Search results

Showing 1 – 50 of 143 results.
Curated
Simple Crosstabs

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

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

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

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

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

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

Curated
Simple Crosstabs

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

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

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

Curated
Restricted

Chicago Community Adult Health Study, 2001-2003 (ICPSR 31142)

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

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

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

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

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

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

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

Curated

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

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

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

Curated

Early Years of Marriage (EYM) Project, Years 1-4, 1986-1989 (ICPSR 4557)

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

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

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

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

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

Curated
Restricted

Extending Health Insurance to the Working Poor: An Assessment of Health Status and Health Care Utilization Effects Among New York City Home Health Attendants, February 1990-June 1991 (ICPSR 9774)

Released/updated on: 2006-01-12
Geographic coverage: New York City
Time period: 1990-02-01--1991-06-01
Using a pre- and post-program design, this survey studied newly-hired home health attendants and their families, most of whom were without medical insurance until they became eligible for health benefits through their union. To assess changes in health status and health services utilization, the attendants were interviewed at the point of union enrollment, and again nine months later. The interview taken prior to enrollment in the benefits program elicited information about concern over health, recent injuries, and self-assessed health status, e.g., the presence or absence of specific health conditions such as diabetes, ulcers, arthritis, stomach trouble, high blood pressure, allergies, asthma, and back problems. Respondents were also queried about the extent and type of previous health coverage (including Medicare and disability insurance), limitations of daily functioning due to poor health, and recent health care utilization, including hospitalization, emergency room usage, and routine ambulatory care. The latter included questions about out-of-pocket expenses and the type of health services received, such as X-rays, CAT scans, sonograms, laboratory tests, electrocardiograms, stress tests, surgery, and setting of bones. Other questions addressed utilization issues of particular relevance to the New York City area, e.g., the use of city hospital clinics. The post-enrollment survey included parallel follow-up questions, as well as questions regarding the respondent's employment status and current benefits. Additional variables in the data collection include respondent's race, Hispanic origin, place of birth, past work experience, date of birth, and sex, plus the sex and dates of birth of family members.
Curated
Restricted

Harvard School of Public Health College Alcohol Study, 1993 (ICPSR 6577)

Released/updated on: 2020-01-30
Geographic coverage: United States
This survey focused on alcohol use and alcohol problems among undergraduate college students. The survey collected information on students' use of alcohol, tobacco, and illicit drugs, views on campus alcohol policies and student alcohol use, reasons for drinking alcohol and reasons for not drinking or limiting drinking, and personal difficulties caused by drinking problems (e.g., missed classes, injury, and trouble with police). Additional topics covered by the survey include overall health status, daily activities, satisfaction with education being received, grade-point average, living arrangements, social life, sexual activity, use of condoms during sexual intercourse, date rape, drunk driving, and attendance in meetings of Alcoholics Anonymous, Alanon, Adult Children of Alcoholics, and Narcotics Anonymous. Background variables include age, height, weight, sex, marital status, religion, mother's and father's education, mother's and father's drinking habits, race, and Hispanic origin.
Curated
Restricted

Harvard School of Public Health College Alcohol Study, 1997 (ICPSR 3163)

Released/updated on: 2020-01-30
Geographic coverage: United States
This study resurveyed colleges that participated in the HARVARD SCHOOL OF PUBLIC HEALTH COLLEGE ALCOHOL STUDY, 1993 (ICPSR 6577). As in the 1993 survey, this survey focused on alcohol use and alcohol problems among undergraduate college students. The survey collected information on students' use of alcohol, tobacco, and illicit drugs, views on campus alcohol policies and student alcohol use, reasons for drinking alcohol and reasons for not drinking or limiting drinking, and personal difficulties caused by drinking problems (e.g., missed classes, injury, and trouble with police). Additional topics covered by the survey include overall health status, daily activities, satisfaction with education being received, grade-point average, living arrangements, social life, sexual activity, use of condoms during sexual intercourse, date rape, drunk driving, and attendance in meetings of Alcoholics Anonymous, Alanon, Adult Children of Alcoholics, and Narcotics Anonymous. Background variables include age, sex, marital status, religion, mother's and father's drinking habits, race, and Hispanic origin.
Curated
Restricted

Harvard School of Public Health College Alcohol Study, 1999 (ICPSR 3818)

