These data are the part of the two National Health Surveys in the Republic of Serbia, conducted in 2006 and 2013, funded by the Ministry of Health. The survey was conducted in accordance with the methodology and instruments of the European Health Interview Survey wave 2. Both surveys were conducted as cross sectional studies. Population presented in the research included adults, aged 19 and more. The researches excluded people living on the territory of Kosovo and Metohija, as well as people with residence addresses in Special institutions (retirement homes, prisons, psychiatric clinics). Data on basic characteristics of the interviewees, health condition of the interviewees, using hospital and non-hospital health care services and prevention check-ups and unachieved need for health care was obtained through a face-to-face interview carried out at home, while information at the level of the household was obtained by means of a household questionnaire. The questions were validated instruments based on the standard questionnaires from similar types of surveys.

The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999, the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements designed to meet current and emerging concerns. The sample for the survey is selected to represent the U.S. population of all ages. Many of the NHANES 2001-2002 questions also were asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups.

In the 2001-2002 wave, the NHANES includes more than 100 datasets. Most have been combined into three datasets for convenience. Each starts with the demographic dataset and includes datasets of a specific type.

1. National Health and Nutrition Examination Survey (NHANES), Demographic & Examination Data, 2001-2002 (the base of the Demographic dataset + all data from medical examinations).

2. National Health and Nutrition Examination Survey (NHANES), Demographic & Laboratory Data, 2001-2002 (the base of the Demographic dataset + all data from medical laboratories).

3. National Health and Nutrition Examination Survey (NHANES), Demographic & Questionnaire Data, 2001-2002 (the base of the Demographic dataset + all data from questionnaires).

Not all files from the 2001-2002 wave are included. This is for two reasons, both of which related to the merging variable (SEQN). For a subset of the files, SEQN is not a unique identifier for cases (i.e. some respondents have multiple cases) or SEQN is not in the file at all. The following datasets from this wave of the NHANES are not included in these three files and can be found individually from the "https://www.cdc.gov/nchs/nhanes/index.html" Target="_blank">NHANES website at the CDC:

Examination: Dietary Interview (Individual Foods File)
Examination: Dual Energy X-ray Absorptiometry (DXX)
Examination: Dual Energy X-ray Absorptiometry (DXX)
Questionnaire: Analgesics Pain Relievers
Questionnaire: Dietary Supplement Use -- Ingredient Information
Questionnaire: Dietary Supplement Use -- Supplement Blend
Questionnaire: Dietary Supplement Use -- Supplement Information
Questionnaire: Drug Information
Questionnaire: Dietary Supplement Use -- Participants Use of Supplement
Questionnaire: Physical Activity Individual Activity File
Questionnaire: Prescription Medications

Variable SEQN is included for merging files within the waves. All data files should be sorted by SEQN.

Additional details of the design and content of each survey are available at the "https://www.cdc.gov/nchs/nhanes/index.html" Target="_blank">NHANES website.

The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. The 1999-2000 NHANES contains data for 9,965 individuals (and MEC examined sample size of 9,282) of all ages. Many questions that were asked in NHANES II, 1976-1980, Hispanic HANES 1982-1984, and NHANES III, 1988-1994, were combined with new questions in the NHANES 1999-2000. The 1999-2000 NHANES collected data on the prevalence of selected chronic conditions and diseases in the population and estimates for previously undiagnosed conditions, as well as those known to and reported by respondents. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The interview includes demographic, socioeconomic, dietary, and health-related questions. The examination component consists of medical, dental, and physiological measurements, as well as laboratory tests. Demographic data file variables are grouped into three broad categories: (1) Status Variables: Provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 1999-2000 data). (2) Recoded Demographic Variables: The variables include age (age in months for persons through age 19 years, 11 months; age in years for 1-84 year olds, and a top-coded age group of 85+ years), gender, a race/ethnicity variable, an education variable (high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), and pregnancy status variable. Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: Sample weights are available for analyzing NHANES 1999-2000 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.

The Research and Development Survey (RANDS) is a platform designed for conducting survey question evaluation and statistical research. RANDS is an ongoing series of surveys from probability-sampled commercial survey panels used for methodological research at the National Center for Health Statistics (NCHS). RANDS estimates are generated using an experimental approach that differs from the survey design approaches generally used by NCHS, including possible biases from different response patterns and sampling frames as well as increased variability from lower sample sizes. Use of the RANDS platform allows NCHS to produce more timely data than would be possible using traditional data collection methods. RANDS is not designed to replace NCHS’ higher quality, core data collections. Below are experimental estimates of reduced access to healthcare for three rounds of RANDS during COVID-19. Data collection for the three rounds of RANDS during COVID-19 occurred between June 9, 2020 and July 6, 2020, August 3, 2020 and August 20, 2020, and May 17, 2021 and June 30, 2021. Information needed to interpret these estimates can be found in the Technical Notes. RANDS during COVID-19 included questions about unmet care in the last 2 months during the coronavirus pandemic. Unmet needs for health care are often the result of cost-related barriers. The National Health Interview Survey, conducted by NCHS, is the source for high-quality data to monitor cost-related health care access problems in the United States. For example, in 2018, 7.3% of persons of all ages reported delaying medical care due to cost and 4.8% reported needing medical care but not getting it due to cost in the past year. However, cost is not the only reason someone might delay or not receive needed medical care. As a result of the coronavirus pandemic, people also may not get needed medical care due to cancelled appointments, cutbacks in transportation options, fear of going to the emergency room, or an altruistic desire to not be a burden on the health care system, among other reasons. The Household Pulse Survey (https://www.cdc.gov/nchs/covid19/pulse/reduced-access-to-care.htm), an online survey conducted in response to the COVID-19 pandemic by the Census Bureau in partnership with other federal agencies including NCHS, also reports estimates of reduced access to care during the pandemic (beginning in Phase 1, which started on April 23, 2020). The Household Pulse Survey reports the percentage of adults who delayed medical care in the last 4 weeks or who needed medical care at any time in the last 4 weeks for something other than coronavirus but did not get it because of the pandemic. The experimental estimates on this page are derived from RANDS during COVID-19 and show the percentage of U.S. adults who were unable to receive medical care (including urgent care, surgery, screening tests, ongoing treatment, regular checkups, prescriptions, dental care, vision care, and hearing care) in the last 2 months. Technical Notes: https://www.cdc.gov/nchs/covid19/rands/reduced-access-to-care.htm#limitations

