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American Communities Project, United States, 2023-2024 (ICPSR 39419)

Released/updated on: 2025-09-08
Geographic coverage: United States
Time period: 2020-01-01--2024-01-01
These are data files from the American Communities Project's study of American Fragmentation. These surveys asked people in 15 different types of communities about their attitudes on a variety of issues and concerns with the goal of identifying where there are commonalities and differences among them. For most of the types, 13 of 15, the surveys were conducted with a probability-based online panel. For two of the communities, where the populations are particularly sparse, the surveys were conducted via RDD (Random Digit Dialing). Those types are the Aging Farmlands and Native American Lands. Because of the cost of RDD, those types were not included on some questions.
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American Health Values Survey (AHVS): Sentinel Communities Segmentation, 5 American communities, 2016-2017 (ICPSR 37910)

Released/updated on: 2021-11-22
Geographic coverage: Baltimore, United States, Phoenix, California, Alabama, Maryland, Mobile, Arizona, Stockton, Nebraska
Time period: 2016-01-01--2017-01-01

The American Health Values Survey (AHVS) was conducted by the National Opinion Research Center (NORC) at the University of Chicago in order to develop a typology of Americans based on their health values and beliefs. The survey, of more than 10,000 adults from five individual communities, examined values and beliefs related to health at both the individual as well as societal levels. The community surveys sought to compare differences between the local typologies, but also to investigate any similarities with national typology groups. The survey assessed the importance of health in:

  • day-to-day personal life (i.e. the amount of effort spent on disease prevention as well as appropriate seeking of medical care);
  • equity, the value placed on the opportunity to succeed generally in life as well as on health equity;
  • social solidarity, the importance of taking into account the needs of others as well as personal needs;
  • health care disparities, views about how easy/hard it is for African Americans, Latinos and low-income Americans to get quality health care;
  • and, the importance of the social determinants of health.

In addition, the survey also explored views about how active government should be in health; collective efficacy, the ease of affecting positive community change by working with others; and health-related civic engagement e.g. the support of health charities and organizations working on health issues.

There are public-use and restricted-use versions of the data provided for each of the five sentinel communities participating in this study. Although each site differs on the number of respondents as listed below, each data file contains the same 143 variables for each site and version of the data. The only difference between the public-use versus restricted-use versions of the data is the variable ZIP, which was MASKED in the public-use version.

  • DS1 and DS2 - Baltimore, Maryland: 2,139
  • DS3 and DS4 - Maricopa County, Arizona: 2,247
  • DS5 and DS6 - Stockton, California: 2,127
  • DS7 and DS8 - Mobile, Alabama: 1,821
  • DS9 and DS10 - North Central counties in Nebraska: 2,846
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American Health Values Survey II, [United States], 2019-2020 (ICPSR 38818)

Released/updated on: 2025-03-05
Geographic coverage: United States
Time period: 2019-01-01--2020-01-01

The Robert Wood Johnson Foundation (RWJF) has a vision to build a Culture of Health (CoH) by making health a shared national priority, one valued and advanced by multiple stakeholders across all sectors of society. This vision embraces a very broadly integrated and comprehensive approach to health, one where well-being lies at the center of every aspect of American life. In 2014, the RWJF commissioned NORC at the University of Chicago to plan and conduct the first American Health Values Survey (AHVS) to understand the extent to which United States adults held views consistent with this vision. The idea was to explore which types of United States adults were more supportive and less supportive of the goal and what the differences were between the more and less supportive groups. To aid in the understanding of these differences, NORC developed a typology of United States adults based on their values and beliefs related to the CoH vision.

Using a large-scale national survey fielded in late 2015 and early 2016, NORC identified six major segments of the population of adults in the United States based on their differing health values and beliefs and developed detailed profiles of each segment that described their pattern of values and beliefs as well as their demographic, political and other characteristics. NORC subsequently replicated the typology development work in five RWJF Sentinel Communities across the nation and also developed a typology of rural America. The same segments, or similar ones, were common across various geographic areas of the United States. Four years have since passed, in which changes occurred in the country. RWJF in 2019 commissioned NORC to conduct a second national, cross-sectional survey (AHVS II) in late 2019 and early 2020.

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American Health Values Survey, [United States], 2015-2016 (ICPSR 37403)

Released/updated on: 2021-12-07
Geographic coverage: United States
The American Health Values Survey was conducted by the National Opinion Research Center (NORC) at the University of Chicago in order to develop a typology of Americans based on their health values and beliefs. The survey examined values and beliefs related to health at both the individual as well as societal levels. The survey assessed the importance of health in day-to-day personal life (i.e. the amount of effort spent on disease prevention as well as appropriate seeking of medical care); equity, the value placed on the opportunity to succeed generally in life as well as on health equity; social solidarity, the importance of taking into account the needs of others as well as personal needs; health care disparities, views about how easy/hard it is for African Americans, Latinos and low-income Americans to get quality health care; and, the importance of the social determinants of health. In addition, the survey also explored views about how active government should be in health; collective efficacy, the ease of affecting positive community change by working with others; and health-related civic engagement e.g. the support of health charities and organizations working on health issues.
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American Life Panel (ALP) (ICPSR 39382)

