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Curated

Aging Statistics (ICPSR 141)

Released/updated on: 2008-03-26
Geographic coverage: United States
Located on the Administration on Aging Web site, Aging Statistics provides links to a variety of tables, reports, databases, studies, and other statistical tools regarding aging populations in the United States. Links are grouped according to topic area, such as estimates and projections for aging populations, minority aging, and disabilities data.
Curated

American National Election Study: 1985 Pilot Study (ICPSR 8476)

Released/updated on: 1999-11-02
Geographic coverage: United States
Time period: 1985-11-01--1986-01-01
This study is part of a time-series collection of national surveys fielded continuously since 1952. The election studies are designed to present data on Americans' social backgrounds, enduring political predispositions, social and political values, perceptions and evaluations of groups and candidates, opinions on questions of public policy, and participation in political life. This pilot study was designed to test instrumentation for the 1986 and 1988 National Election Studies. Special content areas emphasized in the pilot are: political knowledge, group membership, identification of elderly (aged 60 and over) Blacks and women with these social groups, attitudes toward racial issues, and opinions on traditional moral values. In order to experiment with question wording and formats, two forms were used in both waves.
Curated

American National Election Study, 1990-1992: Full Panel Survey (ICPSR 6230)

Released/updated on: 2005-12-15
Geographic coverage: United States
Time period: 1990-01-01--1993-01-01
This study is part of a time-series collection of national surveys fielded continuously since 1952. The American National Election Studies are designed to present data on Americans' social backgrounds, enduring political predispositions, social and political values, perceptions and evaluations of groups and candidates, opinions on questions of public policy, and participation in political life. This collection includes respondents who were first interviewed following the November 1990 general election (see AMERICAN NATIONAL ELECTION STUDY, 1990: POST-ELECTION SURVEY [ICPSR VERSION] [ICPSR 9548]), and then reinterviewed in two subsequent surveys: AMERICAN NATIONAL ELECTION STUDY: 1990-1991 PANEL STUDY OF THE POLITICAL CONSEQUENCES OF WAR/1991 PILOT STUDY [ICPSR VERSION] (ICPSR 9673) and AMERICAN NATIONAL ELECTION STUDY, 1992: PRE- AND POST-ELECTION SURVEY [ENHANCED WITH 1990 AND 1991 DATA] (ICPSR 6067). The purpose of this panel study is to trace the fortunes of the Bush presidency, from post-Gulf War height to November election defeat, and to provide insight into the origins of the Bill Clinton and Ross Perot coalitions. It also allows the panel analyst to do a traditional assessment of panel attrition which is not possible with any of the collections mentioned above. In 1990, respondents answered questions on topics such as presidential performance, the Persian Gulf War, values and individualism, and foreign relations. Post-election vote validation and election administration survey data are also included. In 1991, respondents were reinterviewed several months after hostilities in the Persian Gulf ended. The survey content consisted of a repeat of a subset of questions from the 1990 Post-Election Survey, and additional items especially relevant to the Gulf War. A number of contextual variables also are provided, including summary variables that combine the respondent's recall of his or her senator's and representative's vote on the use of force with that congressperson's actual vote. New pilot questions were also asked in areas such as gender, ethnicity, medical care for the elderly, and social altruism. In 1992, respondents were asked their positions on social issues such as altruism, abortion, the death penalty, prayer in the schools, the rights of homosexuals, sexual harassment, women's rights, and feminist consciousness. Other substantive themes included racial and ethnic stereotypes, opinions on school integration and affirmative action, attitudes towards immigrants (particularly Hispanics and Asians), opinions on immigration policy and bilingual education, assessments of United States foreign policy goals, and United States involvement in the Persian Gulf War. Part 2 provides information on the total number of cases included in the 1990 Post-Election Survey sample (1,980 respondents who were valid interviews and 805 selected respondents who were not interviewed) in order to study survey nonresponse. Variables include reasons for noninterview, the number of calls, and characteristics of the noninterviewed household.
Curated

American National Election Study: 1992-1993 Panel Study on Securing Electoral Success/1993 Pilot Study (ICPSR 6264)

Released/updated on: 2000-01-25
Geographic coverage: United States
Time period: 1992-01-01--1993-01-01
This study is part of a time-series collection of national surveys fielded continuously since 1952. The American National Election Studies are designed to present data on Americans' social backgrounds, enduring political predispositions, social and political values, perceptions and evaluations of groups and candidates, opinions on questions of public policy, and participation in political life. This data collection currently encompasses two waves. The first wave is the 1992 Post-Election Survey. In addition to the standard or core content items, respondents were asked their positions on social issues such as altruism, abortion, the death penalty, prayer in the schools, the rights of homosexuals, sexual harassment, women's rights, and feminist consciousness. Other substantive themes included racial and ethnic stereotypes, opinions on school integration and affirmative action, attitudes toward immigrants (particularly Hispanics and Asians), opinions on immigration policy and bilingual education, assessments of United States foreign policy goals, and United States involvement in the Persian Gulf War. The second wave of this panel, the 1993 Pilot Study, was in the field approximately one year after the first wave. It reexamined a number of items from the 1992 study to give as complete a picture as possible of how President Clinton was faring in the eyes of the coalition that had elected him. It also sought to explore in more detail the strength and depth of the Ross Perot phenomenon and, in particular, the reasons behind his continued support. Finally, this second wave of the panel continued the tradition of all pilot studies in seeking to carry out research and development work for the subsequent year's election study. In this regard, the Pilot Study explored the perceived interests of several groups (e.g., wealthy, poor, middle class, Blacks, whites) in areas such as national health insurance, affirmative action, and school choice, attitudes toward homosexuals and about policies affecting homosexuals, and experiments in the survey response form itself.
Curated
Partially restricted
Simple Crosstabs

Americans' Changing Lives: Waves I, II, III, IV, V, and VI, 1986, 1989, 1994, 2002, 2011, and 2021 (ICPSR 4690)

Released/updated on: 2024-12-12
Geographic coverage: United States
Time period: 1986-01-01--2021-01-01

The Americans' Changing Lives (ACL) survey series is an ongoing, nationally representative, longitudinal study focusing especially on differences between Black and White Americans in middle and late life. These data constitute the first, second, third, fourth, fifth, and sixth waves in a panel survey covering a wide range of sociological, psychological, mental, and physical health items. Wave I of the study began in 1986 with a nation face-to-face survey of 3,617 adults ages 25 and up, with Black Americans and people aged 60 and over over-sampled at twice the rate of the others. Wave II constitutes face-to-face re-interviews in 1989 of those still alive. Survivors have been re-interviewed by telephone, and when necessary face-to-face, in 1994 (Wave III), 2001/02 (Wave IV), 2011 (Wave V), and 2019/21 (Wave VI).

Please note that for Wave VI, the majority of data collection occurred in 2019, with only a small subset (n=39) of participants surveyed in 2021.

ACL was designed and sought to investigate the following: (1) The ways in which a wide range of activities and social relationships that people engage in are broadly "productive," (2) how individuals adapt to acute life events and chronic stresses that threaten the maintenance of health, effective functioning, and productive activity, and (3) sociocultural variations in the nature, meaning, determinants, and consequences of productive activity and relationships. Among the topics covered are interpersonal relationships (spouse/partner, children, parents, friends), sources and levels of satisfaction, social interactions and leisure activities, traumatic life events (physical assault, serious illness, divorce, death of a loved one, financial or legal problems), perceptions of retirement, health behaviors (smoking, alcohol consumption, overweight, rest), and utilization of health care services (doctor visits, hospitalization, nursing home institutionalization, bed days). Also included are measures of physical health, psychological well-being, and indices referring to cognitive functioning.

