integrated cross-national microdatabase that provides a baseline for studies of demographic change. This project improves the NAPP by tripling the size of the database to approximately 365 million records by adding 40 new datasets for the period 1787 to 1930 from Albania, Great Britain, Canada, Denmark, Egypt, Iceland, Ireland, Germany, Norway, Mexico, Sweden, and the United States. It also creates linked national panels and merges NAPP with the Integrated Public Use Microdata Series (IPUMS). NAPP provides a baseline for the study of changes in demography and health of European and North American populations. In each country, it provides the earliest census microdata available. It makes available some of the world's largest and longest-running cross-sectional and longitudinal data sources.
Curated

Mothers, Places, and Preterm Birth (ICPSR 35959)

Released/updated on: 2015-06-12
Geographic coverage: Sweden
This study uses cross-sectional data on adverse birth outcomes and social factors among Swedish mothers from 1973-2005 to create two new databases: WomMed and WomSALLS. These databases link annual census, mortality, hospital, and individual survey data. WomMed contains annual data from prenatal and birth records, hospital admissions, and death records for each mother and child in Sweden, in addition to individual-level sociodemographic characteristics and maternal risk factors. WomSALLS includes data on health behaviors and risk factors, stress and adaptation, social cohesion, and psychological distress based on face-to-face interviews with representative samples of approximately 18,000 mothers aged 15-45, and born between 1928 and 1990.
Curated
Restricted

Study of Dementia in Swedish Twins, 1990-1999 (ICPSR 25963)

Released/updated on: 2010-06-04
Geographic coverage: Sweden, Global
Time period: 1990-05-01--1999-03-01
The Study of Dementia in Swedish Twins was designed to study the relative influence of genetic and environmental factors for Alzheimer's disease and other types of dementia and to test the role of specific environmental exposures that might constitute risk or protective factors for dementia. The first seven years of the Study of Dementia in Swedish Twins was based on the population from the SWEDISH ADOPTION/TWIN STUDY OF AGING (SATSA), 1984, 1987, 1990, and 1993 (ICPSR 3843). SATSA consists of a subset of 3,838 same-sex twins from the population-based Swedish Twin Registry; however, the baseline sample for the Study of Dementia in Swedish Twins consists of 2,394 individuals who were alive and born in 1935 or earlier. The Study of Dementia in Swedish Twins data cover background information (sex, zygosity, rearing status, ages at each data collection point, age at death), cognitive screening (which took place in conjunction with each SATSA wave of data collection), clinical dementia diagnoses for those who received a complete dementia workup (both baseline and longitudinal), cognitive test results (both baseline and longitudinal), medical history and medical risk factors (medical examination; blood pressure; laboratory results; history of neurologic, coronary, mental, and other diseases; smell test; history of head injury, anaesthesia, fevers, medications, dietary history with respect to fish, raw meat, and acidic foods prepared in aluminum pans), residential, occupational, and leisure activities history (including exposure related to welding, hairdressing, agriculture, medical settings, painting and other sources of organic solvents, crystal, carbon monoxide, radiation, raw meat and game; participation in contact sports; antiperspirant containing aluminum; history of smoking; history of use of alcohol), family history of dementia, and APOE genotype. SATSA is archived separately at ICPSR, see ICPSR 3843. The SATSA and the Study of Dementia in Swedish Twins files contain a common ID number that can be used to create a crosswalk between the files.
Curated

Survey of Health, Ageing and Retirement in Europe (SHARE) (ICPSR 24981)

Released/updated on: 2009-02-26
Geographic coverage: Europe, Switzerland, Global, Spain, Greece, Netherlands, Sweden, Austria, Czech Republic, Belgium, Ireland, Denmark, Poland, Italy, Israel, Slovenia, France, Germany

The Survey on Health, Ageing and Retirement in Europe (SHARE) is a multidisciplinary and cross-national panel database of micro data on the health, socio-economic status, and social and family networks of older adults (aged 50 years and over) throughout Europe. Designed to provide a full picture of the aging process, SHARE collects data on a range of topics including health conditions, physical and cognitive functioning, mental health, life satisfaction, employment, income, education, social networks, and social support mechanisms. The first wave of SHARE data collection occurred in 2004-2005, the second wave in 2006-2007, and the third wave in 2008-2009.

SHARE has been harmonized with the United States HEALTH AND RETIREMENT STUDY (HRS) [ICPSR6854], and the ENGLISH LONGITUDINAL STUDY OF AGEING (ELSA) [ICPSR0139].

Curated
Simple Crosstabs

Swedish Adoption/Twin Study on Aging (SATSA), 1984, 1987, 1990, 1993, 2004, 2007, and 2010 (ICPSR 3843)

Released/updated on: 2015-05-13
Geographic coverage: Sweden, Global
Time period: 1984-01-01--2010-01-01
The Swedish Adoption/Twin Study on Aging (SATSA) was designed to study the origins of individual differences in aging and the environmental and genetic factors that are involved. SATSA began in 1984, and six additional waves were conducted in 1987, 1990, 1993, 2004, 2007, and 2010. The questionnaire was initially sent to all twins from the Swedish Twin Registry who were separated at an early age and raised apart; the survey was also administered to a control sample of twins who were raised together. The respondents were surveyed on items that included health status, how they were raised, work environment, alcohol consumption, and dietary and smoking habits, as well as questions about personality and attitudes; this information comprised the first component. The second component was collected from a subsample composed of 150 pairs of twins raised apart and 150 pairs of twins raised together. This subsample participated in seven waves of in-person testing, which included a health examination, structured interviews, and tests on functional capacity, cognitive abilities, and memory. The data are represented according to questionnaire and time number, and correspond to each wave/year: Questionnaire 1 and In-Person Testing Time 1 were in 1984; Questionnaire 2 and In-Person Testing Time 2 were in 1987; Questionnaire 3 and In-Person Testing Time 3 were in 1990; Questionnaire 4 and In-Person Testing Time 4 were in 1993; Questionnaire 5 was in 2003; In-Person Testing Time 5 was in 2004; Questionnaire 6 and In-Person Testing Time 6 were in 2007; In-Person Testing Time 7 was in 2010. The Administrative and Cognitive datasets include data from all years/waves. The Smell Survey dataset only includes data from 1990. No years were specified for the Contact measures and Separation measures datasets. Demographic and background information includes age, sex, education, family history, household composition and employment.
Curated

Twin Studies of the Marriage Benefit: Parsing Selection from Causation (ICPSR 35891)

Released/updated on: 2015-05-14
Geographic coverage: Sweden, United States, Australia
This project collects data from five samples of twins in the United States, Australia, and Sweden. The study uses genetic data and its connection to relationship behaviors, as well as mental and physical health. Finally, the project interviews identical twins about how marriage, romantic relationships, and relationship dissolution may alter the life course.