Released/updated on: 2025-04-11
Geographic coverage: United States
The RAND American Life Panel (ALP) is a nationally representative panel of 11,000 members ages 18 and older who speak English or Spanish. The ALP has expanded from about 800 members in 2003 to its current size. ALP surveys are conducted online to provide quick, affordable, and high-quality results. To enhance the representativeness of the panel, RAND provides internet services and computers to members that would otherwise not be able to participate. ALP members are primarily recruited through probability-based methods. Once in the ALP, participants tend to remain indefinitely, resulting in relatively low attrition rates. ALP panel members are responsive, with survey completion rates generally in the 70%-80% range. All respondent data collected with the American Life Panel are accompanied by demographic information about each respondent. This set of demographics is collected three times a year through a household information survey. The content collected from the household information survey is patterned after the Current Population Survey (CPS) to aid in weighting the data. Files from different studies can be merged using a unique identifier for each panel member. The ALP has conducted more than 450 surveys covering diverse topics, such as financial decision-making, the effect of political events on self-reported well-being, inflation expectations, joint retirement decisions, retirement preferences, health decision-making, Social Security knowledge and expectations, measurement of health utility, and numeracy. All public data are available for free to researchers. Restricted data for the ALP is available to approved researchers at a cost.
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Associated Press Health Care Reform Survey, by Stanford University with the Robert Wood Johnson Foundation, August-September 2010 [United States] (ICPSR 30422)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2010-08-31--2010-09-07
Conducted by Knowledge Networks, this survey measured public opinion about the health care overhaul that was passed by the United States Congress in March 2010. It measured support and opposition to certain general goals of the overhaul, as well as support and opposition to specific parts of the legislation. It had a particular focus on what people knew about the bill and what misperceptions they may have about what was and wasn't in the legislation. In addition, the survey investigated beliefs about the consequences of the legislation on future taxes, health insurance costs, access to health care, and the quality of health care. Other topics investigated by the survey include health status, health insurance status, trust in the federal government, approval/disapproval of the Obama Administration's performance, political ideology, religion, religiosity, and sources of news. The data file also includes demographic information collected by Knowledge Networks' initial KnowledgePanel(R) profile survey, such as age, gender, education, household size and composition, income, marital status, employment status, and ZIP code.
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ASTHO Forces of Change Survey, United States, 2017 (ICPSR 37223)

Released/updated on: 2019-07-30
Geographic coverage: District of Columbia, United States, Marshall Islands, Guam, Virgin Islands of the United States, Northern Mariana Islands, Micronesia (Federated States)

The Forces of Change Survey is an annual survey completed by the state and territorial health agencies that comprise the membership of the Association of State and Territorial Health Officials (ASTHO). ASTHO is the national nonprofit organization representing public health agencies in the United States, the U.S. territories and freely associated states, and the District of Columbia, and the over 100,000 public health professionals these agencies employ. The Forces of Change Survey primarily focuses on emergent and rapidly changing trends. The data collected sought to determine the current climate at state and territorial health agencies as it related to budget, workforce, accreditation, and special interest topics. The 2017 Forces of Change Survey examined the following topics:

  • Health agency resources
  • Activities related to the Zika virus
  • Opioid epidemic response
  • Communicating the value of public health
  • Efforts to advance health equity

The web-based survey, fielded by ASTHO in May of 2017, was administered to state and territorial health agencies through their senior deputies. A total of 52 health agencies responded (from 46 states, Washington, D.C., and five territories and freely associated states). Data included as part of this collection includes one dataset with 122 variables for 52 cases.

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ASTHO Profile Survey of State and Territorial Public Health, United States, 2012 (ICPSR 37823)

Released/updated on: 2022-06-08
Geographic coverage: Puerto Rico, United States, Marshall Islands, Guam, Virgin Islands of the United States, Northern Mariana Islands, Palau, Micronesia (Federated States)
Time period: 2012-10-01--2013-05-01

The 2012 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The 121-question instrument was disseminated electronically in October 2012 and completed by senior deputies at each S/THA. The survey closed in May 2013; the response rate was 96 percent among the 50 states and D.C., and 92 percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

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ASTHO Profile Survey of State and Territorial Public Health, United States, 2016 (ICPSR 37216)

Released/updated on: 2021-05-17
Geographic coverage: Puerto Rico, United States, Marshall Islands, Guam, Virgin Islands of the United States, Northern Mariana Islands, Palau, Micronesia (Federated States)

The 2016 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The 129-question instrument was disseminated electronically in April 2016 and completed by senior deputies at each S/THA. The survey closed in September 2016; the response rate was 98 percent among the 50 states and D.C., and 97 percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

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ASTHO Profile Survey of State and Territorial Public Health, United States, 2019 (ICPSR 37996)

Released/updated on: 2022-07-21
Geographic coverage: Puerto Rico, United States, Marshall Islands, Guam, Virgin Islands of the United States, Northern Mariana Islands, Palau, Micronesia (Federated States)
Time period: 2019-04-09--2020-01-31

The 2019 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The instrument was disseminated electronically in April 2019 and completed by state and territorial health agency staff at each S/THA including senior deputies, chief financial officers, and human resource directors. The survey closed in January 2020; the response rate was 100% percent among the 50 states and D.C., and 98% percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

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ASTHO Profile Survey of State and Territorial Public Health, United States, 2020 (ICPSR 38139)

