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Simple Crosstabs

Midlife in the United States (MIDUS 3), 2013-2014 (ICPSR 36346)

Released/updated on: 2019-04-30
Geographic coverage: Contiguous United States
Time period: 2013-05-01--2014-11-01

In 1995-1996, the MacArthur Midlife Research Network carried out a national survey of over 7,000 Americans aged 25 to 74 [ICPSR 2760]. The purpose of the study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. The study was innovative for its broad scientific scope, its diverse samples (which included siblings of the main sample respondents and a national sample of twin pairs), and its creative use of in-depth assessments in key areas (e.g. daily diary of stressful experiences [ICPSR 3725] and cognitive functioning [ICPSR 3596]) on a subset of participants. A detailed description of the study and findings generated by it are available at: http://www.midus.wisc.edu

With support from the National Institute on Aging, a follow-up of the original Midlife Development in the United States (MIDUS) sample was conducted in 2004 (MIDUS 2 [ICPSR 4652]). The daily stress and cognitive functioning projects were repeated and expanded at MIDUS 2; in addition the protocol was expanded to include biomarkers and neuroscience.

In 2013 a third wave (MIDUS 3) of survey data was collected on longitudinal participants. Data collection for this follow-up wave largely repeated baseline assessments (e.g., phone interview and extensive self-administered questionnaire), with additional questions in selected areas such as economic recession experiences. Cognitive functioning data were also collected at the same time, while data collection for the daily diary, biomarker, and neuroscience projects commenced in 2017.

MIDUS also maintains a Colectica portal, which allows users to interact with variables across waves and create customized subsets. Registration is required.

Curated
Simple Crosstabs

Midlife in the United States (MIDUS 1), 1995-1996 (ICPSR 2760)

Released/updated on: 2020-09-28
Geographic coverage: United States
Time period: 1995-01-01--1996-01-01

The Midlife in the United States (MIDUS) is a collaborative, interdisciplinary investigation of patterns, predictors, and consequences of midlife development in the areas of physical health, psychological well-being, and social responsibility. A description of the study and findings from it are available at http://www.midus.wisc.edu.

The first wave of the MIDUS study (MIDUS 1 or M1) collected survey data from a total of 7,108 participants. The baseline sample was comprised of individuals from four subsamples: (1) a national RDD (random digit dialing) sample (n=3,487); (2) oversamples from five metropolitan areas in the U.S. (n=757); (3) siblings of individuals from the RDD sample (n=950); and (4) a national RDD sample of twin pairs (n=1,914). All eligible participants were non-institutionalized, English-speaking adults in the coterminous United States, aged 25 to 74.

Data from the samples were collected primarily in 1995/96. The survey (Project 1) dataset contains responses from a 30-minute Phone interview and two 50-page Self-Administered Questionnaire (SAQ) instruments. Of the 7,108 respondents who completed the Phone interview, 6,325 also completed the SAQ.

This updated version of the study is comprised of three primary datasets:

Dataset 1, Main, Siblings, and Twin Data, contains responses from the main survey of 7,108 respondents. Respondents were asked to provide extensive information on their physical and mental health throughout their adult lives, and to assess the ways in which their lifestyles, including relationships and work-related demands, contributed to the conditions experienced. Those queried were asked to describe their histories of physical ailments, including heart-related conditions and cancer, as well as the treatment and/or lifestyle changes they went through as a result. A series of questions addressed alcohol, tobacco, and illegal drug use, and focused on history of use, regularity of use, attempts to quit, and how the use of those substances affected respondents' physical and mental well-being. Additional questions addressed respondents' sense of control over their health, their awareness of changes in their medical conditions, commitment to regular exercise and a healthy diet, experience with menopause, the decision-making process used to deal with health concerns, experiences with nontraditional remedies or therapies, and history of attending support groups. Respondents were asked to compare their overall well-being with that of their peers and to describe social, physical, and emotional characteristics typical of adults in their 20's, 40's, and 60's. Information on the work histories of respondents and their significant others was also elicited, with items covering the nature of their occupations, work-related physical and emotional demands, and how their personal health had correlated to their jobs. An additional series of questions focusing on childhood queried respondents regarding the presence/absence of their parents, religion, rules/punishments, love/affection, physical/verbal abuse, and the quality of their relationships with their parents and siblings. Respondents were also asked to consider their personal feelings of accomplishment, desire to learn, sense of control over their lives, interests, and hopes for the future.

The Datasets previously numbered 2 and 3 have been removed to avoid redundancies, and all datasets have been renumbered. Please refer to the readme file.

Dataset 2, Twin Screener Data, provides the first national sample of twin pairs ascertained randomly via the telephone.

Dataset 3, Coded Text Responses, describes how open-ended textual responses in the MIDUS 1 Computer-Assisted Telephone Interview (CATI) and Self-Administered Questionnaire (SAQ) were transformed into categorical numeric codes. These codes are included in a stand-alone dataset containing only those cases (N=3,950) that contained text data in their responses.

Online Analysis Only: Datasets 1, 2, and 3 were merged together by the SU_ID variable to form "Merged Data with Weights (Online Analysis Only)" (Dataset 4) for online analysis capabilities.

MIDUS also maintains a Colectica portal, which allows users to interact with variables across waves and create customized subsets. Registration is required.

Curated
Simple Crosstabs

Midlife in the United States (MIDUS 2), 2004-2006 (ICPSR 4652)

Released/updated on: 2021-09-15
Geographic coverage: United States
Time period: 2004-01-01--2006-01-01

In 1995-1996, the MacArthur Midlife Research Network carried out a national survey of 7,108 Americans aged 25 to 74 (MIDLIFE IN THE UNITED STATES (MIDUS), 1995-1996 [ICPSR 2760]). The purpose of the study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. The study was innovative for its broad scientific scope, its diverse samples (which included twins and the siblings of main sample respondents), and its creative use of in-depth assessments in key areas (e.g., daily stress and cognitive functioning). A description of the study and findings from it are available at http://www.midus.wisc.edu. With support from the National Institute on Aging, a longitudinal follow-up of the original MIDUS samples: core sample (N = 3,487), metropolitan over-samples (N = 757), twins (N = 925 complete pairs), and siblings (N = 950), was conducted in 2004-2006. Guiding hypotheses for it, at the most general level, were that behavioral and psychosocial factors are consequential for physical and mental health. MIDUS 2 respondents were aged 35 to 86. Data collection largely repeated baseline assessments (e.g., phone interview and extensive self-administered questionnaire), with additional questions in selected areas (e.g., cognitive functioning, optimism and coping, stressful life events, and caregiving). To add refinements to MIDUS 2, an African American sample (N = 592) was recruited from Milwaukee, Wisconsin, who participated in a personal interview and completed a questionnaire paralleling the above assessments. Survey data for the Milwaukee sample are available in a separate project [ICPSR 22840]. Also administered was a modified form of the mail questionnaire, via telephone, to respondents who did not complete a self-administered questionnaire.

Curated

Public Use Data on Mexican Immigration (ICPSR 35980)

Released/updated on: 2015-06-18
Geographic coverage: United States, Mexico
This project expands the data collection of the Mexican Migration Project (MMP) to new communities in the western states of Durango, Aguascalientes, Colima, and Sinaloa and in the border states of Nuevo Leon, Baja California and Chihuahua. It also includes new quantitative data files on spouse's work history, macroeconomic and labor market conditions in the USA, and conditions in the Mexican political economy. Moreover, it adds new qualitative data files containing the votive texts of migrants and their families and texts of ethnographic interviews with respondents about their experiences migrating to and from the USA and negotiating U.S. society.
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Partially restricted

Head Start Family and Child Experiences Survey (FACES), Family Engagement Plus Study, United States, 2014-2015 (ICPSR 38027)

Released/updated on: 2022-01-31
Geographic coverage: United States
Time period: 2014-01-01--2015-12-31

The 2014 Head Start Family and Child Experiences Survey, or FACES 2014, is the sixth in a series of national studies of Head Start, with earlier studies conducted in 1997, 2000, 2003, 2006, and 2009. FACES 2014 used a new study design that differs from earlier rounds of FACES in several important ways: (1) it included larger program and classroom samples, (2) all data were collected in a single program year, (3) the baseline sample of children included both children enrolled in their first and second year of Head Start, and (4) several special studies were conducted along with the main (Classroom + Child Outcomes Core and Classroom Core) study to collect more detailed information about a given topic, to study new populations of Head Start programs and participants, and to evaluate measures for possible use in future rounds of FACES. For example, the Family Engagement Plus study collected information from parents and staff (teachers and family services staff) on family engagement efforts and service provision in Head Start programs.

The FACES 2014 Family Engagement Plus study took place in spring 2015 within the 60 programs that participated in the child-level data collection in the Classroom + Child Outcomes Core study. This Plus study describes family engagement practices in Head Start from the perspectives of parents and Head Start staff. It examines how practices align with the Head Start Parent, Family, and Community Engagement (PFCE) Framework and targeted family outcomes. It also explores how programs engage with community partners to provide comprehensive services to families and how parents and staff characterize their relationships with one another. It includes semi-structured interviews with parents and family services staff (FSS) as well as supplemental content added to the Core parent and teacher surveys. This release includes open-ended qualitative data from the semi-structured interviews included in the Family Engagement Plus study.

