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Showing 1 – 50 of 380 results.
Curated

ABC News/Washington Post Poll, March 1987 (ICPSR 8845)

Released/updated on: 1992-02-16
Geographic coverage: United States
This data collection is part of a continuing series of monthly surveys that evaluate the Reagan presidency and solicit opinions on a variety of political and social issues. Topics covered include in-depth questions concerning Reagan's age, health, memory, and honesty, the impact of his advisers on decision-making, the Iran-contra affair, Reagan's involvement and the Tower Commission report, Republican and Democratic presidential candidates, and the disease AIDS. Demographic characteristics of respondents also were recorded.
Curated

ABC News/Washington Post Poll of Public Opinion on Aging, March 1982 (ICPSR 8024)

Released/updated on: 2005-11-04
Geographic coverage: United States
This special topic poll is part of a continuing series of monthly surveys that solicit public opinion on the presidency and on a range of other political and social issues. In this poll, respondents were asked their opinions on problems of the elderly, including Social Security benefits, Medicare coverage, high energy costs, loneliness, and poor health. Also included were questions concerning Ronald Reagan's presidential performance, the automobile industries in Japan and the United States, and United States foreign relations with Israel and other allies. Demographic information on respondents includes race, sex, age, religion, educational and income levels, marital status, and retirement status.
Curated
Restricted

Abstinence Reinforcing Contingency Management to Suppress HIV Viral Load (Project First), New York City, 2012 (ICPSR 39785)

Released/updated on: 2026-04-20
Geographic coverage: New York City, United States, New York (state)

This study is part of the Seek, Test, Treat and Retain (STTR) Collaboration Project that involved over twenty studies in the fields of HIV and drug abuse. All studies were independently developed, but were chosen for the collaboration because they focused on one or more steps of the HIV treatment cascade: Seek, Test, Treat and Retain. As part of STTR Collaboration Project, the studies were grouped into Criminal Justice-related studies and Vulnerable Population-related studies. The data collected by these studies included twelve common domains (e.g., Demographic characteristics, Mental Health) in each of which a shared questionnaire or instrument was taken up by the studies and adapted to fit the study.

Using a randomized controlled study design, this study tested the efficacy of an abstinence-reinforcing CM intervention compared with a control condition (performance feedback) on HIV viral load (VL) suppression. The intervention CM group could receive up to $1320 in vouchers over the 16-week intervention based on drug-free urine. Participants were followed for 28 weeks (44 visits), with research visits occurring twice weekly during the Baseline Period (weeks 1-4, visits 1-8) and Intervention Period (weeks 5-20, visits 9-40), then every two weeks during the Post-Intervention Period (weeks 21-28, visits 41-44).

Curated
Simple Crosstabs

Afrobarometer Round 6: The Quality of Democracy and Governance in Nigeria, 2014-2015 (ICPSR 36721)

Released/updated on: 2017-10-30
Geographic coverage: Africa, Nigeria, Global
Time period: 2014-01-01--2015-01-01

The Afrobarometer is a comparative series of public attitude surveys that collects and disseminates data regarding Africans' views on democracy, governance, the economy, civil society, and related issues. The data are collected from nationally representative samples in face-to-face interviews in the language of the respondent's choice. Standard topics for the Afrobarometers include attitudes toward and evaluations of democracy, governance and economic conditions, political participation, and national identity. In addition, Round 6 surveys include special modules on taxation; tolerance; crime, conflict and insecurity; political corruption; interregional relations; perceptions of China; use of technology; and social service delivery.

This particular data collection is concerned with the attitudes and opinions of the citizens of Nigeria, and also includes a number of "country-specific questions" designed specifically for the respondents of the Nigeria survey. These "country-specific questions" solicited respondents' opinions on topics such as who was supporting extremist groups involved with launching attacks and kidnappings, how effective the government had been in addressing the problem of armed extremists, and whether Nigeria should create more states. Respondents were also asked their opinions on the 2015 elections and how responsive they felt the federal government was to emergencies such as the Ebola virus outbreak, Polio, floods, and insecurities caused by armed robbers and extremist groups.

The surveys also collect a large set of socio-demographic indicators such as age, gender, education level, poverty level, language and ethnicity, and religious affiliation, as well as political party affiliation. Afrobarometer Round 6 surveys were implemented in 36 countries.

Curated
Simple Crosstabs

Age and Generations Study, 2007-2008 (ICPSR 34837)

Released/updated on: 2013-10-07
Geographic coverage: United States
Time period: 2007-01-01--2008-01-01
The Age and Generations Study documented employee and employer outcomes related to the experiences of multi-generational teams in five industry sectors, and examined how the work relationships of these team members might change over time. The five industry sectors included in this collection were retail, pharmaceuticals, finance, health care, and higher education. Various questions focused on the organization and on how the interactions of multi-generational work units affected outcomes for employees in the department/unit, as well as their performance and productivity outcomes. Additionally, the survey requested information on employees' perceptions of their work experience, work that is done by their work groups, opportunities for learning and development, organizational policies, and their assessments of their health and well-being. Demographic variables included gender, birth year, race/ethnicity, education, marital status, number of children, hourly wage, salary, and household income.
Curated

Aging in the Eighties: America in Transition, 1981 (ICPSR 8691)

Released/updated on: 2005-11-04
Geographic coverage: United States
This survey was undertaken to record changes in views about aging among older people as well as younger adults. In the seven years after the benchmark study MYTH AND REALITY OF AGING, 1974 (ICPSR 7657) was conducted, a number of significant social and demographic changes occurred in American society, some profound economic trends continued, suspicions grew about an impending financial crisis in the Social Security system, and new priorities emerged at both the national and local political levels. AGING IN THE EIGHTIES updates topics from MYTH AND REALITY OF AGING with items relating to the experience of aging, social activities and the involvement of the elderly, expectations and attitudes about retirement, and preparation for retirement. Other major issues were explored for the first time, including the economics of aging and retirement, the changing face of retirement and employment after 65, Social Security and the role of government, health status, and health care.
Curated

Aging of Veterans of the Union Army: Military, Pension, and Medical Records, 1820-1940 (ICPSR 6837)

Released/updated on: 2006-06-05
Geographic coverage: Vermont, Indiana, United States, Maine, West Virginia, Massachusetts, Missouri, Wisconsin, District of Columbia, Kentucky, Minnesota, California, Kansas, Delaware, New York (state), New Jersey, Michigan, Pennsylvania, Iowa, New Mexico, Illinois, Connecticut, New Hampshire, Ohio, Maryland
Time period: 1820-01-01--1940-01-01
This data collection constitutes a portion of the historical data collected by the project "Early Indicators of Later Work Levels, Disease, and Death." With the goal of constructing datasets suitable for longitudinal analyses of factors affecting the aging process, the project is collecting military, medical, and socioeconomical data on a sample of white males mustered into the Union Army during the Civil War. The project seeks to examine the influence of environmental and host factors prior to recruitment on the health performance and survival of recruits during military service, to identify and show relationships between socioeconomic and biomedical conditions (including nutritional status) of veterans at early ages and mortality rates from diseases at middle and late ages, and to study the effects of health and pensions on labor force participation rates of veterans at ages 65 and over. This installment of the collection, Version M-5, supersedes any previous version of these data. Collected in this version are data from military service, pension, and medical records of veterans who were originally mustered into the Union Army in California, Connecticut, Delaware, District of Columbia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Vermont, West Virginia, and Wisconsin regiments. Also included are data from a 20-company pilot sample and information on recruits whose pension records were stored at the Veterans Administration (VA) Archives in Washington, DC, but had not been collected previously. Data include date and place of birth, place of residence, marital status, number of children, occupation, wealth and income, muster place and date, length of service, battles fought, medical experiences (e.g., illness, wounds, and hospital stays), health status, pension information, and date, place, and cause of death. Additional variables provide the place and date of birth of the recruits' wives, children, and parents. The data are organized into three sections according to state of enlistment. Section 1 (Parts 1, 2, 3, and 4) contains data from New England, Kansas, Missouri, Minnesota, Iowa, New Jersey, Indiana, Wisconsin, California, New Mexico, and the 20-company pilot sample. Section 2 (Parts 5, 6, 7, and 8) contains data from New York, Michigan, Washington, DC, Delaware, Kentucky, Maryland, and West Virginia, along with pensions data from the VA Archives. Section 3 (Parts 9, 10, 11, and 12) contains data from Ohio, Pennsylvania, and Illinois. The variables in Part 13, Linkage Data, indicate which major document sources were located for each recruit. Also, provided is information regarding death dates (Part 14) for individuals whose death records came from the pension payout cards. Approximate date of death was determined by examining the last record of payment to the pensioner.
Curated
Simple Crosstabs