A panel data set for use in cross-cultural analyses of aging, health, and well-being between the U.S. and Japan. The questionnaires were designed to be partially comparable to many surveys of the aged, including Americans'' Changing Lives; 1984 National Health Interview Survey Supplement on Aging; Health and Retirement Study (HRS), and Well-Being Among the Aged: Personal Control and Self-Esteem (WBA). NSJE questionnaire topics include: * Demographics (age, sex, marital status, education, employment) * Social Integration (interpersonal contacts, social supports) * Health Limitations on daily life and activities * Health Conditions * Health Status (ratings of present health) * Level of physical activity * Subjective Well-Being and Mental Health Status (life satisfaction, morale), * Psychological Indicators (life events, locus of control, self-esteem) * Financial situation (financial status) * Memory (measures of cognitive functioning) * Interviewer observations (assessments of respondents) The NSJE was based on a national sample of 2,200 noninstitutionalized elderly aged 60+ in Japan. This cohort has been interviewed once every 3 years since 1987. To ensure that the data are representative of the 60+ population, the samples in 1990 and 1996 were refreshed to add individuals aged 60-62. In 1999, a new cohort of Japanese adults aged 70+ was added to the surviving members of previous cohorts to form a database of 3,990 respondents 63+, of which some 3,000 were 70+. Currently a 6-wave longitudinal database (1987, 1990, 1993, 1996, 1999, & 2002) is in place; wave 7 began in 2006. Data Availability: Data from the first three waves of the National Survey of the Japanese Elderly are currently in the public domain and can be obtained from ICPSR. Additional data are being prepared for future public release. * Dates of Study: 1987-2006 * Study Features: Longitudinal, International * Sample Size: ** 1987: 2,200 ** 1990: 2,780 ** 1993: 2,780 ** 1996: ** 1999: 3,990 ** 2002: ** 2006: Links: * 1987 (ICPSR): http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/06842 * 1990 (ICPSR): http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/03407 * 1993 (ICPSR): http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/04145 * 1996 (ICPSR): http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/26621

The Research and Development Survey (RANDS) is a platform designed for conducting survey question evaluation and statistical research. RANDS is an ongoing series of surveys from probability-sampled commercial survey panels used for methodological research at the National Center for Health Statistics (NCHS). RANDS estimates are generated using an experimental approach that differs from the survey design approaches generally used by NCHS, including possible biases from different response patterns and sampling frames as well as increased variability from lower sample sizes. Use of the RANDS platform allows NCHS to produce more timely data than would be possible using traditional data collection methods. RANDS is not designed to replace NCHS’ higher quality, core data collections. Below are experimental estimates of telemedicine access and use for three rounds of RANDS during COVID-19. Data collection for the three rounds of RANDS during COVID-19 occurred between June 9, 2020 and July 6, 2020, August 3, 2020 and August 20, 2020, and May 17, 2021 and June 30, 2021. Information needed to interpret these estimates can be found in the Technical Notes. RANDS during COVID-19 included questions about whether providers offered telemedicine (including video and telephone appointments) in the last 2 months—both during and before the pandemic—and about the use of telemedicine in the last 2 months during the pandemic. As a result of the coronavirus pandemic, many local and state governments discouraged people from leaving their homes for nonessential reasons. Although health care is considered an essential activity, telemedicine offers an opportunity for care without the potential or perceived risks of leaving the home. The National Health Interview Survey, conducted by NCHS, added telemedicine questions to its sample adult questionnaire in July 2020. The Household Pulse Survey (https://www.cdc.gov/nchs/covid19/pulse/telemedicine-use.htm), an online survey conducted in response to the COVID-19 pandemic by the Census Bureau in partnership with other federal agencies including NCHS, also reports estimates of telemedicine use during the pandemic (beginning in Phase 3.1, which started on April 14, 2021). The Household Pulse Survey reports telemedicine use in the last 4 weeks among adults and among households with at least one child under age 18 years. The experimental estimates on this page are derived from RANDS during COVID-19 and show the percentage of U.S. adults who have a usual place of care and a provider that offered telemedicine in the past 2 months, who used telemedicine in the past 2 months, or who have a usual place of care and a provider that offered telemedicine prior to the coronavirus pandemic. Technical Notes: https://www.cdc.gov/nchs/covid19/rands/telemedicine.htm#limitations

Abstract copyright UK Data Service and data collection copyright owner.The Health Survey for England (HSE) is a series of surveys designed to monitor trends in the nation's health. It was commissioned by NHS Digital and carried out by the Joint Health Surveys Unit of the National Centre for Social Research and the Department of Epidemiology and Public Health at University College London.The aims of the HSE series are:to provide annual data about the nation’s health;to estimate the proportion of people in England with specified health conditions;to estimate the prevalence of certain risk factors associated with these conditions;to examine differences between population subgroups in their likelihood of having specific conditions or risk factors;to assess the frequency with which particular combinations of risk factors are found, and which groups these combinations most commonly occur;to monitor progress towards selected health targetssince 1995, to measure the height of children at different ages, replacing the National Study of Health and Growth;since 1995, monitor the prevalence of overweight and obesity in children.The survey includes a number of core questions every year but also focuses on different health issues at each wave. Topics are revisited at appropriate intervals in order to monitor change. Further information about the series may be found on the NHS Digital Health Survey for England; health, social care and lifestyles webpage, the NatCen Social Research NatCen Health Survey for England webpage and the University College London Health and Social Surveys Research Group UCL Health Survey for England webpage. Changes to the HSE from 2015:Users should note that from 2015 survey onwards, only the individual data file is available under standard End User Licence (EUL). The household data file is now only included in the Special Licence (SL) version, released from 2015 onwards. In addition, the SL individual file contains all the variables included in the HSE EUL dataset, plus others, including variables removed from the EUL version after the NHS Digital disclosure review. The SL HSE is subject to more restrictive access conditions than the EUL version (see Access information). Users are advised to obtain the EUL version to see if it meets their needs before considering an application for the SL version. The Health Survey for England, 2000 (HSE00) consisted of two samples. The general population sample was a national cross-section sample. Up to two children aged 2-15 years were interviewed in each household, as well as up to 10 adults aged 16 years and over. All private households in the general population sample were eligible for inclusion in the survey (up to a maximum of three households per address). Running alongside the general population sample was a care homes sample, selected from the Laing and Bussion database. The sample contained nursing, residential, dual-registered and small residential homes and covered local authority, voluntary and privately-owned care homes. Up to six people aged 65 and over were selected for interview at each care home, and given a cognitive functioning test to see whether they were capable of being interviewed in person. Proxy interviews for those who were not capable of being interviewed were introduced in June 2000. For the fourth edition (July 2011), the GHQ12 variables were amended to correct errors in the GHQ12 scores. See document 'Note about GHQ12 problems in HSE Data' for details. Main Topics: The interview with informants from the general population sample included the question modules that are asked in most years in the Health Survey ('core' modules), such as general health and longstanding illnesses, use of health services, cigarette smoking, psycho-social health (GHQ12) and accidents. Also included in the 2000 survey were questions on disability (a repeat of the module used in the 1995 Health Survey), the Short-Form Health Outcomes (SF-12) questionnaire (for informants aged 16-64) and a new module on social capital and social exclusion. In addition to the 'core' question modules outlined above, informants in care homes were asked questions about cardiovascular disease (CVD) and respiratory symptoms, eating habits, physical activity and activities in the care home. The disability module was also included in the care home sample interview. A short interview with home managers included details about the type of care home, the number of residents and the availability of services and specialised equipment. Some administrative data and geographic identifiers have been removed from the dataset. Standard Measures:General Health Questionnaire (GHQ12) - copyright David Goldberg, 1978 reproduced by permission of NFER - NELSONMedical Research Council respiratory questionnaireStrengths and Difficulties Questionnaire (SDQ)Short-Form Health Outcomes (SF12) questionnaire Multi-stage stratified random sample Face-to-face interview Self-completion Clinical measurements Physical measurements CAPI 2000 2001 ACCIDENTS ADULTS AGE AGEING ALCOHOL USE ALCOHOLIC DRINKS ALCOHOLISM ANTHROPOMETRIC DATA ANXIETY BEDROOMS BICYCLES BLOOD BUILDING MAINTENANCE CARBOHYDRATES CARDIOVASCULAR DISE... CARDIOVASCULAR SYSTEM CARE OF DEPENDANTS CARE OF THE ELDERLY CAUSES OF DEATH CEREAL PRODUCTS CHILD BENEFITS CHILDREN CHRONIC ILLNESS CLINICAL TESTS AND ... CONCENTRATION CONFECTIONERY CONTRACEPTIVE DEVICES COUGHING CULTURAL IDENTITY DAIRY PRODUCTS DEBILITATIVE ILLNESS DEGREES DEMENTIA DEPRESSION DIABETES DIET AND EXERCISE DISABILITIES DISABLED PERSONS DISEASES DOMESTIC RESPONSIBI... ECONOMIC ACTIVITY EDIBLE FATS EDUCATIONAL BACKGROUND ELDERLY EMPLOYEES EMPLOYMENT EMPLOYMENT HISTORY ETHNIC GROUPS ETHNIC MINORITIES EXAMINATIONS EXERCISE PHYSICAL A... England FAMILIES FAMILY MEMBERS FATHERS FISH AS FOOD FRIENDS FRUIT FULL TIME EMPLOYMENT FURNISHED ACCOMMODA... GARDENING GENDER GENERAL PRACTITIONERS General health and ... HAEMATOLOGIC DISEASES HAPPINESS HEADS OF HOUSEHOLD HEALTH HEALTH ADVICE HEALTH CONSULTATIONS HEALTH PROFESSIONALS HEALTH SERVICES HEART DISEASES HEIGHT PHYSIOLOGY HOME OWNERSHIP HOSPITAL OUTPATIENT... HOSPITAL SERVICES HOSPITAL WAITING LISTS HOSPITALIZATION HOUSEHOLD HEAD S OC... HOUSEHOLDS HOUSEWORK HOUSING HOUSING TENURE Health care service... ILL HEALTH INCOME INDUSTRIAL INJURIES INDUSTRIES INJURIES JOB SEEKER S ALLOWANCE LANDLORDS LEISURE TIME ACTIVI... MANAGERS MARITAL STATUS MEAT MEDICAL CARE MEDICAL DIAGNOSIS MEDICAL HISTORY MEDICAL PRESCRIPTIONS MEMORY MILK MOTHERS MOTOR PROCESSES MOTOR VEHICLES NEIGHBOURHOODS OCCUPATIONAL PENSIONS OCCUPATIONAL QUALIF... OCCUPATIONS OLD AGE PAIN PARENTS PART TIME EMPLOYMENT PASSIVE SMOKING PATIENTS PERSONAL PROTECTIVE... PHYSICAL ACTIVITIES PHYSICIANS PLACE OF BIRTH PREGNANCY PRESCRIPTION DRUGS PRIVATE SECTOR QUALIFICATIONS RELIGIOUS AFFILIATION RENTED ACCOMMODATION RESIDENTIAL CARE OF... RESPIRATORY SYSTEM RESPIRATORY TRACT D... RETIREMENT ROAD ACCIDENTS SALT SAVINGS SAVOURY SNACKS SELF EMPLOYED SELF ESTEEM SHARED HOME OWNERSHIP SICK LEAVE SICK PERSONS SLEEP SMOKING SMOKING CESSATION SOCIAL CLASS SOCIAL HOUSING SOCIAL INTEGRATION SOCIAL SECURITY BEN... SOCIAL SUPPORT SOCIO ECONOMIC STATUS SPORT STATE RETIREMENT PE... STRESS PSYCHOLOGICAL STUDENTS SUPERVISORS SURGERY SYMPTOMS TIED HOUSING TOBACCO TOP MANAGEMENT TRANSPORT ACCIDENTS UNEMPLOYED UNFURNISHED ACCOMMO... VASCULAR DISEASES VEGETABLES VOCATIONAL EDUCATIO... WAGES WALKING WEIGHT PHYSIOLOGY YOUTH