The primary research questions for the Family Engagement Plus study are as follows:

  1. What do family engagement efforts look like in Head Start?
  2. How are families engaged in Head Start and in their children's learning and development at home and in the community?
  3. What staff are involved in family engagement efforts, and in what ways are they involved in those efforts?
  4. How are comprehensive family services provided in Head Start?
  5. How do parents and staff characterize their relationships and interactions with one another?
  6. How do family engagement efforts and service provisions align with the Head Start Parent, Family, and Community Engagement (PFCE) Framework?

The User's Manual provides detailed information about the Family Engagement Plus study design, execution, and data to inform and assist researchers who may be interested in using the data for future analyses or pairing the Family Engagement qualitative data collection sources with other FACES 2014 sources.

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Partially restricted

Time, Love, and Cash in Couples With Children Study (TLC3) [United States], 2000-2005 (ICPSR 22462)

Released/updated on: 2016-01-29
Geographic coverage: Milwaukee, United States, Chicago, New York (state), Wisconsin
Time period: 2000-01-01--2005-01-01
Time, Love, and Cash in Couples with Children (TLC3) consists of four waves of interviews with parents (married and nonmarried) who experienced a birth in the year 2000. Both mothers and fathers participated in semi-structured in-depth interviews individually and as a couple in each of the four waves. Interviewers were encouraged to probe and to be flexible with the order of the questions to foster a more conversational interaction. During the TLC3 interviews respondents were asked their views on parenthood, child-rearing responsibilities and expenditures, family structure and relationships, the amount of time spent with their child, their domestic responsibilities, and household income and expenditures. Questions also focused on the relationship between the parents. Respondents were asked how much time they spend together, what their thoughts were on the future of their relationship, and their general views on marriage, parenthood, and gender roles.
The following results may be significantly less relevant compared to results above.
Curated

Long Beach Longitudinal Study (ICPSR 26561)

Released/updated on: 2011-06-17
Geographic coverage: United States, Long Beach, California
Time period: 1994-01-01--1995-01-01, 2000-01-01--2002-01-01

The Long Beach Longitudinal Study (LBLS) was created in 1978 to obtain normative data for the Schaie-Thurston Adult Mental Abilities Test (STAMAT). From 1994 to 2003 it was extended under the guiding principle that cognitive aging is a largely contextual phenomenon. Individual differences in abilities and change in those abilities over adulthood are associated not only with cognitive mechanisms, but with sociodemographic phenomena such as birth cohort, or gender, and within-individual characteristics, including health, affect, self-efficacy, personality, and other variables that impact health. This principle is reflected in the testing measures added to the original panel. Besides the original ability measures used by Schaie, the Life Complexity Inventory, has been included in all testing. Because these measures were included in the later generations of testing, independent and direct comparisons can be made with Seattle Longitudinal Study (ICPSR 00158) to replicate findings and to generalize longitudinal samples.

Panel 1

The initial panel was sampled in 1978 and consisted of 65 adults aged 28-33 and 518 adults aged 55-84. This sample was tested using the STAMAT, as well as a 20-item list of common English nouns for testing free recall, and a brief essay to test text recall. In 1981, 264 participants from this sample were retested, 106 were again retested from 1994-1995, and 42 in 1997. Finally, 15 participants of the original sample were tested from 2000-2002 using additional tests adopted for the creation of a second panel, described below, as well as a test for measuring executive function.

Panel 2

In 1994, a second panel of 630 participants aged 30-97, a third of which were over 80, was added to the study. The testing for this sample included multiple indices of list recall, text recall, working memory, perceptual speed, and vocabulary for structural equation modeling. Assessment of language, autobiographical memory, personality, depression, health, health behaviors and other measures were also incorporated into the study. In 1997, 352 members of this second panel were retested. From 2000-2002, 179 participants of this second panel completed the 1994-1995 measures, as well as several tests extending the battery to indices of executive function. In 2003, 133 participants were retested.

Panel 3

A third sample was recruited during the 2000-2002 time frame consisting of 911 participants aged 30-98, again approximately a third of which were over the age of 80. In 2003, 513 members of this third panel were retested.

Datasets

The data are provided in 6 datasets.

  1. Panel 1 and 2 1978 - 2003 Longitudinal File

    Dataset 1 is a longitudinal file of data from Panel 1 for tests performed in 1978, 1981, 1994, 1997, and 2000-2002, and data from Panel 2 for tests performed in 1994, 1997, 2000-2002 and 2003.

  2. Panels 1 and 2 1994 STAMAT File

    Dataset 2 contains the STAMAT test variables for Panels 1 and 2.

  3. Panel 1 and 2 1994-2000 Master Data Longitudinal File

    Dataset 3 is a second longitudinal file containing the complete catalog of variables from Panels 1 and 2 for test performed in 1994, 1997 and 2000.

  4. Panel 2 Wave 1 1994 Cross File

    Dataset 4 contains variables for the first wave of Panel 2 which took place in 1994.

  5. Panel 2 Wave 2 1997 Cross File

    Dataset 5 contains variables for the second wave of Panel 2 which took place in 1997.

  6. Panel 3 Wave 1 2000 Master File

    Dataset 6 contains variables from the first wave of Panel 3 which took place in 2000.

Curated

National Maternal and Infant Health Survey, 1988: Longitudinal Follow-up, 1991 (ICPSR 6401)

Released/updated on: 1995-03-16
Geographic coverage: United States
Time period: 1988-01-01--1991-01-01
This follow-up to the NATIONAL MATERNAL AND INFANT HEALTH SURVEY, 1988 (NMIHS) (ICPSR 9730) consists of three components that provide information on early childhood morbidity and health. The Live Birth Survey (Part 1) obtained data on national health issues affecting children, such as child development, effects of low birth weight, childhood injury, child care, pediatric care, health insurance coverage, child safety, and acute and chronic childhood illnesses. For the Medical Provider Survey (Part 12), respondents to the Live Birth Survey were asked to provide the names of all medical providers and hospitals where their children were diagnosed, treated, and/or admitted. Each health care provider was asked to supply information on its organization, the child's health status and history, and each visit or hospitalization. The Fetal and Infant Death Survey (Part 21) interviewed women who were identified through the 1988 NMIHS as having lost a fetus or an infant during the study period. These respondents were reinterviewed to gather information about their health and about any pregnancies since their loss in 1988. The 1991 follow-up data can be merged with data from the 1988 NMIHS, which was designed to explore factors that cause negative pregnancy outcomes.
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Tecumseh Community Health Study, 1959-1969 (ICPSR 8969)

Released/updated on: 1992-02-16
Geographic coverage: United States, Tecumseh, Michigan
The Tecumseh Community Health Study is a longitudinal, ongoing prospective epidemiologic study of a natural community's health and disease status. Data have been collected on the Tecumseh population in southeast Michigan for over 30 years, beginning with a 1957 canvass of all households and adding all newcomers to the community until 1970, after which only previous residents have been followed. The Tecumseh project has conducted over 80 different studies, including both disease-specific investigations and studies concerned with the prevalence and incidence of disease in the community. The core data file for the years 1959-1969 contains data collected in Round I: 1959-1960, Round II: 1962-1965, and Round III: 1967-1969 (referred to as the Cardiovascular Studies I, II, and III, and the General Surveillance Study II). These data include information taken from baseline medical history interviews, medical examinations, clinical measurements, laboratory work, and electrocardiograms. Mortality status of all persons at the time of attempted or actual contact in Round III is also provided. The major variable groups include demographic information, family history of major diseases, systematic review of present and past symptoms and conditions, smoking and drinking habits, physical examinations, measurements and laboratory work, and electrocardiogram results.
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Simple Crosstabs

The Irish Longitudinal Study on Ageing (TILDA), Wave 2, 2012-2013 (ICPSR 37105)

Released/updated on: 2025-05-08
Geographic coverage: Ireland
Time period: 2012-01-01--2013-01-01

This catalog record includes detailed variable-level descriptions, enabling data discovery and comparison. The TILDA Series data, including studies 34315, 38681, 37105, 37106, 38670, 38674, are currently unavailable at the request of the data producer due to concerns related to EU and Irish data privacy and data sharing rules. We are working to determine the best solution to continue to share these data with the research community. Individuals interested in obtaining TILDA data access at this time should reach out to the TILDA project directly (https://tilda.tcd.ie/data/accessing-data/).

The Irish Longitudinal Study on Ageing (TILDA) is a major inter-institutional initiative led by Trinity College Dublin which aims to produce a massive improvement in the quantity and quality of data, research and information relating to older people and ageing in Ireland. Eligible respondents for this study include individuals aged 50 and over and their spouses or partners of any age. The study involves interviews on a two yearly basis with a sample cohort of 8,504 people aged 50 and over (or their spouses/partners) and resident in Ireland, collecting detailed information on all aspects of their lives, including the economic (pensions, employment, living standards), health (physical, mental, service needs and usage) and social aspects (contact with friends and kin, formal and informal care, social participation). Both survey interviews and physical and biological measurements are utilized.

The second wave of TILDA interviews were undertaken between February 2012 and March 2013. Of the 8,504 interviewed in Wave 1, a second interview was obtained for 7,445 respondents. These consisted of the self, proxy and end-of-life interviews types. In addition to the returning respondents, 170 interviews were obtained from eligible household members who had chosen not to take part in Wave 1 or the new spouses/partners of existing respondents.

Demographic and background variables include age, sex, marital status, household composition, education, and employment.

