100+ datasets found
  1. National Survey of Health Attitudes, [United States], 2023

    • icpsr.umich.edu
    ascii, delimited, r +3
    Updated Dec 5, 2024
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    Chandra, Anita (2024). National Survey of Health Attitudes, [United States], 2023 [Dataset]. http://doi.org/10.3886/ICPSR39205.v1
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    delimited, ascii, stata, spss, r, sasAvailable download formats
    Dataset updated
    Dec 5, 2024
    Dataset provided by
    Inter-university Consortium for Political and Social Researchhttps://www.icpsr.umich.edu/web/pages/
    Authors
    Chandra, Anita
    License

    https://www.icpsr.umich.edu/web/ICPSR/studies/39205/termshttps://www.icpsr.umich.edu/web/ICPSR/studies/39205/terms

    Time period covered
    Nov 27, 2023 - Dec 19, 2023
    Area covered
    United States
    Description

    Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH. The National Survey of Health Attitudes (NSHA) is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values. This study includes the results from the 2023 RWJF National Survey of Health Attitudes. The 2023 survey is the third wave of the NSHA. The first wave was conducted in 2015 (ICPSR 37405) and the second wave in 2018 (ICPSR 37633). The 2023 report complements the overview of the 2015 survey described in the RAND report Development of the Robert Wood Johnson Foundation National Survey of Health Attitudes (Carman et al., 2016), and its subsequent topline 2018 Survey of National Health Attitudes: Description and Top-Line Summary (Carman et al., 2019) and is organized similarly for consistency. A companion set of longitudinal surveys during the COVID-19 pandemic was fielded between 2020 and 2021 and is further described in four top-line reports, COVID-19 and the Experiences of Populations at Greater Risk (Carman et al., 2020-2021). The questions in the 2023 survey uniquely capture aspects of American mindset about health, health equity, structural racism, and wellbeing in ways that are not present in other surveys. This version of the NSHA can be viewed in three main sections: (1) individual health experiences, perspectives, and knowledge (making health a shared value); (2) health equity perspectives; and (3) community wellbeing, including climate views and barriers to community engagement. Insights from the surveys referenced above, including this one, have established a baseline and set of cross-sectional pulse checks on where the American public is regarding their recognition of social determinants of health, their understanding of health inequities including structural racism, their willingness to address those inequities and their indication of who in society should be responsible for solving health inequities.

  2. National Health Interview Survey

    • catalog.data.gov
    • healthdata.gov
    • +3more
    Updated Jul 26, 2023
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    Centers for Disease Control and Prevention, Department of Health & Human Services (2023). National Health Interview Survey [Dataset]. https://catalog.data.gov/dataset/national-health-interview-survey
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    Dataset updated
    Jul 26, 2023
    Description

    The National Health Interview Survey (NHIS) is the principal source of information on the health of the civilian noninstitutionalized population of the United States and is one of the major data collection programs of the National Center for Health Statistics (NCHS) which is part of the Centers for Disease Control and Prevention (CDC). The National Health Survey Act of 1956 provided for a continuing survey and special studies to secure accurate and current statistical information on the amount, distribution, and effects of illness and disability in the United States and the services rendered for or because of such conditions. The survey referred to in the Act, now called the National Health Interview Survey, was initiated in July 1957. Since 1960, the survey has been conducted by NCHS, which was formed when the National Health Survey and the National Vital Statistics Division were combined. NHIS data are used widely throughout the Department of Health and Human Services (DHHS) to monitor trends in illness and disability and to track progress toward achieving national health objectives. The data are also used by the public health research community for epidemiologic and policy analysis of such timely issues as characterizing those with various health problems, determining barriers to accessing and using appropriate health care, and evaluating Federal health programs. The NHIS also has a central role in the ongoing integration of household surveys in DHHS. The designs of two major DHHS national household surveys have been or are linked to the NHIS. The National Survey of Family Growth used the NHIS sampling frame in its first five cycles and the Medical Expenditure Panel Survey currently uses half of the NHIS sampling frame. Other linkage includes linking NHIS data to death certificates in the National Death Index (NDI). While the NHIS has been conducted continuously since 1957, the content of the survey has been updated about every 10-15 years. In 1996, a substantially revised NHIS questionnaire began field testing. This revised questionnaire, described in detail below, was implemented in 1997 and has improved the ability of the NHIS to provide important health information.

  3. Consumer Healthcare Experience State Surveys, United States, 2022

    • icpsr.umich.edu
    ascii, delimited, r +3
    Updated May 3, 2023
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    Beaudin-Seiler, Beth (2023). Consumer Healthcare Experience State Surveys, United States, 2022 [Dataset]. http://doi.org/10.3886/ICPSR38596.v1
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    stata, spss, sas, ascii, delimited, rAvailable download formats
    Dataset updated
    May 3, 2023
    Dataset provided by
    Inter-university Consortium for Political and Social Researchhttps://www.icpsr.umich.edu/web/pages/
    Authors
    Beaudin-Seiler, Beth
    License

    https://www.icpsr.umich.edu/web/ICPSR/studies/38596/termshttps://www.icpsr.umich.edu/web/ICPSR/studies/38596/terms

    Time period covered
    2022
    Area covered
    United States, Missouri, Maryland, Illinois, New Jersey
    Description

    Altarum's Consumer Healthcare Experience State Survey (CHESS) and Medical Debt Survey are designed to elicit respondents' unbiased views on a wide range of health system issues, including confidence in using the health system, financial burden, medical debt, and views on fixes that might be needed. The surveys use a web panel from Dynata with a demographically balanced sample of approximately 1,500 respondents who live in a targeted state. The surveys were conducted in English or Spanish and restricted to adults ages 18 and older. Respondents who finished the surveys in less than half the median time were excluded from the final sample.

  4. d

    Washington Health Workforce Survey

    • catalog.data.gov
    • data.virginia.gov
    • +2more
    Updated Sep 6, 2024
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    data.kingcounty.gov (2024). Washington Health Workforce Survey [Dataset]. https://catalog.data.gov/dataset/washington-health-workforce-survey
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    Dataset updated
    Sep 6, 2024
    Dataset provided by
    data.kingcounty.gov
    Area covered
    Washington
    Description

    The Washington State Department of Health presents this information as a service to the public. This includes information on the work status, practice characteristics, education, and demographics of healthcare providers, provided in response to the Washington Health Workforce Survey. This is a complete set of data across all of the responding professions. The data dictionary identifies questions that are specific to an individual profession and aren't common to all surveys. The dataset is provided without identifying information for the responding providers. More information on the Washington Health Workforce Survey can be found at www.doh.wa.gov/workforcesurvey This dataset has been federated from https://data.wa.gov/Health/Washington-Health-Workforce-Survey-Data/cvrw-ujje.

  5. World Health Survey 2003 - Finland

    • apps.who.int
    • catalog.ihsn.org
    • +1more
    Updated Jun 19, 2013
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    World Health Organization (WHO) (2013). World Health Survey 2003 - Finland [Dataset]. https://apps.who.int/healthinfo/systems/surveydata/index.php/catalog/121
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    Dataset updated
    Jun 19, 2013
    Dataset provided by
    World Health Organizationhttps://who.int/
    Authors
    World Health Organization (WHO)
    Time period covered
    2003
    Area covered
    Finland
    Description

    Abstract

    Different countries have different health outcomes that are in part due to the way respective health systems perform. Regardless of the type of health system, individuals will have health and non-health expectations in terms of how the institution responds to their needs. In many countries, however, health systems do not perform effectively and this is in part due to lack of information on health system performance, and on the different service providers.