Abstract copyright UK Data Service and data collection copyright owner.The Health Survey for England (HSE) is a series of surveys designed to monitor trends in the nation's health. It was commissioned by NHS Digital and carried out by the Joint Health Surveys Unit of the National Centre for Social Research and the Department of Epidemiology and Public Health at University College London.The aims of the HSE series are:to provide annual data about the nation’s health;to estimate the proportion of people in England with specified health conditions;to estimate the prevalence of certain risk factors associated with these conditions;to examine differences between population subgroups in their likelihood of having specific conditions or risk factors;to assess the frequency with which particular combinations of risk factors are found, and which groups these combinations most commonly occur;to monitor progress towards selected health targetssince 1995, to measure the height of children at different ages, replacing the National Study of Health and Growth;since 1995, monitor the prevalence of overweight and obesity in children.The survey includes a number of core questions every year but also focuses on different health issues at each wave. Topics are revisited at appropriate intervals in order to monitor change. Further information about the series may be found on the NHS Digital Health Survey for England; health, social care and lifestyles webpage, the NatCen Social Research NatCen Health Survey for England webpage and the University College London Health and Social Surveys Research Group UCL Health Survey for England webpage. Changes to the HSE from 2015:Users should note that from 2015 survey onwards, only the individual data file is available under standard End User Licence (EUL). The household data file is now only included in the Special Licence (SL) version, released from 2015 onwards. In addition, the SL individual file contains all the variables included in the HSE EUL dataset, plus others, including variables removed from the EUL version after the NHS Digital disclosure review. The SL HSE is subject to more restrictive access conditions than the EUL version (see Access information). Users are advised to obtain the EUL version to see if it meets their needs before considering an application for the SL version. The HSE 2006 was designed to provide data at both national and regional level about the population living in private households in England. The sample comprised two components; the core (general population) sample and a boost sample of children aged 2-15. The core sample was designed to be representative of the population living in private households in England and should be used for analyses at the national level. For the HSE core sample, all adults aged 16 years or older at each household were selected for the interview (up to a maximum of ten adults). However, a limit of two was placed on the number of interviews carried out with children aged 0-15. For households with three or more children, interviewers selected two children at random. At boost addresses interviewers screened for households containing at least one child aged 2-15 years. For households which included eligible children, up to two were selected by the interviewer for inclusion in the survey. Interviewing was conducted throughout the year to take account of seasonal differences. For the third edition (April 2010), three new children's Body Mass Index (BMI) variables have been added to the individual data file (bmicat1, bmicat2, bmicat3). The original variables (bmicut, bmicut2, bmicut3) are unreliable and should not be used. Further information is available in the documentation and on the Information Centre for Health and Social Care Health Survey for England web page. For the fourth edition (July 2011), the GHQ12 variables were further amended to correct errors in the GHQ12 scores. See document 'Note about GHQ12 problems in HSE Data' for details. Main Topics: For adult respondents, the HSE 2006 focused on cardiovascular disease (CVD) and risk factors. All adults were asked modules of questions on CVD, general health, alcohol consumption, smoking, fruit and vegetable consumption and physical activities. Adults in the core sample aged 65 years and over were randomly allocated one of two questionnaire versions, to avoid lengthy interviews. These included either the CVD module and a short physical activity module, or a long physical activity module but not the CVD module. Adults aged 16-64 completed both the CVD and long physical activity modules. Questionnaire interviews were followed by a nurse visit. Parents of children aged 0-12 years were asked about their children, with the child interview including questions on physical activity and fruit and vegetable consumption. Children aged 13-15 were interviewed themselves. Standard Measures:General Health Questionnaire (GHQ12)EQ-5D Health StateStrengths and Difficulties Questionnaire (SDQ) Multi-stage stratified random sample Face-to-face interview Self-completion Clinical measurements Physical measurements

Abstract

The Gallup Poll Social Series (GPSS) is a set of public opinion surveys designed to monitor U.S. adults' views on numerous social, economic, and political topics. The topics are arranged thematically across 12 surveys. Gallup administers these surveys during the same month every year and includes the survey's core trend questions in the same order each administration. Using this consistent standard allows for unprecedented analysis of changes in trend data that are not susceptible to question order bias and seasonal effects.