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National Health Interview Survey, 2008 (ICPSR 27341)

Released/updated on: 2010-08-26
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Implementation of a redesigned NHIS, consisting of a basic module, a periodic module, and a topical module, began in 1997 (see NATIONAL HEALTH INTERVIEW SURVEY, 1997 [ICPSR 2954]). The 2008 NHIS contains the Household, Family, Person, Sample Adult, and Sample Child files from the basic module. Each record in Part 1, Household Level, contains data on type of living quarters, number of families in the household responding and not responding, and the month and year of the interview for each sampling unit. Part 2, Family Level, is made up of reconstructed variables from the person-level data of the basic module and includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, and employment status, along with industry and occupation. As part of the basic module, Part 3, Person Level, provides information on all family members with respect to health status, limitation of daily activities, cognitive impairment, and health conditions. Also included are data on years at current residence, region variables, height, weight, bed days, doctor visits, hospital stays, and health care access and utilization. A randomly-selected adult in each family was interviewed for Part 4, Sample Adult, regarding respiratory conditions, renal conditions, AIDS, joint symptoms, health status, limitation of daily activities, and behaviors such as smoking, alcohol consumption, and physical activity. Additionally, questions regarding oral health, asthma, balance, cancer screening, heart disease, HPV, immunization, and vision were fielded. Part 5, Sample Child, provides information from an adult in the household on medical conditions of one child in the household, such as respiratory problems, seizures, allergies, and use of special equipment like hearing aids, braces, or wheelchairs. Also included are variables regarding child behavior, Attention Deficit Hyperactivity Disorder (ADHD), oral health, asthma, indoor tanning, HPV, immunization, mental health, and vision. Part 6, Injury/Poison Episode, is an episode-based file that contains information about the external cause and nature of the injury or poisoning episode and what the person was doing at the time of the injury or poisoning episode, in addition to the date and place of occurrence. Part 7, Injury/Poison Episode Verbatim, contains edited narrative text descriptions of the injury or poisoning, provided by the respondent. Part 8, Paradata, does not contain health related information, but rather data which are related to the interview process, including measures of time, contact-ability, and cooperation.
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Linked Birth/Infant Death Period Data, 1995: [United States, Puerto Rico, Virgin Islands, and Guam] (ICPSR 2285)

Released/updated on: 2006-01-18
Geographic coverage: United States, Guam, Virgin Islands of the United States, Global
This data collection consists of six data files, which can be used to determine infant mortality rates in the United States in 1995. For the first time, data for Puerto Rico, the Virgin Islands, and Guam were included. Another change in 1995 is a change in format of the linked files. They are now released in two different formats, period data and birth cohort data. This collection represents the period data. Parts 1 and 2 are the Denominator files for the United States and for Puerto Rico, the Virgin Islands, and Guam, respectively. These files consist of all births in 1995. Variables in these files include year of birth, state and county of birth, characteristics of the infant (age, sex, race, birth weight, gestation), characteristics of the mother (Hispanic origin, race, age, education, marital status, state of birth), characteristics of the father (Hispanic origin, race, age, education), pregnancy items (prenatal care, live births), and medical data. A new variable in the Denominator files for 1995 is clinical estimate of gestation. Parts 3 and 4 are the Numerator files. They provide records of all infant deaths that occurred in 1995 linked to their corresponding birth certificates, whether the birth occurred in 1995 or 1994. Variables in these files include age at death, underlying cause of death, autopsy, place of accident, infant death identification number, exact age at death, day of birth and death, and month of birth and death. New variables in the linked Numerator files for 1995 include a weight and a clinical estimate of gestation. Parts 5 and 6 are the "unlinked" files. They consist of infant death records that could not be linked to their corresponding birth records.
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Consumer Expenditure Survey, 2009: Diary Survey Files (ICPSR 29883)

Released/updated on: 2010-12-07
Geographic coverage: United States

The Consumer Expenditure Survey (CE) program provides a continuous and comprehensive flow of data on the buying habits of American consumers including data on their expenditures, income, and consumer unit (families and single consumers) characteristics. These data are used widely in economic research and analysis, and in support of revisions of the Consumer Price Index.

The CE program consists of two surveys, the Diary Survey and the quarterly Interview Survey (ICPSR 29884). The Diary Survey is designed to obtain data on frequently purchased smaller items, including food and beverages, both at home and in food establishments, housekeeping supplies, tobacco, nonprescription drugs, and personal care products and services. Each consumer unit (CU) records its expenditures in a diary for two consecutive 1-week periods. Although the diary was designed to collect information on expenditures that could not be easily recalled over time, respondents are asked to report all expenses (except overnight travel) that the CU incurs during the survey week.

The microdata in this collection are available as SAS, STATA, SPSS data sets or ASCII text and comma-delimited files. The 2009 Diary release contains five sets of data files (FMLY, MEMB, EXPN, DTAB, DTID) and three processing files. The FMLY, MEMB, EXPN, DTAB, and DTID files are organized by the quarter of the calendar year in which the data were collected. There are four quarterly data sets for each of these files.

The FMLY files contain CU characteristics, income, and summary level expenditures; the MEMB files contain member characteristics and income data; the EXPN files contain detailed weekly expenditures at the Universal Classification Code (UCC) level; the DTAB files contains the CU's reported annual income values or the mean of the five imputed income values in the multiple imputation method; and the DTID files contain the five imputed income values. The summary level expenditure and income information on the FMLY files permits the data user to link consumer spending, by general expenditure category, and household characteristics and demographics on one set of files.

The three processing files enhance computer processing and tabulation of data, and provide descriptive information on item codes. The three processing files are: (1) an aggregation scheme file used in the published consumer expenditure tables (DSTUB), (2) a UCC file that contains UCCs and their abbreviated titles, identifying the expenditure, income, or demographic item represented by each UCC, and (3) a sample program file that contains the computer program used in Section VII.A. SAMPLE PROGRAM of the Diary User Guide. The processing files are further explained in Section III.E.5. PROCESSING FILES of the same User Guide documentation. There is also a second user guide, "User's Guide to Income Imputation in the CE", which includes information on how to appropriately use the imputed income data.

Demographic and family characteristics data include age, sex, race, marital status, and CU relationships each CU member. Income information, such as wage, salary, unemployment compensation, child support, and alimony, as well as information on the employment of each CU member age 14 and over was also collected.

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Consumer Expenditure Survey, 2010: Diary Survey Files (ICPSR 32482)

Released/updated on: 2011-10-05
Geographic coverage: United States

The Consumer Expenditure Survey (CE) program provides a continuous and comprehensive flow of data on the buying habits of American consumers including data on their expenditures, income, and consumer unit (families and single consumers) characteristics. These data are used widely in economic research and analysis, and in support of revisions of the Consumer Price Index.

The CE program is comprised of two separate components (each with its own survey questionnaire and independent sample), the Diary Survey and the quarterly Interview Survey (ICPSR 32483). This data collection contains the Diary Survey data, which was designed to obtain data on frequently purchased smaller items, including food and beverages, both at home and in food establishments, gasoline, housekeeping supplies, tobacco, nonprescription drugs, and personal care products and services. Each consumer unit (CU) recorded its expenditures in a diary for two consecutive 1-week periods. Although the diary was designed to collect information on expenditures that could not be easily recalled over time, respondents were asked to report all expenses (except overnight travel) that the CU incurred during the survey week.

The microdata in this collection are available as SAS, STATA, SPSS data sets or ASCII text and comma-delimited files. The 2010 Diary release contains five sets of data files (FMLY, MEMB, EXPN, DTAB, DTID) and three processing files. The FMLY, MEMB, EXPN, DTAB, and DTID files are organized by the quarter of the calendar year in which the data were collected. There are four quarterly datasets for each of these files.

The FMLY files contain CU characteristics, income, and summary level expenditures; the MEMB files contain member characteristics and income data; the EXPN files contain detailed weekly expenditures at the Universal Classification Code (UCC) level; the DTAB files contains the CU's reported annual income values or the mean of the five imputed income values in the multiple imputation method; and the DTID files contain the five imputed income values. The summary level expenditure and income information on the FMLY files permits the data user to link consumer spending, by general expenditure category, and household characteristics and demographics on one set of files.

The three processing files enhance computer processing and tabulation of data, and provide descriptive information on item codes. The three processing files are: (1) an aggregation scheme file used in the published consumer expenditure tables (DSTUB), (2) a UCC file that contains UCCs and their abbreviated titles, identifying the expenditure, income, or demographic item represented by each UCC, and (3) a sample program file that contains the computer program used in Section VII.A. SAMPLE PROGRAM of the Diary User Guide. The processing files are further explained in Section III.E.5. PROCESSING FILES of the same User Guide documentation. There is also a second user guide, "User's Guide to Income Imputation in the CE", which includes information on how to appropriately use the imputed income data.

Demographic and family characteristics data include age, sex, race, marital status, and CU relationships for each CU member. Income information, such as wage, salary, unemployment compensation, child support, and alimony, as well as information on the employment of each CU member age 14 and over was also collected.