    The aim of the WHO World Health Survey is to provide empirical data to the national health information systems so that there is a better monitoring of health of the people, responsiveness of health systems and measurement of health-related parameters.

    The overall aims of the survey is to examine the way populations report their health, understand how people value health states, measure the performance of health systems in relation to responsiveness and gather information on modes and extents of payment for health encounters through a nationally representative population based community survey. In addition, it addresses various areas such as health care expenditures, adult mortality, birth history, various risk factors, assessment of main chronic health conditions and the coverage of health interventions, in specific additional modules.

    The objectives of the survey programme are to: 1. develop a means of providing valid, reliable and comparable information, at low cost, to supplement the information provided by routine health information systems. 2. build the evidence base necessary for policy-makers to monitor if health systems are achieving the desired goals, and to assess if additional investment in health is achieving the desired outcomes. 3. provide policy-makers with the evidence they need to adjust their policies, strategies and programmes as necessary.

    Geographic coverage

    The survey sampling frame must cover 100% of the country's eligible population, meaning that the entire national territory must be included. This does not mean that every province or territory need be represented in the survey sample but, rather, that all must have a chance (known probability) of being included in the survey sample.

    There may be exceptional circumstances that preclude 100% national coverage. Certain areas in certain countries may be impossible to include due to reasons such as accessibility or conflict. All such exceptions must be discussed with WHO sampling experts. If any region must be excluded, it must constitute a coherent area, such as a particular province or region. For example if ¾ of region D in country X is not accessible due to war, the entire region D will be excluded from analysis.

    Analysis unit

    Households and individuals

    Universe

    The WHS will include all male and female adults (18 years of age and older) who are not out of the country during the survey period. It should be noted that this includes the population who may be institutionalized for health reasons at the time of the survey: all persons who would have fit the definition of household member at the time of their institutionalisation are included in the eligible population.

    If the randomly selected individual is institutionalized short-term (e.g. a 3-day stay at a hospital) the interviewer must return to the household when the individual will have come back to interview him/her. If the randomly selected individual is institutionalized long term (e.g. has been in a nursing home the last 8 years), the interviewer must travel to that institution to interview him/her.

    The target population includes any adult, male or female age 18 or over living in private households. Populations in group quarters, on military reservations, or in other non-household living arrangements will not be eligible for the study. People who are in an institution due to a health condition (such as a hospital, hospice, nursing home, home for the aged, etc.) at the time of the visit to the household are interviewed either in the institution or upon their return to their household if this is within a period of two weeks from the first visit to the household.

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    SAMPLING GUIDELINES FOR WHS

    Surveys in the WHS program must employ a probability sampling design. This means that every single individual in the sampling frame has a known and non-zero chance of being selected into the survey sample. While a Single Stage Random Sample is ideal if feasible, it is recognized that most sites will carry out Multi-stage Cluster Sampling.

    The WHS sampling frame should cover 100% of the eligible population in the surveyed country. This means that every eligible person in the country has a chance of being included in the survey sample. It also means that particular ethnic groups or geographical areas may not be excluded from the sampling frame.

    The sample size of the WHS in each country is 5000 persons (exceptions considered on a by-country basis). An adequate number of persons must be drawn from the sampling frame to account for an estimated amount of non-response (refusal to participate, empty houses etc.). The highest estimate of potential non-response and empty households should be used to ensure that the desired sample size is reached at the end of the survey period. This is very important because if, at the end of data collection, the required sample size of 5000 has not been reached additional persons must be selected randomly into the survey sample from the sampling frame. This is both costly and technically complicated (if this situation is to occur, consult WHO sampling experts for assistance), and best avoided by proper planning before data collection begins.

    All steps of sampling, including justification for stratification, cluster sizes, probabilities of selection, weights at each stage of selection, and the computer program used for randomization must be communicated to WHO

    STRATIFICATION

    Stratification is the process by which the population is divided into subgroups. Sampling will then be conducted separately in each subgroup. Strata or subgroups are chosen because evidence is available that they are related to the outcome (e.g. health, responsiveness, mortality, coverage etc.). The strata chosen will vary by country and reflect local conditions. Some examples of factors that can be stratified on are geography (e.g. North, Central, South), level of urbanization (e.g. urban, rural), socio-economic zones, provinces (especially if health administration is primarily under the jurisdiction of provincial authorities), or presence of health facility in area. Strata to be used must be identified by each country and the reasons for selection explicitly justified.

    Stratification is strongly recommended at the first stage of sampling. Once the strata have been chosen and justified, all stages of selection will be conducted separately in each stratum. We recommend stratifying on 3-5 factors. It is optimum to have half as many strata (note the difference between stratifying variables, which may be such variables as gender, socio-economic status, province/region etc. and strata, which are the combination of variable categories, for example Male, High socio-economic status, Xingtao Province would be a stratum).

    Strata should be as homogenous as possible within and as heterogeneous as possible between. This means that strata should be formulated in such a way that individuals belonging to a stratum should be as similar to each other with respect to key variables as possible and as different as possible from individuals belonging to a different stratum. This maximises the efficiency of stratification in reducing sampling variance.

    MULTI-STAGE CLUSTER SELECTION

    A cluster is a naturally occurring unit or grouping within the population (e.g. enumeration areas, cities, universities, provinces, hospitals etc.); it is a unit for which the administrative level has clear, nonoverlapping boundaries. Cluster sampling is useful because it avoids having to compile exhaustive lists of every single person in the population. Clusters should be as heterogeneous as possible within and as homogenous as possible between (note that this is the opposite criterion as that for strata). Clusters should be as small as possible (i.e. large administrative units such as Provinces or States are not good clusters) but not so small as to be homogenous.

    In cluster sampling, a number of clusters are randomly selected from a list of clusters. Then, either all members of the chosen cluster or a random selection from among them are included in the sample. Multistage sampling is an extension of cluster sampling where a hierarchy of clusters are chosen going from larger to smaller.

    In order to carry out multi-stage sampling, one needs to know only the population sizes of the sampling units. For the smallest sampling unit above the elementary unit however, a complete list of all elementary units (households) is needed; in order to be able to randomly select among all households in the TSU, a list of all those households is required. This information may be available from the most recent population census. If the last census was >3 years ago or the information furnished by it was of poor quality or unreliable, the survey staff will have the task of enumerating all households in the smallest randomly selected sampling unit. It is very important to budget for this step if it is necessary and ensure that all households are properly enumerated in order that a representative sample is obtained.

    It is always best to have as many clusters in the PSU as possible. The reason for this is that the fewer the number of respondents in each PSU, the lower will be the clustering effect which

  6. Health Interview Surveys (HIS)

    • healthinformationportal.eu
    html
    Updated Sep 6, 2022
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    Institute of Health Information and Statistics of the Czech Republic (2022). Health Interview Surveys (HIS) [Dataset]. https://www.healthinformationportal.eu/health-information-sources/health-interview-survey-his
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    htmlAvailable download formats
    Dataset updated
    Sep 6, 2022
    Dataset authored and provided by
    Institute of Health Information and Statistics of the Czech Republic
    License

    MIT Licensehttps://opensource.org/licenses/MIT
    License information was derived automatically

    Variables measured
    sex, title, topics, country, language, data_owners, description, contact_name, geo_coverage, contact_email, and 12 more
    Measurement technique
    Survey/interview data
    Description

    Since 1993, the Czech Republic has carried out the so-called Sample Survey on the Health Status of the Czech Population, referred to as the HIS CR. This survey was conducted by the Institute of Health Information and Statistics of the Czech Republic every three years until 2002. In subsequent years, it was followed up by the European Health Sample Survey (EHIS), which took place in the Czech Republic in 2008 and 2014.