Released/updated on: 2021-10-07
Geographic coverage: Puerto Rico, United States, Marshall Islands, Guam, Virgin Islands of the United States, Northern Mariana Islands, Palau, Micronesia (Federated States)
Time period: 2020-12-01--2021-03-01

The 2020 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The instrument was significantly shortened for this data collection and separated into three separate surveys. The surveys were administered in December 2020 and completed by state and territorial health agency staff at each S/THA including senior deputies, chief financial officers, and human resource directors. The survey closed in March 2021; 80% of states and DC responded to at least one survey, of which 40% of states and DC responded to all three surveys; 38% of territories responded to at least one survey, of which 11% responded to all three surveys.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

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ASTHO Profile Survey of State and Territorial Public Health, United States, 2022 (ICPSR 39285)

Released/updated on: 2025-06-16
Geographic coverage: Puerto Rico, United States, Marshall Islands, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands, Palau, Micronesia (Federated States)

The 2022 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The Profile aims to define the scope of S/THA services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The Profile began in 2007 and was fielded on average every three years between 2007 and 2022. The data collected through the Profile represent the breadth of work overseen by health agencies and shows how the public health field has shifted in response to societal changes and emergent needs. Data also reflect the structural nuances and limitations in which agencies conduct their work.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

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Bridging the Gap, Elementary School Data (Food and Fitness Survey) (ICPSR 36356)

Released/updated on: 2018-01-15
Geographic coverage: United States
Time period: 2006-01-01--2013-01-01
The Food and Fitness Survey is part of the larger Bridging the Gap (BTG) research program, which is a research initiative funded by the Robert Wood Johnson Foundation. The primary goals of the Food and Fitness survey project were to obtain nationally representative information on school practices, and to obtain information about the association between district-level wellness policies and practices in those schools. Food and Fitness involved annual surveys of school-level respondents at elementary schools from the 2006-07 to the 2012-13 school years. This study contains data from these surveys for public and private elementary schools from the 2006-07 to the 2012-13 school years. Topics of the surveys include school characteristics, school meal options and prices, food advertisements in schools, food practices in classrooms and school functions, meal times during the day, physical education facilities and curriculum, methods of transportation to and from school, school wellness policies, school beverage guidelines, the "Nutritional Guidelines for Competitive Foods", school vending machines, and a la carte as well as school store food and beverage offerings.
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Consumer Healthcare Experience State Surveys, United States, 2022 (ICPSR 38596)

Released/updated on: 2023-05-03
Geographic coverage: United States, Illinois, Missouri, Maryland, New Jersey

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.

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Consumer Healthcare Experience State Surveys, United States, 2023 (ICPSR 39031)

Released/updated on: 2026-04-16
Geographic coverage: Mississippi, United States, Louisiana, Florida, Utah
Altarum's Consumer Healthcare Experience State Survey (CHESS) is designed to elicit respondents' unbiased views on a wide range of health system issues, including confidence in using the health system, financial burden, and views on fixes that might be needed. The survey uses a web panel from Dynata with a demographically balanced sample of approximately 1500 respondents who live in a targeted state. The survey was conducted in English or Spanish and restricted to adults ages 18 and older. Respondents who finished the survey in less than half the median time were excluded from the final sample.
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COVID-19 and the Experiences of Populations at Greater Risk: Wave 1 General Population, United States, 2020-2021 (ICPSR 38736)

Released/updated on: 2023-09-25
Geographic coverage: United States
Time period: 2020-06-29--2020-07-22

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation have partnered to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low-to moderate-income backgrounds.

Questions in this COVID-19 survey focused specifically on experiences related to the pandemic (e.g., financial, physical, emotional), how respondents viewed the disproportionate impacts of the pandemic, whether and how respondents' views and priorities regarding health actions and investments are changing (including the roles of government and the private sector), and how general values about such issues as freedom and racism may be related to pandemic views and response expectations.

This study includes the results for Wave 1 for the general population.

Demographic information includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

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COVID-19 and the Experiences of Populations at Greater Risk: Wave 1, United States, 2020-2021 (ICPSR 38732)

Released/updated on: 2023-07-13
Geographic coverage: United States
Time period: 2020-06-29--2020-07-22

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation have partnered to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low-to moderate-income backgrounds.

This is the first of a four-wave survey intended for individuals and organizations interested in learning more about public attitudes about a Culture of Health and how COVID-19 specifically may influence views about health, health investments, and how different populations are affected. This a longitudinal study, collecting data in four waves. The study also included 2 populations: A sample of populations at greater risk, and a general population sample. This study includes the results for Wave 1 for populations at greater risk.

Demographic info includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.
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COVID-19 and the Experiences of Populations at Greater Risk: Wave 2, United States, 2020-2021 (ICPSR 38733)

Released/updated on: 2023-07-12
Geographic coverage: United States
Time period: 2020-10-09--2020-11-02

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation partnered again to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low- to moderate-income backgrounds.

The study is a longitudinal study, collecting data in four waves. The study also included 2 populations: A sample of populations at greater risk, and a general population sample. This study includes the results for Wave 2 for populations at greater risk.

One previous wave and two future waves were conducted. The questions in the surveys were largely similar across all four waves. All respondents who participated in Wave 1 were invited to participate in the future waves.