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Mortality Detail and Multiple Cause of Death, 1981 (ICPSR 3874)

Released/updated on: 2007-07-12
Geographic coverage: North Carolina, Indiana, Wyoming, Utah, Guam, Virgin Islands of the United States, Arizona, Montana, Kentucky, California, Kansas, Florida, Delaware, Pennsylvania, Mississippi, Iowa, Illinois, Texas, Connecticut, Georgia, Virginia, Maryland, Idaho, Oregon, Vermont, Puerto Rico, United States, Oklahoma, Tennessee, Maine, American Samoa, Alabama, Arkansas, Washington, South Carolina, Nebraska, West Virginia, Massachusetts, Colorado, Missouri, Alaska, North Dakota, Wisconsin, Nevada, New York, District of Columbia, Rhode Island, South Dakota, Hawaii, Minnesota, New Jersey, Michigan, New Mexico, New Hampshire, Louisiana, Ohio
This data collection presents information about the causes of deaths occurring during 1981. Part 1, the Mortality Detail file, describes every death or fetal death registered in the United States for 1981. Part 2, Multiple Cause of Death, provides information about the causes of all recorded deaths occurring in the United States, Puerto Rico, the Virgin Islands, Guam, and American Samoa during 1981. Data are provided concerning underlying causes of death, multiple conditions that caused the death, place of death, residence of the deceased (e.g., region, division, state, county), whether an autopsy was performed, and the month and day of death. In addition, data are supplied on the sex, race, age, marital status, education, usual occupation, and origin or descent of the deceased. The multiple cause of death fields were coded from the MANUAL OF THE INTERNATIONAL STATISTICAL CLASSIFICATION OF DISEASES, INJURIES, AND CAUSE-OF-DEATH, NINTH REVISION (ICD-9), VOLUMES 1 AND 2.
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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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Conflict of Interest in the Alcoholic Drinks Industry: How Much Alcohol Consumption Do "Unhealthy Drinkers" Account for in the United Kingdom, 2000-2001? (ICPSR 24701)

Released/updated on: 2009-02-05
Geographic coverage: Great Britain, United Kingdom
Time period: 2000-01-01--2001-01-01
The alcohol industry has been advancing an agenda of corporate social responsibility, claiming that there is no conflict between commercial interests and public health goals. This study subjects this claim to critical scrutiny by estimating the share of total alcohol sales that are due to "unhealthy drinkers" in the United Kingdom, extending previous studies geographically, methodologically and conceptually. Includes secondary analysis of the amount of alcohol consumption above various official guidelines in four British datasets for 2000-2002: the National Diet and Nutrition Survey; the General Household Survey; Smoking, Drinking and Drug Use Among Young People; and the March 2002 ONS Omnibus Survey.
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International Data Base, February 1990 (ICPSR 8490)

Released/updated on: 1992-02-16
Geographic coverage: Global
This dataset contains information from tables of demographic, economic and social data for the countries of the world. Information presented includes population, health, nutrition, mortality, fertility, family planning and contraceptive use, literacy, housing, and economic activity data. Tabular data are broken down by such variables as age, sex, and urban/rural residence.
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National Health Interview Survey, 2007 (ICPSR 27201)

Released/updated on: 2010-08-26
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Implementation of a redesigned NHIS, consisting of a basic module, a periodic module, and a topical module, began in 1997 (see NATIONAL HEALTH INTERVIEW SURVEY, 1997 [ICPSR 2954]). The 2007 NHIS contains the Household, Family, Person, Sample Adult, and Sample Child files from the basic module. Each record in Part 1, Household Level, contains data on type of living quarters, number of families in the household responding and not responding, and the month and year of the interview for each sampling unit. Part 2, Family Level, is made up of reconstructed variables from the person-level data of the basic module and includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, and employment status, along with industry and occupation. As part of the basic module, Part 3, Person Level, provides information on all family members with respect to health status, limitation of daily activities, cognitive impairment, and health conditions. Also included are data on years at current residence, region variables, height, weight, bed days, doctor visits, hospital stays, and health care access and utilization. A randomly-selected adult in each family was interviewed for Part 4, Sample Adult, regarding respiratory conditions, use of nasal spray, renal conditions, AIDS, joint symptoms, health status, limitation of daily activities, and behaviors such as smoking, alcohol consumption, and physical activity in addition to questions regarding stroke, diabetes, arthritis, and weight control. Part 5, Sample Child, provides information from an adult in the household on medical conditions of one child in the household, such as respiratory problems, seizures, allergies, and use of special equipment like hearing aids, braces, or wheelchairs. Also included are variables regarding child behavior, the use of mental health services, and Attention Deficit Hyperactivity Disorder (ADHD), as well as responses to the SDQ, the Strengths and Difficulties questionnaire on child mental health. The 2007 data contain the Child Conditions - Limitation of Activity and Health Status (CHS), Child Health Care Access and Utilization (CAU), Child Mental Health Brief (CMB), Child Mental Health Services (CMS) and Child Influenza Immunization (CFI) sections. Part 6, Injury/Poison Episode, is an episode-based file that contains information about the external cause and nature of the injury or poisoning episode and what the person was doing at the time of the injury or poisoning episode, in addition to the date and place of occurrence. Part 7, Injury/Poison Episode Verbatim, contains edited narrative text descriptions of the injury or poisoning, provided by the respondent. Part 8, Adult Complementary and Alternative Medicine, and Part 9, Child Complementary and Alternative Medicine, provide information regarding the use of 17 nonconventional health care practices, including acupuncture, movement therapies, and relaxation techniques, for sample adults and sample children, respectively. Supplemental Sample Child, Part 10, and Supplemental Sample Child Alternative Medicine, Part 11, are supplemental files for the 2007 data release. These files provide dummy records to fill in the missing information for Part 5, Sample Child, and Part 9, Child Complementary and Alternative Medicine. Part 12, Paradata, does not contain health related information, but rather data which are related to the interview process, including measures of time, contact-ability, and cooperation. RAT_CAT3 Update, Part 13, corrects an error in the 2007 Family Level variable RAT_CAT3.
Curated

Nineteenth Century Family History in Michigan: 1850-1880 (ICPSR 32)

Released/updated on: 2008-03-26
Geographic coverage: Detroit, Flint, United States, Lansing, Michigan
This data collection provides information on the characteristics of 1,194 Michigan families in rural places, towns and villages, and the urban areas of Detroit in 1850 and 1880. Data are provided on the geographic location of each household and type of locale, total number of residents in the household, and total number of children of the head of each household. Demographic variables provide information on age, race, place of birth, and occupation of the household head and their spouse, place of birth of father and mother of the household head and of their spouse, sex of the household head and their children, and age of the children. Additional variables provide information on the number of children listed as unemployed, the number of parents or parents-in-law of the household head residing in the household, the number of other related adults aged 14 and older, other related children aged 14 and younger living in the household, the number of servants or employees in the household, and the number of boarders or roomers in the household.
Curated

Norwegian Ecological Data, 1949-1961 (ICPSR 40)

Released/updated on: 1992-02-16
Geographic coverage: Norway, Europe
Time period: 1949-01-01--1961-01-01
This study contains election and census data for 732 Norwegian communes in the period 1949-1961. Election returns are available for the elections of 1949, 1953, 1957, and 1961. In addition, data from the censuses of 1950 and 1960 are presented, including information on demography, education, modernization, the economy, and occupational structure, and contextual information about clusters of neighboring communes. Data are provided on the total number of registered voters and the total number of votes cast for the Norwegian Communist Party, the Norwegian Labour Party, the Liberal Party (Venstre), the Christian People's Party, the Agrarian Party (the Centre Party), the Conservative Party (Hoyre), and other political parties. Additional variables provide information on age and educational levels for males and females, the total number of economically active population employed in agriculture, forestry, fisheries, manufacturing, and construction, the total value of industrial production, and the total number of private households and occupied housing units.
Curated

Multiple Cause of Death, 1996 (ICPSR 2702)

Released/updated on: 2009-03-05
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States
This data collection includes information about the cause of all recorded deaths occurring in the United States, Puerto Rico, the Virgin Islands, and Guam during 1996. Data are provided concerning underlying causes of death, multiple conditions that caused the death, place of death, residence of the deceased (e.g., region, division, state, county), whether an autopsy was performed, and the month and day of the week of the death. In addition, data are supplied on the sex, race, age, marital status, education, usual occupation, and origin or descent of the deceased. Mortality Detail data for 1996 also can be extracted from this file. The Mortality Detail records are contained in the first 159 positions of these Multiple Cause records. The multiple cause of death fields were coded from the MANUAL OF THE INTERNATIONAL STATISTICAL CLASSIFICATION OF DISEASES, INJURIES, AND CAUSE-OF-DEATH, NINTH REVISION (ICD-9), VOLUMES 1 AND 2.
Curated
Partially restricted

Study of Disability Services Coordinators in Head Start, 2022 (DSC Study), National Data, Regions I-XII, [United States] (ICPSR 39415)

Released/updated on: 2025-10-08
Geographic coverage: United States
The 2022 Study of Disability Services Coordinators (DSCs) in Head Start was the first nationally representative study of the Early Head Start (EHS) and Head Start (HS) DSC workforce, their roles, and the activities they support. NORC at the University of Chicago, along with their partners at SRI International and consultant Amanda Schwartz, conducted the study under contract from the Office of Planning, Research, and Evaluation (OPRE) at the Administration for Children and Families (ACF) within the United States Department of Health and Human Services (HHS). The study was developed in close collaboration with the Office of Head Start (OHS), with OHS staff and EHS and HS staff providing review and feedback on the constructs of interest and the developing study measures. The study explored who fulfills the roles and responsibilities of a DSC in EHS and HS programs and how they work with program staff, local education agencies, service providers, and families to support children with disabilities and suspected delays in their programs. Data from this study sought to inform ACF and OHS about how programs were implementing the DSC efforts and topics for technical and training assistance. Further, programs can examine how their current practices compared to national and regional approaches to disability services.
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Consumer Expenditure Survey, 2009: Interview Survey and Detailed Expenditure Files (ICPSR 29884)

Released/updated on: 2011-01-03
Geographic coverage: United States
Time period: 2008-01-01--2010-01-01

The Consumer Expenditure Survey (CE) program provides a continuous and comprehensive flow of data on the buying habits of American consumers including data on their expenditures, income, and consumer unit (families and single consumers) characteristics. These data are used widely in economic research and analysis, and in support of revisions of the Consumer Price Index.