  7. World Health Survey 2003, Wave 0 - China

    • apps.who.int
    • catalog.ihsn.org
    • +2more
    Updated Jun 19, 2013
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    World Health Organization (WHO) (2013). World Health Survey 2003, Wave 0 - China [Dataset]. https://apps.who.int/healthinfo/systems/surveydata/index.php/catalog/78
    Explore at:
    Dataset updated
    Jun 19, 2013
    Dataset provided by
    World Health Organizationhttps://who.int/
    Authors
    World Health Organization (WHO)
    Time period covered
    2003
    Area covered
    China
    Description

    Abstract

    Different countries have different health outcomes that are in part due to the way respective health systems perform. Regardless of the type of health system, individuals will have health and non-health expectations in terms of how the institution responds to their needs. In many countries, however, health systems do not perform effectively and this is in part due to lack of information on health system performance, and on the different service providers.

    The aim of the WHO World Health Survey is to provide empirical data to the national health information systems so that there is a better monitoring of health of the people, responsiveness of health systems and measurement of health-related parameters.

    The overall aims of the survey is to examine the way populations report their health, understand how people value health states, measure the performance of health systems in relation to responsiveness and gather information on modes and extents of payment for health encounters through a nationally representative population based community survey. In addition, it addresses various areas such as health care expenditures, adult mortality, birth history, various risk factors, assessment of main chronic health conditions and the coverage of health interventions, in specific additional modules.

    The objectives of the survey programme are to: 1. develop a means of providing valid, reliable and comparable information, at low cost, to supplement the information provided by routine health information systems. 2. build the evidence base necessary for policy-makers to monitor if health systems are achieving the desired goals, and to assess if additional investment in health is achieving the desired outcomes. 3. provide policy-makers with the evidence they need to adjust their policies, strategies and programmes as necessary.

    Geographic coverage

    The survey sampling frame must cover 100% of the country's eligible population, meaning that the entire national territory must be included. This does not mean that every province or territory need be represented in the survey sample but, rather, that all must have a chance (known probability) of being included in the survey sample.

    There may be exceptional circumstances that preclude 100% national coverage. Certain areas in certain countries may be impossible to include due to reasons such as accessibility or conflict. All such exceptions must be discussed with WHO sampling experts. If any region must be excluded, it must constitute a coherent area, such as a particular province or region. For example if ¾ of region D in country X is not accessible due to war, the entire region D will be excluded from analysis.

    Analysis unit

    Households and individuals

    Universe

    The WHS will include all male and female adults (18 years of age and older) who are not out of the country during the survey period. It should be noted that this includes the population who may be institutionalized for health reasons at the time of the survey: all persons who would have fit the definition of household member at the time of their institutionalisation are included in the eligible population.

    If the randomly selected individual is institutionalized short-term (e.g. a 3-day stay at a hospital) the interviewer must return to the household when the individual will have come back to interview him/her. If the randomly selected individual is institutionalized long term (e.g. has been in a nursing home the last 8 years), the interviewer must travel to that institution to interview him/her.

    The target population includes any adult, male or female age 18 or over living in private households. Populations in group quarters, on military reservations, or in other non-household living arrangements will not be eligible for the study. People who are in an institution due to a health condition (such as a hospital, hospice, nursing home, home for the aged, etc.) at the time of the visit to the household are interviewed either in the institution or upon their return to their household if this is within a period of two weeks from the first visit to the household.

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    SAMPLING GUIDELINES FOR WHS

    Surveys in the WHS program must employ a probability sampling design. This means that every single individual in the sampling frame has a known and non-zero chance of being selected into the survey sample. While a Single Stage Random Sample is ideal if feasible, it is recognized that most sites will carry out Multi-stage Cluster Sampling.

    The WHS sampling frame should cover 100% of the eligible population in the surveyed country. This means that every eligible person in the country has a chance of being included in the survey sample. It also means that particular ethnic groups or geographical areas may not be excluded from the sampling frame.

    The sample size of the WHS in each country is 5000 persons (exceptions considered on a by-country basis). An adequate number of persons must be drawn from the sampling frame to account for an estimated amount of non-response (refusal to participate, empty houses etc.). The highest estimate of potential non-response and empty households should be used to ensure that the desired sample size is reached at the end of the survey period. This is very important because if, at the end of data collection, the required sample size of 5000 has not been reached additional persons must be selected randomly into the survey sample from the sampling frame. This is both costly and technically complicated (if this situation is to occur, consult WHO sampling experts for assistance), and best avoided by proper planning before data collection begins.

    All steps of sampling, including justification for stratification, cluster sizes, probabilities of selection, weights at each stage of selection, and the computer program used for randomization must be communicated to WHO

    STRATIFICATION

    Stratification is the process by which the population is divided into subgroups. Sampling will then be conducted separately in each subgroup. Strata or subgroups are chosen because evidence is available that they are related to the outcome (e.g. health, responsiveness, mortality, coverage etc.). The strata chosen will vary by country and reflect local conditions. Some examples of factors that can be stratified on are geography (e.g. North, Central, South), level of urbanization (e.g. urban, rural), socio-economic zones, provinces (especially if health administration is primarily under the jurisdiction of provincial authorities), or presence of health facility in area. Strata to be used must be identified by each country and the reasons for selection explicitly justified.

    Stratification is strongly recommended at the first stage of sampling. Once the strata have been chosen and justified, all stages of selection will be conducted separately in each stratum. We recommend stratifying on 3-5 factors. It is optimum to have half as many strata (note the difference between stratifying variables, which may be such variables as gender, socio-economic status, province/region etc. and strata, which are the combination of variable categories, for example Male, High socio-economic status, Xingtao Province would be a stratum).

    Strata should be as homogenous as possible within and as heterogeneous as possible between. This means that strata should be formulated in such a way that individuals belonging to a stratum should be as similar to each other with respect to key variables as possible and as different as possible from individuals belonging to a different stratum. This maximises the efficiency of stratification in reducing sampling variance.

    MULTI-STAGE CLUSTER SELECTION

    A cluster is a naturally occurring unit or grouping within the population (e.g. enumeration areas, cities, universities, provinces, hospitals etc.); it is a unit for which the administrative level has clear, nonoverlapping boundaries. Cluster sampling is useful because it avoids having to compile exhaustive lists of every single person in the population. Clusters should be as heterogeneous as possible within and as homogenous as possible between (note that this is the opposite criterion as that for strata). Clusters should be as small as possible (i.e. large administrative units such as Provinces or States are not good clusters) but not so small as to be homogenous.

    In cluster sampling, a number of clusters are randomly selected from a list of clusters. Then, either all members of the chosen cluster or a random selection from among them are included in the sample. Multistage sampling is an extension of cluster sampling where a hierarchy of clusters are chosen going from larger to smaller.

    In order to carry out multi-stage sampling, one needs to know only the population sizes of the sampling units. For the smallest sampling unit above the elementary unit however, a complete list of all elementary units (households) is needed; in order to be able to randomly select among all households in the TSU, a list of all those households is required. This information may be available from the most recent population census. If the last census was >3 years ago or the information furnished by it was of poor quality or unreliable, the survey staff will have the task of enumerating all households in the smallest randomly selected sampling unit. It is very important to budget for this step if it is necessary and ensure that all households are properly enumerated in order that a representative sample is obtained.