Introduced in 2001, the GPSS is the primary method Gallup uses to update several hundred long-term Gallup trend questions, some dating back to the 1930s. The series also includes many newer questions added to address contemporary issues as they emerge.

The dataset currently includes responses from up to and including 2025.

Methodology

Gallup conducts one GPSS survey per month, with each devoted to a different topic, as follows:

January: Mood of the Nation

February: World Affairs

March: Environment

April: Economy and Finance

May: Values and Beliefs

June: Minority Rights and Relations (discontinued after 2016)

July: Consumption Habits

August: Work and Education

September: Governance

October: Crime

November: Health

December: Lifestyle (conducted 2001-2008)

The core questions of the surveys differ each month, but several questions assessing the state of the nation are standard on all 12: presidential job approval, congressional job approval, satisfaction with the direction of the U.S., assessment of the U.S. job market, and an open-ended measurement of the nation's "most important problem." Additionally, Gallup includes extensive demographic questions on each survey, allowing for in-depth analysis of trends.

Interviews are conducted with U.S. adults aged 18 and older living in all 50 states and the District of Columbia using a dual-frame design, which includes both landline and cellphone numbers. Gallup samples landline and cellphone numbers using random-digit-dial methods. Gallup purchases samples for this study from Survey Sampling International (SSI). Gallup chooses landline respondents at random within each household based on which member had the next birthday. Each sample of national adults includes a minimum quota of 70% cellphone respondents and 30% landline respondents, with additional minimum quotas by time zone within region. Gallup conducts interviews in Spanish for respondents who are primarily Spanish-speaking.

Gallup interviews a minimum of 1,000 U.S. adults aged 18 and older for each GPSS survey. Samples for the June Minority Rights and Relations survey are significantly larger because Gallup includes oversamples of Blacks and Hispanics to allow for reliable estimates among these key subgroups.

Gallup weights samples to correct for unequal selection probability, nonresponse, and double coverage of landline and cellphone users in the two sampling frames. Gallup also weights its final samples to match the U.S. population according to gender, age, race, Hispanic ethnicity, education, region, population density, and phone status (cellphone only, landline only, both, and cellphone mostly).

Demographic weighting targets are based on the most recent Current Population Survey figures for the aged 18 and older U.S. population. Phone status targets are based on the most recent National Health Interview Survey. Population density targets are based on the most recent U.S. Census.

Usage

The year appended to each table name represents when the data was last updated. For example, January: Mood of the Nation - 2025** **has survey data collected up to and including 2025.

For more information about what survey questions were asked over time, see the Supporting Files.

Bulk Data Access

Data access is required to view this section.

Abstract copyright UK Data Service and data collection copyright owner.The Health Survey for England (HSE) is a series of surveys designed to monitor trends in the nation's health. It was commissioned by NHS Digital and carried out by the Joint Health Surveys Unit of the National Centre for Social Research and the Department of Epidemiology and Public Health at University College London.The aims of the HSE series are:to provide annual data about the nation’s health;to estimate the proportion of people in England with specified health conditions;to estimate the prevalence of certain risk factors associated with these conditions;to examine differences between population subgroups in their likelihood of having specific conditions or risk factors;to assess the frequency with which particular combinations of risk factors are found, and which groups these combinations most commonly occur;to monitor progress towards selected health targetssince 1995, to measure the height of children at different ages, replacing the National Study of Health and Growth;since 1995, monitor the prevalence of overweight and obesity in children.The survey includes a number of core questions every year but also focuses on different health issues at each wave. Topics are revisited at appropriate intervals in order to monitor change. Further information about the series may be found on the NHS Digital Health Survey for England; health, social care and lifestyles webpage, the NatCen Social Research NatCen Health Survey for England webpage and the University College London Health and Social Surveys Research Group UCL Health Survey for England webpage. Changes to the HSE from 2015:Users should note that from 2015 survey onwards, only the individual data file is available under standard End User Licence (EUL). The household data file is now only included in the Special Licence (SL) version, released from 2015 onwards. In addition, the SL individual file contains all the variables included in the HSE EUL dataset, plus others, including variables removed from the EUL version after the NHS Digital disclosure review. The SL HSE is subject to more restrictive access conditions than the EUL version (see Access information). Users are advised to obtain the EUL version to see if it meets their needs before considering an application for the SL version. The Health Survey for England, 2016: Special Licence Access is available from the UK Data Archive under SN 9084. Latest edition information: For the fourth edition (May 2023), a number of corrections were made to the data file and the data documentation file. Further information is available in the documentation file '8334_hse_2016_eul_v5_corrections_to_ukds.pdf'. Main Topics: Data collection involved an interview, followed by a visit from a specially trained nurse for all those in the core sample who agreed. The 2016 survey included additional topics for adults on physical activity, weight management, kidney and liver disease and problem gambling. The survey also provided updates on repeated core topics, including general health, long standing illness, smoking and drinking. The nurse visit covered height and weight measurement, blood pressure measurement, waist and hip circumference measurement, taking of blood samples for cholesterol and glycated haemoglobin, and taking of adult and child saliva samples. In 2016, urine samples were also collected from adult participants. Multi-stage stratified random sample Face-to-face interview: Computer-assisted (CAPI/CAMI) Self-administered questionnaire

Analysis of ‘Access and Use of Telemedicine During COVID-19’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://catalog.data.gov/dataset/62ae3836-5b7b-4d97-b8e7-7e853aa39df0 on 26 January 2022.

--- Dataset description provided by original source is as follows ---

The Research and Development Survey (RANDS) is a platform designed for conducting survey question evaluation and statistical research. RANDS is an ongoing series of surveys from probability-sampled commercial survey panels used for methodological research at the National Center for Health Statistics (NCHS). RANDS estimates are generated using an experimental approach that differs from the survey design approaches generally used by NCHS, including possible biases from different response patterns and sampling frames as well as increased variability from lower sample sizes. Use of the RANDS platform allows NCHS to produce more timely data than would be possible using traditional data collection methods. RANDS is not designed to replace NCHS’ higher quality, core data collections. Below are experimental estimates of telemedicine access and use for three rounds of RANDS during COVID-19. Data collection for the three rounds of RANDS during COVID-19 occurred between June 9, 2020 and July 6, 2020, August 3, 2020 and August 20, 2020, and May 17, 2021 and June 30, 2021. Information needed to interpret these estimates can be found in the Technical Notes. RANDS during COVID-19 included questions about whether providers offered telemedicine (including video and telephone appointments) in the last 2 months—both during and before the pandemic—and about the use of telemedicine in the last 2 months during the pandemic. As a result of the coronavirus pandemic, many local and state governments discouraged people from leaving their homes for nonessential reasons. Although health care is considered an essential activity, telemedicine offers an opportunity for care without the potential or perceived risks of leaving the home. The National Health Interview Survey, conducted by NCHS, added telemedicine questions to its sample adult questionnaire in July 2020. The Household Pulse Survey (https://www.cdc.gov/nchs/covid19/pulse/telemedicine-use.htm), an online survey conducted in response to the COVID-19 pandemic by the Census Bureau in partnership with other federal agencies including NCHS, also reports estimates of telemedicine use during the pandemic (beginning in Phase 3.1, which started on April 14, 2021). The Household Pulse Survey reports telemedicine use in the last 4 weeks among adults and among households with at least one child under age 18 years. The experimental estimates on this page are derived from RANDS during COVID-19 and show the percentage of U.S. adults who have a usual place of care and a provider that offered telemedicine in the past 2 months, who used telemedicine in the past 2 months, or who have a usual place of care and a provider that offered telemedicine prior to the coronavirus pandemic. Technical Notes: https://www.cdc.gov/nchs/covid19/rands/telemedicine.htm#limitations