Aging of Veterans of the Union Army: Surgeons' Certificates, United States, 1862-1940 (ICPSR 2877)

Released/updated on: 2018-05-18
Geographic coverage: United States
Time period: 1862-01-01--1940-01-01

This data collection, Aging of Veterans of the Union Army: Surgeons' Certificates, United States, 1862-1940, constitutes a portion of the historical data collected by the project "Early Indicators of Later Work Levels, Disease, and Death." With the goal of constructing datasets suitable for longitudinal analyses of factors affecting the aging process, the project collects military, medical, and socioeconomic data on a sample of white males mustered into the Union Army during the Civil War. The surgeons' certificates contain information from examining physicians to determine eligibility for pension benefits. Also included are questions regarding the age, occupation, residence, and military experience of the veterans. These data can be linked to "Aging of Veterans of the Union Army: Military, Pension, and Medical Records, 1820-1940" (ICPSR 6837) and "Aging of Veterans of the Union Army: United States Federal Census Records, 1850, 1860, 1900, 1910" (ICPSR 6836) using the variable "recidnum."

Curated

Aging of Veterans of the Union Army: United States Federal Census Records, 1850, 1860, 1900, 1910 (ICPSR 6836)

Released/updated on: 2006-06-13
Geographic coverage: Vermont, Indiana, United States, Maine, West Virginia, Massachusetts, Missouri, Wisconsin, District of Columbia, Kentucky, Minnesota, California, Kansas, Delaware, New York (state), New Jersey, Michigan, Pennsylvania, Iowa, New Mexico, Illinois, Connecticut, New Hampshire, Ohio, Maryland
This data collection constitutes a portion of the historical data collected by the project "Early Indicators of Later Work Levels, Disease, and Death." With the goal of constructing datasets suitable for longitudinal analyses of factors affecting the aging process, the project is collecting military, medical, and socioeconomical data on a sample of white males mustered into the Union Army during the Civil War. The project seeks to examine the influence of environmental and host factors prior to recruitment on the health performance and survival of recruits during military service, to identify and show relationships between socioeconomic and biomedical conditions (including nutritional status) of veterans at early ages and mortality rates from diseases at middle and late ages, and to study the effects of health and pensions on labor force participation rates of veterans at ages 65 and over. This installment of the collection, Version C-3, supersedes all previous collections (Versions C-1 and C-2), and contains data from the censuses of 1850, 1860, 1900, and 1910 on veterans who were originally mustered into the Union Army in Connecticut, Delaware, District of Columbia, Illinois, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Vermont, and West Virginia. This version of the collection also contains observations from Wisconsin, Indiana, California, and New Mexico. Census Data, Part 1, includes place of residence, relationship to head of household, date and place of birth, number of children, education, disability status, employment status, number of years in the United States, literacy, marital status, occupation, parents' birthplace, and property/home ownership. The variables in Part 2, Linkage Data, indicate which document sources were located for each recruit.
Curated

Aging, Status, and Sense of Control (ASOC), 1995, 1998, 2001 [United States] (ICPSR 3334)

Released/updated on: 2005-12-15
Geographic coverage: United States
The Aging, Status, and Sense of Control (ASOC) was conducted during 1995, 1998 and 2001 and examined the relationship between age and changes in the sense of control over one's life. Part I contains data for Waves I and II. Respondents were queried about their physical health, including activities of daily living such as shopping, walking, and doing housework, along with medical conditions such as heart disease, high blood pressure, lung disease, breast cancer, diabetes, arthritis or rheumatism, osteoporosis, and allergies or asthma. Questions regarding mental health investigated difficulties staying focused, feelings of sadness or anxiety, and enjoyment of life. Respondents were also asked about their health behaviors, including use of tobacco and alcohol, frequency of exercise, use of medical services including insurance coverage, and the number of prescription medications used. Also examined was respondents' sense of control over their lives, including social support and participation, and history of adversity, which covered such topics as home or apartment break-ins or assaults, major natural disasters, unemployment longer than six months, and times without enough money for clothes, food, rent, bills, or other necessities. Demographic questions included age, sex, marital status, education, work status, marital and family relations, and socioeconomic status. Wave III (Part 2) was collected in 2001 and contains data on the same questions such as physical health, mental health and health behaviors.
Curated
Simple Crosstabs

American Family Health Study (AFHS), [United States], 2020-2022 (ICPSR 38838)

Released/updated on: 2023-11-15
Geographic coverage: United States
Time period: 2020-01-01--2022-01-01
The American Family Health Study (AFHS) focuses on a special group of households from across the United States that were randomly selected to take part in a study aimed at assessing the health of American individuals and families from 2020-2022. Randomly selected households initially received a link enabling a household member to complete a short questionnaire online, where researchers collected some simple information about the people who usually live in the sampled household.
Curated

Australian [Adelaide] Longitudinal Study of Aging, Wave 6: [1999-2000] (ICPSR 3679)

Released/updated on: 2006-01-18
Geographic coverage: Australia, Global
Time period: 1999-01-01--2000-01-01
The general purpose of the Australian [Adelaide] Longitudinal Study of Aging (ALSA) is to gain further understanding of how social, biomedical, and environmental factors are associated with age-related changes in the health and well-being of persons aged 70 years and older. Emphasis is given to the effects of social and economic factors on morbidity, disability, acute and long-term care service use, and mortality. The aim is to analyze the complex relationships between individual and social factors and changes in health status, health care needs, and service utilization dimensions. Components of Wave 6 (1999-2000) (Part 1) include a comprehensive personal interview conducted via the Computer-Assisted Personal Interview (CAPI) system, a home-based assessment of physiological functions, self-completed questionnaires, and additional clinical studies. In Part 2, Wave 6 Clinical Data, information about the health histories of the respondents was elicited, including information on medication, blood pressure, and physical and mental disabilities.
Curated

Australian [Adelaide] Longitudinal Study of Aging, Waves 1-5 [1992-1997] (ICPSR 6707)

Released/updated on: 2005-11-04
Geographic coverage: Australia, Global
Time period: 1992-01-01--1997-01-01
The general purpose of the Australian Longitudinal Study of Aging (ALSA) is to gain further understanding of how social, biomedical, and environmental factors are associated with age-related changes in the health and well-being of persons aged 70 years and older. Emphasis is given to the effects of social and economic factors on morbidity, disability, acute and long-term care service use, and mortality. The aim is to analyze the complex relationships between individual and social factors and changes in health status, health care needs, and service utilization dimensions. Components of Wave 1 (1992-1993) (Part 1) included a comprehensive personal interview conducted via the Computer-Assisted Personal Interview (CAPI) system, a home-based assessment of physiological functions, self-completed questionnaires, and additional clinical studies. Wave 2 (1993-1994), Wave 3 (1994-1995), Wave 4 (1995-1996), and Wave 5 (1996-1997) (Parts 2, 7, 8, and 10, respectively) included questions regarding changes in domicile, current health and functional status, new morbidity conditions, changes in medication, major life events, general life satisfaction, and changes in economic circumstances. For Wave 3 Clinical Data (Part 9) information about the health histories of the respondents was elicited, including information on medication, blood pressure, and physical and mental disabilities.
Curated
Simple Crosstabs

Behavioral Risk Factor Surveillance System (BRFSS), 2003 (ICPSR 34085)