Demographic info includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

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COVID-19 and the Experiences of Populations at Greater Risk: Wave 3, United States, 2020-2021 (ICPSR 38734)

Released/updated on: 2023-06-21
Geographic coverage: United States
Time period: 2021-02-22--2021-03-23

In the context of COVID-19, RAND and RWJF partnered again to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low to moderate-income backgrounds.

The questions in this COVID-19 survey focused specifically on experiences related to the pandemic (e.g., financial, physical, emotional), how respondents viewed the disproportionate impacts of the pandemic, whether and how respondents' views and priorities regarding health actions and investments are changing (including the roles of government and the private sector), and how general values about such issues as freedom and racism may be related to pandemic views and response expectations. The study is a longitudinal study, which collected data in four waves. The study also included 2 populations: A sample of populations at greater risk, and a general population sample. This study included the results for Wave 2 for populations at greater risk. The questions in the surveys were largely similar across all four waves.

Demographic info includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

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COVID-19 and the Experiences of Populations at Greater Risk: Wave 4 General Population, United States, 2020-2021 (ICPSR 38737)

Released/updated on: 2023-10-19
Geographic coverage: United States
Time period: 2021-09-07--2021-10-04

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation partnered again to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how these health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low- to moderate-income backgrounds.

The questions in this COVID-19 survey focused specifically on experiences related to the pandemic (e.g., financial, physical, emotional), how respondents viewed the disproportionate impacts of the pandemic, whether and how respondents' views and priorities regarding health actions and investments are changing (including the roles of government and the private sector), and how general values about such issues as freedom and racism may be related to pandemic views and response expectations.

This study includes the results for Wave 4 for the general population.

Demographic information includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

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COVID-19 and the Experiences of Populations at Greater Risk: Wave 4, United States, 2020-2021 (ICPSR 38735)

Released/updated on: 2023-09-18
Geographic coverage: United States
Time period: 2021-09-07--2021-10-04

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation (RWJF) partnered again to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low to moderate-income backgrounds.

The questions in this COVID-19 survey focused specifically on experiences related to the pandemic (e.g., financial, physical, emotional), how respondents viewed the disproportionate impacts of the pandemic, whether and how respondents' views and priorities regarding health actions and investments are changing (including the roles of government and the private sector), and how general values about such issues as freedom and racism may be related to pandemic views and response expectations. Some questions used in the NSHA are fielded in this COVID-19 survey while others are newly used from other COVID-19 surveys or newly developed for this effort. The study is a longitudinal study, collecting data in four waves. The study also included 2 populations: A sample of populations at greater risk, and a general population sample. This study includes the results for Wave 4 for populations at greater risk. The questions in the surveys were largely similar across all four waves.

Demographic info includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

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Developing the PROMIS-Preference Score for Monitoring Population Health Outcomes, United States, 2017 (ICPSR 37516)

Released/updated on: 2020-03-25
Geographic coverage: United States

This is a United States nationally representative survey of 4142 respondents age 18 and older from the National Opinion Research Center Amerispeak panel. The study survey includes self rated health, 4 summary measures of health, questions about chronic conditions, and questions about social determinants of health. Basic demographic information is included in this study regarding age, education, race/ethnicity, gender, household size, housing type, household income, marital status, and employment status.

The National Opinion Research Center also provided the latitude and longitude of the participant's household which were used to get census tract level information and scores from walkscore.com (walkability, transportation, and opportunity scores).

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Employer Perspectives on the Health Insurance Market: A Survey of Businesses in the United States, 2014 (ICPSR 36175)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2014-08-19--2014-10-08
This survey investigated health insurance benefits offered by private-sector employers as key components of the Affordable Care Act (ACA) were implemented. The employers were interviewed about the types of health benefits they offered to employees and dependents, reasons for offering health insurance, and key considerations when choosing health insurance plans with an emphasis on sources of information used to evaluate health insurance plan quality. Additional topics covered by the survey include the use of brokers to assist in choosing health insurance plans, changes in insurance carriers or decisions to offer additional plans with a new insurance carrier, and how employers planned to react to the ACA requirement that employers with 50 or more full-time employees offer coverage to at least 70 percent of full-time employees or face financial penalties.
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Forces of Change Survey, United States, 2018 (ICPSR 38307)

Released/updated on: 2023-02-01
Geographic coverage: United States

The National Association of County and City Health Officials' (NACCHO) Forces of Change Survey is an evolution of NACCHO's Job Losses and Program Cuts Surveys (also known as the Economic Surveillance Surveys) which measured the impact of the economic recession on local health departments' (LHD) budgets, staff, and programs. The Forces of Change Survey continues to measure changes in LHD budgets, staff, and programs and assess more broadly the impact of forces affecting change in local health departments, such as health reform and accreditation. The 2018 Forces of Change survey was distributed to a stratified random sample of 966 LHDs in the United States.

The survey included six topics: (1) Budget Cuts and Job Losses, (2) Response to Opioid Use and Abuse, (3) Population Health Activities, (4) Influenza Preparedness and Response, (5) Informatics Capacity, and (6) Environmental Health Activities.

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Forces of Change Survey, United States, 2020 (ICPSR 39356)

Released/updated on: 2026-04-07
Geographic coverage: United States

The National Association of County and City Health Officials' (NACCHO) Forces of Change Survey was developed as an evolution to NACCHO's Job Losses and Program Cuts Surveys (also known as the Economic Surveillance Surveys), which measured the impact of the economic recession on local health departments' (LHDs) budgets, staff, and programs.