    It is always best to have as many clusters in the PSU as possible. The reason for this is that the fewer the number of respondents in each PSU, the lower will be the clustering effect which

  8. o

    National Survey of Healthcare Organizations and Systems Summary Public Use...

    • openicpsr.org
    Updated Mar 16, 2022
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    Ellen Meara (2022). National Survey of Healthcare Organizations and Systems Summary Public Use Datasets 2017-2018 [Dataset]. http://doi.org/10.3886/E165241V1
    Explore at:
    Dataset updated
    Mar 16, 2022
    Dataset provided by
    Harvard University, T.H. Chan School of Public Health; The Dartmouth Institute for Health Policy and Clinical Practice, Geisel School of Medicine at Dartmouth
    Authors
    Ellen Meara
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Area covered
    United States
    Description

    The National Survey of Healthcare Organizations and Systems (NSHOS) was developed by researchers at Dartmouth College in collaboration with Harvard University; University of California, Berkeley; Mayo Clinic and the High Value Healthcare Collaborative. The NSHOS was fielded from June 2017-August 2018 with funding from the Agency for Healthcare Research and Quality's Comparative Health System Performance Initiative. This suite of nationally representative surveys aimed to characterize the structure, ownership, leadership, and care delivery capabilities of health care systems, primary and multispecialty care physician practices, and hospitals. The surveys assess ownership, mental and behavioral health, information collection for quality improvement, and ACO participation, among other topics. Practice managers and physicians at practices and C-suite leaders at hospitals were contacted with up to four mailings with invitations to complete the survey on paper or electronically. Email and telephone outreach were conducted when possible. Most respondents completed the survey on paper. Up to three individuals in each practice were contacted for practices that had not already completed the survey.These public versions of the practice and hospital surveys include a subset of survey questions and scales to prevent identification of respondents.

  9. H

    Healthcare Survey Tools Report

    • datainsightsmarket.com
    doc, pdf, ppt
    Updated May 1, 2025
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    Data Insights Market (2025). Healthcare Survey Tools Report [Dataset]. https://www.datainsightsmarket.com/reports/healthcare-survey-tools-1429545
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    pdf, ppt, docAvailable download formats
    Dataset updated
    May 1, 2025
    Dataset authored and provided by
    Data Insights Market
    License

    https://www.datainsightsmarket.com/privacy-policyhttps://www.datainsightsmarket.com/privacy-policy

    Time period covered
    2025 - 2033
    Area covered
    Global
    Variables measured
    Market Size
    Description

    Discover the booming Healthcare Survey Tools market! This in-depth analysis reveals a CAGR of 15-20%, driven by patient-centric care and digital health. Explore market size, key trends, top companies (SurveyMonkey, Qualtrics, etc.), and regional insights to unlock growth opportunities. Get the data-driven perspective you need!

  10. w

    Service Delivery Indicators Health Survey 2018 - Harmonized Public Use Data...

    • microdata.worldbank.org
    • catalog.ihsn.org
    Updated Jul 20, 2021
    + more versions
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    Statistics Sierra Leone (2021). Service Delivery Indicators Health Survey 2018 - Harmonized Public Use Data - Sierra Leone [Dataset]. https://microdata.worldbank.org/index.php/catalog/4038
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    Dataset updated
    Jul 20, 2021
    Dataset authored and provided by
    Statistics Sierra Leone
    Time period covered
    2018
    Area covered
    Sierra Leone
    Description

    Abstract

    The Service Delivery Indicators (SDI) are a set of health and education indicators that examine the effort and ability of staff and the availability of key inputs and resources that contribute to a functioning school or health facility. The indicators are standardized, allowing comparison between and within countries over time.

    The Health SDIs include healthcare provider effort, knowledge and ability, and the availability of key inputs (for example, basic equipment, medicines and infrastructure, such as toilets and electricity). The indicators provide a snapshot of the health facility and assess the availability of key resources for providing high quality care.

    The Sierra Leone SDI Health survey team visited a sample of 536 health facilities across Sierra Leone between January and April 2018. The survey team collected rosters covering 5,055 workers for absenteeism and assessed 829 health workers for competence using patient case simulations.

    Geographic coverage

    National

    Analysis unit

    Health facilities and healthcare providers

    Universe

    All health facilities providing primary-level care

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    The sampling strategy for SDI surveys is designed towards attaining indicators that are accurate and representative at the national level, as this allows for proper cross-country (i.e. international benchmarking) and across time comparisons, when applicable. In addition, other levels of representativeness are sought to allow for further disaggregation (rural/urban areas, public/private facilities, subregions, etc.) during the analysis stage.

    The sampling strategy for SDI surveys follows a multistage sampling approach. The main units of analysis are facilities (schools and health centers) and providers (health and education workers: teachers, doctors, nurses, facility managers, etc.). The multi-stage sampling approach makes sampling procedures more practical by dividing the selection of large populations of sampling units in a step-by-step fashion. After defining the sampling frame and categorizing it by stratum, a first stage selection of sampling units is carried out independently within each stratum. Often, the primary sampling units (PSU) for this stage are cluster locations (e.g. districts, communities, counties, neighborhoods, etc.) which are randomly drawn within each stratum with a probability proportional to the size (PPS) of the cluster (measured by the location’s number of facilities, providers or pupils). Once locations are selected, a second stage takes place by randomly selecting facilities within location (either with equal probability or with PPS) as secondary sampling units. At a third stage, a fixed number of health and education workers and pupils are randomly selected within facilities to provide information for the different questionnaire modules.

    Detailed information about the specific sampling process is available in the associated SDI Country Report included as part of the documentation that accompany these datasets.

    Mode of data collection

    Face-to-face [f2f]

    Research instrument

    The SDI Health Survey Questionnaire consists of four modules:

    Module 1: General Information - Administered to the health facility manager to collect information on equipment, medicines, infrastructure and other facets of the health facility.

    Module 2: Provider Absence - A roster of healthcare providers is collected and absence measured.

    Module 3: Clinical Vignettes – A selection of providers are given clinical vignettes to measure knowledge of common medical conditions.

    Module 4: Facility finances – Information on facility revenue and expenditures is collected from the health facility manager.

    Weights: Weights for facilities, absentee-related analyses and clinical vignette analyses.

    Cleaning operations

    Quality control was performed in Stata.

  11. World Health Survey

    • datacatalog.hshsl.umaryland.edu
    Updated Apr 24, 2024
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    World Health Organization (2024). World Health Survey [Dataset]. https://datacatalog.hshsl.umaryland.edu/dataset/83
    Explore at:
    Dataset updated
    Apr 24, 2024
    Dataset authored and provided by
    World Health Organizationhttps://who.int/
    Time period covered
    Jan 1, 2002 - Dec 31, 2004
    Area covered
    Global
    Description

    The World Health Survey was implemented by WHO in 2002–2004 in partnership with 70 countries to generate information on the health of adult populations and health systems. The total sample size in these cross-sectional studies includes over 300,000 individuals. Survey materials and data are available through the WHO World Health Survey Data Archive accessible from the WHS webpage. (From the WHO World Health Survey webpage).