--- Original source retains full ownership of the source dataset ---

Abstract

The Indonesia Demographic and Health Survey (IDHS) is part of the worldwide Demographic and Health Surveys program, which is designed to collect data on fertility, family planning, and maternal and child health. The 2002-2003 IDHS follows a sequence of several previous surveys: the 1987 National Indonesia Contraceptive Prevalence Survey (NICPS), the 1991 IDHS, the 1994 IDHS, and the 1997 IDHS. The 2002-2003 IDHS is expanded from the 1997 IDHS by including a collection of information on the participation of currently married men and their wives and children in the health care.

The main objective of the 2002-2003 IDHS is to provide policymakers and program managers in population and health with detailed information on population, family planning, and health. In particular, the 2002-2003 IDHS collected information on the female respondents’ socioeconomic background, fertility levels, marriage and sexual activity, fertility preferences, knowledge and use of family planning methods, breastfeeding practices, childhood and adult mortality including maternal mortality, maternal and child health, and awareness and behavior regarding AIDS and other sexually transmitted infections in Indonesia.

The 2002-2003 IDHS was specifically designed to meet the following objectives: - Provide data concerning fertility, family planning, maternal and child health, maternal mortality, and awareness of AIDS/STIs to program managers, policymakers, and researchers to help them evaluate and improve existing programs - Measure trends in fertility and contraceptive prevalence rates, analyze factors that affect such changes, such as marital status and patterns, residence, education, breastfeeding habits, and knowledge, use, and availability of contraception - Evaluate achievement of goals previously set by the national health programs, with special focus on maternal and child health - Assess men’s participation and utilization of health services, as well as of their families - Assist in creating an international database that allows cross-country comparisons that can be used by the program managers, policymakers, and researchers in the area of family planning, fertility, and health in general.

Geographic coverage

National

Analysis unit

• Household
• Children under five years
• Women age 15-49
• Men age 15-54

Kind of data

Sample survey data

Sampling procedure

SAMPLE DESIGN AND IMPLEMENTATION

Administratively, Indonesia is divided into 30 provinces. Each province is subdivided into districts (regency in areas mostly rural and municipality in urban areas). Districts are subdivided into subdistricts and each subdistrict is divided into villages. The entire village is classified as urban or rural.

The primary objective of the 2002-2003 IDHS is to provide estimates with acceptable precision for the following domains: · Indonesia as a whole; · Each of 26 provinces covered in the survey. The four provinces excluded due to political instability are Nanggroe Aceh Darussalam, Maluku, North Maluku and Papua. These provinces cover 4 percent of the total population. · Urban and rural areas of Indonesia; · Each of the five districts in Central Java and the five districts in East Java covered in the Safe Motherhood Project (SMP), to provide information for the monitoring and evaluation of the project. These districts are: - in Central Java: Cilacap, Rembang, Jepara, Pemalang, and Brebes. - in East Java: Trenggalek, Jombang, Ngawi, Sampang and Pamekasan.

The census blocks (CBs) are the primary sampling unit for the 2002-2003 IDHS. CBs were formed during the preparation of the 2000 Population Census. Each CB includes approximately 80 households. In the master sample frame, the CBs are grouped by province, by regency/municipality within a province, and by subdistricts within a regency/municipality. In rural areas, the CBs in each district are listed by their geographical location. In urban areas, the CBs are distinguished by the urban classification (large, medium and small cities) in each subdistrict.

Note: See detailed description of sample design in APPENDIX B of the survey report.

Mode of data collection

Face-to-face

Research instrument

The 2002-2003 IDHS used three questionnaires: the Household Questionnaire, the Women’s Questionnaire for ever-married women 15-49 years old, and the Men’s Questionnaire for currently married men 15-54 years old. The Household Questionnaire and the Women’s Questionnaire were based on the DHS Model “A” Questionnaire, which is designed for use in countries with high contraceptive prevalence. In consultation with the NFPCB and MOH, BPS modified these questionnaires to reflect relevant issues in family planning and health in Indonesia. Inputs were also solicited from potential data users to optimize the IDHS in meeting the country’s needs for population and health data. The questionnaires were translated from English into the national language, Bahasa Indonesia.

The Household Questionnaire was used to list all the usual members and visitors in the selected households. Basic information collected for each person listed includes the following: age, sex, education, and relationship to the head of the household. The main purpose of the Household Questionnaire was to identify women and men who were eligible for the individual interview. In addition, the Household Questionnaire also identifies unmarried women and men age 15-24 who are eligible for the individual interview in the Indonesia Young Adult Reproductive Health Survey (IYARHS). Information on characteristics of the household’s dwelling unit, such as the source of water, type of toilet facilities, construction materials used for the floor and outer walls of the house, and ownership of various durable goods were also recorded in the Household Questionnaire. These items reflect the household’s socioeconomic status.

The Women’s Questionnaire was used to collect information from all ever-married women age 15-49. These women were asked questions on the following topics: • Background characteristics, such as age, marital status, education, and media exposure • Knowledge and use of family planning methods • Fertility preferences • Antenatal, delivery, and postnatal care • Breastfeeding and infant feeding practices • Vaccinations and childhood illnesses • Marriage and sexual activity • Woman’s work and husband’s background characteristics • Childhood mortality • Awareness and behavior regarding AIDS and other sexually transmitted infections (STIs) • Sibling mortality, including maternal mortality.

The Men’s Questionnaire was administered to all currently married men age 15-54 in every third household in the IDHS sample. The Men’s Questionnaire collected much of the same information included in the Women’s Questionnaire, but was shorter because it did not contain questions on reproductive history, maternal and child health, nutrition, and maternal mortality. Instead, men were asked about their knowledge and participation in the health-seeking practices for their children.

Cleaning operations

All completed questionnaires for IDHS, accompanied by their control forms, were returned to the BPS central office in Jakarta for data processing. This process consisted of office editing, coding of open-ended questions, data entry, verification, and editing computer-identified errors. A team of about 40 data entry clerks, data editors, and two data entry supervisors processed the data. Data entry and editing started on November 4, 2002 using a computer package program called CSPro, which was specifically designed to process DHS-type survey data. To prepare the data entry programs, two BPS staff spent three weeks in ORC Macro offices in Calverton, Maryland in April 2002.