Released/updated on: 2020-01-30
Geographic coverage: United States
This survey interviewed students at colleges that participated in the first two rounds of the HARVARD SCHOOL OF PUBLIC HEALTH COLLEGE ALCOHOL STUDY, which were conducted in 1993 and 1997 (ICPSR 6577 and 3163). As in the previous surveys, the 1999 survey focused on alcohol use and alcohol problems among undergraduate college students. The survey collected information on students' use of alcohol, tobacco, and illicit drugs, views on campus alcohol policies and student alcohol use, reasons for drinking alcohol and reasons for not drinking or limiting drinking, and personal difficulties caused by drinking problems (e.g., missed classes, trouble with police, and health problems). Additional topics covered by the survey include overall health status, daily activities, satisfaction with education being received, grade-point average, living arrangements, social life, sexual activity (heterosexual, homosexual, and bisexual), use of condoms during sexual intercourse, date rape, drunk driving, and attendance in meetings of Alcoholics Anonymous. Background variables include age, height, weight, sex, marital status, religion, mother's and father's education, mother's and father's drinking habits, race, and Hispanic origin.
Curated
Restricted

Harvard School of Public Health College Alcohol Study, 2001 (ICPSR 4291)

Released/updated on: 2008-02-05
Geographic coverage: United States
The Harvard School of Public Health College Alcohol Study (CAS), a multi-round survey that interviewed students in four-year colleges, examined key issues in alcohol abuse and other high risk behaviors among college students, including the relationship of state alcohol control measures and college policies to alcohol use and the role of fraternities and sororities, easy access to alcohol, and low alcohol prices. As in the previous rounds of CAS, which were conducted in 1993 (ICPSR 6577), 1997 (ICPSR 3163), and 1999 (ICPSR 3818), this round collected information on students' use of alcohol, tobacco, and illicit drugs, views on campus alcohol policies and student alcohol use, reasons for drinking alcohol and reasons for not drinking or limiting drinking, and personal difficulties caused by drinking problems (e.g., missed classes and trouble with police). Additional topics covered by the survey include overall health status, daily activities, satisfaction with education being received, grade-point average, living arrangements, social life, sexual activity (heterosexual, homosexual, and bisexual), use of condoms during sexual intercourse, rape, and drunk driving. Background variables include age, height, weight, sex, marital status, religion, mother's and father's education, mother's and father's drinking habits, race, and Hispanic origin.
Curated
Restricted

Health Insurance Coverage Among Working Latinos in California, 2001 (ICPSR 3572)

Released/updated on: 2003-02-19
Geographic coverage: United States, California
To learn why Latinos often lack health insurance in California, this survey interviewed a sample of employed Hispanics in that state. Respondents were interviewed about their health status, health insurance coverage, access to health care, and health care utilization. For insured respondents, the survey measured satisfaction with one's current health plan and collected information on the plan type, length of coverage with the plan, and the plan's co-pays and deductibles. Uninsured respondents were asked why they did not have health insurance, if they had tried to obtain insurance in the past year, how long it was since they last had coverage, whether or not their employer offered health insurance, and what they would expect to pay for it. Additionally, the survey gauged attitudes regarding control of one's fate, acceptability of community and free-care clinics as sources for care, the desirability of getting regular check-ups, and health insurance as a good versus a bad value for the money. Demographic and socioeconomic characteristics collected by the survey include age, sex, household size, educational attainment, religious preference, county of birth, ancestry, citizenship, number of years in the United States, ability to speak English, income, number of jobs held, size of employer (number of employees), length of time at job, industry, occupation, and labor union membership.
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