Demographic information provided for individuals includes household composition, number of children and grandchildren, employment status, occupation and work history, income, family financial situation, religious beliefs and practices, ethnicity, race, education, sex, and region of residence.

Curated

County-Level Estimates of the Population Aged Sixty Years and Over by Age, Sex, and Race, 1977-1980 (ICPSR 7955)

Released/updated on: 1992-02-16
Geographic coverage: North Carolina, Indiana, Wyoming, Utah, Arizona, Montana, Kentucky, California, Kansas, Florida, Delaware, Pennsylvania, Mississippi, Iowa, Illinois, Texas, Connecticut, Georgia, Virginia, Maryland, Idaho, Oregon, Vermont, Oklahoma, Tennessee, Maine, Alabama, Arkansas, Washington, South Carolina, Nebraska, West Virginia, Massachusetts, Colorado, Missouri, Alaska, North Dakota, Wisconsin, Nevada, District of Columbia, Rhode Island, South Dakota, Hawaii, Minnesota, New York (state), New Jersey, Michigan, New Mexico, New Hampshire, Louisiana, Ohio
Time period: 1977-01-01--1980-01-01
Preparation of this data collection was funded by grant #90-A-1279 from the United States Department of Health and Human Services, Administration on Aging. Estimates of the population of persons 60 years old and older were received from the Census Bureau in printed form and were made machine-readable by staff at ICPSR. Other variables contained in this dataset were merged from existing machine-readable census files. The data concerning racial composition of counties were taken from the CENSUS OF POPULATION AND HOUSING, 1980 [UNITED STATES]: P.L. 94-171 POPULATION COUNTS (ICPSR 7854). The figures concerning per capita income were taken from the Bureau of the Census, GENERAL REVENUE SHARING, 1978 POPULATION ESTIMATES (ICPSR 7840). Variables include Federal Information Processing Standard (FIPS) state and county codes, 1978 per capita income of county, and total population of county broken down by sex, race, and age (in four-year increments with a category for persons 75 years old and older).
Curated

Detroit Area Study, 1988: Perspectives on the Care of the Elderly (ICPSR 6411)

Released/updated on: 1995-10-12
Geographic coverage: Detroit, United States, Michigan

The 1988 Detroit Area Study addressed attitudes toward issues such as retirement age, Social Security, funding for the care of the elderly, perceptions of the elderly, and personal experiences with care of the elderly. Respondents were also asked about their views regarding government spending on elderly assistance, health care, welfare, and job programs. Demographic characteristics of respondents include employment status, years of residency in the Detroit area, education, religion, age, sex, race, and income.

Curated

Detroit Area Study, 1993: Health and Aging (ICPSR 2839)

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

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

Curated

General Social Survey Cumulative File, 1972-1986 (ICPSR 8609)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1972-01-01--1986-01-01
The General Social Survey has been conducted by the National Opinion Research Center annually since 1972 except for the years 1979 and 1981. The Roper Center for Public Opinion Research has prepared a cumulative dataset which merges thirteen years of the General Social Survey into a single file, with each year constituting a subfile. The content of each year's survey changes slightly as some items are added to or deleted from the interview schedule. The most notable addition to the 1986 wave of the survey was a group of questions related to the feminization of poverty. Respondents were asked if they had ever received income from various governmental assistance programs or from alimony or child support payments. Attitudes toward welfare were also probed through agreement or disagreement with a series of statements concerning the welfare system. On this same subject, factorial vignettes were conducted in 1986 and are included as a supplemental file to this collection. These vignettes, which describe hypothetical situations presented in brief descriptive passages, required each respondent to evaluate ten different sets of circumstances relating to family life and the need for public assistance. Seven of the vignettes related to the conditions of young families and three pertained to older women. The respondent's task was to determine whether or not the family's income should be augmented with government assistance. Each record in the supplementary file contains all the choices made by a single respondent to all ten vignettes.
Curated

Health and Retirement Study (HRS) (ICPSR 6854)

Released/updated on: 2006-04-06
Geographic coverage: United States

The University of Michigan Health and Retirement Study (HRS) is a longitudinal panel study that surveys a representative sample of approximately 20,000 people in America, supported by the National Institute on Aging and the Social Security Administration.

The HRS aims to provide multidisciplinary data that researchers can use to address important questions about the challenges and opportunities of aging. The HRS includes the "original" HRS and the Asset and Health Dynamics Among the Oldest-Old (AHEAD) study. These studies were merged in 1998 and now represent the United States population over age 50. Two new cohorts were added in 1998: the Children of the Depression (born 1924-1930) and the War Babies (1942-1947). A fourth cohort, the Early Baby Boomers (1948-1953), was added in 2004; a fifth cohort, the Mid Baby Boomers (1954-1959), was added in 2010; and in 2016, the Late Baby Boomers cohort (1960-1965) became the sixth.

Questionnaire topics include physical and cognitive functioning, retirement plans, family structure and transfers, demographic characteristics, housing, employment status, income, disability, health insurance, pension plans, job history, and attitudes, preferences, and expectations for the future. The survey data are linked with administrative records from the Employer Pension Study (1993 and 1999), National Death Index, Social Security Administration earnings and projected benefits data and W-2 self-employment data, and Medicare files.

Curated
Simple Crosstabs

Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE) Frailty Study: 2006-2009 (ICPSR 36321)

Released/updated on: 2016-03-29
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2006-01-01--2009-01-01
The Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE) Frailty Study sought to apply a standard definition of frailty in a well-defined sample of Mexican American older adults and to examine the impact of frailty on disability, health related quality of life, institutionalization, and mortality in this population over time. This project is a continuation of a prior study (the Hispanic EPESE) examining the enabling-disabling process in this same population of aging Mexican Americans; data were collected from 1,031 older adults who were participating in the Hispanic EPESE. Only subjects who were physically capable of safely completing the muscle strength measures were included. Baseline interviews were collected for this subsample in 2006/2007 during Wave 6 (ICPSR 29654) of the Hispanic EPESE study. This collection includes data about respondents' health status, activities of daily living and their ability to perform tasks. Two-year follow-up data were collected in 2008/2009 from 731 participants in Wave 1. Demographic and background information include age, relationship status, gender, marital status and household composition.
Curated

Hispanic Established Populations for Epidemiologic Studies of the Elderly, Wave II, 1995-1996: [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 3385)