Response rate

A total of 34,738 households were selected for the survey, of which 33,419 were found. Of the encountered households, 33,088 (99 percent) were successfully interviewed. In these households, 29,996 ever-married women 15-49 were identified, and complete interviews were obtained from 29,483 of them (98 percent). From the households selected for interviews with men, 8,740 currently married men 15-54 were identified, and complete interviews were obtained from 8,310 men, or 95 percent of all eligible men. The generally high response rates for both household and individual interviews (for eligible women and men) were due mainly to the strict enforcement of the rule to revisit the originally selected household if no one was at home initially. No substitution for the originally selected households was allowed. Interviewers were instructed to make at least three visits in an effort to contact the household, eligible women, and eligible men.

Note: See summarized response rates by place of residence in Table 1.2 of the survey report.

Sampling error estimates

The estimates from a sample survey are affected by two types of errors: (1) nonsampling errors, and (2) sampling errors. Nonsampling errors are the results of mistakes made in implementing data collection and data processing, such as failure to locate and interview the correct household, misunderstanding of the questions on the part of either the interviewer or the respondent, and data entry errors. Although numerous efforts were made during the implementation of the 2002-2003 Indonesia Demographic and Health Survey (IDHS) to minimize this type of error, nonsampling errors are impossible to avoid and difficult to evaluate statistically.

Sampling errors, on the other hand, can be evaluated statistically. The sample of respondents

Analysis of ‘Reduced Access to Care During COVID-19’ provided by Analyst-2 (analyst-2.ai), based on source dataset retrieved from https://catalog.data.gov/dataset/3f716763-bea5-4d84-989a-b1e688150d3d on 26 January 2022.

--- Dataset description provided by original source is as follows ---

The Research and Development Survey (RANDS) is a platform designed for conducting survey question evaluation and statistical research. RANDS is an ongoing series of surveys from probability-sampled commercial survey panels used for methodological research at the National Center for Health Statistics (NCHS). RANDS estimates are generated using an experimental approach that differs from the survey design approaches generally used by NCHS, including possible biases from different response patterns and sampling frames as well as increased variability from lower sample sizes. Use of the RANDS platform allows NCHS to produce more timely data than would be possible using traditional data collection methods. RANDS is not designed to replace NCHS’ higher quality, core data collections. Below are experimental estimates of reduced access to healthcare for three rounds of RANDS during COVID-19. Data collection for the three rounds of RANDS during COVID-19 occurred between June 9, 2020 and July 6, 2020, August 3, 2020 and August 20, 2020, and May 17, 2021 and June 30, 2021. Information needed to interpret these estimates can be found in the Technical Notes. RANDS during COVID-19 included questions about unmet care in the last 2 months during the coronavirus pandemic. Unmet needs for health care are often the result of cost-related barriers. The National Health Interview Survey, conducted by NCHS, is the source for high-quality data to monitor cost-related health care access problems in the United States. For example, in 2018, 7.3% of persons of all ages reported delaying medical care due to cost and 4.8% reported needing medical care but not getting it due to cost in the past year. However, cost is not the only reason someone might delay or not receive needed medical care. As a result of the coronavirus pandemic, people also may not get needed medical care due to cancelled appointments, cutbacks in transportation options, fear of going to the emergency room, or an altruistic desire to not be a burden on the health care system, among other reasons. The Household Pulse Survey (https://www.cdc.gov/nchs/covid19/pulse/reduced-access-to-care.htm), an online survey conducted in response to the COVID-19 pandemic by the Census Bureau in partnership with other federal agencies including NCHS, also reports estimates of reduced access to care during the pandemic (beginning in Phase 1, which started on April 23, 2020). The Household Pulse Survey reports the percentage of adults who delayed medical care in the last 4 weeks or who needed medical care at any time in the last 4 weeks for something other than coronavirus but did not get it because of the pandemic. The experimental estimates on this page are derived from RANDS during COVID-19 and show the percentage of U.S. adults who were unable to receive medical care (including urgent care, surgery, screening tests, ongoing treatment, regular checkups, prescriptions, dental care, vision care, and hearing care) in the last 2 months. Technical Notes: https://www.cdc.gov/nchs/covid19/rands/reduced-access-to-care.htm#limitations

--- Original source retains full ownership of the source dataset ---

A dataset that permits examination of health, economic, work, and retirement trajectories for a representative national sample of men from middle to old age. The original sample of 5,020 men, first interviewed in 1966, was re-interviewed periodically until 1983 under a contract with the US Department of Labor. The study provided a detailed longitudinal record of their labor market activity, health, financial status, family structure, and attitudes toward and experience in retirement. The NIA grant made possible a re-interview in 1990 with the surviving men and the widows (or other next-of-kin) of the decedents. The merging of the 1990 data includes death certificate information for the decedents, Blacks were over-represented in the original sample in a ratio of about three or four to one, resulting in about 500 surviving black men in the sample. Information on labor market activity, income, and assets also is available for a sample of about 1,350 widows, 90 percent of whom are between 60 and 89 years of age. This information can be linked to earlier data on the women''s health and work activity that was reported by their late husbands. Due to the original sample selection, other NLS cohorts contain wives and daughters of the older men. These other surveys also hold a wealth of detailed information on aging and retirement issues, especially on income transfers. * Dates of Study: 1966-1990 * Study Features: Longitudinal, Minority Oversamples * Sample Size: ** 1966: 5,020 men (baseline) ** 1990: 2,092 surviving men, 1,341 widows, 865 other next-of-kin Links: * BLS Website on NLS: http://www.bls.gov/nls/ * ICPSR: http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/04675

Overview

The Associated Press is sharing data from the COVID Impact Survey, which provides statistics about physical health, mental health, economic security and social dynamics related to the coronavirus pandemic in the United States.

Conducted by NORC at the University of Chicago for the Data Foundation, the probability-based survey provides estimates for the United States as a whole, as well as in 10 states (California, Colorado, Florida, Louisiana, Minnesota, Missouri, Montana, New York, Oregon and Texas) and eight metropolitan areas (Atlanta, Baltimore, Birmingham, Chicago, Cleveland, Columbus, Phoenix and Pittsburgh).

The survey is designed to allow for an ongoing gauge of public perception, health and economic status to see what is shifting during the pandemic. When multiple sets of data are available, it will allow for the tracking of how issues ranging from COVID-19 symptoms to economic status change over time.

The survey is focused on three core areas of research:

• Physical Health: Symptoms related to COVID-19, relevant existing conditions and health insurance coverage.
• Economic and Financial Health: Employment, food security, and government cash assistance.
• Social and Mental Health: Communication with friends and family, anxiety and volunteerism. (Questions based on those used on the U.S. Census Bureau’s Current Population Survey.) ## Using this Data - IMPORTANT This is survey data and must be properly weighted during analysis: DO NOT REPORT THIS DATA AS RAW OR AGGREGATE NUMBERS!!

Instead, use our queries linked below or statistical software such as R or SPSS to weight the data.

Queries

If you'd like to create a table to see how people nationally or in your state or city feel about a topic in the survey, use the survey questionnaire and codebook to match a question (the variable label) to a variable name. For instance, "How often have you felt lonely in the past 7 days?" is variable "soc5c".

Nationally: Go to this query and enter soc5c as the variable. Hit the blue Run Query button in the upper right hand corner.