Released/updated on: 2013-08-05
Geographic coverage: Oregon, Vermont, Puerto Rico, Indiana, United States, Oklahoma, Maine, Utah, Nebraska, West Virginia, Massachusetts, North Dakota, Wisconsin, Arizona, Nevada, District of Columbia, Rhode Island, Montana, Hawaii, Kansas, New York (state), New Jersey, Michigan, Iowa, New Mexico, Illinois, Texas, Connecticut, New Hampshire, Louisiana, Ohio, Georgia, Virginia, Maryland
The Behavioral Risk Factor Surveillance System (BRFSS) is a state-based system of health surveys that collects information on health risk behaviors, preventive health practices, and health care access primarily related to chronic disease and injury. For many states, the BRFSS is the only available source of timely, accurate data on health-related behaviors. BRFSS was established in 1984 by the Centers for Disease Control and Prevention (CDC); currently data are collected monthly in all 50 states, the District of Columbia, Puerto Rico, the United States Virgin Islands, and Guam. More than 350,000 adults are interviewed each year, making the BRFSS the largest telephone health survey in the world. States use BRFSS data to identify emerging health problems, establish and track health objectives, and develop and evaluate public health policies and programs. The BRFSS is a cross-sectional telephone survey conducted by state health departments with technical and methodologic assistance provided by CDC. States conduct monthly telephone surveillance using a standardized questionnaire to determine the distribution of risk behaviors and health practices among adults. Responses are forwarded to CDC, where the monthly data are aggregated for each state, returned with standard tabulations, and published at the year's end by each state. The BRFSS questionnaire was developed jointly by CDC's Behavioral Surveillance Branch (BSB) and the states. When combined with mortality and morbidity statistics, these data enable public health officials to establish policies and priorities and to initiate and assess health promotion strategies.
Curated

Behavioral Risk Factor Surveillance System (BRFSS) Asthma Call-Back Survey, 2009 (ICPSR 34300)

Released/updated on: 2012-08-09
Geographic coverage: North Carolina, Oregon, Vermont, Puerto Rico, Indiana, United States, Oklahoma, Maine, Utah, Washington, Nebraska, West Virginia, Massachusetts, North Dakota, Wisconsin, Arizona, Nevada, District of Columbia, Rhode Island, Montana, Hawaii, California, Kansas, Florida, New York (state), New Jersey, Michigan, Iowa, New Mexico, Illinois, Texas, Connecticut, New Hampshire, Louisiana, Ohio, Georgia, Virginia, Maryland

Asthma is one of the nation's most common and costly chronic conditions, affecting over 38 million Americans at some time in their lives. Managing asthma requires a long term, multifaceted approach, including patient education, behavior changes, asthma trigger avoidance, pharmacological therapy, and frequent medical follow-up. This study provides asthma data available at the state and local level to direct and evaluate interventions undertaken by asthma control programs located in the state health departments. Improved tracking for asthma is critical for planning and evaluating efforts to reduce the health burden from the disease.

The Behavioral Risk Factor Surveillance System (BRFSS) is a state-based system of health surveys that collects information on health risk behaviors, preventive health practices, and health care access primarily related to chronic disease and injury. For many states, the BRFSS is the only available source of timely, accurate data on health-related behaviors. BRFSS was established in 1984 by the Centers for Disease Control and Prevention (CDC); currently data are collected monthly in all 50 states, the District of Columbia, Puerto Rico, the United States Virgin Islands, and Guam. More than 350,000 adults are interviewed each year, making the BRFSS the largest telephone health survey in the world. States use BRFSS data to identify emerging health problems, establish and track health objectives, and develop and evaluate public health policies and programs. The BRFSS is a cross-sectional telephone survey conducted by state health departments with technical and methodological assistance provided by CDC. States conduct monthly telephone surveillance using a standardized questionnaire to determine the distribution of risk behaviors and health practices among adults. Responses are forwarded to CDC, where the monthly data are aggregated for each state, returned with standard tabulations, and published at the year's end by each state. The BRFSS questionnaire was developed jointly by CDC's Behavioral Surveillance Branch (BSB) and the states. Data derived from the questionnaire provide health departments, public health officials, and policymakers with necessary behavioral information. When combined with mortality and morbidity statistics, these data enable public health officials to establish policies and priorities and to initiate and assess health promotion strategies. Demographic variables include race, age, sex, education level, marital status, employment status, and income level.

Curated
Simple Crosstabs

Behavioral Risk Factor Surveillance System (BRFSS), United States, 2017 (ICPSR 37989)

Released/updated on: 2023-07-10
Geographic coverage: District of Columbia, Puerto Rico, United States, Guam

The Behavioral Risk Factor Surveillance System (BRFSS) is a system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. Established in 1984 with 15 states, BRFSS now collects data in all 50 states as well as the District of Columbia and three U.S. territories. BRFSS completes more than 400,000 adult interviews each year.

Curated

Better Rehabilitation Through Better Characterization of Treatments: Development of the Manual for Rehabilitation Treatment Specification [Methods Study], United States, 2014-2018 (ICPSR 39571)

Released/updated on: 2025-11-24
Geographic coverage: United States
Time period: 2014-01-01--2018-01-01

Many people have health problems that affect how well they can do normal activities, either for a short time or for their lifetime. These problems may be present from birth or result from illness, injury, or aging. Rehabilitation, or rehab, can help patients regain the ability to do normal activities. Rehab providers include doctors, nurses, psychologists, and physical, occupational, speech, or language therapists.

Rehab treatments often lack a common definition. Rehab providers often name treatments by the type of professional who delivers them or the problem they treat, rather than by the content of the treatment. Also, treatments can vary across rehab providers. Using a standard way to define rehab treatments may help researchers compare these treatments.

In this study, the research team created and tested a manual to help rehab providers use standard ways to define rehab treatments.

Curated

Bicol Multipurpose Survey (BMS), 1983: [Philippines] (ICPSR 6889)

Released/updated on: 2006-01-12
Geographic coverage: Philippines, Global
Time period: 1978-01-01--1982-01-01
The 1983 Bicol Multipurpose Survey (BMS) was designed to revisit the residents of the Bicol Region of the Philippines who were surveyed during 1978 in an effort to review the progress of the Bicol River Basin Development Project (BRBDP). The Bicol Multipurpose Survey (BMS) was designed to assess the impact of the BRBDP on one of the poorest regions in the Philippines. Using data collected from both semi-urban and rural areas of the Bicol Region, the BMS sought to examine the impact not only of the various development projects of the BRBDP such as irrigation, electricity, and road repair, but also the economic, social, and health issues faced by the residents of the Bicol Region. The survey gathered data for 17 project areas and 3 cities in the provinces of Albay, Camarines Sur, and Sorsogon. The 1983 BMS follows the same design as BICOL MULTIPURPOSE SURVEY (BMS), 1978: [PHILIPPINES] (ICPSR 6878), with the data being organized into 31 "blocks" or series of questions. A total of 1,901 households were surveyed in 1983, most of which were previously surveyed in 1978. An additional replacement sample of 420 was drawn from the 1978 rosters for the 1983 survey. Respondents were again asked about income, employment, education, health status, and health services. Additionally, the 1983 survey gathered extensive information on fishing, business expenses, and small business activities, along with fertility, pregnancy, and mortality histories. Due to time and cost considerations, detailed questions on credit, some health-related items regarding beliefs, chronic illnesses, and breast-feeding, and detailed questions on crops were not included in the 1983 BMS. Section I, Household Data (Parts 1-32), focused on background information, transportation, environment, morbidity, and health services. Information was gathered about people living in the household six months prior to the survey as well as people who had left the household five years prior to the survey. Expenditure data on schooling were gathered for individuals 6-30 years of age. Marriage and pregnancy histories were elicited from women aged 15-49 along with family planning and birth interval information. Section II, Agriculture/Income/Labor Data (Parts 33-87), posed questions on employment, wages, and hired labor for men, women, and children aged 6-15. Data on coconut, sugar cane, and abaca crop production were also gathered, along with information about livestock and poultry, and extensive data were collected about fishing activities. Fishing boat owners were interviewed, along with capture fisherman who fished both inland and marine waters. The Barangay Survey (Parts 88-96) provided information about characteristics of the barangay in which the respondent lived (a barangay is a political subdivision equivalent to a village in rural areas and to a neighborhood in urban areas), services available in the community, types of social services or practitioners, the availability of public utilities and transportation, different types of organizations present within the barangay, employment conditions, and environmental sanitation conditions.
Curated