Released/updated on: 2007-01-17
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 1995-01-01--1996-01-01
The baseline Hispanic Established Populations for the Epidemiologic Studies of the Elderly (Hispanic EPESE, ICPSR 2851) was modeled after the design of ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1981-1993: [EAST BOSTON, MASSACHUSETTS, IOWA AND WASHINGTON COUNTIES, IOWA, NEW HAVEN, CONNECTICUT, AND NORTH CENTRAL NORTH CAROLINA] (ICPSR 9915) and ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1996-1997: PIEDMONT HEALTH SURVEY OF THE ELDERLY, FOURTH IN-PERSON SURVEY [DURHAM, WARREN, VANCE, GRANVILLE, AND FRANKLIN COUNTIES, NORTH CAROLINA] (ICPSR 2744). This data collection contains the two-year follow-up of the baseline Hispanic EPESE, which collected data on a representative sample of community-dwelling Mexican-American elderly, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the study was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE attempted to determine whether certain risk factors for mortality and morbidity operate differently in Mexican Americans than in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public-use data cover demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. This two-year follow-up is a cross-sectional examination of the predictors of mortality, changes in health outcomes, institutionalization, and other changes in living arrangements, as well as changes in life situations and quality of life issues. The Medications file (Part 2) includes a listing of the medications, by brand name and classification of the drug, which were prescribed for the respondent. The vital status of respondents from baseline to this round of the survey may be determined using the Vital Status file (Part 3). This file contains interview dates from the baseline as well as vital status at Wave II (respondent survived, date of death if deceased, proxy-assisted, proxy-true).
Curated

Hispanic Established Populations for Epidemiologic Studies of the Elderly, Wave III, 1998-1999: [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 4102)

Released/updated on: 2007-01-23
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 1998-01-01--1999-01-01
This dataset comprises the second follow-up of the baseline Hispanic EPESE, HISPANIC ESTABLISHED POPULATIONS FOR THE EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1993-1994: [ARIZONA, CALIFORNIA, COLORADO, NEW MEXICO, AND TEXAS] (ICPSR 2851), and provides information on 1,980 of the original respondents. The Hispanic EPESE collected data on a representative sample of community-dwelling Mexican-American elderly, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the series was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE attempted to determine whether certain risk factors for mortality and morbidity operate differently in Mexican Americans than in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public-use data cover background characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. The follow-ups provide a cross-sectional examination of the predictors of mortality, changes in health outcomes, and institutionalization and other changes in living arrangements, as well as changes in life situations and quality of life issues. The vital status of respondents from baseline to this round of the survey may be determined using the Vital Status file (Part 2). This file contains interview dates from the baseline as well as vital status at Wave III (respondent survived, date of death if deceased, proxy-assisted, proxy-true). The first follow-up of the baseline data (Hispanic EPESE Wave II, 1995-1996 [ICPSR 3385]) followed 2,438 of the original 3,050 respondents. Hispanic EPESE, ICPSR 2851, was modeled after the design of ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1981-1993: [EAST BOSTON, MASSACHUSETTS, IOWA AND WASHINGTON COUNTIES, IOWA, NEW HAVEN, CONNECTICUT, AND NORTH CENTRAL NORTH CAROLINA] (ICPSR 9915) and ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1996-1997: PIEDMONT HEALTH SURVEY OF THE ELDERLY, FOURTH IN-PERSON SURVEY [DURHAM, WARREN, VANCE, GRANVILLE, AND FRANKLIN COUNTIES, NORTH CAROLINA] (ICPSR 2744).
Curated

Hispanic Established Populations for Epidemiologic Studies of the Elderly, Wave IV, 2000-2001 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 4314)

Released/updated on: 2009-11-25
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2000-01-01--2001-01-01
This dataset comprises the third follow-up of the baseline Hispanic EPESE, HISPANIC ESTABLISHED POPULATIONS FOR THE EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1993-1994: [ARIZONA, CALIFORNIA, COLORADO, NEW MEXICO, AND TEXAS] (ICPSR 2851), and provides information on 1,682 of the original respondents. The Hispanic EPESE collected data on a representative sample of community-dwelling Mexican-American elderly, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the series was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE attempted to determine whether certain risk factors for mortality and morbidity operate differently in Mexican Americans than in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public-use data cover background characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. The follow-ups provide a cross-sectional examination of the predictors of mortality, changes in health outcomes, and institutionalization and other changes in living arrangements, as well as changes in life situations and quality of life issues. The vital status of respondents from baseline to this round of the survey may be determined using the Vital Status file (Part 2). This file contains interview dates from the baseline as well as vital status at Wave IV (respondent survived, date of death if deceased, proxy-assisted, proxy-reported cause of death, proxy-true). The first follow-up of the baseline data (Hispanic EPESE Wave II, 1995-1996 [ICPSR 3385]) followed 2,438 of the original 3,050 respondents, and the second follow-up (Hispanic EPESE Wave III, 1998-1999 [ICPSR 4102]) followed 1,980 of these respondents. Hispanic EPESE, 1993-1994 (ICPSR 2851), was modeled after the design of ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1981-1993: [EAST BOSTON, MASSACHUSETTS, IOWA AND WASHINGTON COUNTIES, IOWA, NEW HAVEN, CONNECTICUT, AND NORTH CENTRAL NORTH CAROLINA] (ICPSR 9915) and ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1996-1997: PIEDMONT HEALTH SURVEY OF THE ELDERLY, FOURTH IN-PERSON SURVEY [DURHAM, WARREN, VANCE, GRANVILLE, AND FRANKLIN COUNTIES, NORTH CAROLINA] (ICPSR 2744).
Curated

Hispanic Established Populations for the Epidemiologic Studies of the Elderly, 1993-1994: [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 2851)

Released/updated on: 2009-12-14
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 1993-01-01--1994-01-01
The Hispanic Established Populations for the Epidemiologic Studies of the Elderly (Hispanic EPESE) was modeled after the design of the ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1981-1993: [EAST BOSTON, MASSACHUSETTS, IOWA AND WASHINGTON COUNTIES, IOWA, NEW HAVEN, CONNECTICUT, AND NORTH CENTRAL NORTH CAROLINA] (ICPSR 9915) and ESTABLISHED POPULATIONS FOR EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1996-1997: PIEDMONT HEALTH SURVEY OF THE ELDERLY, FOURTH IN-PERSON SURVEY [DURHAM, WARREN, VANCE, GRANVILLE, AND FRANKLIN COUNTIES, NORTH CAROLINA] (ICPSR 2744). The Hispanic EPESE collected baseline data beginning in September 1993 through June 1994 on a representative sample of community-dwelling Mexican-American elderly, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the study was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE attempted to determine whether certain risk factors for mortality and morbidity operate differently in Mexican Americans than in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public use baseline data cover demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression.
Curated

Hispanic Established Populations for the Epidemiologic Study of the Elderly (HEPESE) Wave 5, 2004-2005 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 25041)

Released/updated on: 2009-09-23
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2004-01-01--2005-01-01
This dataset comprises the fourth follow-up of the baseline Hispanic EPESE (HISPANIC ESTABLISHED POPULATIONS FOR THE EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1993-1994: [ARIZONA, CALIFORNIA, COLORADO, NEW MEXICO, AND TEXAS] [ICPSR 2851]). The baseline Hispanic EPESE collected data on a representative sample of community-dwelling Mexican-Americans, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the series was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE provides data on risk factors for mortality and morbidity in Mexican Americans in order to contrast how these factors operate differently in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public-use data cover demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Subsequent follow-ups provide a cross-sectional examination of the predictors of mortality, changes in health outcomes, and institutionalization, and other changes in living arrangements, as well as changes in life situations and quality of life issues. During this 5th Wave, 2004-2005, reinterviews were conducted either in person or by proxy, with 1,167 of the original respondents. This 4th follow-up includes an additional sample of 902 Mexican Americans aged 75 and over with higher average-levels of education than those of the surviving cohort, increasing the total number of respondents to 2,069. By diversifying the cohort of those aged 75 and older, a better understanding can be gained of the influence of socioeconomic and cultural variations on the lives and health of older Mexican Americans.
Curated