  12. World Health Survey 2003 - Chad

    • apps.who.int
    • catalog.ihsn.org
    • +1more
    Updated Jun 19, 2013
    + more versions
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    World Health Organization (WHO) (2013). World Health Survey 2003 - Chad [Dataset]. https://apps.who.int/healthinfo/systems/surveydata/index.php/catalog/77
    Explore at:
    Dataset updated
    Jun 19, 2013
    Dataset provided by
    World Health Organizationhttps://who.int/
    Authors
    World Health Organization (WHO)
    Time period covered
    2003
    Area covered
    Chad
    Description

    Abstract

    Different countries have different health outcomes that are in part due to the way respective health systems perform. Regardless of the type of health system, individuals will have health and non-health expectations in terms of how the institution responds to their needs. In many countries, however, health systems do not perform effectively and this is in part due to lack of information on health system performance, and on the different service providers.

    The aim of the WHO World Health Survey is to provide empirical data to the national health information systems so that there is a better monitoring of health of the people, responsiveness of health systems and measurement of health-related parameters.

    The overall aims of the survey is to examine the way populations report their health, understand how people value health states, measure the performance of health systems in relation to responsiveness and gather information on modes and extents of payment for health encounters through a nationally representative population based community survey. In addition, it addresses various areas such as health care expenditures, adult mortality, birth history, various risk factors, assessment of main chronic health conditions and the coverage of health interventions, in specific additional modules.

    The objectives of the survey programme are to: 1. develop a means of providing valid, reliable and comparable information, at low cost, to supplement the information provided by routine health information systems. 2. build the evidence base necessary for policy-makers to monitor if health systems are achieving the desired goals, and to assess if additional investment in health is achieving the desired outcomes. 3. provide policy-makers with the evidence they need to adjust their policies, strategies and programmes as necessary.

    Geographic coverage

    The survey sampling frame must cover 100% of the country's eligible population, meaning that the entire national territory must be included. This does not mean that every province or territory need be represented in the survey sample but, rather, that all must have a chance (known probability) of being included in the survey sample.

    There may be exceptional circumstances that preclude 100% national coverage. Certain areas in certain countries may be impossible to include due to reasons such as accessibility or conflict. All such exceptions must be discussed with WHO sampling experts. If any region must be excluded, it must constitute a coherent area, such as a particular province or region. For example if ¾ of region D in country X is not accessible due to war, the entire region D will be excluded from analysis.

    Analysis unit

    Households and individuals

    Universe

    The WHS will include all male and female adults (18 years of age and older) who are not out of the country during the survey period. It should be noted that this includes the population who may be institutionalized for health reasons at the time of the survey: all persons who would have fit the definition of household member at the time of their institutionalisation are included in the eligible population.

    If the randomly selected individual is institutionalized short-term (e.g. a 3-day stay at a hospital) the interviewer must return to the household when the individual will have come back to interview him/her. If the randomly selected individual is institutionalized long term (e.g. has been in a nursing home the last 8 years), the interviewer must travel to that institution to interview him/her.

    The target population includes any adult, male or female age 18 or over living in private households. Populations in group quarters, on military reservations, or in other non-household living arrangements will not be eligible for the study. People who are in an institution due to a health condition (such as a hospital, hospice, nursing home, home for the aged, etc.) at the time of the visit to the household are interviewed either in the institution or upon their return to their household if this is within a period of two weeks from the first visit to the household.

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    SAMPLING GUIDELINES FOR WHS

    Surveys in the WHS program must employ a probability sampling design. This means that every single individual in the sampling frame has a known and non-zero chance of being selected into the survey sample. While a Single Stage Random Sample is ideal if feasible, it is recognized that most sites will carry out Multi-stage Cluster Sampling.

    The WHS sampling frame should cover 100% of the eligible population in the surveyed country. This means that every eligible person in the country has a chance of being included in the survey sample. It also means that particular ethnic groups or geographical areas may not be excluded from the sampling frame.

    The sample size of the WHS in each country is 5000 persons (exceptions considered on a by-country basis). An adequate number of persons must be drawn from the sampling frame to account for an estimated amount of non-response (refusal to participate, empty houses etc.). The highest estimate of potential non-response and empty households should be used to ensure that the desired sample size is reached at the end of the survey period. This is very important because if, at the end of data collection, the required sample size of 5000 has not been reached additional persons must be selected randomly into the survey sample from the sampling frame. This is both costly and technically complicated (if this situation is to occur, consult WHO sampling experts for assistance), and best avoided by proper planning before data collection begins.

    All steps of sampling, including justification for stratification, cluster sizes, probabilities of selection, weights at each stage of selection, and the computer program used for randomization must be communicated to WHO

    STRATIFICATION

    Stratification is the process by which the population is divided into subgroups. Sampling will then be conducted separately in each subgroup. Strata or subgroups are chosen because evidence is available that they are related to the outcome (e.g. health, responsiveness, mortality, coverage etc.). The strata chosen will vary by country and reflect local conditions. Some examples of factors that can be stratified on are geography (e.g. North, Central, South), level of urbanization (e.g. urban, rural), socio-economic zones, provinces (especially if health administration is primarily under the jurisdiction of provincial authorities), or presence of health facility in area. Strata to be used must be identified by each country and the reasons for selection explicitly justified.

    Stratification is strongly recommended at the first stage of sampling. Once the strata have been chosen and justified, all stages of selection will be conducted separately in each stratum. We recommend stratifying on 3-5 factors. It is optimum to have half as many strata (note the difference between stratifying variables, which may be such variables as gender, socio-economic status, province/region etc. and strata, which are the combination of variable categories, for example Male, High socio-economic status, Xingtao Province would be a stratum).

    Strata should be as homogenous as possible within and as heterogeneous as possible between. This means that strata should be formulated in such a way that individuals belonging to a stratum should be as similar to each other with respect to key variables as possible and as different as possible from individuals belonging to a different stratum. This maximises the efficiency of stratification in reducing sampling variance.

    MULTI-STAGE CLUSTER SELECTION

    A cluster is a naturally occurring unit or grouping within the population (e.g. enumeration areas, cities, universities, provinces, hospitals etc.); it is a unit for which the administrative level has clear, nonoverlapping boundaries. Cluster sampling is useful because it avoids having to compile exhaustive lists of every single person in the population. Clusters should be as heterogeneous as possible within and as homogenous as possible between (note that this is the opposite criterion as that for strata). Clusters should be as small as possible (i.e. large administrative units such as Provinces or States are not good clusters) but not so small as to be homogenous.

    In cluster sampling, a number of clusters are randomly selected from a list of clusters. Then, either all members of the chosen cluster or a random selection from among them are included in the sample. Multistage sampling is an extension of cluster sampling where a hierarchy of clusters are chosen going from larger to smaller.

    In order to carry out multi-stage sampling, one needs to know only the population sizes of the sampling units. For the smallest sampling unit above the elementary unit however, a complete list of all elementary units (households) is needed; in order to be able to randomly select among all households in the TSU, a list of all those households is required. This information may be available from the most recent population census. If the last census was >3 years ago or the information furnished by it was of poor quality or unreliable, the survey staff will have the task of enumerating all households in the smallest randomly selected sampling unit. It is very important to budget for this step if it is necessary and ensure that all households are properly enumerated in order that a representative sample is obtained.

    It is always best to have as many clusters in the PSU as possible. The reason for this is that the fewer the number of respondents in each PSU, the lower will be the clustering effect which

  13. w

    Service Delivery Indicators Health Survey 2016 - Harmonized Public Use Data...