Boston Rehabilitative Impairment Study of the Elderly (Boston RISE), 2009-2015 (ICPSR 37045)

Released/updated on: 2021-01-28
Geographic coverage: Massachusetts, Boston
Time period: 2009-01-01--2015-01-01
The Boston Rehabilitative Impairment Study of the Elderly (Boston RISE) was a prospective cohort study of older primary care patients, aged 65 years and older, who were at risk for declining mobility and disability at baseline. The study was designed to investigate which combinations of neuromuscular impairments are most responsible for mobility decline and disability over 2 years of follow up. Through additional funding, Boston RISE continued to collect follow up data on the Late Life Function and Disability Instrument (LLFDI) and mobility-related and healthcare utilization outcomes over the phone as part of a 2-year extension. Several ancillary measures were also collected throughout the course of the study.
Curated

Building Infrastructure for Comparative Effectiveness Protocols (BICEP), 2002-2012 [Connecticut] (ICPSR 34447)

Released/updated on: 2013-11-11
Geographic coverage: United States, Connecticut
Time period: 2002-01-01--2012-01-01

CCPC's long term vision is to use pragmatic comparative effectiveness methods, linked to an extensive primary care practice data repository, to establish evidence about best practices for complex real world patients and deliver appropriate, real-time decision support at point of service for primary care practitioners (PCPs) in a way that will account for individualized management of conditions and choice of treatments in order to provide optimal care.

The primary aim of BICEP was to advance analytical methods of observational Comparative Effectiveness Research (CER) to support evidentiary needs of primary care practitioners in answering important questions related to care of patient populations with Multiple Complex Conditions (MCCs).

The secondary aim of BICEP was to conduct a pilot study to demonstrate the feasibility and value of using the analytic methods for conducting CER among complex patients.

BICEP sought to answer the following clinical research questions: In adults with Type 2 Diabetes Mellitus (T2DM) coupled with additional chronic diseases,

  1. What is the comparative effectiveness of T2DM medications in achieving glycemic control?
  2. What is the comparative effectiveness of T2DM medications on intermediate outcomes, adverse events, side effects, tolerability?
  3. Does the effectiveness and safety of the diabetic treatment options differ across subgroups of patients based on patient demographic characteristics, complex co-morbidities, or the use of other concurrent therapies?
Curated
Simple Crosstabs

Canadian COVID-19 Response Survey of People with Disabilities and Health Conditions, 2020, 2021 (ICPSR 38875)

Released/updated on: 2023-10-16
Geographic coverage: Canada
Time period: 2020-06-11--2020-06-22, 2021-07-15--2021-07-31
The Canadian COVID-19 Response Survey of People with Disabilities and Health Conditions was administered to obtain a sample of people with disabilities and health conditions across 10 Canadian provinces and their views on government response to the COVID-19 pandemic.
Curated

Candidate Countries Eurobarometer 2004.1, February-March 2004 (ICPSR 4350)

Released/updated on: 2006-08-17
Geographic coverage: Romania, Cyprus, Hungary, Global, Malta, Czech Republic, Latvia, Turkey, Poland, Slovenia, Slovakia, Bulgaria, Lithuania, Estonia
Time period: 2004-02-01--2004-03-01
The Candidate Countries Eurobarometer (CCEB) series, first conducted in 2001, gathers information from the countries applying to become members of the European Union (EU) in a way that allows direct comparison with the standard Eurobarometer series carried out in the existing EU countries. The CCEB provides decision-makers and the European public with opinion data on the similarities and differences between the EU and the candidate countries. The CCEB continuously tracks support for EU membership in each country and records changes in attitudes related to European issues in the candidate countries. This round of the CCEB surveys was conducted between February 20 and March 17, 2004, in the 13 candidate countries: Bulgaria, Cyprus, Czech Republic, Estonia, Hungary, Latvia, Lithuania, Malta, Poland, Romania, Slovakia, Slovenia, and Turkey. The three main topics covered were opinions regarding the European Union (EU), health, and Internet use by the respondents' children. For the first topic, respondents were asked about the enlargement of the EU, its policies, and its institutions. They were asked several questions to discern the impact the EU would have on their lives when their residing country joined the EU. Other questions focused on the European Parliament, its elections, and its voting intent. Further questions included national decision-making policies of the EU, statements on EU policies -- particularly foreign and defense policies -- and the EU's role in globalization. For the second main topic, health, the respondents were asked about health care and the health care system in their residing country. Other questions asked about the respondent's role in the care of a person with a long-term illness, a person with a handicap, or the elderly. They were further asked about their own health situations. The third topic was Internet usage. The questions focused on ways to protect children from possible dangers and risks associated with the Internet such as pornographic, discriminatory, or violent content. Respondents answered questions concerning Internet rules in their homes, Internet safety, and procedures for reporting harmful content. Demographic and other background information provided includes each respondent's age, gender, nationality, marital status, left-right political self-placement, occupation, age at completion of education, household income, region of residence, subjective size of community, and religious affiliation.
Curated

CBS News/New York Times Monthly Poll #2, February 2007 (ICPSR 23021)

Released/updated on: 2008-10-06
Geographic coverage: United States
This poll, fielded February 23-27, 2007, is a part of a continuing series of monthly surveys that solicits public opinion on the presidency and on a range of other political and social issues. Respondents were asked whether they approved of the way George W. Bush was handling his job as president and other issues such as foreign policy. They also were asked to rate the condition of the national economy, what was the most important domestic policy for the president and Congress to focus on, and whether they approved of the way Congress was handling its job. Opinions were solicited on the topic of health care, including how well the United States health care system works, the cost of health care, the federal government's responsibility to guarantee health care for all Americans, whether taxes should be increased in order to expand health care to all Americans, and whether employers should be required to provide insurance for all their workers. A series of questions asked for respondents' opinions on advertisements by drug companies, including whether they are helpful to consumers, whether prescription drug advertisements on television should be limited by the government, whether it was acceptable for doctors to be paid by drug companies to promote prescription drugs, and whether Congress should change the law to allow Americans to buy lower cost prescription drugs from Canada. Respondents were asked whether the government would do a better job than private insurance companies in providing medical coverage and holding down health care costs, which issues they would like most to hear the 2008 presidential candidates talk about over the next two years regarding health care, and whether they had confidence in each presidential candidate's ability to make decisions about health care. Information was also collected about the status of respondents and their household members' health care coverage and health care costs, their health status and treatment for common conditions, life expectancy, whether they had an employer-sponsored pension plan, and whether they were concerned about not having enough money for retirement. Additional information was collected on respondents' opinions of the Republican and Democratic parties, international trade, globalization, and the United States military situation with Iraq and Iran. Demographic information includes sex, age, race, education level, household income, marital status, religious preference, type of residential area (e.g., urban or rural), political party affiliation, political philosophy, voter registration status and participation history, the presence of children under 18 and household members between the ages of 18 and 24, and whether respondents had children attending a four-year college.
Curated
Simple Crosstabs

CBS News/New York Times Poll, December #2, 2013 (ICPSR 36065)

Released/updated on: 2015-10-19
Geographic coverage: United States
Time period: 2013-12-04--2013-12-15
This poll, the last of two fielded in December 2013, is part of a continuing series of monthly surveys that solicit public opinion on a range of political and social issues. Respondents were asked about their general attitudes toward the government, economy, the direction of the country, and health care issues including the Affordable Care Act (ACA) health care reform law of 2010. Opinions were collected on the coverage, quality, affordability, and source of respondents' health insurance, along with reasons for being uninsured. Furthermore, respondents provided speculation on the impacts, both personal and nationwide, of the health care law (ACA) passed in 2010, as well as their approval of components of the law. Additional topics of the poll include use and understanding of health care online exchange Web sites, specifically Healthcare.gov, and the problems respondents faced using the sites. Demographic information includes sex, age, race, marital status, education level, household income, religious affiliation, type of residential area (e.g., urban or rural), political party, and political philosophy.
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Center for Research on Social Reality [Spain] Survey, February 1994: Health (ICPSR 2031)