The CE program consists of two surveys, the quarterly Interview Survey and the Diary Survey (ICPSR 29883). The quarterly Interview survey is designed to collect data on major items of expense which respondents can be expected to recall for 3 months or longer. These include relatively large expenditures, such as those for property, automobiles, and major durable goods, and those that occur on a regular basis, such as rent or utilities. The Interview survey does not collect data on expenses for housekeeping supplies, personal care products, and nonprescription drugs, which contribute about 5 to 15 percent of total expenditures.

The microdata in this collection are available as SAS, STATA, SPSS data sets or ASCII text and comma-delimited files. The 2009 Interview release contains seven groups of Interview data files (FMLY, MEMB, MTAB, ITAB, ITAB_IMPUTE, FPAR, and MCHI), 50 EXPN files, and processing files.

The FMLY, MEMB, MTAB, ITAB, and ITAB_IMPUTE files are organized by the calendar quarter of the year in which the data were collected. There are five quarterly data sets for each of these files, running from the first quarter of 2009 through the first quarter of 2010. The FMLY file contains consumer unit (CU) characteristics, income, and summary level expenditures; the MEMB file contains member characteristics and income data; the MTAB file contains expenditures organized on a monthly basis at the Universal Classification Code (UCC) level; the ITAB file contains income data converted to a monthly time frame and assigned to UCCs; and the ITAB_IMPUTE file contains the five imputation variants of the income data converted to a monthly time frame and assigned to UCCs.

The FPAR and MCHI datasets are grouped as 2-year datasets (2008 and 2009), plus the first quarter of the 2010. The FPAR file contains CU level data about the Interview survey, including paradata collected about the interview within the interview collection instrument (CAPI). This data includes information on the amount of time required to collect each interview and interview section, as well as other interviewer entered information about the resulting survey. The MCHI file contains data about each interview contact attempt, including reasons for refusal and times of contact. Both FPAR and MCHI files contain five quarters of data.

Each of the 50 EXPN files contains five quarters of data. The EXPN files contain data directly derived from their respective questionnaire sections.

The processing files enhance computer processing and tabulation of data, and provide descriptive information on item codes. The processing files are: (1) aggregation scheme files used in the published consumer expenditure survey interview tables and integrated tables (ISTUB and INTSTUB), (2) a UCC file that contains UCCs and their abbreviated titles, identifying the expenditure, income, or demographic item represented by each UCC, (3) a vehicle make file (CAPIVEHI), and (4) files containing sample programs. The processing files are further explained in the Interview User Guide, Section III.F.6. PROCESSING FILES. There is also a second user guide, "User's Guide to Income Imputation in the CE", which includes information on how to appropriately use the imputed income data.

Demographic and family characteristics data include age, sex, race, marital status, and CU relationships each CU member. Income information, such as wage, salary, unemployment compensation, child support, and alimony, as well as information on the employment of each CU member age 14 and over was also collected.

Curated

Consumer Expenditure Survey, 2010: Interview Survey and Detailed Expenditure Files (ICPSR 32483)

Released/updated on: 2011-10-05
Geographic coverage: United States
Time period: 2009-01-01--2011-01-01

The Consumer Expenditure Survey (CE) program provides a continuous and comprehensive flow of data on the buying habits of American consumers including data on their expenditures, income, and consumer unit (families and single consumers) characteristics. These data are used widely in economic research and analysis, and in support of revisions of the Consumer Price Index.

The CE program is comprised of two separate components (each with its own questionnaire and independent sample), the quarterly Interview Survey and the Diary Survey (ICPSR 32482). This data collection contains the quarterly Interview Survey data, which was designed to collect data on major items of expense which respondents could be expected to recall for 3 months or longer. These included relatively large expenditures, such as those for property, automobiles, and major durable goods, and those that occurred on a regular basis, such as rent or utilities. The Interview Survey does not collect data on expenses for housekeeping supplies, personal care products, and nonprescription drugs, which contribute about 5 to 15 percent of total expenditures.

The microdata in this collection are available as SAS, STATA, SPSS data sets or ASCII text and comma-delimited files. The 2010 Interview Survey release contains seven groups of Interview data files (FMLY, MEMB, MTAB, ITAB, ITAB_IMPUTE, FPAR, and MCHI), 50 EXPN files, and processing files.

The FMLY, MEMB, MTAB, ITAB, and ITAB_IMPUTE files are organized by the calendar quarter of the year in which the data were collected. There are five quarterly data sets for each of these files, running from the first quarter of 2010 through the first quarter of 2011. The FMLY file contains consumer unit (CU) characteristics, income, and summary level expenditures; the MEMB file contains member characteristics and income data; the MTAB file contains expenditures organized on a monthly basis at the Universal Classification Code (UCC) level; the ITAB file contains income data converted to a monthly time frame and assigned to UCCs; and the ITAB_IMPUTE file contains the five imputation variants of the income data converted to a monthly time frame and assigned to UCCs.

The FPAR and MCHI datasets are grouped as 2-year datasets (2009 and 2010), plus the first quarter of the 2011. The FPAR file contains CU level data about the Interview survey, including paradata collected about the interview within the interview collection instrument (CAPI). This data includes information on the amount of time required to collect each interview and interview section, as well as other interviewer entered information about the resulting survey. The MCHI file contains data about each interview contact attempt, including reasons for refusal and times of contact. Both FPAR and MCHI files contain five quarters of data.

Each of the 50 EXPN files contains five quarters of data. The EXPN files contain data directly derived from their respective questionnaire sections.

The processing files enhance computer processing and tabulation of data, and provide descriptive information on item codes. The processing files are: (1) aggregation scheme files used in the published consumer expenditure survey interview tables and integrated tables (ISTUB and INTSTUB), (2) a UCC file that contains UCCs and their abbreviated titles, identifying the expenditure, income, or demographic item represented by each UCC, (3) a vehicle make file (CAPIVEHI), and (4) files containing sample programs. The processing files are further explained in the Interview User Guide, Section III.F.6. PROCESSING FILES. There is also a second user guide, "User's Guide to Income Imputation in the CE", which includes information on how to appropriately use the imputed income data.

Demographic and family characteristics data include age, sex, race, marital status, and CU relationships for each CU member. Income information, such as wage, salary, unemployment compensation, child support, and alimony, as well as information on the employment of each CU member age 14 and over was also collected.

Curated

Health Interview Survey, 1964 (ICPSR 28663)

Released/updated on: 2010-07-06
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this year's survey, each in a separate data file. The Family file (Part 1) includes information on family size, sex, race, education, health status of family members, and total health expenses for the family. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The X-ray file (Part 5) includes information on X-ray records, doctor visits, height and weight, and total medical X-ray visits.
Curated

Health Interview Survey, 1963 (ICPSR 28381)

Released/updated on: 2010-11-11
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in this year's survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Family file (Part 2) includes information on family size, sex, race, education, health status of family members, and total health expenses for the family. The Person file (Part 3) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 4) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 5) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Health Expenditure file (Part 6) includes medical and health related expenses, such as hospital bills, medicine costs, dental bills, doctor bills, as well as insurance coverage and costs.
Curated

Norwegian Ecological Data, 1868-1903 (ICPSR 41)

Released/updated on: 2006-01-12
Geographic coverage: Norway, Europe
Time period: 1868-01-01--1903-01-01
This data collection provides economic, social, political, and demographic information on 431 communes (or electoral parishes) of Norway in the period 1868-1903. There are four parts to this collection. Part 1 contains information from the censuses of 1875, 1891, and 1900 and the electoral censuses of 1868 and 1876 on occupation, income distribution, taxation, age, household, total population by sex, place of birth, and religious affiliation, and information about political participation, such as the number of eligible voters, registered votes, and votes cast in the Storting (unicameral parliament) elections of 1868, 1870, 1873, 1876, 1879, 1882, 1885, 1888, 1891, 1894, 1897, 1900 and 1903. Part 2 provides information from the educational censuses of 1875 and 1885 on school enrollment, the number of male and female teachers, and school expenditures. Part 3 provides information on births, miscarriages, deaths, the number of live births from unwed mothers, the number of married couples, and the number of persons emigrating overseas and to the United States in 1868, 1875, 1891 to 1895, 1896 to 1900, and 1901 to 1905. Part 4 provides information on inter-communal communication and transportation, such as railways and steamships.
Curated

National Mortality Followback Survey, 1993 (ICPSR 2900)

Released/updated on: 2005-02-21
Geographic coverage: United States
The National Mortality Followback Survey (NMFS) Program, begun in the 1960s by the National Center for Health Statistics (NCHS), uses a sample of United States residents who die in a given year, supplementing information derived from the death certificate with information from the next of kin or another person familiar with the decedent's life history. This information, sometimes enhanced by administrative records, is collected in order to study the etiology of disease, demographic trends in mortality, and other health issues. The 1993 National Mortality Followback Survey (NMFS) sampled individuals aged 15 years and over who died in 1993. Forty-nine of the 50 state vital registration areas, as well as the independent vital registration areas of the District of Columbia and New York City, granted approval to sample their death certificates. (South Dakota declined to participate due to a state law restricting the use of death certificate information.) A sample of 22,957 death certificates from 1993 was then drawn. To obtain reliable numbers for important population subgroups, such as persons under age 35, women, and the Black population, death certificates from those subgroups were oversampled. The 1993 NMFS survey focused on five subject areas: (1) socioeconomic differentials in mortality, (2) associations between risk factors and cause of death (use of tobacco, alcohol, drugs, firearms, motor vehicles), (3) disability (medical condition and cognitive functioning during the last year of life), (4) access and utilization of health care facilities during the last year of life (number of doctor visits, days bedridden, nursing home experiences, use of assistive medical devices, availability of health insurance), and (5) reliability of certain items reported on the death certificate. Demographic variables include age, gender, race, marital status, birthplace, education, occupation and industry, and income and assets. The 1993 NMFS survey differed from the previous mortality followback surveys in several ways: First, it emphasized deaths due to homicide, suicide, and unintentional injury. Second, the subject areas were considerably broader (many previously-surveyed subject areas, however, are included for trend analysis). This survey was also the first to acquire national-level information from medical examiners and coroners. Finally, the complexity of the questionnaire necessitated telephone or in-person interviews. The 1993 NMFS was designed in collaboration with other agencies of the Public Health Service, Department of Health and Human Services, and the National Highway Traffic Safety Administration.
Curated