Local or State: To find figures for that response in a specific state, go to this query and type in a state name and soc5c as the variable, and then hit the blue Run Query button in the upper right hand corner.

The resulting sentence you could write out of these queries is: "People in some states are less likely to report loneliness than others. For example, 66% of Louisianans report feeling lonely on none of the last seven days, compared with 52% of Californians. Nationally, 60% of people said they hadn't felt lonely."

Margin of Error

The margin of error for the national and regional surveys is found in the attached methods statement. You will need the margin of error to determine if the comparisons are statistically significant. If the difference is:

• At least twice the margin of error, you can report there is a clear difference.
• At least as large as the margin of error, you can report there is a slight or apparent difference.
• Less than or equal to the margin of error, you can report that the respondents are divided or there is no difference. ## A Note on Timing Survey results will generally be posted under embargo on Tuesday evenings. The data is available for release at 1 p.m. ET Thursdays.

About the Data

The survey data will be provided under embargo in both comma-delimited and statistical formats.

Each set of survey data will be numbered and have the date the embargo lifts in front of it in the format of: 01_April_30_covid_impact_survey. The survey has been organized by the Data Foundation, a non-profit non-partisan think tank, and is sponsored by the Federal Reserve Bank of Minneapolis and the Packard Foundation. It is conducted by NORC at the University of Chicago, a non-partisan research organization. (NORC is not an abbreviation, it part of the organization's formal name.)

Data for the national estimates are collected using the AmeriSpeak Panel, NORC’s probability-based panel designed to be representative of the U.S. household population. Interviews are conducted with adults age 18 and over representing the 50 states and the District of Columbia. Panel members are randomly drawn from AmeriSpeak with a target of achieving 2,000 interviews in each survey. Invited panel members may complete the survey online or by telephone with an NORC telephone interviewer.

Once all the study data have been made final, an iterative raking process is used to adjust for any survey nonresponse as well as any noncoverage or under and oversampling resulting from the study specific sample design. Raking variables include age, gender, census division, race/ethnicity, education, and county groupings based on county level counts of the number of COVID-19 deaths. Demographic weighting variables were obtained from the 2020 Current Population Survey. The count of COVID-19 deaths by county was obtained from USA Facts. The weighted data reflect the U.S. population of adults age 18 and over.

Data for the regional estimates are collected using a multi-mode address-based (ABS) approach that allows residents of each area to complete the interview via web or with an NORC telephone interviewer. All sampled households are mailed a postcard inviting them to complete the survey either online using a unique PIN or via telephone by calling a toll-free number. Interviews are conducted with adults age 18 and over with a target of achieving 400 interviews in each region in each survey.Additional details on the survey methodology and the survey questionnaire are attached below or can be found at https://www.covid-impact.org.

Attribution

Results should be credited to the COVID Impact Survey, conducted by NORC at the University of Chicago for the Data Foundation.

AP Data Distributions

​To learn more about AP's data journalism capabilities for publishers, corporations and financial institutions, go here or email kromano@ap.org.

Abstract copyright UK Data Service and data collection copyright owner.The Health Survey for England (HSE) is a series of surveys designed to monitor trends in the nation's health. It was commissioned by NHS Digital and carried out by the Joint Health Surveys Unit of the National Centre for Social Research and the Department of Epidemiology and Public Health at University College London.The aims of the HSE series are:to provide annual data about the nation’s health;to estimate the proportion of people in England with specified health conditions;to estimate the prevalence of certain risk factors associated with these conditions;to examine differences between population subgroups in their likelihood of having specific conditions or risk factors;to assess the frequency with which particular combinations of risk factors are found, and which groups these combinations most commonly occur;to monitor progress towards selected health targetssince 1995, to measure the height of children at different ages, replacing the National Study of Health and Growth;since 1995, monitor the prevalence of overweight and obesity in children.The survey includes a number of core questions every year but also focuses on different health issues at each wave. Topics are revisited at appropriate intervals in order to monitor change. Further information about the series may be found on the NHS Digital Health Survey for England; health, social care and lifestyles webpage, the NatCen Social Research NatCen Health Survey for England webpage and the University College London Health and Social Surveys Research Group UCL Health Survey for England webpage. Changes to the HSE from 2015:Users should note that from 2015 survey onwards, only the individual data file is available under standard End User Licence (EUL). The household data file is now only included in the Special Licence (SL) version, released from 2015 onwards. In addition, the SL individual file contains all the variables included in the HSE EUL dataset, plus others, including variables removed from the EUL version after the NHS Digital disclosure review. The SL HSE is subject to more restrictive access conditions than the EUL version (see Access information). Users are advised to obtain the EUL version to see if it meets their needs before considering an application for the SL version. The HSE 2005 was designed to provide data at both national and regional level about the population living in private households in England. The sample comprised three components: the core (general population) sample; a boost sample of people aged 65 years and over (those living in institutions were not included); and a boost sample of children aged 2-15. The core sample was designed to be representative of the population living in private households in England and should be used for analyses at the national level. All private households in the general population sample are eligible for inclusion in the survey (up to a maximum of three households per address). For the core sample, up to two children aged 0-15 are interviewed in each household, as well as up to 10 adults aged 16 and over. At boost sample addresses, interviewers screened for households containing at least one person of either of the age groups covered in the boost: persons aged 65 and over, or (for certain months) children aged 2-15 years. Because of funding restrictions, the boost sample only included children during fieldwork conducted in January, February, October, November and December. At each household where people of the eligible ages were found, all persons aged 65 and over, and up to two eligible children were selected by the interviewer for inclusion in the survey. Interviewing was conducted throughout the year to take account of seasonal differences. For the second edition (April 2010), three new children's Body Mass Index (BMI) variables have been added to the individual data file (bmicat1, bmicat2, bmicat3). The original variables (bmicut, bmicut2, bmicut3) are unreliable and should not be used. Further information is available in the documentation and on the Information Centre for Health and Social Care Health Survey for England web page. For the third edition (July 2011), the GHQ12 variables were amended to correct errors in the GHQ12 scores. See document 'Note about GHQ12 problems in HSE Data' for details. Main Topics: For adult respondents, the HSE 2005 focused on the health of older people. All adults were asked modules of questions on general health, alcohol consumption, smoking, fruit and vegetable consumption and complementary and alternative medicine. Older informants were also asked about use of health, dental and social care services, cardiovascular disease (CVD), chronic diseases and quality of care, disabilities and falls. Older informants in the boost sample received a slightly shorter questionnaire, omitting questions about fruit and vegetable consumption and complementary and alternative medicines. An interview with each eligible person was followed by a nurse visit. Children aged 13-15 years were interviewed themselves, and parents of children aged 0-12 were asked about their children. The child interview included questions on physical activity, and fruit and vegetable consumption. Standard Measures:General Health Questionnaire (GHQ12)Strengths and Difficulties Questionnaire (SDQ)Geriatric Depression ScoreEQ-5D Health State Multi-stage stratified random sample Face-to-face interview Self-completion Clinical measurements Physical measurements