Released/updated on: 1997-12-19
Geographic coverage: Europe, Global, Spain
Time period: 1994-02-07--1994-02-12
This data collection is part of a series of nationwide surveys conducted from October 1990 to June 1996 in Spain. The questionnaires for each of these surveys consisted of three sections. The first section collected information on respondents' attitudes regarding personal, national, and international issues, and included questions on respondents' level of life satisfaction and frequency of visits with relatives, neighbors, and friends. The second section contained a topical module of questions that varied from survey to survey, with this survey's topic focusing on health. Among the issues investigated were respondents' health status, utilization of medical care and alternative medicine, health insurance coverage, attitudes toward health and medical care, and habits and lifestyle choices related to health. Questions in the third section of the questionnaire elicited socioeconomic information, such as respondent's sex, age, marital status, size of household, occupation, education, religion, religiosity, place of birth, and income.
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Center for Research on Social Reality [Spain] Survey, November 1990: Health and Health Culture (ICPSR 6977)

Released/updated on: 1997-12-19
Geographic coverage: Europe, Global, Spain
This data collection is part of a series of nationwide surveys conducted from October 1990 to June 1996 in Spain. The questionnaires for each of these surveys consisted of three sections. The first section collected information on respondents' attitudes regarding personal, national, and international issues, and included questions on respondents' level of life satisfaction and frequency of visits with relatives, neighbors, and friends. The second section contained a topical module of questions that varied from survey to survey, with this survey's topic focusing on health and health culture. Among the issues investigated were respondents' health status, utilization of medical care, health insurance coverage, attitudes toward health and medical care, and habits and lifestyle choices related to health. Questions in the third section of the questionnaire elicited socioeconomic information, such as respondent's sex, age, marital status, size of household, occupation, education, religion, religiosity, place of birth, and income.
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Charleston Heart Study, Charleston, South Carolina, 1960-2000 (ICPSR 4050)

Released/updated on: 2021-06-03
Geographic coverage: Charleston (South Carolina), United States, South Carolina
Time period: 1960-01-01--2000-01-01
The Charleston Heart Study (CHS) represents data collected over a 41-year period (1960-2000) in order to provide an understanding of the natural progression of aging in a community-based cohort. In 1960 the CHS began enrolling a random selection of community residents who were 35 years of age and older -- including men and women, Black and White. The primary hypothesis of the original study was to investigate racial differences in the manifestation and risk factors for coronary disease. Over the ensuing 40+ years, a variety of outcome measurements were incorporated into the re-examination of the participants, including psychosocial, behavioral, aging, and functional measures. As a longitudinal study, the CHS allows for the study of the risk factors, correlates, and consequences of aging, while simultaneously allowing for exploration of racial disparity in the manifestation of putative risk factors and outcomes. The CHS began with baseline data and added a special cohort of Black men. In subsequent years three separate follow-ups were conducted. The data include death information for respondents and background characteristics (age, race, sex, occupation, education, and marital status).
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Chicago Community Adult Health Study, 2001-2003 (ICPSR 31142)

Released/updated on: 2012-07-11
Geographic coverage: United States, Chicago, Illinois
Time period: 2001-01-01--2003-01-01

The Chicago Community Adult Health Study (CCAHS) consists of four interrelated components that were conducted simultaneously: (1) a survey of adult health on a probability sample of 3,105 Chicago adults, including direct physical measurements of their blood pressure and heart rate and of height, weight, waist and hip circumference, and leg length; (2) a biomedical supplement which collected blood and/or saliva samples on a subset of 661 survey respondents; (3) a community survey in which individuals described aspects of the social environment of all survey respondents' neighborhoods; and (4) a systematic social observation (SSO) of the blocks in which potential survey respondents resided, including a lost letter drop (Milgram et al. 1965) as an unobtrusive measure of neighborhood social capital/sense of responsibility to help others. The latter two extend a community survey and SSO of neighborhoods carried out by the Project on Human Development in Chicago Neighborhoods (PHDCN) in 1995. The adult health survey and the community survey were conducted jointly through face-to-face interviews with a stratified, multistage probability sample of 3,105 individuals aged 18 and over and living in the city of Chicago, with a response rate of 72 percent that is about the highest currently attainable in large urban areas. In addition, blood pressure, heart rate, and physical measurements (of height, weight, waist and hips, and leg length) were collected during the survey interview, and blood and saliva samples from 661 respondents or 60 percent of those doing the survey in the 80 "focal" neighborhood clusters (NCs). SSOs were conducted on 1,663 of the 1,672 city blocks on which each respondent lived. The CCAHS is the largest of five projects under the NIH-funded Michigan Interdisciplinary Center on Social Inequalities, Mind and Body Mind (#P50HD38986), one of five Mind-Body Centers funded by the National Institutes of Health in late 1999. This study will advance the understanding of socioeconomic and racial/ethnic disparities in health, a major priority of the Public Health Service and the National Institutes of Health.

The PI-supplied summary mentions that the study is comprised of four components. However, for the purposes of this data release there are three distinct datasets. Demographic variables include age, birth year, race, ethnicity, number of children in the household, number of children living elsewhere, number of times the respondent has been married, and relationship status, religious preference, and sex.

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Chicago Health Aging and Social Relations Study: Attrition (ICPSR 36950)

Released/updated on: 2017-11-03
Geographic coverage: United States, Chicago, Illinois, Florida, Michigan
Time period: 2002-09-01--2013-08-31
The Chicago Health, Aging, and Social Relations Study (CHASRS) is a ten-wave longitudinal, population-based study of 229 Caucasian, African American, and Hispanic men and women who ranged from 50-68 years of age at baseline. The study identifies characteristics of respondents that predict attrition in order to permit evaluation of potential selection biases. Respondents were required to spend one day per wave to complete interviews, surveys, and physiological testing in a university laboratory. Analyses of baseline measures of demographic factors, health, cognitive function, loneliness, and social contact indicated that attrition was higher for older respondents, and lower for respondents with better cognitive function and more social contacts. The results replicated age and cognitive function as predictors of attrition in an ethnically diverse sample, and extended this work to include the number of social contacts as protective against attrition.
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Children and Neighborhoods: Randomized Study of Mobility (Continuation-Revised) (ICPSR 36000)

Released/updated on: 2015-06-19
Geographic coverage: United States
This project collects follow-up survey data on the physical and mental health of youth whose families were randomly assigned the HUD's Moving to Opportunity (MTO) housing vouchers. Youth are surveyed roughly ten years after randomization.
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China Health and Nutrition Survey (CHNS) (ICPSR 176)

Released/updated on: 2006-03-08
Geographic coverage: Asia, China (Peoples Republic), Global
The China Health and Nutrition Survey (CHNS), an ongoing open cohort, international collaborative project between the Carolina Population Center at the University of North Carolina at Chapel Hill and the National Institute of Nutrition and Food Safety at the Chinese Center for Disease Control and Prevention, was designed to examine the effects of the health, nutrition, and family planning policies and programs implemented by national and local governments and to see how the social and economic transformation of Chinese society is affecting the health and nutritional status of its population. The impact on nutrition and health behaviors and outcomes is gauged by changes in community organizations and programs as well as by changes in sets of household and individual economic, demographic, and social factors.
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Cleveland Study of the Elderly: a Follow-Up, 1984-1988 (ICPSR 6985)