Hispanic Established Populations for the Epidemiologic Study of the Elderly (HEPESE) Wave 6, 2006-2007 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 29654)

Released/updated on: 2012-02-23
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2006-01-01--2007-01-01
This dataset comprises the fifth follow-up of the baseline Hispanic EPESE (HISPANIC ESTABLISHED POPULATIONS FOR THE EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1993-1994: [ARIZONA, CALIFORNIA, COLORADO, NEW MEXICO, AND TEXAS] [ICPSR 2851]). The baseline Hispanic EPESE collected data on a representative sample of community-dwelling Mexican Americans, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas. The primary purpose of the series was to provide estimates of the prevalence of key physical health conditions, mental health conditions, and functional impairments in older Mexican Americans and to compare these estimates with those for other populations. The Hispanic EPESE provides data on risk factors for mortality and morbidity in Mexican Americans in order to contrast how these factors operate differently in non-Hispanic White Americans, African Americans, and other major ethnic groups. The public-use data cover demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Subsequent follow-ups provide a cross-sectional examination of the predictors of mortality, changes in health outcomes, and institutionalization, and other changes in living arrangements, as well as changes in life situations and quality of life issues. During this 6th Wave, 2006-2007, reinterviews were conducted either in person or by proxy, with 921 of the original respondents. This fifth follow-up includes an additional sample of 621 Mexican Americans aged 75 years and over with higher average-levels of education than those of the surviving cohort, increasing the total number of respondents to 1,542. By diversifying the cohort of those aged 75 and older, a better understanding can be gained of the influence of socioeconomic and cultural variations on the lives and health of older Mexican Americans.
Curated
Simple Crosstabs

Hispanic Established Populations for the Epidemiologic Study of the Elderly (HEPESE) Wave 9, 2016 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 39038)

Released/updated on: 2024-06-05
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2016-01-26--2016-11-10

The Hispanic EPESE provides data on risk factors for mortality and morbidity in older Mexican Americans in order to contrast how these factors operate differently than in non-Hispanic Whites, African Americans, and other major ethnic groups.

The Wave 9 dataset comprises the eighth follow-up of the baseline Hispanic Established Populations for the Epidemiologic Studies of the Elderly, 1993-1994: [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 2851). The baseline Hispanic EPESE collected data on a representative sample of community-dwelling Mexican Americans, aged 65 years and older, residing in the five Southwestern states of Arizona, California, Colorado, New Mexico, and Texas.

The public-use data covers demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health behaviors, self-reported use of dental, hospital, and nursing home services, and depression. Subsequent follow-ups allow examination of the predictors of mortality, changes in health outcomes, institutionalization, changes in living arrangements, as well as changes in life situations and quality of life.

During this 9th Wave (Dataset 1), 2016, 480 re-interviews were conducted either in person or by proxy, with 283 of the original respondents interviewed in 1993-1994. This Wave also includes 197 re-interviews from the 902 new respondents added at Wave 5 in 2004-2005. All respondents were aged 85 and over at Wave 9.

The Wave 9 Informant Interviews dataset (Dataset 2) includes data from interviews with 460 respondents who provided information on themselves as well as the older respondents. The older respondents were asked to provide the name and contact information of the person they are "closer to" or they "depend on the most for help." These INFORMANTS, many of whom provide caregiving support to the older respondents, were contacted, and interviewed regarding the health, function, social situation, finances, and general well-being of the older Hispanic EPESE respondents. Information was also collected on the informant's health, function, and caregiver responsibilities and burden. This dataset includes information from the 460 informants, more than two-thirds of whom were children of the respective respondents. Thus, there are 460 respondent-informant dyads that provide opportunities for caregiving research.

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National Health and Nutrition Examination Survey I: Epidemiologic Followup Study, 1986 (ICPSR 9466)

Released/updated on: 1992-02-17
Geographic coverage: United States
The NHANES I Epidemiologic Followup Study (NHEFS) is a longitudinal study of adults originally examined, measured, and interviewed in 1971-1975 as part of the first National Health and Nutrition Examination Survey (NHANES I). The NHEFS was jointly initiated by the National Center for Health Statistics (NCHS), the National Institute on Aging, and other components of the National Institutes of Health and Public Health Service. The primary purpose of the followup study is to investigate longitudinal relationships between the extensive data on physiological, nutritional, behavioral, and demographic characteristics collected during NHANES I and subsequent morbidity or mortality from specific diseases and conditions. The 1982-1984 wave of data collection for NHEFS followed all medically examined respondents who had been 25 to 74 years in 1971-1975. The 1986 NHEFS wave focused on older members of the NHANES I NHEFS cohorts, those who had been 55-74 years of age at their baseline examinations in 1971-1975 and were not known to be deceased at the time of the 1982-1984 NHEFS. In the 1986 NHEFS, the surviving respondents were 65-89 years of age. Data were collected on changes in vital, health, and functional status and use of health care services that had occurred since the last contact, whether the contact was in 1982-1984 or 1971-1975. The vital and tracing status file documents efforts to trace all subjects who had been 55 years of age and over at NHANES I (N = 5,677) and ascertain their vital status and demographic data. Further data collection was aimed at the 3,980 subjects who were not known to be deceased by 1982-1984. Thirty-minute telephone interviews were conducted with either sample members (N = 2,558) or with proxies for the incapacitated (N = 469) and deceased (N = 581) subjects. Questions were asked on household composition, self-reports of physician-diagnosed medical conditions (with detail on reports of cancer, bone fractures, and non-hospital health facility stays), death if applicable, functional limitations, use of health care facilities, and interviewer observations about the respondent. Items on coronary bypass surgery, pacemaker procedures, and community services utilization were 1986 additions to the NHEFS questionnaire. For those respondents who had not been interviewed in 1982-1984, questions were included on smoking and alcohol use, vision and hearing, exercise and weight, and pregnancy and menstrual history. Health care facility records were abstracted to provide diagnostic and summary information on single or multiple overnight stays in hospitals and nursing homes for 2,021 subjects reporting such stays. Death certificate data, including International Classification of Diseases, 9th Revision codes for multiple causes of death, were added for 661 decedents reported since the 1982-1984 wave, for a total of 2,266 decedents.
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National Health and Nutrition Examination Survey I: Epidemiologic Follow-Up Study, 1987 (ICPSR 9854)