Natality Detail File, 1997: [United States] (ICPSR 3389)

Released/updated on: 2006-01-18
Geographic coverage: United States
This collection provides information on live births in the United States during calendar year 1997. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Geographic variables describing residence for births include the state, county, city, county and city population, standard metropolitan statistical area (SMSA), and metropolitan/nonmetropolitan county. Other variables specify the race and sex of the child, the age of the mother, place of delivery, person in attendance, and live-birth order. The natality tabulations in the documentation include live births by age of mother, live-birth order, and race of child, live births by marital status of mother, age of mother, and race of child, and live births by attendant and place of delivery.
Curated

Indonesian Family Life Survey, 1993 (ICPSR 6706)

Released/updated on: 2006-01-12
Geographic coverage: Kalimantan, Java, Bali, Sumatra, West Nusa Tenggara, Global, Indonesia, Sulawesi

This release of the 1993 Indonesian Family Life Survey (IFLS-1-PR) is a revised and restructured version of the Wave 1 data. This data collection provides a broad range of economic, demographic, and health information at both the household and community levels across 13 provinces on the islands of Java, Sumatra, Bali, West Nusa Tenggara, Kalimantan, and Sulawesi. A sample of 7,224 households was interviewed during August 1993 through January 1994. Household-level data cover topics such as household characteristics, income, education of both adults and children, marriage histories, inter-household transfers, pregnancy history, and knowledge and use of contraceptives. At the community-facility level, information was gathered from village leaders and heads of village women's groups in each of the 321 enumeration areas (EAs) where the households were located. Questions were asked regarding community characteristics (transportation, water and sanitation, history of schools, and availability of health facilities), nurses, midwives, and paramedics (facility management and family planning history, vignettes on types of care), and traditional health practitioners (buying or making herbal medicines or using services of traditional practitioners, rituals, and incantations). When the household data are combined with the community-facility data, the 1993 Indonesian Family Life Survey provides a unique look at areas of fertility, family planning, infant and child health, education, migration, employment, and the social, economic, and health status of over 7,000 households in a diverse setting during a period of rapid demographic and socioeconomic change.

As of June 2015, there are four waves of data for the IFLS. However, a fifth wave of data collection has begun. Please see the IFLS Web site for more information on how to obtain these data.

Curated

Malawi Journals Project (MJP), 1999-2015 (ICPSR 37347)

Released/updated on: 2019-06-27
Geographic coverage: Malawi, Africa
Time period: 1999-01-01--2015-01-01

The Malawi Journals Project provides a unique perspective on a contemporary epidemic in Africa. Begun in 1999, when HIV incidence and prevalence peaked, it tracked contradictions between survey data and qualitative data. After the first round of the Malawi Longitudinal Study of Families and Health (MLSFH) (ICPSR 20840), in 1998, the researchers had a great deal of data about the composition and structure of local social networks in which rural Malawians talked about AIDS. They had not; however, learned much about the content of the social interactions--what people said to each other, rather than to interviewers, about AIDS or their strategies for avoiding infection and death--and even less about the wider everyday interactions that shaped responses to the epidemic.

In 1999 Susan Watkins instituted "The Malawi Journals Project" as a complement to a longitudinal survey that she was conducting in rural Malawi. At that time, Malawians were suffering and dying from a major AIDS epidemic. After the first round of the survey, she found evidence of social desirability bias. For example, when survey interviewers asked men under age 35 how many sexual partners they had, the typical response was that they had only one sexual partner, their wife. In the context of Malawi, as well as other African countries; however, a man with only one partner was so unusual that his survey response was not believable.

Watkins thus developed a new approach to data collection: learning what men and women said to each other rather than to an interviewer. After the first round of the survey the researchers had a great deal of data about the composition and structure of the social networks in which rural Malawians talked about AIDS. They had not; however, learned much about the content of the social interactions--what people said to each other, rather than to interviewers, about AIDS or their strategies for avoiding infection and death--and even less about the wider everyday interactions that shaped responses to the epidemic. Thus, the researchers improvised by commissioning 10 high school graduates, both men and women, who had worked for the survey to be participant observers as they went about their daily routines. They were to pay attention to what their peers said about the AIDS epidemic in their informal social networks, such as walking to a funeral or drinking at a bar, and to write the conversation word for word in a private space. If they overheard anything concerning AIDS, they were to make mental notes of what people said and did, and then write their recollections word-for-word in commonplace school notebooks that evening or soon thereafter. The notebooks were given to a local intermediary who mailed them to the researchers. In 2005, Watkins invited a colleague, Adam Ashforth, an ethnographer who had conducted research in Malawi, to join the Malawi Journals Project

More than 1,000 journals have been written since 1999, each approximately 12 single-spaced typed pages, and each usually covering several different conversations or incidents. Since there are frequently several people conversing, the reader can overhear, at second hand, several thousand people. Twenty-two journalists (9 females, 13 males) have contributed to the corpus of texts, with three (two males, one female) contributing very frequently, 13 frequently, and six only occasionally. The diarists wrote in English, a language learned in school, and used parentheses or carets to set off their explanatory comments or untranslatable expressions in the local language. The handwriting and repetitions suggest they often wrote rapidly. We have retained locutions that reflect local adaptations of English. English is taught in Malawian public schools starting in Standard 5, equivalent to U.S. fifth grade, and has become somewhat indigenized. For example, to be sexually promiscuous is to be "movious" and one who has multiple partners is said to be "moving around," an Anglicization of a Chichewa expression, woyendayenda, derived from the earlier association of multiple partners with migrant labor. The naturalness with which the journalists adapt English to Chichewa, chiYao, or chiTumbuka linguistic forms means that their English is somewhat closer to local languages than is the standard English in which a Canadian, British or American ethnographer might translate local languages. In our publications, we have retained most of the idiosyncrasies in grammar and spelling, although on occasion we insert obviously missing words in brackets and make minor corrections.

Initially, Malawians were convinced that all would die of AIDS, and were skeptical about the attempts of the government and international organizations to reduce new HIV infections. Over the subsequent years, this began to change as conversational partners advised each other to be careful to select their sexual partners with care. By 2017, men and women speaking about AIDS in their social networks acknowledged that times had changed, and the number of new HIV infections had steeply declined.

Curated

National Survey of Family Growth, Cycle IV, 1990 Telephone Reinterview (ICPSR 6643)

Released/updated on: 2006-01-18
Geographic coverage: United States
The NSFG Cycle IV telephone reinterviews have been divided into two files. The Respondent File (Part 1) contains one record for each woman in the survey, while the Interval File (Part 2) contains one record for each completed pregnancy experienced by a woman in the survey. An interval can be defined as any of the following: the time between a first intercourse at last contact (in 1988) and a pregnancy that ended after last contact, or the time between a pregnancy that ended before last contact and one that was in progress at the time of the interview. Part 1 offers data on the respondent's marital history/update, education, family background, sex education, births and pregnancies, first sexual intercourse, sterilizing operations, contraceptive history/update, family planning services, infertility services, births intended and expected, adoption, sexually transmitted diseases/AIDS, religion, race/ethnicity, employment/occupation, income, and insurance. Part 2 supplies information on outcomes of pregnancies and other pregnancy-related information, use of birth control methods during intervals, and "wantedness" of pregnancies.
Curated
Partially restricted

Pathways to Adulthood: A Three-Generation Urban Study, 1960-1994: [Baltimore, Maryland] (ICPSR 2420)