Released/updated on: 2006-03-30
Geographic coverage: United States, Ohio, Cleveland
Time period: 1984-01-01--1988-01-01
This follow-up survey, funded under two separate grants from the National Institute on Aging (NIA), reinterviewed survivors of STUDY OF THE WELL-BEING OF OLDER PEOPLE IN CLEVELAND, OHIO, 1975-1976 (ICPSR 7773). The first part of the project, "Cleveland GAO Study of the Elderly: A Follow-Up", was conducted from 1983 to 1986, and reinterviewed survivors (n = 647) of the original 1975 sample (n = 1,834) to determine the impact of gender on the quality of life for elders, along with stability and change in measures of mental health. During 1984, a subset of the interview subjects were visited at their homes to validate self-reported impairment and disability. These data are presented in Part 1, Cleveland GAO Study of the Elderly: A Follow-Up, 1984 Data for Survivors of 1975 Sample. The second phase of the project, "Cleveland Elderly 12 Years Later," describes changes in disease, disability, and mortality since 1975 and attempted to determine if differences were related to changes in social support, use of health services, or economic status. The study also sought to assess levels of social, economic, mental, and physical well-being reported by respondents, and examined daily activities, the use and quality of services, and the characteristics of service providers. The "Cleveland Elderly 12 Years Later" data were collected in 1987 and again in 1988. Data collected in 1987 consist of interviews with survivors of the original 1975 sample (Part 2) along with interviews from an additional sample drawn from the 1977 Medicare rolls (Part 3). During 1988, interviews were again conducted with survivors of the original 1975 sample (Part 4) and survivors of the Medicare sample (Part 5). Data collected in 1984, 1987, and 1988 for survivors of the 1975 sample may be merged with the original data collected in 1975-1976 using the ID number.
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Cognition and Aging in the USA (CogUSA) 2007-2009 (ICPSR 36053)

Released/updated on: 2015-04-16
Geographic coverage: United States
Time period: 2007-01-01--2009-01-01
Cognition and Aging in the USA (CogUSA) is a national longitudinal study of cognition, focused on the age-related changes in cognition across cohorts and on the impact of cognition on key health and economic outcomes. The aim of the CogUSA Study was to evaluate the effectiveness of a variety of tests in assessing cognitive skills on a sample mirroring the Health and Retirement Survey (HRS) (ICPSR 6854). Data were derived in three waves, with each wave utilizing a variety of measures. In Waves 1 and 3, these measures included an adaptive number series test. The Woodcock-Johnson (WJ-III) number series test and the Wechsler Abbreviated Scale of Intelligence (WASI) were used in Wave 2. Waves 1 and 3 were conducted as telephone interviews, while Wave 2 was conducted as an in-person interview. This collection includes indicators of cognitive abilities and functioning as well as a variety of demographic, health, and economic variables. Dataset 1 presents participant demographic information, and Dataset 2 presents scores calculated for the cognitive tests administered to the respondents in each of the three waves.
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College and Beyond II (CBII) Alumni Survey, [United States], 2021 (ICPSR 38299)

Released/updated on: 2022-12-12
Geographic coverage: United States

The purpose of College and Beyond II (CBII) is to better understand how students' undergraduate experiences in and out of the classroom relate to their long-run development. The CBII Alumni Survey provides data collected from graduates ten years after earning their bachelor's degrees. It serves as the main source of information on students' long-run development for the study series. Domains covered by the CBII Alumni Survey include arts appreciation and engagement; health and well-being; labor market participation and wealth; civic engagement; beliefs about diversity and pluralism; and democratic participation. The survey also asks about respondents' recollections of their college experiences, as well as their current family structure, social identities, educational attainment, experiences with discrimination, and political and religious identification. The survey contains scales that are widely used in various disciplines such as education, economics, political science, and psychology.

The CBII Alumni Survey data can be linked to other studies in the CBII series using the ID_PERSON anonymized student identifier. These CBII studies provide information about respondents' academic backgrounds, undergraduate course transcripts, descriptions of courses taken, and postsecondary enrollment and degree attainment. Contextual data about respondents' neighborhoods can be linked to the National Neighborhood Data Archive using current zip codes, and contextual data about the colleges respondents applied to can be linked to the Integrated Postsecondary Education Data System using U.S. Department of Education UNITID identifiers.

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Communities in Charge Survey, 2001-2003 [Alameda County, California, Austin, Texas, and Southern Maine] (ICPSR 4638)

Released/updated on: 2007-03-01
Geographic coverage: Texas, Maine, California, Austin
Time period: 2001-01-01--2003-01-01
This three-wave survey was conducted as part of an evaluation of the Communities in Charge (CIC) initiative, a competitive grants program funded by the Robert Wood Johnson Foundation (RWJF). CIC provided funding and technical assistance to help communities design and implement new or expand existing approaches for supplying health care to the uninsured. Three of the 14 CIC sites funded by RWJF in 2001 were selected for the survey: Alameda County, California, Austin, Texas, and southern Maine. With CIC grant support, all three created programs that provided fairly comprehensive health benefits to low-income, uninsured participants, who were interviewed by the survey within three months of enrollment (Wave 1) and again at about six months and 12 months after enrollment (Waves 2 and 3). Conducted in English in southern Maine, English and Spanish in Austin, and English, Spanish, and Cantonese in Alameda County, the survey collected information on demographic and socioeconomic characteristics, health status, health insurance coverage, access to health services, and health services utilization. Additional topics covered by the survey include out-of-pocket spending on health care, unmet health care needs, and satisfaction with and opinions about health care. There are two data files for each wave, one with the data from the Cantonese interviews and one with the data from the English and Spanish interviews.
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Community Hospital Program (CHP) Access Impact Evaluation Surveys, 1978-1979, 1981 (ICPSR 8245)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1978-01-01--1979-01-01
This data collection evaluates group medical practices and the ways in which they affect both access to and use of medical services. Group practices, sponsored by the Robert Wood Johnson Foundation Community Hospital Program (CHP), were selected for use in this assessment. The data were collected by the Center for Health Administration Studies at the University of Chicago, with the assistance of Chilton Research Services. Two surveys were conducted for the study: a baseline survey in 1978-1979 and a follow-up in 1981. Community residents and CHP patients in 12 communities were interviewed. Demographic and medical care data were collected for selected individuals and families in the survey areas. Data on regular sources of medical care for individuals include the type of organization used, type of practice, accessibility, frequency of visits, types of health care professionals seen, cost, and satisfaction. Also in the collection are data on perceived health, episodes of illness (including symptoms, duration, disability days, and doctors consulted), use of preventive health care services, and insurance coverage. Demographic data for individuals and families include age, sex, race, educational attainment, employment, and income. Of the 198 files in this collection, 88 are "raw" data files and 110 are frequencies. The data files consist of four types. The first type are Sample Person files. These contain the responses of group practice patients and community members. The second type are Doctor Episode files, which record doctors and episodes of illness. Family files make up the third type of file, and consist of family members' responses to the survey. Analysis files, linking patient and doctor data, are the fourth type of file. The SPSS frequency files correspond to the data files: two per file for the Sample Person files, and one per file for the remaining three types of files.
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Connecticut Health Care Survey, 2012-2013 (ICPSR 35475)

Released/updated on: 2014-11-05
Geographic coverage: United States, Connecticut
Time period: 2012-06-01--2013-02-01
The Connecticut Health Care Survey was a statewide, random-digit dial telephone survey conducted from June 2012 to February 2013. The goal of the survey was to gather health-related experiences, information, and perspectives from Connecticut residents about themselves and children within their households. The survey provides state-level data on the health and health care of Connecticut residents, including health insurance coverage, access and sources of care, continuity of care, health status, and patient-provider experience and communication. Demographic variables include gender, age, race/ethnicity, and health reference group.
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Cross-National Equivalent File (CNEF), 1970-2009 (ICPSR 145)

Released/updated on: 2006-06-19
Geographic coverage: Canada, South Korea, Great Britain, United States, Australia, Switzerland, Germany, Russia
The Cross-National Equivalent File 1970-2009 contains equivalently defined variables for the British Household Panel Study (BHPS), the Household Income and Labour Dynamics in Australia (HILDA), the Korea Labor and Income Panel Study (KLIPS), the Panel Study of Income Dynamics (PSID), the Russia Longitudinal Monitoring Survey (RLMS-HSE), the Swiss Household Panel (SHP), the Canadian Survey of Labour and Income Dynamics (SLID), and the German Socio-Economic Panel (G-SOEP). The data are designed to allow cross-national researchers not experienced in panel data analysis to access a simplified version of these panels, while providing experienced panel data users with guidelines for formulating equivalent variables across countries. Most importantly, the equivalent file provides a set of constructed variables (for example pre- and post-government income and United States and international household equivalence weights) that are not directly available on the original surveys. Since the Cross-National Equivalent File 1970-2009 can be merged with the original surveys, PSID-CNEF users can easily incorporate these constructed variables into current analyses.
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Daily Experience in Adolescence and Biomarkers of Early Risk for Adult Health (ICPSR 35952)