    • microdata.worldbank.org
    • catalog.ihsn.org
    • +1more
    Updated Apr 1, 2021
    + more versions
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    Waly Wane (2021). Service Delivery Indicators Health Survey 2016 - Harmonized Public Use Data - Tanzania [Dataset]. https://microdata.worldbank.org/index.php/catalog/3873
    Explore at:
    Dataset updated
    Apr 1, 2021
    Dataset authored and provided by
    Waly Wane
    Time period covered
    2016
    Area covered
    Tanzania
    Description

    Abstract

    The Service Delivery Indicators (SDI) are a set of health and education indicators that examine the effort and ability of staff and the availability of key inputs and resources that contribute to a functioning school or health facility. The indicators are standardized, allowing comparison between and within countries over time.

    The Health SDIs include healthcare provider effort, knowledge and ability, and the availability of key inputs (for example, basic equipment, medicines and infrastructure, such as toilets and electricity). The indicators provide a snapshot of the health facility and assess the availability of key resources for providing high quality care.

    The Tanzania SDI Health survey team visited a sample of 383 health facilities across Tanzania between August and October 2016. The survey team collected rosters covering 5,160 workers for absenteeism and assessed 498 health workers for competence using patient case simulations. The technical report and field manual are unavailable for Tanzania 2016. The questionnaire is the same as Tanzania 2014.

    Geographic coverage

    National

    Analysis unit

    Health facilities and healthcare providers

    Universe

    All health facilities providing primary-level care

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    The sampling strategy for SDI surveys is designed towards attaining indicators that are accurate and representative at the national level, as this allows for proper cross-country (i.e. international benchmarking) and across time comparisons, when applicable. In addition, other levels of representativeness are sought to allow for further disaggregation (rural/urban areas, public/private facilities, subregions, etc.) during the analysis stage.

    The sampling strategy for SDI surveys follows a multistage sampling approach. The main units of analysis are facilities (schools and health centers) and providers (health and education workers: teachers, doctors, nurses, facility managers, etc.). The multi-stage sampling approach makes sampling procedures more practical by dividing the selection of large populations of sampling units in a step-by-step fashion. After defining the sampling frame and categorizing it by stratum, a first stage selection of sampling units is carried out independently within each stratum. Often, the primary sampling units (PSU) for this stage are cluster locations (e.g. districts, communities, counties, neighborhoods, etc.) which are randomly drawn within each stratum with a probability proportional to the size (PPS) of the cluster (measured by the location’s number of facilities, providers or pupils). Once locations are selected, a second stage takes place by randomly selecting facilities within location (either with equal probability or with PPS) as secondary sampling units. At a third stage, a fixed number of health and education workers and pupils are randomly selected within facilities to provide information for the different questionnaire modules.

    The Tanzania 2016 survey is a repeated panel of the 2014 survey.

    Mode of data collection

    Face-to-face [f2f]

    Research instrument

    The SDI Health Survey Questionnaire consists of four modules:

    Module 1: General Information - Administered to the health facility manager to collect information on equipment, medicines, infrastructure and other facets of the health facility.

    Module 2: Provider Absence - A roster of healthcare providers is collected and absence measured.

    Module 3: Clinical Vignettes – A selection of providers are given clinical vignettes to measure knowledge of common medical conditions.

    Module 4: Facility finances – Information on facility revenue and expenditures is collected from the health facility manager.

    Weights: Weights for facilities, absentee-related analyses and clinical vignette analyses.

    Cleaning operations

    Quality control was performed in Stata.

  14. Serbian National Health Survey Database .xlsx

    • figshare.com
    xlsx
    Updated Nov 29, 2016
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    Natasa Mihailovic; Sanja Kocic; Goran Trajkovic; Mihajlo (Michael) Jakovljevic MD, PhD, MAE (2016). Serbian National Health Survey Database .xlsx [Dataset]. http://doi.org/10.6084/m9.figshare.4265117.v1
    Explore at:
    xlsxAvailable download formats
    Dataset updated
    Nov 29, 2016
    Dataset provided by
    Figsharehttp://figshare.com/
    Authors
    Natasa Mihailovic; Sanja Kocic; Goran Trajkovic; Mihajlo (Michael) Jakovljevic MD, PhD, MAE
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Area covered
    Serbia
    Description

    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.

  15. Population Health (BRFSS: HRQOL)

    • kaggle.com
    zip
    Updated Dec 14, 2022
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    The Devastator (2022). Population Health (BRFSS: HRQOL) [Dataset]. https://www.kaggle.com/datasets/thedevastator/unlock-population-health-needs-with-brfss-hrqol
    Explore at:
    zip(2247473 bytes)Available download formats
    Dataset updated
    Dec 14, 2022
    Authors
    The Devastator
    Description

    Population Health (BRFSS: HRQOL)

    Examining Trends, Disparities and Determinants of Health in the US Population

    By Health [source]

    About this dataset

    The Behavioral Risk Factor Surveillance System (BRFSS) offers an expansive collection of data on the health-related quality of life (HRQOL) from 1993 to 2010. Over this time period, the Health-Related Quality of Life dataset consists of a comprehensive survey reflecting the health and well-being of non-institutionalized US adults aged 18 years or older. The data collected can help track and identify unmet population health needs, recognize trends, identify disparities in healthcare, determine determinants of public health, inform decision making and policy development, as well as evaluate programs within public healthcare services.

    The HRQOL surveillance system has developed a compact set of HRQOL measures such as a summary measure indicating unhealthy days which have been validated for population health surveillance purposes and have been widely implemented in practice since 1993. Within this study's dataset you will be able to access information such as year recorded, location abbreviations & descriptions, category & topic overviews, questions asked in surveys and much more detailed information including types & units regarding data values retrieved from respondents along with their sample sizes & geographical locations involved!

    More Datasets

    For more datasets, click here.

    Featured Notebooks

    • 🚨 Your notebook can be here! 🚨!

    How to use the dataset

    This dataset tracks the Health-Related Quality of Life (HRQOL) from 1993 to 2010 using data from the Behavioral Risk Factor Surveillance System (BRFSS). This dataset includes information on the year, location abbreviation, location description, type and unit of data value, sample size, category and topic of survey questions.

    Using this dataset on BRFSS: HRQOL data between 1993-2010 will allow for a variety of analyses related to population health needs. The compact set of HRQOL measures can be used to identify trends in population health needs as well as determine disparities among various locations. Additionally, responses to survey questions can be used to inform decision making and program and policy development in public health initiatives.

    Research Ideas

    • Analyzing trends in HRQOL over the years by location to identify disparities in health outcomes between different populations and develop targeted policy interventions.
    • Developing new models for predicting HRQOL indicators at a regional level, and using this information to inform medical practice and public health implementation efforts.
    • Using the data to understand differences between states in terms of their HRQOL scores and establish best practices for healthcare provision based on that understanding, including areas such as access to care, preventative care services availability, etc

    Acknowledgements

    If you use this dataset in your research, please credit the original authors. Data Source

    License

    See the dataset description for more information.

    Columns

    File: rows.csv | Column name | Description | |:-------------------------------|:----------------------------------------------------------| | Year | Year of survey. (Integer) | | LocationAbbr | Abbreviation of location. (String) | | LocationDesc | Description of location. (String) | | Category | Category of survey. (String) | | Topic | Topic of survey. (String) | | Question | Question asked in survey. (String) | | DataSource | Source of data. (String) | | Data_Value_Unit | Unit of data value. (String) | | Data_Value_Type | Type of data value. (String) | | Data_Value_Footnote_Symbol | Footnote symbol for data value. (String) | | Data_Value_Std_Err | Standard error of the data value. (Float) | | Sample_Size | Sample size used in sample. (Integer) | | Break_Out | Break out categories used. (String) | | Break_Out_Category | Type break out assessed. (String) | | **GeoLocation*...