The Forces of Change Survey continues to measure changes in LHD budgets, staff, and programs and assess more broadly the impact of forces affecting change in LHDs. For the 2020 Forces of Change survey, the core set of questions were distributed to a total of 2392 LHDs in the United States, with a stratified random sample of 905 LHDs receiving the module questionnaire.

More specifically, the survey collected information about LHD staffing levels, workforce reductions, and changes in budget sizes; provided services or functions; changes in the level of service delivery; billing for clinical services; efforts to help people enroll in health insurance from exchanges under the Affordable Care Act; awareness of and involvement in the State Innovation Models Initiative; participation in the Public Health Accreditation Board's national accreditation program for LHDs; and whether LHDs are part of a combined health and human services agency.

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Forces of Change Survey, United States, 2023 (ICPSR 39352)

Released/updated on: 2025-08-20
Geographic coverage: United States
The National Association of County and City Health Officials' (NACCHO's) Forces of Change Survey was developed as an evolution to NACCHO's Job Losses and Program Cuts surveys, which measured the impact of the economic recession on local health departments' (LHDs) budgets, staff, and programs. Beginning in 2014, NACCHO began conducting the Forces of Change survey yearly in years that the National Profile Study of Local Health Departments (Profile) was not fielded. The Forces of Change Survey continues to measure changes in LHD budgets, staff, programs, and assess more broadly the impact of forces affecting change in LHDs.
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Forces of Change Survey, United States, 2024 (ICPSR 39672)

Released/updated on: 2026-06-02
Geographic coverage: United States

The National Association of County and City Health Officials' (NACCHO's) Forces of Change Survey was developed as an evolution to NACCHO's Job Losses and Program Cuts surveys, which measured the impact of the economic recession on local health departments' (LHDs) budgets, staff, and programs.

Beginning in 2014, NACCHO began conducting the Forces of Change survey yearly in years that the National Profile Study of Local Health Departments (Profile) was not fielded. The Forces of Change Survey continues to measure changes in LHD budgets, staff, programs, and assess more broadly the impact of forces affecting change in LHDs.

More specifically, the survey collected information about staffing and budget changes, agency governance, engagement with fellowship/training programs, public health nursing activities, evaluation capacity, and services to address the infectious disease consequences of the opioid crisis.

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The Future of Families and Child Wellbeing Study (FFCWS), Public Use, United States, 1998-2024 (ICPSR 31622)

Released/updated on: 2026-04-06
Geographic coverage: United States
Time period: 1998-01-01--2024-01-01

The Future of Families and Child Wellbeing Study (FFCWS, formerly known as the Fragile Families and Child Wellbeing Study) follows a cohort of nearly 5,000 children born in large, U.S. cities between 1998 and 2000. The study oversampled births to unmarried couples; and, when weighted, the data are representative of births in large U.S. cities at the turn of the century. The FFCWS was originally designed to address four questions of great interest to researchers and policy makers:

  1. What are the conditions and capabilities of unmarried parents, especially fathers?
  2. What is the nature of the relationships between unmarried parents?
  3. How do children born into these families fare?
  4. How do policies and environmental conditions affect families and children?

The FFCWS consists of interviews with mothers, fathers, and/or primary caregivers at birth and again when children are ages 1, 3, 5, 9, 15, and 22. The parent interviews collected information on attitudes, relationships, parenting behavior, demographic characteristics, health (mental and physical), economic and employment status, neighborhood characteristics, and program participation. Beginning at age 9, children were interviewed directly (either during the home visit or on the telephone). The direct child interviews collected data on family relationships, home routines, schools, peers, and physical and mental health, as well as health behaviors.

A collaborative study of the FFCWS, the In-Home Longitudinal Study of Pre-School Aged Children (In-Home Study) collected data from a subset of the FFCWS Core respondents at the Year 3 and 5 follow-ups to ask how parental resources in the form of parental presence or absence, time, and money influence children under the age of 5. The In-Home Study collected information on a variety of domains of the child's environment, including: the physical environment (quality of housing, nutrition and food security, health care, adequacy of clothing and supervision) and parenting (parental discipline, parental attachment, and cognitive stimulation). In addition, the In-Home Study also collected information on several important child outcomes, including anthropometrics, child behaviors, and cognitive ability. This information was collected through interviews with the child's primary caregiver, and direct observation of the child's home environment and the child's interactions with his or her caregiver.

Similar activities were conducted during the Year 9 follow-up. At the Year 15 follow-up, a condensed set of home visit activities were conducted with a subsample of approximately 1,000 teens. Teens who participated in the In-Home Study were also invited to participate in a Sleep Study and were asked to wear an accelerometer on their non-dominant wrist for seven consecutive days to track their sleep (Sleep Actigraphy Data) and that day's behaviors and mood (Daily Sleep Actigraphy and Diary Survey Data).

An additional collaborative study collected data from the child care provider (Year 3) and teacher (Years 9 and 15) through mail-based surveys. Saliva samples were collected at Year 9 and 15 (Biomarker file and Polygenic Scores). The Study of Adolescent Neural Development (SAND) COVID Study began data collection in May 2020 following the onset of the COVID-19 pandemic. It included online surveys with the young adult and their primary caregiver.