Hispanic Health and Nutrition Examination Survey, 1982-1984 (ICPSR 8535)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1982-07-01--1984-12-01
Sixteen components focusing on nutritional practices and physical health comprise this survey of Hispanic Americans. The Body Measurements file includes anthropometric data on individuals such as skeletal and skin fold measurements, body circumferences, height, and weight. The Dental Health data provide dental history information, including the frequency of and reasons for visits to a dental hygienist, fluoride treatments, and the results of a clinical examination. The Blood and Urine Assessments component of the study contains clinical data such as red and white blood cell counts, serum iron and vitamin levels, amount of lead, and other assays. The Physician's Examination file provides the results of a basic physical exam, and the Dietary Practices/Food Frequency component includes information on food recall, special diets, frequency of meals, and consumption of various types of foods. The Adolescent and Adult History Questionnaire file supplies information on health care and problems getting care, dental care, health status, conditions, medical treatment, pesticide exposure, smoking, acculturation, meal programs for school-age children, reproductive history, and health status of children. Measures of Depression provides data on feelings of depression, how depression affected everyday life, help sought during depression, and weight changes and sleep loss due to depression. The Alcohol Consumption Data section includes information on the amount and kind of alcohol consumed, reasons for drinking, and self-perception of drinking habits. The Drug Abuse file offers information on the use of barbiturates and other sedatives, marijuana and hash, inhalants, and cocaine. The Hearing data were collected during the physical examination and provide information on respondents' ability to hear and the condition of their hearing organs. The Gallbladder Ultrasound data include information on disease, history of symptoms, findings of ultrasounds, and physical examinations of the gallbladder. Diabetes and OGTT (oral glucose tolerance test) data were also collected. Respondents were asked whether they had diabetes and were also questioned about age of onset, medication taken, diet, and if the OGTT had been administered. The file also contains detailed information on the OGTT, diet before the testing, time intervals between blood drawings, and plasma glucose values in milligrams and deciliters. The Vision section furnishes information on the respondent's eyesight, whether he or she had a problem seeing, appliances worn, age when corrective lenses were first worn, if a doctor had been visited for sight problems, and findings from a physician's examination. Measurements of the respondent's visual acuity with and without correction are also included in the data. The Child History section includes information on health status, health care utilization, infant feeding practices, participation in meal programs, school attendance, and language use. The 24-Hour Recall lists amounts of calories, protein, total fat, fatty acids, cholesterol, carbohydrates, dietary fiber, alcohol, vitamins, and minerals for each food item consumed by each person. It also contains a description of the food, ingestion period, approximate time of consumption, and food source. The data from the Measurement and Interpretation of Electrocardiograms file give an objective measure of the cardiac health status of individuals examined in the survey. Despite the limitations of such data, the electrocardiographic variables are carefully and completely defined. Also, an extensive process was used to ensure the accuracy of the findings. In addition, each part of this collection provides sociodemographic data, such as age, race, national origin, birthplace, education, employment, insurance, and use of public assistance. Also included are family data including number of people in the family, family income, poverty index, use of food stamps, and size of residence.
Curated
Restricted

Hurricane Katrina Community Advisory Group Study [United States] (ICPSR 22325)

Released/updated on: 2010-06-10
Geographic coverage: Mississippi, United States, Louisiana, New Orleans, Alabama
Hurricane Katrina was the most destructive and costliest natural disaster to occur in the United States. Nearly 5 million people lived in the path of Katrina. An additional 1.3 million lived in the New Orleans metropolitan area at the time of the hurricane. Although not in the direct path of Katrina, New Orleans was devastated by a massive flood that occurred as a result. The purpose of this study is to inform policy-makers of the impact of Hurricane Katrina on survivors' physical and mental health and barriers to treatment, as well as assist in future natural disaster planning efforts. This will be achieved by monitoring, over time, a group of people who represent those affected by Katrina. The Hurricane Katrina Community Advisory Group consists of a broad cross-section of people affected by Katrina, including separate samples of people who resided in the New Orleans metropolitan area at the time of the hurricane and those who resided in the counties or parishes of Alabama, Louisiana, and Mississippi that were in the path of the hurricane. Follow-up interviews conducted with the Advisory Group members to monitor the pace of recovery, as well as reports prepared for policy-makers, press releases, and digitally recorded oral histories are being posted on the Hurricane Katrina Community Advisory Group Web site as they become available. Demographic variables include gender, age, race, ethnicity, pre-hurricane residence (place), pre-hurricane type of housing (detached home, mobile home, apartment, etc.), pre-hurricane employment, family income, marital status, education, home ownership (owned with mortgage, owned without mortgage, rented, etc.), where the respondent lived at time of interview, religious preference, and religiosity.
Curated

Mexican Origin People in the United States: the 1979 Chicano Survey (ICPSR 8436)

Released/updated on: 2005-11-04
Geographic coverage: United States, Chicago, New Mexico, Illinois, Texas, Colorado, California, Arizona
The 1979 Chicano Survey, conducted by the Institute for Social Research, University of Michigan, was a household survey of persons of Mexican descent living in California, Arizona, New Mexico, Colorado, Texas, and Chicago, Illinois. The purpose of the survey was to compile a statistically representative and comprehensive body of empirical information about the social, economic, and psychological status of Chicanos. Interviews were conducted in Spanish or English, depending upon the respondent's preference. Major topics covered were mental and physical health and use of health services, family background and composition, customary practices and values, language use and attitudes, employment history, social identity, group consciousness, and political opinions and participation.
Curated
Simple Crosstabs