Released/updated on: 2006-01-12
Geographic coverage: United States
The National Health and Nutrition Examination Survey I Epidemiologic Follow-Up Study (NHEFS) is a longitudinal study which uses as its baseline those adult persons aged 25 to 74 years who were examined in the first National Health and Nutrition Examination Survey (NHANES I). The NHEFS surveys were designed to investigate the association between factors measured at the baseline and the development of specific health conditions. The NHEFS is comprised of a series of follow-up surveys, three of which have been completed. The first wave of data collection, the 1982-1984 NHEFS (ICPSR 8900), included all persons who were between 25 and 74 years of age at their NHANES I examination. The second wave of data collection, the 1986 NHEFS (ICPSR 9466), included the NHEFS cohort who were 55-74 years at their baseline examination and not known to be deceased at the time of the 1982-1984 NHEFS. The third wave, the 1987 NHEFS, was conducted for the entire nondeceased NHEFS cohort. The 1982-1984 NHEFS consisted of five steps. The first step focused on tracing and locating all subjects in the cohort or their proxies and determining their vital status. The second step involved obtaining death certificates for subjects who were deceased. Interviews with the participants or their proxies constituted the third phase of the follow-up. The fourth phase of the follow-up included measurements of pulse, blood pressure, and weight for interviewed respondents, and the fifth step was the acquisition of relevant hospital and nursing home records, including pathology reports and electrocardiograms. The 1986 NHEFS assessed changes to the health and functional status of the oldest members of the NHEFS cohort since the last contact period. The 1987 NHEFS also collected information on changes in the health and functional status of the NHEFS cohort since the last contact period. The Vital and Tracing Status file contains summary information about the status of the entire NHEFS cohort. The Health Care Facility Record file contains information on reports of stays in hospitals and nursing homes as well as information abstracted from facility medical records. The Mortality Data file contains data abstracted from the death certificates from all three NHEFS surveys. The Interview Data file contains information on selected aspects of the subject's health history since the time of the NHANES I exam.
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National Health and Nutrition Examination Survey II: Mortality Study, 1992 (ICPSR 2631)

Released/updated on: 2006-03-30
Geographic coverage: United States
The National Health and Nutrition Examination Survey II: Mortality Study, 1992 (NH2MS) followed a subset of the participants in the second National Health and Nutrition Examination Survey (NHANES II). The NH2MS cohort is comprised of adult respondents to the NHANES II who were 30-75 years of age at the time of the NHANES II, and who were interviewed and examined for NHANES II. Some participants who were 74 years of age during their interview turned 75 years old between their interview and the examination. The NHANES series of data collections included standardized physical examinations, laboratory tests, and interviews that covered various health-related topics. The NH2MS was designed to investigate the association between factors measured at baseline and overall mortality or death from specific causes. The NH2MS involved searching national databases containing information about mortality and causes of death. The study was entirely passive: participants were not recontacted, nor were all death certificates obtained. Instead, mortality status was ascertained solely by computerized matching to national databases and evaluation of the resulting matches. Furthermore, no recontact is planned in the future. Rather, matching to the National Death Index (NDI) and to other national databases will continue on a periodic basis. The Mortality Status file (Part 1) contains mortality status and demographic data for all NH2MS participants who were 30-75 years of age at their NHANES II examination. The Cause of Death file (Part 2) contains one record for each known decedent for whom multiple causes of death were obtained (2,103 out of the 2,145 participants identified as deceased). Cause of death is missing for some decedents either because there was no matching record on the NCHS Multiple Cause of Death files or the death certificate was not found through the state vital statistics office.
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National Health Interview Survey, 1984 (ICPSR 8659)

Released/updated on: 2011-04-19
Geographic coverage: United States
The basic 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. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, region, and type of sampling area. The Person File (Part 2) includes sex, age, race, marital status, veteran status, and education. These variables are found in the Condition, Doctor Visit, 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 (Part 3), Doctor Visit (Part 4), and Hospital Episode (Part 5) Files contain information on each reported acute or chronic condition, doctor visit, or hospitalization, respectively. A sixth, seventh, and eighth file have been provided. The Health Insurance Supplement File (Part6) contains information on the type of health insurance held by each respondent from the Person file. Parts 7-8 comprise the Supplement on Aging (SOA) Files divided into Condition and Person Public Use Files respectively, and contain data on a subset of the NHIS population, those aged 55 and over. These files contain the same Condition and Person variables as Parts 2-3 but are supplemented by questions pertaining specifically to the subpopulation of older respondents. These additional variables cover family relationships and support, community and social support, occupation and retirement, nursing home stays, help with care, health opinions, and other health-related and social information about middle-aged and older people.
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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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National Medical Care Expenditure Survey, 1977: Health Insurance/Employer Survey Data (ICPSR 8627)

Released/updated on: 2006-03-30
Geographic coverage: United States
The purpose of the National Medical Care Expenditure Survey (NMCES) was to assess the cost and extent of health insurance in the United States. Information on health insurance coverage was obtained in a household survey, then verified and supplemented with information from the Health Insurance/Employer Survey (HIES). Insurance companies, employers, unions, and other organizations identified in the household survey as sources of private insurance coverage were asked to verify reported coverage, to provide information on each subscriber's coverage and its cost, the parties responsible for payment of premiums, and the availability of alternative or optional plans. This release includes two distinct datasets. One contains information for each individual respondent in the NMCES component on private health insurance status as verified in the HIES, and includes data on premiums and sources of premium payment. The other contains information for each individual respondent 65 years or older with private insurance as verified in the HIES, as well as information on the services covered by their private insurance benefits.
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National Nursing Home Survey, 1977 (ICPSR 7946)

Released/updated on: 1992-02-16
Geographic coverage: United States
Data for the 1977 National Nursing Home Survey were collected in a nationwide sample of nursing homes, personal care homes (with or without nursing), and domicilary care homes. Information on staff, residents, and discharges was collected via a combination of personal interviews and self-enumerated forms. Four files are contained within this data collection. Part 1, Facility-Expense File, contains information on type of facility, certification, bed size, services and therapy routinely provided to residents or non-residents, regular and temporary admissions, vacant staff positions, facility income, and expenditures. Parts 2 and 3, Current and Discharged Resident Files, supply data on residents regarding admissions, impairments, conditions, behavioral problems, visits to a physician, services, therapy or treatments received, use of aids or need of assistance, level of care received, total charges for care, and sources and amount of payments. Part 4, Staff File, contains information on employees' job experience, services performed, hours worked, educational background, non-degree training, salaries, and benefits.
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National Nursing Home Survey, 1995 (ICPSR 6998)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1995-07-01--1995-12-01
The National Nursing Home Survey (NNHS) is a survey of nursing homes and related care facilities in the United States. Between July and December 1995, information regarding facility and financial characteristics was gathered from 1,409 facilities, along with current resident information for 8,056 residents. For Part 1, Facility Questionnaire Data, personal interviews with facility administrators provided information on topics such as certification, availability of beds, and kinds of services provided, including dental, hospice, and nutrition. Through interviews with staff persons, current residents provided information on their age, race, marital status, level of care, and use of aids such as walkers, hearing aids, and crutches. These data are contained in Part 2, Current Resident Questionnaire Data. Financial data for facilities in Part 3, Expense Questionnaire Data, were supplied by accountants and bookkeepers using self-enumerated questionnaires pertaining to payroll expenses, drug costs, total revenues, and Medicare/Medicaid payments.
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National Nursing Home Survey, 1999 (ICPSR 3268)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1999-07-01--1999-12-01
The National Nursing Home Survey (NNHS) is a survey of nursing homes and related care facilities in the United States. Between July and December 1999, information regarding facility and financial characteristics was gathered from 1,423 facilities, along with current resident information for 8,215 residents. For Part 1, Facility Questionnaire Data, personal interviews with facility administrators provided information on topics such as certification, availability of beds, and kinds of services provided, including dental, hospice, and nutrition. Part 2, Current Resident Questionnaire Data, provides information on age, race, marital status, level of care, and use of aids such as walkers, hearing aids, and crutches. Part 3, Discharged Resident Questionnaire Data, includes date of admission, reason for discharge, admission diagnosis, discharge diagnosis, assistive devices used, help needed with daily activities, services provided (health, mental health, transportation, social, educational), and payment sources.
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National Nursing Home Survey, 2004 (ICPSR 4651)