Released/updated on: 2015-06-05
Geographic coverage: United States
This project conducts a 3-wave longitudinal study of adolescents and their caregivers from Mexican, Chinese, and European backgrounds in order to assess the impact of daily experience on biological indicators of early risk for adult health. It includes intensive behavioral assessments and detailed biological markers of health risk from both adolescents and their parents. Approximately 540 pairs of adolescents and their primary caregivers (180 from each ethnic group) are assessed when the adolescents are approximately 15-16, 17-18, and 19-20 years old. Each year, both adolescents and caregivers participate in interviews that include measures of global social factors and potential protective factors. Participants report daily experiences using a nightly diary checklist for 9 consecutive days. Salivary cortisol is obtained at 4 time points each day for 4 of these days in order to analyze HPA activity, and participants wear wrist actigraphs for the same 4 days to measure objective sleep behaviors. Blood pressure, BMI, and waist/hip ratio are assessed, and dried blood spots are obtained for the assessment of c-reactive-protein (CRP), cholesterol, and high density lipoproteins (HDL). Finally, peripheral blood samples are provided by a subsample of 120 families for the assessment of plasma interleukin-6 (IL-6), a pro-inflammatory cytokine, and for gene expression analyses of molecular signaling pathways driving inflammatory biology.
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Danish 1905 Cohort Study, 1998 (ICPSR 3960)

Released/updated on: 2016-08-22
Geographic coverage: Denmark, Global
Time period: 1905-01-01--1998-01-01
This data collection provides information on individuals born in Denmark in 1905 and who were still living in Denmark in 1998. The overall goal of the study was to establish a genetic-epidemiological database to shed light on the aging process among the extremely old. The data focus on their physical and cognitive functioning. Respondents were asked if they had been previously diagnosed with diseases such as diabetes, arthritis, asthma, migraine, cancer, stroke, heart attack, or depression, and if they were experiencing such ailments as cough, body pains, and bone fracture and were taking medication for them. Questions probed respondents' feelings about their health, life, and future. To assess respondents' general health and functioning, they were asked if they needed assistance with toileting, bathing, dressing, and mobility around the house; how often they needed to use the bathroom during the night; and if they used physical aids such as wheelchairs, eyeglasses, crutches, catheters, or diapers. They were also tested for memory and cognition, mobility, vision, speech, hearing, and lung functioning. Information was also elicited on respondents' mental state and awareness, energy level, menopause, frequency of visits with children and family, visits from a nurse, use of home care services, sleeping patterns, smoking and drinking habits, weight gain or loss, exercises, social activities, hobbies, reading habits, television viewing, and recent deaths in the family. Demographic information includes age, education, and marital status.
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Detroit Area Old Age Study, 1966 (ICPSR 7669)

Released/updated on: 1992-02-16
Geographic coverage: Detroit, United States, Michigan
This data collection contains information about health gathered in interviews with persons aged 65 and over living in the Detroit area (Wayne, Oakland, and Macomb counties as well as the city of Detroit) in 1966. The majority of questions concerned the respondent's physical health, e.g., illnesses, symptoms, history of medical care, type of medical care received currently, satisfaction with care, mental health, dental health, hospitalization costs, medicine costs, health insurance costs, welfare status, attitudes toward assistance and welfare programs, and past sources of payment for medical care and hospitalization other than insurance. Also asked were questions about income and personal finances, past and present employment and earnings, attitudes about retirement, cost of household utilities, amount paid in taxes, sources and history of financial assistance, and housing and living conditions. Other questions probed for place of birth and place where raised, daily activities, attitudes about surrounding area, number of times per week visiting or shopping in surrounding area in both the past and present, contact with family members, family history, family health history, attitudes about role in family, memberships, leisure activities, hobbies, presidential voting history, past and current political affiliation, and attitudes toward the federal government's response to social problems, as well as the respondent's race, education, number of children, marital status, and religious affiliation.
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Detroit Area Study, 1993: Health and Aging (ICPSR 2839)

Released/updated on: 2001-03-26
Geographic coverage: Detroit, United States, Michigan

The 1993 Detroit Area Study explored a variety of issues related to health, the effects of aging, living conditions, and participation in civic life in the Michigan tri-county area of Wayne, Oakland, and Macomb counties. A battery of questions probed respondents' perceptions of their health and mental state and those of their spouse, their ability to perform certain physical and mental activities, and the effect of their emotional state on their appetite and sleeping patterns. Other explored their feelings about neighborhood safety, means of transportation, relationships, accommodation, the portrayal of older people on television programs, and the treatment of older people by employers. The survey also sought respondents' opinions about government, their personal financial situation and problems, money management, savings and investments, and their life as a whole. Additional items questioned respondents about the frequency of their visits to the doctor, overnight hospitalization, chronic health conditions, smoking and drinking habits, and medical coverage, as well as electoral participation, political party preference, ideological leanings, class self-identification, assistance received from community organizations, family, and friends, personal regrets, and time spent watching television and engaging in pleasurable activities. Other questions gauged respondents' memory, vision, and motor skills. Respondents also provided demographic information on sex, age, marital status, race, ethnicity, religion, and education.

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Detroit Area Study, 1995: Social Influence on Health: Stress, Racism, and Health Protective Resources (ICPSR 3272)

Released/updated on: 2002-08-16
Geographic coverage: Detroit, United States, Michigan

This survey explored the ways in which social influences, such as stress and racism, affected health, and the impact these influences had on the respondents' outlook on life. Respondents were questioned about their health status and their exercise, smoking, sleeping, and dieting habits, as well as about diagnosed health problems and depression and their effects on daily activities. Respondents were also asked a series of questions regarding their employment status, type of job and whether it was a supervisory position, the racial makeup of their workgroup, their perceptions of their position and job, the likelihood of their finding another job, hassles experienced while at work, and whether they had any trouble balancing family and work. Another series of questions asked respondents whether they had been a victim of a serious physical attack or assault, robbery, or home burglary, if they had ever been unfairly searched, stopped, or questioned by police, why they felt they had been treated this way, and if they felt they had ever been treated unfairly by a teacher, landlord, or neighbor. Opinions were also solicited on the respondents' experience with depression and anxiety. Respondents were asked whether they felt it was possible to reach their goals, how satisfied they were with their present situation, how often they felt depressed and how long this feeling lasted, whether they lost weight or sleep due to this feeling, how this feeling of depression made them view themselves, how often and how long they were worried about things that were not likely to happen, how often they worried about non-serious things, and how they felt physically when they were anxious or depressed. Another set of questions queried respondents on alcohol and drug use. Respondents were asked how often they drank alcohol, the most they had to drink at one time, whether they had experienced any addiction to alcohol or experienced any emotional or psychological problems associated with drinking, whether they had any problem controlling their drinking, whether they had used drugs outside of a doctor's order, what types of drugs they had used, how often and in what type of situations they had used these drugs, and whether they had any addiction to the drugs. Respondents were also asked whether they had a regular doctor, whether they went to a doctor's office or clinic to seek medical attention, the last time they had gone for a checkup, how they were treated by staff at the visit, whether they trusted their doctor, the reasons why they did or did not receive medical attention, and whether they had health insurance. Respondents were also asked for their perceptions of differences between Blacks and whites, attitudes toward affirmative action with regard to employment, and their attitude toward interracial relationships. Another battery of questions queried respondents on any fears or phobias they had, such as a fear of animals, water, or visiting a doctor or dentist. Questions focused on the severity of these fears, how long they had had these fears, and how much these fears interfered in daily activities. A final set of questions gathered demographic information on respondents such as highest level of education completed, political affiliation, religious affiliation, level of religious participation, importance of religion, birth date, whether they owned their own home or rented, how much they spent on food each week, total family income for the year 1994, and the height and weight of respondents.