Midlife in the United States (MIDUS 2): Cognitive Project, 2004-2006 (ICPSR 25281)

Released/updated on: 2023-02-21
Geographic coverage: United States
Time period: 2004-01-01--2006-01-01

In 1994/1995, the MacArthur Midlife Research Network carried out a national survey of over 7,000 Americans aged 25 to 74. The purpose of the study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. A description of the study and findings from it are available at the MIDUS website.

With support from the National Institute on Aging, a longitudinal follow-up of the original MIDUS samples (core sample (N = 3,487), metropolitan over-samples (N = 757), twins (N = 957 pairs), and siblings (N = 950)) was conducted in 2004-2006. Guiding hypotheses, at the most general level, were that behavioral and psychosocial factors are consequential for health (physical and mental). The purpose of the Cognitive Project was to determine how cognition is related to overall mental and physical health. Specific goals were: (1) to characterize the nature and range of midlife cognitive performance, relative to those younger and older, across multiple domains in a nationally representative sample (MIDUS); and (2) to examine the relationship between biopsychosocial factors (e.g., SES, health status, health-promoting behaviors, metabolic and cardiovascular biomarkers, depression, personality, control beliefs, stressful life events) and individual differences in cognitive functioning.

The development of a cognitive battery for the second wave of testing of the Midlife Development in the United States (MIDUS) study provided an opportunity to examine the cognitive performance of young, middle-aged and older adults from a wide range of education levels in a large-scale, national sample. As part of the Cognitive Project of the MIDUS II the Brief Test of Adult Cognition by Telephone (BTACT) (Lachman & Tun, 2008; Tun & Lachman, 2006) was administered. More information about the BTACT can be found at the Brandeis website. The BTACT represents the first comprehensive cognitive battery, including measures of speed and reaction time, to be administered by telephone to a national sample across the adult years and into later life. With a response rate of over 86 percent for the cognitive testing component of the MIDUS II, a cognitive data set of unprecedented range in terms of age, gender, socioeconomic status (SES), education, and geographic diversity was produced.

Curated
Partially restricted

Midlife in the United States (MIDUS 2): Milwaukee African American Sample, 2005-2006 (ICPSR 22840)

Released/updated on: 2024-02-26
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2005-01-01--2006-01-01
As a refinement to Midlife in the United States (MIDUS 2), 2004-2006 (ICPSR 4652), a sample of African Americans from Milwaukee was included to examine health issues in minority populations. Areas of the city of Milwaukee, Wisconsin, were stratified according to the proportion of the population that were African American. Those areas with high concentrations were sampled at higher rates than areas with lower concentrations. Area probability sampling methods were used along with population counts from the 2000 United States Census to identify potential respondents. Field interviewers screened households to determine if they contained any African American adults. There was additional screening to achieve an appropriate age/gender distribution in a manner similar to what was done for the original MIDUS sample Midlife in the United States (MIDUS 1), 1995-1996 (ICPSR 2760). Milwaukee respondents were interviewed in their homes using a Computer Assisted Personal Interview (CAPI) protocol and afterwards asked to complete a Self-Administered Questionnaire (SAQ). All measures paralleled those used in the larger MIDUS 1 and 2 samples. After successful completion of the Project 1 survey, some participants were eligible to participate in other MIDUS projects (2 through 5). Survey data was collected for 592 individuals.
Curated
Restricted

Midlife in the United States (MIDUS 3): Milwaukee African American Sample, 2016-2017 (ICPSR 37120)

Released/updated on: 2023-03-16
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2016-01-01--2017-01-01

In 2005, 592 African Americans from Milwaukee were added to the MIDUS sample to examine health issues in minority populations (for more details, see Midlife in the United States (MIDUS 2): Milwaukee African American Sample [ICPSR #22840]). Respondents were interviewed in their homes using a Computer Assisted Personal Interview (CAPI) survey protocol and asked to complete and return a Self-Administered Questionnaire (SAQ). Afterwards these individuals were eligible for participation in the same research protocol as the national MIDUS 2 sample, including cognitive, daily stress, biomarker, and neuroscience projects.