Released/updated on: 2007-03-23
Geographic coverage: United States
Time period: 2004-08-01--2004-12-01
The National Nursing Home Survey (NNHS) is a survey of nursing homes and related care facilities in the United States. During 2004, information regarding facility and financial characteristics was gathered from 1,174 facilities, along with current resident information for 13,507 residents, with additional information from 3,017 Nursing Assistants. The 2004 NNHS, conducted between August and December of 2004, was reintroduced into the field after a five-year break, during which time the survey was redesigned and expanded to collect many new data items using the National Nursing Assistant Survey (NNAS), which was sponsored by the Office of the Assistant Secretary for Planning and Evaluation (APSE) and is the first national study of nursing assistants working in nursing facilities in the United States. Facilities (DS 1) information was gathered through personal interviews with facility administrators and provided information on topics such as certification, availability of beds, and kinds of services provided, including dental, hospice, and nutrition. Current Residents (DS 2) information includes questions regarding age, race, marital status, level of care, and use of aids such as walkers, hearing aids, and crutches. Nursing Assistants (Part 3) information looked at the important role of nursing assistants in providing long-term care services for the growing population of the elderly and chronically ill. The NNAS gathered information regarding recruitment, education, training and licensure, job history, and family life, along with client relations, job satisfaction, and workplace environment.
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National Survey of Hispanic Elderly People, 1988 (ICPSR 9289)

Released/updated on: 2005-11-04
Geographic coverage: United States
Time period: 1987-01-01--1988-01-01
This survey, conducted as an extension of the NATIONAL SURVEY OF PROBLEMS FACING ELDERLY AMERICANS LIVING ALONE, 1986 (ICPSR 9379) (NSPFEALA), was designed to investigate specific problems of the elderly in order to gain a better understanding of the economic, health, and social status of this group. The survey focused on many of the same issues investigated by the NSPFEALA to allow comparisons between Hispanic elderly and the elderly population as a whole. Respondents were given their choice of English or Spanish as the interview language. Elderly Hispanics were asked if they had serious problems with family relationships, loneliness, anxiety, care of a sick spouse or relative, paying for medical bills, having enough money to live on, or dependence on others. In the same vein, respondents were asked if they had disabilities that affected their daily activities such as bathing, dressing, walking, eating, and shopping, and who, if anyone, helped them to perform these functions. Respondents were also asked if they were generally satisfied with their lives and if they felt excited, restless, proud, pleased, bored, depressed, optimistic, or upset during the few weeks preceding the interview. In addition, the survey inquired about willingness to accept various changes in Social Security benefits and taxation and also queried respondents about their living arrangements (actual and preferred), social networks, general health, doctor visits and hospital stays during the last 12 months, coverage by and utilization of social programs and services, income and sources of income, fluency in English and Spanish, current and past employment, usual means of transportation, home ownership, ancestry, country of birth, year of immigration, religion, education, number of living children, age, sex, and marital status.
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National Survey of the Aged, 1975 (ICPSR 7945)

Released/updated on: 1992-02-16
Geographic coverage: United States
This survey was conducted during the spring and summer of 1975 under a grant from the Administration on Aging and with supplemental funding from the Social Security Administration. It surveyed noninstitutionalized Americans aged 65 and older with a special focus on developing national estimates of the economic needs and social concerns of the elderly. The survey attempted to describe the aged population and to indicate the degree of health, financial independence, and familial support of 2,143 older Americans. Also studied were the work status of respondents, their past and present attitudes toward work, their desire for gainful employment, their income and assets, their evaluation of their own financial status, and their reported use of health and welfare services. The data collection comprises three files. Part 1 contains the general survey, Part 2 is a survey of proxy respondents, and Part 3 supplies information on persons who could not complete an interview.
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National Survey of the Aged [United States], 1957 (ICPSR 7686)

Released/updated on: 2006-03-30
Geographic coverage: United States
This survey, sponsored by the Health Information Foundation at the University of Chicago and conducted at the National Opinion Research Center, consists of three component parts. Part 1, the Health Needs of Older Persons, covers health, the use of medical facilities, the cost of medical care, the older person's sources of income, his/her social relationships, attitudes toward younger family members, work, religion, and a self-evaluation of health status for persons aged 60 and over. Part 2, Household Enumeration: Noninterviewed Individuals, contains information describing persons located during the enumeration process who were unable to complete an interview. For Part 3, Public Attitudes on Older People, a cross-section of adult Americans was surveyed. This survey was mainly concerned with the level of responsibility younger and middle-aged people assumed for older relatives, the kinds of plans they were making for their own maintenance in later years, and overall attitudes on the part of all age groups toward certain situations that are commmon in later life.
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National Survey of the Aged [United States], 1962 (ICPSR 7687)

Released/updated on: 1992-02-16
Geographic coverage: United States
This data collection contains the results of a survey of the aged in the United States in 1962. The study gathered information on the health, economic status, living arrangements, and family relationships of persons aged 65 years and older. The emphasis of the survey was on the general physical capacity of older people, the relationship of physical capacity to economic conditions, employment and retirement patterns, housing, and family and social relationships. The survey was designed to produce national estimates of the needs of older persons. In particular, the services that facilitate continued independent living arrangements were examined. The survey was conducted by the National Opinion Research Center and was part of a three-nation study in Denmark, Great Britain, and the United States (see NATIONAL SURVEY OF THE AGED [UNITED STATES], 1957 [ICPSR 7686] and NATIONAL SURVEY OF THE AGED, 1975 [ICPSR 7945]). In personal interviews respondents who were currently employed (and those who were retired or housewives) were asked for employment details and occupational history, their attitudes about work and retirement, and descriptions of their physical health, with specific questions asked of both nonambulatory and housebound persons, (e.g., if they needed and/or received help with various personal care tasks, what specific illness kept them indoors, and who provided their in-home care). Respondents were also asked for information about their children and relatives (e.g., the amount of financial help received from them, the number of times each sibling and child visited, and the amount of time it would take each to make the trip to the respondent's dwelling) and their finances (e.g., living expenses, life insurance, value of property, amount of mortgage payment or rent, and amount and sources of income). Other questions concerned attitudes about aging (e.g., if respondents were satisfied with their life accomplishments, if they believed in an afterlife, and how often they experienced feelings of loneliness and isolation). The interviewers provided observational data about respondents (e.g., level of cooperation and alertness and ability to hear and see). Demographic data gathered include age, sex, marital status, relationship to head of household, number of persons in household, type of household, country of origin, age when arrived in the United States, last grade or year of school completed, religious preference, and if living on a farm.
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Old Age in the United States, 1880 (ICPSR 8427)