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Detroit Area Study, 1997: Social Change in Religion and Child Rearing (ICPSR 4120)

Released/updated on: 2005-06-02
Geographic coverage: Detroit, United States, Michigan

For this survey, respondents from three counties in the Detroit, Michigan, area were queried about their work, health, marriage and family, finances, political views, religion, and child rearing. With respect to finances, respondent views were elicited on credit card purchases, recording expenditures, and savings and investments. Regarding political views, respondents were questioned about political preferences, presidential values, freedom of speech, nuclear war, and the interest of public officials. Questions also addressed religious beliefs and experiences, including the religiosity of respondents' parents, belief in and relationship with God, the relationship between science and religion, school prayer, divorce, and homosexuality. Additional religious questions -- based on the respondents' religious preference (i.e., Protestant, Catholic, Jew, Other Religion, or No Preference/Agnostic/Atheist Only) -- also were asked, covering topics such as interfaith marriages, religion of friends, and observance of religious holy days. Questions were asked about the views of respondents' religious leaders on issues including drinking, abortion, and test-tube fertilization. Regarding child rearing, views were elicited on issues including religious preference of child(ren) raised, religious training given to child(ren), and frequency of prayer before meals. Background information includes marital status, employment, political orientation, and income.

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Detroit Metro Area Communities Study (DMACS) Wave 14, Michigan, 2021 (ICPSR 38970)

Released/updated on: 2025-03-31
Geographic coverage: Detroit, United States, Michigan
Time period: 2021-11-03--2021-12-15

The Detroit Metro Area Communities Study (DMACS) is a panel survey of Detroit residents aged 18 and older. The original panel of respondents was drawn from an address-based probability sample of all occupied Detroit households in 2016 and has since been refreshed through additional address-based sampling annually. Between November 3 and December 15, 2021, 2,662 previously-enrolled panelists were invited to participate in a self-administered online or interviewer-administered telephone survey. A total of 1,900 Detroit residents completed the survey, yielding an overall response rate of 72% (using AAPOR Response Rate 1).

Topics include experience with COVID-19; COVID-19 vaccine receipt, attitudes and trust; employment and economic precarity; neighborhood satisfaction; neighborhood change; as well as healthcare usage; the Child Tax Credit; and Digital Inclusion.

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Do Older Adults Know Their Spouses' End-of-Life Treatment Preferences? (ICPSR 25701)

Released/updated on: 2009-06-23
Geographic coverage: United States
When terminally ill patients become mentally incapacitated, their surrogates often make treatment decisions in collaboration with health care providers. The authors examined how surrogates' errors in reporting their spouses' preferences are affected by their gender, status as durable power of attorney for health care (DPAHC), whether they and their spouses discussed end-of-life preferences, and their spouses' health status. Structural equation models were applied to data from married couples in their mid-60s from the 2004 wave of the Wisconsin Longitudinal Study. Surrogates reported their spouses' preferences incorrectly 13 percent and 26 percent of the time in end-of-life scenarios involving cognitive impairment and physical pain, respectively. Surrogates projected their own preferences onto their spouses'. Similar patterns emerged regardless of surrogate gender and status as DPAHC, marital discussions about end-of-life preferences, or spousal health status. Implications for the process of surrogate decision-making and for future research are discussed.
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Early Years of Marriage (EYM) Project, Years 1-4, 1986-1989 (ICPSR 4557)

Released/updated on: 2007-10-03
Geographic coverage: United States, Michigan

The purpose of the Early Years of Marriage (EYM) Project was to determine ways in which the early development of marriage for Black couples and White couples affect the mental and physical health of spouses, marital stability, long-term marital outcomes, patterns of family life and, for those who divorce, individual adjustment to family disruption. The EYM Project began in 1986 with 373 newlywed couples--174 White couples and 199 Black couples. The marriages were all intra-racial and it was the first marriage for both spouses.

Year 1 interviews, which queried the couples on various aspects of married life, began after four to nine months into the marriage. Very few respondents who originally participated in Year 1 of the study refused to participate in subsequent phases of the study. In 1986 (Year 1) and 1988 (Year 3) spouses were interviewed in their homes separately and together, with the interviews conducted by interviewers of the same race. In 1987 (Year 2) and 1989 (Year 4) shorter individual telephone interviews were conducted.

In all four years, respondents were queried on a wide variety of topics such as feelings and perceptions of their own family, spouse, in-laws, and their spouse's friends, family planning, how many children they should have, how the children should be reared, childcare, and household roles and responsibilities. A series of questions was asked about reasons for getting married, how satisfying married life was, what, if any, were the special pleasures and good feelings that came from being married, how often arguments and disagreements occurred, main reasons for arguments, and how they were eventually resolved. A series of questions were also asked regarding the mental and physical health of the spouse, job satisfaction, job security, and how the job affected the family. In Year 2 and Year 4 interviews (Parts 2-4), a series of questions regarding separation and divorce were also asked.

Demographic variables include race, gender, age, level of education, occupation, income, and religious preference.

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East Asian Social Survey (EASS), Cross-National Survey Data Sets: Work Life in East Asia, 2015 (ICPSR 38160)

Released/updated on: 2022-03-22
Geographic coverage: Asia, Japan, Taiwan, China (Peoples Republic), Global

The East Asian Social Survey (EASS) is a biennial social survey project that serves as a cross-national network of the following four General Social Survey type surveys in East Asia: Chinese General Social Survey (CGSS), Japanese General Social Survey (JGSS), Korean General Social Survey (KGSS), Taiwan Social Change Survey (TSCS), and comparatively examines diverse aspects of social life in these regions. Since its 1st module survey in 2006, EASS produces and disseminates its module survey datasets and this is the harmonized data for the 4th module survey, called 'Work Life in East Asia,' which was carried out during 2015 in China, Japan, and Taiwan.

Survey information in this module focuses on work related issues such as equity at work place, work orientation, and work-family balance. Additionally, respondents were asked about global economic crisis, social disparity and mobility as well as entrepreneurship.

Demographic information specific to the respondent and their spouse includes age, sex, marital status, education, employment status and hours worked, occupation, earnings and income, religion, class, size of community, and region.

Curated

Elucidating Biopsychosocial Mediators of HIV Progression (ICPSR 35912)

Released/updated on: 2015-06-09
Geographic coverage: United States
This project conducts biopsychosocial assessments of at least 100 HIV-infected participants at baseline and at 6, 12, 18, 24, and 36 months. Measures include Type C coping (emotionally inexpressive, not recognizing own needs or feelings); stress and reactivity; beta-chemokines and cytokines; and clinical variables including CD4 cell count, HIV-1 RNA (viral load, VL). Medical status is assessed at 48 months.
Curated

English Longitudinal Study of Ageing (ELSA) (ICPSR 139)

Released/updated on: 2006-06-19
Geographic coverage: Great Britain, Global

The English Longitudinal Study of Ageing is a study of aging and quality of life for people over the age of 50. Established in 2002, the original sample was drawn from households that had previously responded to the Health Survey for England (HSE) between 1998 and 2001. The same group of respondents are surveyed every two years to see how their health, economic, and social circumstances may change over time. One of the study's aims is to determine the relationships between functioning and health, social networks, resources, and economic position as people plan for, move into, and progress beyond retirement. It is patterned after the Health and Retirement Study, a similar study based in the United States.

Although new topics can be introduced at different waves, every module has been reviewed to ensure that it will provide data that can measure change over time. This is achieved by repeating some measures exactly, by asking directly about change, and by adopting questions to allow people to update or amend past responses.

The information collected provides data about: Household and individual demographics; Health - physical and psychosocial; Social care (from Wave 6); Work and pensions; Income and assets; Housing; Cognitive function; Social participation; Effort and Reward (voluntary work and caring); Expectations; Walking speed; Weight.