Released/updated on: 2019-11-26
Geographic coverage: Baltimore, United States, Maryland
Time period: 1960-01-01--1994-01-01
This collection incorporates both prospective and retrospective data on three generations of families initially living in inner-city Baltimore, Maryland. The prospective data were selected from data collected as part of the Johns Hopkins Collaborative Perinatal Study (JHCPS), a survey of pregnant women seeking prenatal care and delivery at Johns Hopkins Hospital during 1960-1964. JHCPS studied these women (the first-generation mothers, abbreviated as G1) and the children born to them during 1960-1965 (the second-generation children, abbreviated as G2) until the children were 8 years old. The retrospective data come from a follow-up study, conducted in 1992-1994, of G1, G2, and the children born to G2 (the third-generation children, abbreviated as G3). Data from JHCPS on G1 include obstetrical and reproductive history at registration for prenatal care, sociological/family history variables at or around delivery of G2, observations of mother with child when G2 was 4 months old and 8 months old, and family history, demographic, and sociological variables when G2 was age 7. For G2, the data from JHCPS include delivery room observations at birth, pediatric examination data at age 4 months, developmental evaluation data at age 8 months, pediatric-neurological examination data at age 12 months, language, hearing, and speech evaluation summary data at age 36 months, psychological, behavior profile, physical growth, and other tests at age 48 months, psychological, motor, behavior, neurological, vision, physical, and other tests at age 7-1/2 years, and language, hearing, and speech evaluations, physical growth, interval medical history, and other tests at age 8 years. Retrospective data from the follow-up study on G1 include variables on education, employment, family composition, health and health care usage, housing conditions, income and income sources, marital status, partnerships and changes, neighborhood characteristics at registration to JHCPS and current, and reproductive history. For G2, data from the follow-up include information on aspirations, education, schooling, employment, family composition, health and health care usage, housing conditions, income and income sources, legal problems, living arrangements, marriage, partnership and changes, neighborhood characteristics at birth, at ages 11/12 and 16/17, and current, reproductive history, social relationships, smoking, and substance abuse. Data for the assessed third-generation children, i.e., G3s who were 7-8 years old during the follow-up period, include information on cognitive development, academic achievement and behavior, prenatal care, health, day care, and parental aspirations.
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National Survey of Family Growth, Cycle II, 1976: Couple File (ICPSR 7902)

Released/updated on: 2008-11-26
Geographic coverage: United States
This data collection contains information on fertility, family planning, and related aspects of maternal and child health for 8,611 women aged 15-44 living in the coterminous United States who were either currently married, previously married, or never married but had offspring living in the household in 1976. The data have been utilized by the National Center for Health Statistics as the basis for a series of reports on the determinants and consequences of patterns of family formation and fertility in the United States. This release of Cycle II of the 1976 Survey of Family Growth data contains extensive information on respondents' methods of family planning, prenatal and postnatal health care, family size preferences, and child care usage. Other demographic variables provide information on respondent's family, marital, and employment histories, date of birth, race, ethnicity, religion, education, occupation, and income. Additional information about the respondents can be found in the related collection, NATIONAL SURVEY OF FAMILY GROWTH, CYCLE II, 1976: INTERVAL FILE (ICPSR 8181).
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National Ambulatory Medical Care Survey, 2008 (ICPSR 29921)

Released/updated on: 2011-10-11
Geographic coverage: United States
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. The 2008 survey contains information from 28,741 patient visits to 1,187 physicians' offices. Data are available on the patient's smoking habits, reason for the visit, expected source of payment, the physician's diagnosis, and the kinds of diagnostic and therapeutic services rendered. Other variables include information on the following: drugs/medications ordered, administered, or provided during office visits; information on medication code, generic name and code, brand name, entry status, prescription status, federal controlled substance status, composition status, and related ingredient codes. Information is also included on the physician's specialization and geographic location. Demographic information on patients, such as age, sex, race, and ethnicity, was also collected.
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National Hospital Ambulatory Medical Care Survey, 2007 (ICPSR 28442)

Released/updated on: 2010-06-24
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Survey (NHAMCS) provides data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2007 survey, data were collected from 202 OPDs and 432 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit, physician's diagnoses, cause of injury, surgical procedures (OPDs only), medication therapy, and expected source of payment. For 2007, additional updates and revisions have been made to both the emergency department and outpatient department data, including modifications to pre-existing variables pertaining but not limited to electronic medical records.
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National Hospital Ambulatory Medical Care Survey, 2008 (ICPSR 29922)

Released/updated on: 2011-01-18
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Surveys (NHAMCS) provide data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2008 survey, data were colected from 209 OPDs and 431 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit physician's diagnoses, cause of injury, surgical procedures (OPD's only), medication therapy, and expected source of payment. The 2008 survey remains unchanged from the previous year.
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National Ambulatory Medical Care Survey, 2009 (ICPSR 31482)

Released/updated on: 2011-11-17
Geographic coverage: United States
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. The 2009 survey contains information from 32,281 patient visits to 1,293 physicians' offices. Data are available on the patient's smoking habits, reason for the visit, expected source of payment, the physician's diagnosis, and the kinds of diagnostic and therapeutic services rendered. Other variables include information on the following: drugs/medications ordered, administered, or provided during office visits; information on medication code, generic name and code, brand name, entry status, prescription status, federal controlled substance status, composition status, and related ingredient codes. Information is also included on the physician's specialization and geographic location. Demographic information on patients, such as age, sex, race, and ethnicity, was also collected.
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National Hospital Ambulatory Medical Care Survey, 2005 (ICPSR 28261)

Released/updated on: 2010-06-08
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Survey (NHAMCS) provides data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2005 survey, data were collected from 205 OPDs and 417 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit, physician's diagnoses, cause of injury, surgical procedures (OPDs only), medication therapy, and expected source of payment. For 2005, additional updates and revisions have been made to both the emergency department and outpatient department data, including modifications to preexisting variables and the inclusion of new variables pertaining but not limited to patient pregnancy, height, and weight.
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Growth of American Families, 1955 (ICPSR 20000)

Released/updated on: 2009-11-17
Geographic coverage: United States
The 1955 Growth of American Families survey was the first in a series of surveys (later becoming the National Fertility Survey) that measured women's attitudes on various topics related to fertility and family planning. The sample was composed of 2,713 married women aged 18-39 living in the United States. The survey included the following main subjects: residence history, marital history, education, income, occupation and employment, religiosity, family background, attitude toward contraception, contraception use, pregnancies and births, fecundity, opinions on childbearing and rearing, and fertility expectations. Respondents were asked questions pertaining to their residence history, including if they owned or rented their home, and if they lived on a farm. A series of questions also dealt with the respondents' marital history, including when they first married and the month and year of subsequent marriages. Respondents were also asked to describe the level of education they had attained and that of their husbands. Respondents were also asked to give information with respect to income, both individual and household, and if their financial situation was better now compared to five years ago. Respondents were queried on their occupation, specifically on what exactly they did and in what kind of business. Similar questions were asked about their husbands' occupations. Also, they were asked what their reasons were for working. The survey sought information about the respondents' religious affiliation and with what frequency they attended church. Respondents were asked how many brothers and sisters they had as well as their attitude about the number of siblings in their household. Also included was a series of questions regarding the respondents' attitudes toward family planning. Respondents were asked if they and their husband thought it was acceptable for couples to use contraceptives to limit the size of their family. They were also queried about what specific methods of contraception they had used in the past, and after which pregnancy they started using a particular method. Respondents were asked whether they or their husband had had surgery to make them sterile and if there was any other reason to believe that they could not have children. Respondents were also asked if they thought raising a family was easier or harder now than when they were a child. Respondents were also asked what they believed was the ideal number of children for the average American family and what the ideal number of children would be, if at age 45, they could start their married life over. Other questions addressed how many children respondents expected to have before their family was completed and their reason for not wanting more or less than that number. Each respondent was also asked when she expected her next child.
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National Ambulatory Medical Care Survey, 2006 (ICPSR 28403)

Released/updated on: 2011-10-12
Geographic coverage: United States
The National Ambulatory Medical Care Surveys (NAMCS) supply data on ambulatory medical care provided in physicians' offices. The 2006 survey contains information from 29,392 patient visits to 1,455 physicians' offices. Data are available on the patient's smoking habits, reason for the visit, expected source of payment, the physician's diagnosis, and the kinds of diagnostic and therapeutic services rendered. Other variables cover drugs/medications ordered, administered, or provided during office visits, with information on medication code, generic name and code, brand name, entry status, prescription status, federal controlled substance status, composition status, and related ingredient codes. Information is also included on the physician's specialization and geographic location. Demographic information on patients, such as age, sex, race, and ethnicity, was also collected. In addition, the 2006 survey contains two new sampling strata which are from 104 Community Health Centers (CHCs) and 200 oncologists.
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National Health Interview Survey: Longitudinal Study of Aging, 70 Years and Over, 1984-1990 (ICPSR 8719)

Released/updated on: 2011-08-18
Geographic coverage: United States
Time period: 1984-01-01--1990-01-01
This study, commonly known as the Longitudinal Study of Aging (LSOA), was conducted by the National Center for Health Statistics (NCHS) in collaboration with the National Institute on Aging (NIA) and designed to (1) provide mortality rates by demographic, social, economic, and health characteristics that are not available from the vital statistics system, (2) measure change in the functional status and living arrangements of older people, and (3) provide measures of health care use. It was also designed to describe the continuum from functionally independent living in the community through dependence, possible institutionalization, and finally death. The LSOA is an extension of the National Health Interview Survey (NHIS) of 1984, following its sample of 16,148 noninstitutionalized elderly people (55 years and over) living in the United States, with a special focus on those who were 70 years and over in 1984. This release of the LSOA contains data on those respondents who had been 70 years and older at the time of their 1984 interviews. The data include 1986, 1988, and 1990 reinterviews, National Death Index matches from 1984-1989, and 1987 interviews with contact persons named by decedents, as well as selected variables from the 1984 NHIS core questionnaire and its two supplements, Health Insurance and the Supplement on Aging (SOA). Two Medicare files are also included: Part 2, Medicare Hospital Records, and Part 3, Other Medicare Use Records (which covers home health care, hospice, and outpatient use). Links also are provided to allow merging of additional variables from the NATIONAL HEALTH INTERVIEW SURVEY, 1984 (ICPSR 8659).
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Guatemalan Survey of Family Health (EGSF), 1995 (ICPSR 2344)

Released/updated on: 2025-11-06
Geographic coverage: Guatemala, Global
Time period: 1995-05-01--1995-10-01

The Guatemalan Survey of Family Health (EGSF) was undertaken to investigate the health of children under the age of five and women during pregnancy and childbirth residing in 60 communities within the departments (geopolitical units) of Chimaltenango, Suchitepequez, Totonicapan, and Jalapa in Guatemala. Data were collected at the household, individual, and community levels to gain an in-depth understanding of the way residents in these rural populations think about their health, treatment, and family relations.