The FFCWS began its seventh wave of data collection in October 2020, around the focal child's 22nd birthday. Data collection and interviews continued through January 2024. The Year 22 wave included a young adult (YA) survey with the original focal child and a primary caregiver (PCG) survey. Data were also collected on the children of the original focal child (referred to as Generation 3, or G3).

In 2017, the FFCWS team announced the Fragile Families (FF) Challenge, a collaborative effort in which participants were tasked with using machine learning methods and FFCWS data (Baseline to Year 9) to build a model that would predict six key outcomes at Year 15. Materials used in the FF Challenge have been archived in this collection.

Documentation for these files is available on the FFCWS website under Data and Documentation. For details of updates made to the FFCWS data files, please see the project's Data Alerts page.

Data collection for the Future of Families and Child Wellbeing Study was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) of the National Institutes of Health under award numbers R01HD36916, R01HD39135, and R01HD40421, as well as a consortium of private foundations.

Below is the citation for use of the FFCWS data accessed through ICPSR. For information on additional citation requirements when using FFCWS in publications, please refer to this FAQ on the FFCWS project site.

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Health Reform Monitoring Survey, United States, April 2021 (ICPSR 38526)

Released/updated on: 2023-04-12
Geographic coverage: United States
Time period: 2021-04-01--2021-04-30
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 20th round of the survey (April 2021) include self-reported health status, health insurance coverage, access to health care, awareness of Marketplace and Medicaid coverage options, use of public benefits, telehealth, COVID-19 vaccine attitudes, forgone care because of the COVID-19 pandemic, and unfair treatment in health care settings. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race and ethnicity, United States citizenship, housing type, home ownership, internet access, income, and employment status.
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Health Reform Monitoring Survey, United States, First Quarter 2013 (ICPSR 35624)

Released/updated on: 2019-05-16
Geographic coverage: United States
Time period: 2013-01-31--2013-02-11, 2013-02-26--2013-03-11
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the first round of the survey (first quarter 2013) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, and health care affordability. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, First Quarter 2014 (ICPSR 35614)

Released/updated on: 2019-08-19
Geographic coverage: United States
Time period: 2014-02-28--2014-03-20
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the fifth round of the survey (first quarter 2014) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, health care affordability, awareness of key provisions of the ACA, sources of information about the health plans in the new ACA health insurance exchanges (healthcare.gov), the importance of various criteria in choosing health insurance plans, and whether the respondent enrolled in health insurance through healthcare.gov. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, First Quarter 2015 (ICPSR 36364)

Released/updated on: 2019-08-22
Geographic coverage: United States
Time period: 2015-03-04--2015-03-22
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the first quarter 2015 survey (the ninth round of the HRMS) include self-reported health status, awareness of key provisions of the ACA, sources of information about the health plans offered in the ACA marketplace, whether health insurance was purchased through the ACA marketplace, difficulties with access to health care and paying for medical bills and housing costs, out-of-pocket health care costs, type of health insurance coverage if any, and reasons for not having health insurance. Respondents who enrolled in a health insurance plan through the ACA marketplace in 2014 were asked if and why they renewed or changed their plan in 2015. Additional information collected by the survey includes age, gender, sexual orientation, marital status, family size, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size. The data file also records whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral health condition and whether the respondent or a family member received Social Security, Supplemental Security Income, unemployment insurance benefits or benefits though the Supplement Nutrition Assistance Program, Earned Income Tax Credit, Temporary Assistance for Needy Families, or child care services or child care assistance from a local welfare agency or case manager.
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Health Reform Monitoring Survey, United States, First Quarter 2016 (ICPSR 36744)

Released/updated on: 2019-08-22
Geographic coverage: United States
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 11th round of the survey (first quarter 2016) include self-reported health status, type of health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, health insurance literacy, feelings of unfair treatment by doctors and other health care providers, experience with health insurance marketplaces, awareness of ACA provisions, and rating of neighborhood characteristics. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, employer size, body mass index, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, First Quarter 2017 (ICPSR 37031)

Released/updated on: 2019-07-01
Geographic coverage: United States
Time period: 2017-01-01--2017-03-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 13th round of the survey (first quarter 2017) include self-reported health status, health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, health insurance literacy, dental care, opinions of the ACA, and rating of neighborhood characteristics. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Health Reform Monitoring Survey, United States, First Quarter 2018 (ICPSR 37304)

Released/updated on: 2019-06-10
Geographic coverage: United States
Time period: 2018-01-01--2018-03-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 15th round of the survey (first quarter 2018) include self-reported health status, health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, work experience, consumer experiences with health insurance marketplaces, the individual mandate, attitudes toward health plans that are not ACA-compliant, attitudes toward Medicaid work requirements, trust in health care providers, and plan quality ratings. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Health Reform Monitoring Survey, United States, First Quarter 2019 (ICPSR 37630)

Released/updated on: 2020-07-14
Geographic coverage: United States
Time period: 2019-01-01--2019-03-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 17th round of the survey (first quarter 2019) include self-reported health status, health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, work experience, awareness of Medicaid work requirements, attitudes toward proposals to expand health insurance coverage, and short-term health plans. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Health Reform Monitoring Survey, United States, First Quarter 2020 (ICPSR 38110)