Released/updated on: 1992-10-31
Geographic coverage: United States
This data collection describes the social conditions of the older population of the United States in the late nineteenth century. Variables include personal characteristics such as age, sex, marital status, race, birthplace, number of children, and occupation of sampled older persons. Detailed information, extracted from the 1880 United States Census manuscript census schedules, is provided on household composition and family structure. In addition, occupational and ethnic characteristics of family heads appearing on the same sampled census page as the older person (on census pages grouped by street location) are reported. The data collection consists of three independent samples: (1) a national sample, (2) a Southern urban sample, and (3) a Southern Black sample. Older Blacks are over-represented in the Southern urban and Southern Black samples in order to focus on their family experiences in the urban and rural South.
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Old Age in the United States, 1900 (ICPSR 8428)

Released/updated on: 1993-02-14
Geographic coverage: United States
This data collection describes the social conditions of the older population of the United States at the turn of the century. Detailed information, extracted from the 1900 United States Census manuscript schedules, is provided on household composition and family structure for each sampled older person. Ecological characteristics of the county of residence, e.g., the percentage of the county's population that is foreign born, are provided for most sampled older persons. In addition, occupational and ethnic characteristics of family heads appearing on the same sampled census page as the older person (on census pages grouped by street location) are reported.
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Simple Crosstabs

Puerto Rican Elderly: Health Conditions (PREHCO) Project, 2002-2003, 2006-2007 (ICPSR 34596)

Released/updated on: 2013-09-13
Geographic coverage: Puerto Rico, United States
Time period: 2002-01-01--2007-01-01
The Puerto Rican Elderly: Health Conditions (PREHCO) study investigates issues affecting the elderly (individuals over 60 years of age) population in Puerto Rico: health status, housing arrangements, functional status, transfers, labor history, migration, income, childhood characteristics, health insurance, use of health services, marital history, mistreat, sexuality, etc. It is an island-wide, longitudinal sample survey of target individuals and their spouses with two waves of data collection: 2002-2003 and 2006-2007.
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Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001, Baseline and Follow-Up Data (ICPSR 3678)

Released/updated on: 2006-09-26
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-01
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Baseline data (ICPSR 3253) were collected through randomized clinical trials at six sites: University of Alabama-Birmingham, The Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee-Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions such as psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services varied by site. This collection contains baseline data along with follow-up data at 6-, 12-, and 18-month intervals from each site with focus on the impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization. Also included are follow-up batteries, transition batteries (placement, bereavement, discontinued), and data reporting missed visits. Parts 1 through 5 contain screening data and responses to a short mental status questionnaire. Parts 6 through 34 contain baseline data along with follow-up data at 6, 12, and 18-month intervals and cover activities of daily living, anxiety, and caregiver health and health behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 35 through 40 contain tracking data and also include an examination of interventions.
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Resources for Enhancing Alzheimer's Caregiver Health (REACH II), 2001-2004 (ICPSR 4354)

Released/updated on: 2006-10-27
Geographic coverage: Palo Alto, United States, Tennessee, Memphis, California, Alabama, Florida, Birmingham, Philadelphia, Pennsylvania, Miami
Time period: 2001-01-01--2004-01-01
Built upon the findings of RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH, 1996-2001, BASELINE AND FOLLOW-UP DATA [ICPSR 3678], REACH II designed and tested a single multi-component intervention among family caregivers of persons with Alzheimer's disease or related disorders. The overall objectives were (1) to identify and reduce modifiable risk factors among diverse family caregivers of patients with Alzheimer's Disease or a related disorder, (2) to enhance the quality of care provided to the care recipients, and (3) to enhance the well-being of the caregivers. REACH II is the first project to simultaneously test a comprehensive caregiver intervention in three distinct racial/ethnic groups: Hispanic/Latino, Black/African-American, and White/Caucasian. The intervention was based on a risk-appraisal approach in which five areas of risk--depression, burden, self-care, social support, and patient problem behaviors--that are central to caregiver well-being and quality of life were matched to corresponding intervention components. These components included education, skills to manage troublesome care-recipient behaviors, social support, cognitive strategies for reframing negative emotional responses, and strategies for enhancing healthy behaviors and managing stress. Consistent with this approach, the primary outcome was a multivariate quality of life indicator that assessed caregiver depression, burden, self-care, social support, and patient problem behaviors. Two hallmarks of caregiver intervention studies--caregiver clinical depression and patient institutionalization--were assessed as secondary outcomes. The dataset names listed in this collection include the shortened name of the form administered.
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Partially restricted

Sacramento Area Latino Study on Aging (SALSA Study), 1996-2008 (ICPSR 22760)

Released/updated on: 2009-06-29
Geographic coverage: Sacramento, United States, California
Time period: 1996-01-01--2008-01-01

The Sacramento Area Latino Study on Aging (SALSA Study) project tracked the incidence of physical and cognitive impairment as well as dementia and cardiovascular diseases in elderly Latinos in the Sacramento, California, region. The SALSA project aimed to assess cognitive, physical and social functions, which include the ability to follow instructions, to perform certain movements, and to interact with others. The study explored the effects that cultural, nutritional, social and cardiovascular risk factors have on overall health and dementia, and examined the association between diabetes and functional status. Demographic information includes age given at follow-up visits, country of birth, language, religion, marital status, educational level, occupation, household income, and size of household.

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Partially restricted
Simple Crosstabs

Sacramento Area Latino Study on Aging (SALSA Study), 1996-2008: Demographic Data (ICPSR 34483)

Released/updated on: 2012-12-11
Geographic coverage: Sacramento, United States, California
Time period: 1996-01-01--2008-01-01

This study contains demographic variables for the the Sacramento Area Latino Study on Aging (SALSA) Series and can be used with ICPSR studies 22760, 29321, 29322, 29323. Demographic variables include gender, primary language, country of origin, state of birth, cause of death, 2000 census tract codes, birth date, date of death, and age given at follow-up visits.

About SALSA: The Sacramento Area Latino Study on Aging (SALSA Study) project tracked the incidence of physical and cognitive impairment as well as dementia and cardiovascular diseases in elderly Latinos in the Sacramento, California, region. The SALSA project aimed to assess cognitive, physical, and social functions, which include the ability to follow instructions, to perform certain movements, and to interact with others. The study explored the effects that cultural, nutritional, social, and cardiovascular risk factors have on overall health and dementia, and examined the association between diabetes and functional status.

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Partially restricted

Sacramento Area Latino Study on Aging (SALSA Study), 1996-2008: Neuroclinical Exam Data (ICPSR 29322)

Released/updated on: 2017-02-23
Geographic coverage: Sacramento, United States, California
Time period: 1996-01-01--2008-01-01

The Sacramento Area Latino Study on Aging (SALSA Study) project tracked the incidence of physical and cognitive impairment as well as dementia and cardiovascular diseases in elderly Latinos in the Sacramento, California, region. The SALSA project aimed to assess cognitive, physical, and social functions, which include the ability to follow instructions, to perform certain movements, and to interact with others. The study explored the effects that cultural, nutritional, social, and cardiovascular risk factors have on overall health and dementia, and examined the association between diabetes and functional status. This study contains the neuroclinical exam data from the SALSA project. Demographic information includes age given at follow-up visits, country of birth, language, religion, marital status, educational level, occupation, household income, and size of household.