Data at the household level (Parts 1-5, 90-92) provide information on household members, relation to household head, age, education, and language used.

The individual-level data (Parts 6-37) describe the respondent's background, marital/relationship history, social ties and social support, and economic status, along with health beliefs, a complete birth history, knowledge and use of contraception, health problems and treatment during the last two pregnancies, and anthropometry on mothers and children. Extensive data were gathered regarding the health problems and treatment for each of the two youngest children born since January 1990, with particular focus on diarrhea and respiratory infections.

The community data (Parts 41-60) supply information gathered from three knowledgeable individuals called "key informants" about occupations in the community, crops grown, wages, utilities and community services, and the history of the community. Parts 61-89 contain information regarding Health Posts (health care centers) through interviews conducted with key informants, doctors (Parts 72-80), and other health service providers (Parts 81-89), including traditional providers such as curers, midwives, and bone setters, regarding their practices, patients, referrals, fees, payment, and the use of specific treatments.

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RAND Health Insurance Experiment [in Metropolitan and Non-Metropolitan Areas of the United States], 1974-1982 (ICPSR 6439)

Released/updated on: 2005-11-04
Geographic coverage: Charleston (South Carolina), Seattle, United States, Massachusetts, Ohio, Washington, South Carolina, Dayton
Time period: 1974-01-01--1982-01-01
The Health Insurance Experiment (HIE) was conducted from 1974 to 1982 in six sites across the country: Dayton, Ohio, Seattle, Washington, Fitchburg-Leominster and Franklin County, Massachusetts, and Charleston and Georgetown County, South Carolina. These sites represent four census regions (Midwest, West, Northeast, and South), as well as urban and rural areas. The HIE attempted to determine what effects alternative cost-sharing plans and a staff-model Health Maintenance Organization (HMO) had on the use of medical services and individual health outcomes. The main purpose of the experiment was to assess how the cost of health services affected individuals' use of services, their satisfaction with health care, the quality of their care, and the state of their health. To study the effects of health insurance coverage, a comprehensive method for measuring health and monitoring changes in health over time was developed. Health status was seen as having four dimensions: physical, mental, social, and physiological. Physical health focused on five categories of activities: self-care, mobility, exertion, role fulfillment, and leisure pursuits. Mental health focused on mood and anxiety disorders along with loss of control over feelings, thoughts, and behavior. Social health was assessed by the frequency of several kinds of participation, interaction, and resources, covering family and home, social life, and community involvement. Physiologic health was determined by looking at a number of physical disorders both in adults (aged 14 to 61) and children (aged 0 to 13) that would be easily traced over time and would be responsive to changes in the level and quality of medical care. For adults, acne, congestive heart failure, and sleeping pill and tranquilizer use were considered. For children, variables included allergic conditions (asthma, eczema, hay fever), anemia, middle ear disease, hearing impairment, and vision impairment. Also included were general health measures based on single questions about health-related pain and worry, and a rating of health (excellent, good, fair, poor). Health habits described aspects of smoking, consumption of alcohol, weight, height, and exercise.
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Border Contraceptive Access Study, El Paso, Texas 2005-2008 (ICPSR 32561)

Released/updated on: 2011-11-07
Geographic coverage: El Paso, Ciudad Juarez, United States, Texas, Mexico, Chihuahua
Time period: 2005-01-01--2008-01-01

Oral contraceptive (OC) users living in El Paso, Texas were interviewed to assess motivations for patronizing a United States clinic or a Mexican pharmacy with over-the-counter (OTC) pills and to determine which women were likely to use the OTC option. The experiences of OC users who obtained their contraception from Mexican pharmacies were compared with those of women who obtained their pills from family planning clinics in El Paso, Texas, where eligible low-income women often pay nothing. 532 clinic users and 514 pharmacy users were surveyed about background characteristics, motivations for choosing their oral contraception source, and satisfaction with this source. For more information, please see the Border Contraceptive Access Study website.

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Simple Crosstabs

Families of Newtown, New York, 1642-1790 (ICPSR 35005)

Released/updated on: 2016-06-22
Geographic coverage: United States, New York (state)
Time period: 1642-01-01--1790-01-01
This dataset focuses on economic, social, and geographic mobility of town residents, and life events (marriage, birth and mortality). Church records supplemented with genealogies, wills, inventories, probate records, cemetery data, town books, court books, censuses, and tax lists were used to reconstitute families along the lines of previous French and English work (e.g. Fleury, M. and L. Henry, Nouveau manuel de dépouillement et d'exploitation de l'état civil ancient (1965) and Wrigley, E.A, "Family Reconstitution" in E.A. Wrigley, ed. An Introduction to English Historical Demography (1966). Family reconstitution is a method for studying demographic behavior in the absence of modern censuses and vital registration, providing for both observation of demographic events, as well as the population and time at risk. This dataset includes information about 202 couples and their 1094 children. The data on couples focus on demographic details for mothers and fathers, including birth, baptism, marriage and death dates, residence and religion. The data on children includes demographic information for the child, as well as marriage age and residence. Not all families have complete information.
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Simple Crosstabs

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

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

A Place In Time: Colonial Middlesex County, VA, 1650-1750 (ICPSR 35057)

Released/updated on: 2016-06-15
Geographic coverage: United States, Virginia
Time period: 1650-01-01--1750-01-01
This dataset was produced by Darrett B. and Anita H. Rutman while researching their book A Place in Time: Middlesex County Virginia, 1650-1750 and the companion volume, A Place in Time: Explicatus (both New York: Norton, 1984). Together, these works were intended as an ethnography of the English settlers of colonial Middlesex County, which lies on the Chesapeake Bay. The Rutmans created this dataset by consulting documentary records from Middlesex and Lancaster Counties (Middlesex was split from Lancaster in the late 1660s) and material artifacts, including gravestones and house lots. The documentary records include information about birth, marriage, death, migration, land patents and conveyances, probate, church matters, and government matters. The Rutmans organized this material by person involved in the recorded events, producing over 12,000 individual biographical sheets. The biographical sheets contain as much information as could be found for each individual, including dates of birth, marriage, and death; children's names and dates of birth and death; names of parents and spouses; appearance in wills, transaction receipts, and court proceedings; occupation and employers; and public service. This process is described in detail in Chapter 1 of A Place in Time: Middlesex County Virginia, 1650-1750. The Rutmans' biographical sheets have been archived at the Virginia Historical Society in Richmond, Virginia. To produce this dataset, most of the sheets were photographed (those with minimal information -- usually only a name and one date -- were omitted). Information from the sheets was then hand-keyed and organized into two data tables: one containing information about the individuals who were the main subjects of each sheet, and one containing information about children listed on those sheets. Because individuals appear several times, data for the same person frequently appears in both tables and in more than one row in each table. For example, a woman who lived all her life in Middlesex and married once would have two rows in the children's table -- one for her appearance on her mother's sheet and one for her appearance on her father's sheet -- and two rows in the individual table -- one for the sheet with her maiden name and one for the sheet with her married name. After entry, records were linked in order to associate all appearances of the same individual and to associate individuals with spouses, parents, children, siblings, and other relatives. Sheets with minimal information were not included in the dataset. The data includes information on 6586 unique individuals. There are 4893 observations in the individual file, and 7552 in the kids file.
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Simple Crosstabs

European-origin and Mexican-origin Populations in Texas, 1850, 1860, 1870, 1880, 1900, 1910 (ICPSR 35032)

Released/updated on: 2016-06-20
Geographic coverage: United States, Texas
This dataset was produced in the 1990s by Myron Gutmann and others at the University of Texas to assess demographic change in European- and Mexican-origin populations in Texas from the mid-nineteenth to early-twentieth centuries. Most of the data come from manuscript records for six rural Texas counties - Angelina, DeWitt, Gillespie, Jack, Red River, and Webb - for the U.S. Censuses of 1850-1880 and 1900-1910, and tax records where available. Together, the populations of these counties reflect the cultural, ethnic, economic, and ecological diversity of rural Texas. Red River and Angelina Counties, in Eastern Texas, had largely native-born white and black populations and cotton economies. DeWitt County in Southeast Texas had the most diverse population, including European and Mexican immigrants as well as native-born white and black Americans, and its economy was divided between cotton and cattle. The population of Webb County, on the Mexican border, was almost entirely of Mexican origin, and economic activities included transportation services as well as cattle ranching. Gillespie County in Central Texas had a mostly European immigrant population and an economy devoted to cropping and livestock. Jack County in North-Central Texas was sparsely populated, mainly by native-born white cattle ranchers. These counties were selected to over-represent the European and Mexican immigrant populations. Slave schedules were not included, so there are no African Americans in the samples for 1850 or 1860. In some years and counties, the Census records were sub-sampled, using a letter-based sample with the family as the primary sampling unit (families were chosen if the surname of the head began with one of the sample letters for the county). In other counties and years, complete populations were transcribed from the Census microfilms. For details and sample sizes by county, see the County table in the Original P.I. Documentation section of the ICPSR Codebook, or see Gutmann, Myron P. and Kenneth H. Fliess, How to Study Southern Demography in the Nineteenth Century: Early Lessons of the Texas Demography Project (Austin: Texas Population Research Center Papers, no. 11.11, 1989).