  16. d

    New York City Community Health Survey

    • catalog.data.gov
    • data.cityofnewyork.us
    • +1more
    Updated May 24, 2024
    + more versions
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    data.cityofnewyork.us (2024). New York City Community Health Survey [Dataset]. https://catalog.data.gov/dataset/dohmh-community-health-survey-2010-2016
    Explore at:
    Dataset updated
    May 24, 2024
    Dataset provided by
    data.cityofnewyork.us
    Area covered
    New York
    Description

    The New York City Community Health Survey (CHS) is a telephone survey conducted annually by the DOHMH, Division of Epidemiology, Bureau of Epidemiology Services. CHS provides robust data on the health of New Yorkers, including neighborhood, borough, and citywide estimates on a broad range of chronic diseases and behavioral risk factors. The data are analyzed and disseminated to influence health program decisions, and increase the understanding of the relationship between health behavior and health status. For more information see EpiQuery, https://a816-health.nyc.gov/hdi/epiquery/visualizations?PageType=ps&PopulationSource=CHS

  17. r

    National public health survey, Health on equal terms - 2014

    • researchdata.se
    • data.europa.eu
    Updated Feb 28, 2017
    + more versions
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    Public Health Agency of Sweden (2017). National public health survey, Health on equal terms - 2014 [Dataset]. https://researchdata.se/en/catalogue/dataset/ext0118-1
    Explore at:
    (357267), (836135), (504761), (205668), (5216060)Available download formats
    Dataset updated
    Feb 28, 2017
    Dataset authored and provided by
    Public Health Agency of Sweden
    Area covered
    Sweden
    Description

    The Public Health Agency of Sweden annually conducts a national public health survey, Health on Equal Terms, including a sample of 20 000 people aged 16-84 years. The survey, which was conducted for the first time in 2004, is an on going collaboration between the The Public Health Agency of Sweden and county councils/regions in Sweden and is carried out with help from Statistics Sweden (SCB). All studies, since 2004, can be found under the tab Related studies.

    The survey is voluntary and done with the purpose to investigate the health in the population and to show changes in the population's health over time as a follow up of the national health politics.

    The sample is randomly drawn from the Statistics Sweden's population register and includes 20 000 people aged 16-84 years. The personal data is confidential and protected by law and those working with this survey are obliged to practice professional secrecy. Individual answers can not be identified in the results.

    The study participants are since 2007 given the opportunity to answer the survey on the web. Since 2012, the web survey is also in English, and since 2014 also in Finnish.

    The questionnaire includes about 85 questions. Each county council has its own introduction letter and the questions has been prepared in collaboration with representatives from a number of different community medicine units. The origin and quality of the questions are described in the report "Objective and background of the questions in the national public health survey". Most questions recur each year, but questions can in particular cases be replaced by other questions of good quality and national relevance.

    The questions in the national public health survey cover physical and mental health, consumption of pharmaceuticals, contact with healthcare services, dental health, living habits, financial conditions, work and occupation, work environment, safety and social relationships. Data regarding education is collected from the education register, and data of income, economic support, sickness benefits and pensions from the income an taxation register.

    Purpose:

    The aim is to investigate the health in the population and to show changes in the population's health over time as a follow up of the national health politics.

    The data collection is ongoing, during the year 2014.

  18. Data from: Health Information National Trends Survey (HINTS)

    • catalog.data.gov
    • data.virginia.gov
    • +2more
    Updated Jul 26, 2023
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    National Institutes of Health (NIH), Department of Health & Human Services (2023). Health Information National Trends Survey (HINTS) [Dataset]. https://catalog.data.gov/dataset/health-information-national-trends-survey-hints
    Explore at:
    Dataset updated
    Jul 26, 2023
    Dataset provided by
    United States Department of Health and Human Serviceshttp://www.hhs.gov/
    Description

    The Health Information National Trends Survey (HINTS) is a biennial, cross-sectional survey of a nationally-representative sample of American adults that is used to assess the impact of the health information environment. The survey provides updates on changing patterns, needs, and information opportunities in health; Identifies changing communications trends and practices; Assesses cancer information access and usage; Provides information about how cancer risks are perceived; and Offers a testbed to researchers to test new theories in health communication.

  19. World Health Survey 2003 - France

    • microdata.worldbank.org
    • datacatalog.ihsn.org
    • +2more
    Updated Oct 17, 2013
    + more versions
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    World Health Organization (WHO) (2013). World Health Survey 2003 - France [Dataset]. https://microdata.worldbank.org/index.php/catalog/1712
    Explore at:
    Dataset updated
    Oct 17, 2013
    Dataset provided by
    World Health Organizationhttps://who.int/
    Authors
    World Health Organization (WHO)
    Time period covered
    2003
    Area covered
    France
    Description

    Abstract

    Different countries have different health outcomes that are in part due to the way respective health systems perform. Regardless of the type of health system, individuals will have health and non-health expectations in terms of how the institution responds to their needs. In many countries, however, health systems do not perform effectively and this is in part due to lack of information on health system performance, and on the different service providers.

    The aim of the WHO World Health Survey is to provide empirical data to the national health information systems so that there is a better monitoring of health of the people, responsiveness of health systems and measurement of health-related parameters.

    The overall aims of the survey is to examine the way populations report their health, understand how people value health states, measure the performance of health systems in relation to responsiveness and gather information on modes and extents of payment for health encounters through a nationally representative population based community survey. In addition, it addresses various areas such as health care expenditures, adult mortality, birth history, various risk factors, assessment of main chronic health conditions and the coverage of health interventions, in specific additional modules.

    The objectives of the survey programme are to: 1. develop a means of providing valid, reliable and comparable information, at low cost, to supplement the information provided by routine health information systems. 2. build the evidence base necessary for policy-makers to monitor if health systems are achieving the desired goals, and to assess if additional investment in health is achieving the desired outcomes. 3. provide policy-makers with the evidence they need to adjust their policies, strategies and programmes as necessary.

    Geographic coverage

    The survey sampling frame must cover 100% of the country's eligible population, meaning that the entire national territory must be included. This does not mean that every province or territory need be represented in the survey sample but, rather, that all must have a chance (known probability) of being included in the survey sample.

    There may be exceptional circumstances that preclude 100% national coverage. Certain areas in certain countries may be impossible to include due to reasons such as accessibility or conflict. All such exceptions must be discussed with WHO sampling experts. If any region must be excluded, it must constitute a coherent area, such as a particular province or region. For example if ¾ of region D in country X is not accessible due to war, the entire region D will be excluded from analysis.

    Analysis unit

    Households and individuals

    Universe

    The WHS will include all male and female adults (18 years of age and older) who are not out of the country during the survey period. It should be noted that this includes the population who may be institutionalized for health reasons at the time of the survey: all persons who would have fit the definition of household member at the time of their institutionalisation are included in the eligible population.

    If the randomly selected individual is institutionalized short-term (e.g. a 3-day stay at a hospital) the interviewer must return to the household when the individual will have come back to interview him/her. If the randomly selected individual is institutionalized long term (e.g. has been in a nursing home the last 8 years), the interviewer must travel to that institution to interview him/her.

    The target population includes any adult, male or female age 18 or over living in private households. Populations in group quarters, on military reservations, or in other non-household living arrangements will not be eligible for the study. People who are in an institution due to a health condition (such as a hospital, hospice, nursing home, home for the aged, etc.) at the time of the visit to the household are interviewed either in the institution or upon their return to their household if this is within a period of two weeks from the first visit to the household.