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Partially restricted

Sacramento Area Latino Study on Aging (SALSA Study), 1996-2008: Neuropsychological Exam Data (ICPSR 29323)

Released/updated on: 2017-02-23
Geographic coverage: Sacramento, United States, California
Time period: 1996-01-01--2008-01-01
The Sacramento Area Latino Study on Aging (SALSA Study) project tracked the incidence of physical and cognitive impairment as well as dementia and cardiovascular diseases in elderly Latinos in the Sacramento, California, region. The SALSA project aimed to assess cognitive, physical, and social functions, which include the ability to follow instructions, to perform certain movements, and to interact with others. The project explored the effects that cultural, nutritional, social, and cardiovascular risk factors have on overall health and dementia, and examined the association between diabetes and functional status. This study contains the neuropsychological exam data from the SALSA project, which includes data reflecting tests of respondents' verbal and non-verbal semantic memory object naming, spatial abilities pattern recognition, verbal attention span, and verbal conceptual thinking. Demographic information includes age given at follow-up visits, language, and educational level.
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Partially restricted
Simple Crosstabs

Sacramento Area Latino Study on Aging (SALSA Study), 1996-2008: Semi-Annual Phone Call Data (ICPSR 29321)

Released/updated on: 2018-08-17
Geographic coverage: Sacramento, United States, California
Time period: 1998-01-01--2004-01-01

The Sacramento Area Latino Study on Aging (SALSA Study) was a longitudinal cohort study of 1,789 community-dwelling Mexican Americans residing in California's Sacramento Valley who were aged 60-101 years at baseline in 1998-1999. Participants were followed every 12-15 months via home visits that included clinical and cognitive assessments. A semiannual phone call was made to obtain updates on medications, health events, and some sociodemographic risk factors. This study, Semi-Annual Phone Call Data, contains data from the six-month follow-up calls of the SALSA project.

The SALSA project tracked the incidence of physical and cognitive impairment as well as dementia and cardiovascular diseases in elderly Latinos in the Sacramento, California region. The SALSA project aimed to assess cognitive, physical, and social functions, which include the ability to follow instructions, to perform certain movements, and to interact with others. The project explored the effects that cultural, nutritional, social, and cardiovascular risk factors have on overall health and dementia, and examined the association between diabetes and functional status.

Demographic information collected in these data includes language and age given at follow-up visits.

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Study of Women's Health Across the Nation (SWAN), 1998-2001: Family Medical History From Visits 02, 03, and 04 (ICPSR 30181)

Released/updated on: 2014-02-13
Geographic coverage: Inkster, Hackensack, United States, Chicago, Ypsilanti, California, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 1998-02-15--2001-06-01
The Study of Women's Health Across the Nation (SWAN) is a multisite longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers, and women learn how mid-life experiences affect health and quality of life during aging. The study is co-sponsored by the National Institute on Aging (NIA) and the National Institute of Health (NIH), Office of Research on Women's Health. The study began in 1994. Between 1998 and 2001, 2,829 of the 3,302 women that joined SWAN participated in a collection of family history data. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Almeda and Contra Costa County, CA (University of California, Davis and Kaiser Permanente); Los Angeles, CA (University of California, Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures.
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Study of Women's Health Across the Nation (SWAN), 2001-2003: Visit 05 Dataset (ICPSR 30501)

Released/updated on: 2025-08-05
Geographic coverage: Inkster, Hackensack, United States, Chicago, Ypsilanti, California, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2001-03-01--2003-02-15
The Study of Women's Health Across the Nation (SWAN), is a multisite longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological, and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers, and women learn how mid-life experiences affect health and quality of life during aging. The data include questions about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2001 and 2003, 2,617 of the 3,302 women that joined SWAN were seen for their fifth follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis, and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Simple Crosstabs

Study of Women's Health Across the Nation (SWAN), 2002-2004: Visit 06 Dataset (ICPSR 31181)

Released/updated on: 2025-06-30
Geographic coverage: Inkster, Hackensack, Contra Costa County, Alameda County, United States, Chicago, Ypsilanti, California, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2002-03-15--2004-02-15
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2002 and 2004, 2,448 of the 3,302 women that joined SWAN were seen for their sixth follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Simple Crosstabs

Study of Women's Health Across the Nation (SWAN), 2003-2005: Visit 07 Dataset (ICPSR 31901)

Released/updated on: 2025-07-10
Geographic coverage: Inkster, Contra Costa County, Alameda County, United States, Chicago, Ypsilanti, California, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2003-05-15--2005-01-31
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2003 and 2005, 2,327 of the 3,302 women that joined SWAN were seen for their seventh follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Though the New Jersey site was still part of the study, data was not collected from this site for the seventh visit. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Study of Women's Health Across the Nation (SWAN), 2004-2006: Visit 08 Dataset (ICPSR 32122)

Released/updated on: 2018-11-20
Geographic coverage: Inkster, Contra Costa County, Alameda County, United States, Chicago, Ypsilanti, California, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2004-03-15--2006-01-31
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2004 and 2006, 2,278 of the 3,302 women that joined SWAN were seen for their eighth follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Though the New Jersey site was still part of the study, data was not collected from this site for the eighth visit. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Simple Crosstabs

Study of Women's Health Across the Nation (SWAN), 2005-2007: Visit 09 Dataset (ICPSR 32721)

Released/updated on: 2018-11-20
Geographic coverage: Inkster, Contra Costa County, Alameda County, United States, Chicago, Ypsilanti, California, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2005-02-15--2007-01-31
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2005 and 2007, 2,255 of the 3,302 women that joined SWAN were seen for their ninth follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Though the New Jersey site was still part of the study, data was not collected from this site for the ninth visit. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Study of Women's Health Across the Nation (SWAN), 2006-2008: Visit 10 Dataset (ICPSR 32961)

Released/updated on: 2018-11-15
Geographic coverage: Inkster, Hackensack, United States, Chicago, Ypsilanti, California, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2006-02-15--2008-01-31
The Study of Women's Health Across the Nation (SWAN) is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2006 and 2008, 2,245 of the 3,302 women that joined SWAN were seen for their tenth follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan), Boston, MA (Massachusetts General Hospital), Chicago, IL (Rush Presbyterian-St. Luke's Medical Center), Almaeda and Contra Costa County, CA (University of California, Davis and Kaiser Permanente), Los Angeles, CA (University of California, Los Angeles), Hackensack, NJ (Hackensack University Medical Center) and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Though the New Jersey site was still part of the study, data was not collected from this site for the tenth visit. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Simple Crosstabs

Study of Women's Health Across the Nation (SWAN): Baseline Dataset, [United States], 1996-1997 (ICPSR 28762)

Released/updated on: 2019-05-15
Geographic coverage: Detroit, United States, Chicago, California, Oakland, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Newark, Boston, Pittsburgh
Time period: 1996-01-01--1997-11-30

The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological, and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers, and women learn how mid-life experiences affect health and quality of life during aging. The data include questions about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause.

The study is co-sponsored by the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR), the National Institutes of Health (NIH), and the NIH Office of Research on Women's Health. The study began in 1994. Between 1996 and 1997, 3,302 participants joined SWAN through 7 designated research centers. The research centers are located in the following communities: Detroit, MI; Boston, MA; Chicago, IL; Oakland and Los Angeles, CA; Newark, NJ; and Pittsburgh, PA. SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. This is the next phase of data collection after the original collection of the screening data (ICPSR 4368).