BackgroundThe combined impact of multiple healthy behaviors on health exceeds that of single behaviors. This study aimed to estimate trends in the prevalence of a healthy lifestyle among adults in Germany.MethodsA data set of 18,058 adults aged 25–69 years from three population-based national health examination surveys 1990–92, 1997–99 and 2008–11 with complete information for five healthy behavior factors was used. A ‘daily intake of both fruits and vegetables, ‘sufficient physical exercise’, ‘no current smoking’ and ‘no current risk drinking’ were assessed with self-reports and ‘normal body weight’ was calculated based on measured body weight and height. A dichotomous ‘healthy lifestyle’ indicator was defined as meeting at least four out of five healthy behaviors. Age-standardized prevalence was calculated stratified by sex, age groups (25–34, 35–44, 45–54 and 55–69 years) and education level (low, medium and high). Trends were expressed in relative change (RC) between 1990–92 and 2008–11.ResultsIn Germany, the overall prevalence of healthy lifestyle increased from 9.3% in 1990–92 to 13.5% in 1997–99 and to 14.7% in 2008–11 (RC: +58.1%). The prevalence increased among men and women and in all age groups, with the exception of men aged 45–54 years. The RC of increasing healthy lifestyle prevalence between 1990–92 and 2008–11 was stronger albeit on a higher level among women compared to men. Therefore, the gender difference in healthy lifestyle has increased, but age-related differences have overall decreased in this period. Among high educated men the prevalence of a healthy lifestyle increased between 1990–92 and 2008–11 from 10.6% to 16.3% (p = 0.01) and among high educated women from 16.4% to 30.3% and also among medium educated women (10.9 to 16.6, p

The 1998 South Africa Demographic and Health Survey (SADHS) is the first study of its kind to be conducted in South Africa and heralds a new era of reliable and relevant information in South Africa. The SADHS, a nation-wide survey has collected information on key maternal and child health indicators, and in a first for international demographic and health surveys, the South African survey contains data on the health and disease patterns in adults. Plans to conduct the South Africa Demographic and Health Survey go as far back as 1995, when the Department of Health National Health Information Systems of South Africa (NHIS/SA) committee, recognised serious gaps in information required for health service planning and monitoring. Fieldwork was conducted between late January and September 1998, during which time 12,247 households were visited, 17,500 people throughout nine provinces were interviewed and 175 interviewers were trained to interview in 11 languages. The aim of the 1998 South Africa Demographic and Health Survey (SADHS) was to collect data as part of the National Health Information System of South Africa (NHIS/SA). The survey results are intended to assist policymakers and programme managers in evaluating and designing programmes and strategies for improving health services in the country. A variety of demographic and health indicators were collected in order to achieve the following general objectives: (i) To contribute to the information base for health and population development programme management through accurate and timely data on a range of demographic and health indicators. (ii) To provide baseline data for monitoring programmes and future planning. (iii) To build research and research management capacity in large-scale national demographic and health surveys. The primary objective of the SADHS is to provide up-to-date information on: basic demographic rates, particularly fertility and childhood mortality levels, awareness and use of contraceptive methods, breastfeeding practices, maternal and child health, awareness of HIV/AIDS, chronic health conditions among adults, lifestyles that affect the health status of adults, and anthropometric indicators.

The 1991 Health Activity Limitation Survey (HALS) is a post-censal survey used to identify the number and distribution of persons with disabilities in Canada and the barriers experienced by them in such areas as housing, employment, transportation, education, community support, and recreation. The Health and Activity Limitation Survey (HALS) was designed to collect data for a national database on disability. HALS is a post-censal survey, i.e., its survey frame is provided by the answers to two filter questions on the census questionnaire. It was first conducted after the 1986 Census of Population, and repeated after the 1991 census. It was not conducted after the 1996 census due to budget constraints. Survey year: 1991. Although there are some differences between the 1986 HALS and the 1991 HALS with respect to content and levels of geography, the objectives of the two surveys remain largely the same. The objectives for HALS are: to include persons with disabilities residing in the Yukon and Northwest Territories; to interview a sufficient number of persons with disabilities to enable the release of data for subprovincial areas (e.g. 17 Census Metropolitan Areas) as well as data on disabilities due to conditions that have a low prevalence. The target population of the 1991 HALS consisted of all persons with a physical, sensory, or psychological disability who were living in Canada at the 1991 Census, including residents of the Yukon and Northwest Territories, and permanent residents of most collective dwellings and health-care institutions. Although Indian reserves and settlements were included in the 1986 HALS, they were excluded from the 1991 HALS. Disablity data for Indian reserves and settlements may be obtained from the 1991 Aboriginal Peoples Survey, also conducted by Statistics Canada. Persons excluded for operational reasons were residents of penal institutions, correctional facilities, military camps, campgrounds and parks, soup kitchens, merchant and coastguard ships, and children's group homes. Data collection for the Household Survey took place in the Fall of 1991, immediately after the 1991 Census. Approximately 35,000 individuals were selected for the "yes" sample and 113,000 for the "no" sample, yielding a total of 148,000 adults and children for the household survey. Approximately 20% (or 7,000) of persons in the "yes" sample proved to have no disability according to HALS' criteria. For the 1986 HALS both a "yes" and a "no" sample were also selected. The "yes" sample size of 112,000 was significally larger in 1986 than in 1991, while the "no" sample of 72,5000 was smaller for the 1986 HALS. Due to a larger sample size for the 1986 HALS, data are available from the 1986 HALS for 200 sub-provincial areas and 19 CMAs. For detailed description of the differences between the 1986 and the 1991 HALS, please refer to Appendix B. The Household Survey was carried out in two stages. The first stage involved adding two questions to the 1991 Census long questionnaire, and the second involved conducting the actual survey for adults and children. Data collection for the Institutions Survey was carried out from January to March, 1992. All interviews were conducted in person and, whenever possible, with the selected individual. However, due to their conditions, many residents were not able to answer the questions themselves. In these cases the interviews were conducted with the help of institutional staff or next-of-kin. The response rate for the Institutions Survey was 96%.

Abstract copyright UK Data Service and data collection copyright owner. The Welsh Health Survey (WHS), which ran from 1995-1998 and then 2003/04-2015, collected information about the health of people living in Wales, the way they use health services, and then things that can affect their health. This dataset covers the twelfth and last year of the WHS. From April 2016 health and health related lifestyles are reported on using the National Survey for Wales. The WHS replaced two previous surveys; the former Welsh Health Survey (undertaken in 1995 (not held at the UK Data Archive) and 1998 (SN 4176)) and the former Health in Wales Survey (undertaken every two to three years between 1985 and 1996). Results from this survey are not comparable with those from the previous surveys because of differences in the questionnaires and survey methodology. The survey was designed to: provide national estimates of health and health-related lifestyleexamine differences between population sub-groups and local areasprovide evidence to inform and monitor policies and strategies for promoting better healthprovide data for setting and monitoring targets and indicatorsprovide local authority level information for development of joint local health, social care and well-being strategiesThe WHS was based on a representative sample of adults aged 16 and over living in private households in Wales. In addition, up to two children aged 0 to 15 were randomly selected from each household. Further information about the WHS, including links to publications, may be found on the Welsh Government's Welsh Health Survey web pages. Main Topics: The main topics covered for adults are: general health and wellbeinghealth service usemedicines and illnessesuntreated problems or symptomsalcohol and smokingfruit and vegetable consumptionexercisecarersheight and weightdemographicsinfant feedingThe main topics covered for children are: general health and well-beingGP, hospital and other service useaccidentsillnesses and other health problemseating habitsphysical activitystrengths and difficulties (SDQ) One-stage stratified or systematic random sample Face-to-face interview Self-completion Physical measurements