    Kind of data

    Sample survey data [ssd]

    Sampling procedure

    SAMPLING GUIDELINES FOR WHS

    Surveys in the WHS program must employ a probability sampling design. This means that every single individual in the sampling frame has a known and non-zero chance of being selected into the survey sample. While a Single Stage Random Sample is ideal if feasible, it is recognized that most sites will carry out Multi-stage Cluster Sampling.

    The WHS sampling frame should cover 100% of the eligible population in the surveyed country. This means that every eligible person in the country has a chance of being included in the survey sample. It also means that particular ethnic groups or geographical areas may not be excluded from the sampling frame.

    The sample size of the WHS in each country is 5000 persons (exceptions considered on a by-country basis). An adequate number of persons must be drawn from the sampling frame to account for an estimated amount of non-response (refusal to participate, empty houses etc.). The highest estimate of potential non-response and empty households should be used to ensure that the desired sample size is reached at the end of the survey period. This is very important because if, at the end of data collection, the required sample size of 5000 has not been reached additional persons must be selected randomly into the survey sample from the sampling frame. This is both costly and technically complicated (if this situation is to occur, consult WHO sampling experts for assistance), and best avoided by proper planning before data collection begins.

    All steps of sampling, including justification for stratification, cluster sizes, probabilities of selection, weights at each stage of selection, and the computer program used for randomization must be communicated to WHO

    STRATIFICATION

    Stratification is the process by which the population is divided into subgroups. Sampling will then be conducted separately in each subgroup. Strata or subgroups are chosen because evidence is available that they are related to the outcome (e.g. health, responsiveness, mortality, coverage etc.). The strata chosen will vary by country and reflect local conditions. Some examples of factors that can be stratified on are geography (e.g. North, Central, South), level of urbanization (e.g. urban, rural), socio-economic zones, provinces (especially if health administration is primarily under the jurisdiction of provincial authorities), or presence of health facility in area. Strata to be used must be identified by each country and the reasons for selection explicitly justified.

    Stratification is strongly recommended at the first stage of sampling. Once the strata have been chosen and justified, all stages of selection will be conducted separately in each stratum. We recommend stratifying on 3-5 factors. It is optimum to have half as many strata (note the difference between stratifying variables, which may be such variables as gender, socio-economic status, province/region etc. and strata, which are the combination of variable categories, for example Male, High socio-economic status, Xingtao Province would be a stratum).

    Strata should be as homogenous as possible within and as heterogeneous as possible between. This means that strata should be formulated in such a way that individuals belonging to a stratum should be as similar to each other with respect to key variables as possible and as different as possible from individuals belonging to a different stratum. This maximises the efficiency of stratification in reducing sampling variance.

    MULTI-STAGE CLUSTER SELECTION

    A cluster is a naturally occurring unit or grouping within the population (e.g. enumeration areas, cities, universities, provinces, hospitals etc.); it is a unit for which the administrative level has clear, nonoverlapping boundaries. Cluster sampling is useful because it avoids having to compile exhaustive lists of every single person in the population. Clusters should be as heterogeneous as possible within and as homogenous as possible between (note that this is the opposite criterion as that for strata). Clusters should be as small as possible (i.e. large administrative units such as Provinces or States are not good clusters) but not so small as to be homogenous.

    In cluster sampling, a number of clusters are randomly selected from a list of clusters. Then, either all members of the chosen cluster or a random selection from among them are included in the sample. Multistage sampling is an extension of cluster sampling where a hierarchy of clusters are chosen going from larger to smaller.

    In order to carry out multi-stage sampling, one needs to know only the population sizes of the sampling units. For the smallest sampling unit above the elementary unit however, a complete list of all elementary units (households) is needed; in order to be able to randomly select among all households in the TSU, a list of all those households is required. This information may be available from the most recent population census. If the last census was >3 years ago or the information furnished by it was of poor quality or unreliable, the survey staff will have the task of enumerating all households in the smallest randomly selected sampling unit. It is very important to budget for this step if it is necessary and ensure that all households are properly enumerated in order that a representative sample is obtained.

    It is always best to have as many clusters in the PSU as possible. The reason for this is that the fewer the number of respondents in each PSU, the lower will be the clustering effect which

  20. Demographic and Health Surveys

    • datacatalog.med.nyu.edu
    Updated Feb 12, 2025
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    United States - Agency for International Development (USAID) (2025). Demographic and Health Surveys [Dataset]. https://datacatalog.med.nyu.edu/dataset/10110
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    Dataset updated
    Feb 12, 2025
    Dataset provided by
    United States Agency for International Developmenthttp://usaid.gov/
    Authors
    United States - Agency for International Development (USAID)
    Area covered
    International
    Description

    The Demographic and Health Surveys (DHS) Program overseen by the US Agency for International AID (USAID) uses nationally representative surveys, biomarker testing, and geographic location to collect data on monitoring and impact evaluation indicators for individual countries and for cross-country comparisons.

    Standardized DHS surveys include the Demographic and Health Survey, Service Provision Assessment, HIV/AIDS Indicator Survey, Malaria Indicator Survey, and Key Indicators Survey. The DHS Program also collects biomarkers and geographic data. Data availability varies by year and country. A table that lists all currently available data can be found here.

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Chandra, Anita (2024). National Survey of Health Attitudes, [United States], 2023 [Dataset]. http://doi.org/10.3886/ICPSR39205.v1
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National Survey of Health Attitudes, [United States], 2023

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2 scholarly articles cite this dataset (View in Google Scholar)
delimited, ascii, stata, spss, r, sasAvailable download formats
Dataset updated
Dec 5, 2024
Dataset provided by
Inter-university Consortium for Political and Social Researchhttps://www.icpsr.umich.edu/web/pages/
Authors
Chandra, Anita
License

https://www.icpsr.umich.edu/web/ICPSR/studies/39205/termshttps://www.icpsr.umich.edu/web/ICPSR/studies/39205/terms

Time period covered
Nov 27, 2023 - Dec 19, 2023
Area covered
United States
Description

Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH. The National Survey of Health Attitudes (NSHA) is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values. This study includes the results from the 2023 RWJF National Survey of Health Attitudes. The 2023 survey is the third wave of the NSHA. The first wave was conducted in 2015 (ICPSR 37405) and the second wave in 2018 (ICPSR 37633). The 2023 report complements the overview of the 2015 survey described in the RAND report Development of the Robert Wood Johnson Foundation National Survey of Health Attitudes (Carman et al., 2016), and its subsequent topline 2018 Survey of National Health Attitudes: Description and Top-Line Summary (Carman et al., 2019) and is organized similarly for consistency. A companion set of longitudinal surveys during the COVID-19 pandemic was fielded between 2020 and 2021 and is further described in four top-line reports, COVID-19 and the Experiences of Populations at Greater Risk (Carman et al., 2020-2021). The questions in the 2023 survey uniquely capture aspects of American mindset about health, health equity, structural racism, and wellbeing in ways that are not present in other surveys. This version of the NSHA can be viewed in three main sections: (1) individual health experiences, perspectives, and knowledge (making health a shared value); (2) health equity perspectives; and (3) community wellbeing, including climate views and barriers to community engagement. Insights from the surveys referenced above, including this one, have established a baseline and set of cross-sectional pulse checks on where the American public is regarding their recognition of social determinants of health, their understanding of health inequities including structural racism, their willingness to address those inequities and their indication of who in society should be responsible for solving health inequities.

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