Released/updated on: 2022-02-10
Geographic coverage: United States
Time period: 2020-03-01--2020-04-30
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 19th round of the survey (first quarter 2020) include self-reported health status, health insurance coverage, access to health care, trust in the health care system, use of public benefits, material hardship, and the COVID-19 pandemic. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race and ethnicity, United States citizenship, housing type, home ownership, internet access, income, and employment status.
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Health Reform Monitoring Survey, United States, Fourth Quarter 2013 (ICPSR 35621)

Released/updated on: 2019-08-07
Geographic coverage: United States
Time period: 2013-12-06--2013-12-23
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the fourth round of the survey (fourth quarter 2013) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, health care affordability, use of information about the health insurance plans offered through the health insurance exchanges created by the ACA, enrollment in health plans or Medicaid through the ACA exchanges, the importance of various criteria in choosing health insurance plans, whether the respondent received notice that his/her current insurance policy was cancelled or would no longer be offered after 2013, worries about future health insurance coverage, and expectations about one's health insurance coverage in 2014. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, Fourth Quarter 2014 (ICPSR 36287)

Released/updated on: 2019-08-19
Geographic coverage: United States
Time period: 2014-12-02--2014-12-29
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the eight round of the survey (fourth quarter 2014) include self-reported health status, type of and satisfaction with health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, and awareness of various provisions of the ACA. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, receipt of government benefits, employment status, and employer size.
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Health Reform Monitoring Survey, United States, June 2022 (ICPSR 38774)

Released/updated on: 2024-08-08
Geographic coverage: United States
Time period: 2022-06-01--2022-07-31
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 21st round of the survey (June 2022) include self-reported health status, health insurance coverage, access to health care, disability, COVID-19, awareness of the Medicaid continuous coverage requirement, past-due medical debt, unfair treatment in health care settings, food security, and access to transportation. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race and ethnicity, United States citizenship, housing type, home ownership, internet access, income, and employment status.
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Health Reform Monitoring Survey, United States, Second Quarter 2013 (ICPSR 35623)

Released/updated on: 2019-07-10
Geographic coverage: United States
Time period: 2013-06-27--2013-07-24
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the second round of the survey (second quarter 2013) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, health care affordability, whether the respondent considered purchasing or tried to purchase health insurance coverage directly from an insurance company, whether the respondent considered obtaining coverage through Medicaid or other government sponsored assistance plan based on income or disability, sources of information about health insurance, and the importance of various criteria in choosing a health insurance plan. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, number of employees at place of work, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, Second Quarter 2014 (ICPSR 36045)

Released/updated on: 2019-08-07
Geographic coverage: United States
Time period: 2014-06-03--2014-06-20
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the sixth round of the survey (second quarter 2014) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, health care affordability, awareness of key provisions of the ACA, opinions about the ACA, sources of information about the health plans in the ACA health insurance exchanges (healthcare.gov), the importance of various criteria in choosing health insurance plans, whether the respondent enrolled in health insurance through healthcare.gov, and how easy or hard it was to use healthcare.gov. Additional information collected by the survey includes income, employment status, age, education, race, gender, housing type, marital status, home ownership, internet access, ability to read and work with numbers, and sexual orientation. The data file also records whether the respondent reported an ambulatory care sensitive condition or reported a mental or behavioral health condition, and whether the respondent or a family member received unemployment insurance benefits or benefits though the Supplement Nutrition Assistance Program, Earned Income Tax Credit, Temporary Assistance for Needy Families, or child care services or child care assistance from a local welfare agency or case manager.
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Health Reform Monitoring Survey, United States, Third Quarter 2013 (ICPSR 35622)

Released/updated on: 2019-05-14
Geographic coverage: United States
Time period: 2013-09-11--2013-09-30
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the third round of the survey (third quarter 2013) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, health care affordability, opinions about the ACA, awareness of key provisions of the ACA, expected health insurance coverage in 2014, and whether the respondent or respondent's family were affected by provisions of the ACA. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, Third Quarter 2014 (ICPSR 36208)

Released/updated on: 2019-08-29
Geographic coverage: United States
Time period: 2014-09-11--2014-09-30
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the seventh round of the survey (third quarter 2014) include self-reported health status, health insurance coverage, access to and use of health care, health care affordability, and awareness of various provisions of the ACA. Additional information collected by the survey includes income, employment status, age, education, race, Hispanic origin, United States citizenship, gender, housing type, marital status, home ownership, internet access, and sexual orientation.
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Health Reform Monitoring Survey, United States, Third Quarter 2015 (ICPSR 36743)

Released/updated on: 2019-09-05
Geographic coverage: United States
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the third quarter 2015 survey (the tenth round of the HRMS) include self-reported health status, type of and satisfaction with health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, health insurance literacy, feelings of unfair treatment by doctors and other health care providers, and rating of neighborhood characteristics. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, employer size, body mass index, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, Third Quarter 2016 (ICPSR 36842)

Released/updated on: 2019-06-27
Geographic coverage: United States
Time period: 2016-09-01--2016-11-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 12th round of the survey (third quarter 2016) include self-reported health status, type of health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, health insurance literacy, feelings of unfair treatment by doctors and other health care providers, experience with health insurance marketplaces, awareness of ACA provisions, and rating of neighborhood characteristics. Demographic information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, employer size, body mass index, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.
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Health Reform Monitoring Survey, United States, Third Quarter 2017 (ICPSR 37298)