With support from the National Institute on Aging, a second wave of survey data collection on the Milwaukee sample was begun in 2016. The survey consisted of a 2.5 hour CAPI interview followed by a 45-page mailed SAQ. CAPI survey data was collected for 389 individuals, realizing a 78 percent response rate, adjusted for mortality and other eligibility criteria. Data collection for this follow-up wave largely repeated baseline assessments, with additional questions in selected areas (e.g., economic recession experiences, childhood experience with race, etc.). Following successful completion of the CAPI and SAQ protocols, individuals were eligible for participation in cognitive, daily stress, biomarker, and neuroscience projects.

Curated
Restricted

Midlife in the United States (MIDUS Refresher 1): Milwaukee African American Sample, 2012-2013 (ICPSR 36722)

Released/updated on: 2025-09-11
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2012-01-01--2013-01-01

In 2012-2013, the MIDUS Milwaukee Refresher study recruited a sample of 508 Milwaukee African American adults, aged 25 to 64, designed to replenish the Midlife Development in the United States (MIDUS 2): Milwaukee African American Sample, 2005-2006 (ICPSR 22840). This sample was also designed to increase the number of racial minorities included in the broader MIDUS study. The MIDUS Milwaukee Refresher survey employed the same assessments (demographic, psycho-social, and physical and mental health) as those assembled on the existing MIDUS sample, but with additional questions about the effect of the economic recession of 2008-09. A sample of African Americans from Milwaukee County, Wisconsin, was stratified by age, gender, and income.

Area probability sampling methods were used to identify potential respondents. Field interviewers screened households to determine if they contained any African American adults. There was additional screening to achieve an appropriate age/gender distribution in a manner similar to what was done for the original MIDUS sample (Midlife in the United States (MIDUS 1), 1995-1996 [ICPSR 2760]). Milwaukee respondents were interviewed in their homes using a 2.5-hour Computer Assisted Personal Interview (CAPI) protocol and afterwards asked to complete a self-administered questionnaire (SAQ). All measures paralleled those used in the larger MIDUS samples. In addition to successful completion of the survey, participants were asked to complete a cognitive assessment by phone. Some respondents were eligible to participate in additional MIDUS projects: daily diary assessments, biomarker assessments, and neuroscience assessments.

Curated
Restricted

Midlife in the United States (MIDUS Refresher 2): Milwaukee African American Sample, 2023-2024 (ICPSR 39583)

Released/updated on: 2025-11-19
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2023-01-01--2024-01-01

In 2012-2013, the MIDUS Milwaukee Refresher study recruited a sample of 508 Milwaukee African American adults, aged 25 to 64, designed to replenish the original MIDUS Milwaukee 1 survey that was designed to increase the number of racial minorities in 2005. The MIDUS Milwaukee Refresher survey employed the same comprehensive assessments (demographic, psycho-social, and physical and mental health) as those on the existing MIDUS sample, with additional questions about the effect of the Great Recession in 2008-09.

In 2023-2024, the second wave of survey data was collected from 327 longitudinal Refresher Milwaukee participants, including the questions (1) repeated from the Refresher 1, (2) new impacts of the COVID-19 pandemic replacing the questions related to the Great Recession in the Refresher 1, and (3) the additional questions in selected areas (e.g., AD8, IADL, family history of dementia). This new longitudinal MIDUS Refresher Milwaukee data allow examination of period effects on health and well-being related to the COVID-19 pandemic by comparing the pre-pandemic MIDUS Refresher Milwaukee 1 data with the post-pandemic MIDUS Refresher Milwaukee 2 data. Further, the longitudinal MIDUS Refresher datasets (wave 1 and wave 2) allow investigation of the two major macro-level historic events, the Great Recession and the COVID-19 pandemic, on health and well-being.