Released/updated on: 2019-06-10
Geographic coverage: United States
Time period: 2017-07-01--2017-09-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 14th round of the survey (third quarter 2017) include self-reported health status, type of and satisfaction with health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, health insurance literacy, health plan network, opinions about the ACA and health insurance, surprise medical bills, distance and travel time to usual source of care, and rating of neighborhood characteristics. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Health Reform Monitoring Survey, United States, Third Quarter 2018 (ICPSR 37487)

Released/updated on: 2020-02-25
Geographic coverage: United States
Time period: 2018-07-01--2018-09-30
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 16th round of the survey (third quarter 2018) include self-reported health status, health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, work experience, awareness of Medicaid work requirements, experiences with health care and social service providers, and health plan choice. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Health Reform Monitoring Survey, United States, Third Quarter 2019 (ICPSR 37922)

Released/updated on: 2021-01-21
Geographic coverage: United States
Time period: 2019-07-01--2019-09-01
In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the 18th round of the survey (third quarter 2019) include self-reported health status, health insurance coverage, access to and use of health care, out-of-pocket health care costs, health care affordability, awareness of and attitudes toward Medicaid work requirements, health savings accounts, flexible spending accounts, access to behavioral health care and dental care, and attitudes toward proposals to expand health insurance coverage. Additional information collected by the survey includes age, gender, sexual orientation, marital status, education, race, Hispanic origin, United States citizenship, housing type, home ownership, internet access, income, employment status, and employer size.
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Healthy Schools Program Evaluation, 2006-2014 (ICPSR 33541)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2006-01-01--2014-01-01

These data were collected as part of the evaluation of the Healthy School Program (HSP), a program that provides support to elementary, middle, and high schools in the United States as they work to create healthy school environments that promote physical activity and healthy eating for students and staff. HSP was created in 2006 by the Alliance for a Healthier Generation with funding from the Robert Wood Johnson Foundation. The HSP evaluation addressed both process and impact outcomes:

  1. Is the HSP technical assistance and training model effective in increasing the implementation of policies and programs that promote and provide access to healthier foods and more physical activity before, during and after school?

  2. Are there distinctive or common school-level characteristics that hasten or hinder school-level implementation of policies and programs that promote and provide access to healthy foods and physical activity in the school setting in HSP schools?

  3. Does participation in HSP contribute to an increase in healthy eating behaviors and physical activity participation among students? Does participation in HSP contribute to a decrease in body mass index (BMI) among students?

The evaluation used a mixed-method design incorporating both quantitative and qualitative components. The quantitative component of the evaluation was a longitudinal design that measured student changes in eating and physical activity behaviors and BMI and schools' implementation of policies and practices promoted by HSP. For the qualitative component the evaluation team conducted site visits in a sample of HSP schools.

Nine data files constitute this data collection:

  1. HSP Participation and Inventory Data File, 2006-2011 (originally called the Inventory Data File)

  2. Pilot Student Survey Data File

  3. Pilot Student Height and Weight Measurements Data File

  4. Survey of Students in Boston and Miami-Dade Public Schools Data File

  5. HSP Participation and Inventory Data File, 2006-2014

  6. Arizona, Prince George's County and Nevada Healthy Schools Youth Survey Data File

  7. Arizona and Prince George's County Youth Height and Weight Measurements Data File

  8. Arizona Academic Achievement Data File

  9. Prince George's County School Wellness Coordinator Survey Data File

Dataset 1 contains data on school characteristics, HSP engagement indicators, baseline and follow-up responses to the Healthy Schools Inventory, and indices derived from the Inventory for all HSP schools as of August 2011. The Inventory collected information about each school's adherence to the Healthy Schools Program Framework, a set of best practice guidelines that promote physical activity and healthy eating among students and staff.

Datasets 2, 4 and 6 contain data from baseline and follow-up administrations of the Healthy Schools Youth Survey questionnaire in three samples of HSP schools: students in grades 5-12 in the initial pilot cohort of HSP schools; students in grades 5, 8 and 10 in the 2007-2008 cohort of HSP schools in Boston, Massachusetts and Miami-Dade County, Florida; and students in grades 5, 8 and 10 or 11 in HSP schools in Arizona, Nevada and Prince George's County, Maryland. Topics covered by the Healthy Schools Youth Survey questionnaire include eating and physical activity habits, attitudes about healthy eating and physical activity, health knowledge, and school food environments.

Datasets 3 and 7 contain baseline and follow-up height and weight measurements and derived BMIs, the former for students in grades 4-12 in schools sampled by the Pilot Student Survey and the latter for students in grades 5, 8, and 10 in Arizona and grades 1-12 in Prince George's County in schools sampled by the Arizona, Prince George's County and Nevada Healthy Schools Youth Survey.

Dataset 5 is an update to Dataset 1. Like Dataset 1 it contains data on HSP participation and engagement and school characteristics. Dataset 5 covers 8,500 schools that participated in HSP through fall 2014. It includes 4,028 of the 4,542 schools in Dataset 1.

Dataset 8 contains average math, reading and language scores for grades in HSP and comparable non-HSP schools in Arizona. Every record in the data file represents a grade (one or more of the grades 2-9) within a school (150 schools) for a given school year (up to seven years 2007-2008 to 2013-2014).

Dataset 9 contains data from a survey of HSP school coordinators in Prince Georges County. The coordinators were interviewed about the implementation of HSP in their schools.

ICPSR did not receive the site visit data.