Curated
Simple Crosstabs

Midlife in the United States (MIDUS): Survey of Minority Groups [Chicago and New York City], 1995-1996 (ICPSR 2856)

Released/updated on: 2018-03-21
Geographic coverage: New York City, United States, Chicago, Illinois, New York (state)
Time period: 1995-01-01--1996-01-01
This survey of minority groups was part of a larger project to investigate the patterns, predictors, and consequences of midlife development in the areas of physical health, psychological well-being, and social responsibility. Conducted in Chicago and New York City, the survey was designed to assess the well-being of middle-aged, urban, ethnic minority adults living in both hyper-segregated neighborhoods and in areas with lower concentrations of minorities. Respondents' views were sought on issues relevant to quality of life, including health, childhood and family background, religion, race and ethnicity, personal beliefs, work experiences, marital and close relationships, financial situation, children, community involvement, and neighborhood characteristics. Questions on health explored the respondents' physical and emotional well-being, past and future attitudes toward health, physical limitations, energy level and appetite, amount of time spent worrying about health, and physical reactions to those worries. Questions about childhood and family background elicited information on family structure, the role of the parents with regard to child rearing, parental education, employment status, and supervisory responsibilities at work, the family financial situation including experiences with the welfare system, relationships with siblings, and whether as a child the respondent slept in the same bed as a parent or adult relative. Questions on religion covered religious preference, whether it is good to explore different religious teachings, and the role of religion in daily decision-making. Questions about race and ethnicity investigated respondents' backgrounds and experiences as minorities, including whether respondents preferred to be with people of the same racial group, how important they thought it was to marry within one's racial or ethnic group, citizenship, reasons for moving to the United States and the challenges faced since their arrival, their native language, how they would rate the work ethic of certain ethnic groups, their views on race relations, and their experiences with discrimination. Questions on personal beliefs probed for respondents' satisfaction with life and confidence in their opinions. Respondents were asked whether they had control over changing their life or their personality, and what age they viewed as the ideal age. They also rated people in their late 20s in the areas of physical health, contribution to the welfare and well-being of others, marriage and close relationships, relationships with their children, work situation, and financial situation. Questions on work experiences covered respondents' employment status, employment history, future employment goals, number of hours worked weekly, number of nights away from home due to work, exposure to the risk of accident or injury, relationships with coworkers and supervisors, work-related stress, and experience with discrimination in the workplace. A series of questions was posed on marriage and close relationships, including marital status, quality and length of relationships, whether the respondent had control over his or her relationships, and spouse/partner's education, physical and mental health, employment status, and work schedule. Questions on finance explored respondents' financial situation, financial planning, household income, retirement plans, insurance coverage, and whether the household had enough money. Questions on children included the number of children in the household, quality of respondents' relationships with their children, prospects for their children's future, child care coverage, and whether respondents had changed their work schedules to accommodate a child's illness. Additional topics focused on children's identification with their culture, their relationships with friends of different backgrounds, and their experiences with racism. Community involvement was another area of investigation, with items on respondents' role in child-rearing, participation on a jury, voting behavior, involvement in charitable organizations, volunteer experiences, whether they made monetary or clothing donations, and experiences living in an institutional setting or being homeless. Respondents were also queried about their neighborhoods, with items on neighborhood problems including racism, vandalism, crime, drugs, poor schools, teenage pregnancy, the existence of social networks, the frequency of contact with family members, social interaction with neighbors, sense of community, whether the respondent owned or rented their home, and the financial, legal, and medical problems of family members. A final set of questions sought respondents' assessments of their life and their expectations for the future. Additional background information on respondents includes age, ethnicity, and gender.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Arthritis (ICPSR 8060)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Audiometric Test (ICPSR 8067)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Biochemistry, Serology, Hematology, Peripheral Blood Slide, and Urinary Data (ICPSR 8069)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Chest X-ray, Pulmonary Diffusion, and Tuberculin Test Results (ICPSR 8507)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1971-01-01--1975-01-01
Information for all examined sampled persons in each of these National Health and Nutrition Examination Surveys (NHANES I) was obtained by means of a household interview, a general medical history, a 24-hour dietary intake recall interview, a food frequency interview, a food program questionnaire, a general medical examination, dental, dermatological and ophthalmological examinations, anthropometric measurement, hand-wrist x-rays (of persons ages 1-17 only) and 24 hematological, blood chemistry, and urological laboratory determinations. In addition to this information, some respondents were given more specific tests such as x-rays of the chest and hip and knee joints, audiometry, electrocariography, goniometry, spirometry, pulmonary diffusion and tuberculin tests, and additional laboratory determinations. This data set contains demographic characteristics for 6913 examinees ages 25-74 who had received the detailed examination during NHANES I. Additional information includes their lung and heart size measurements, three expert x-ray readings for lung and heart pathology, pulmonary diffusion measurements, and tuberculin test results.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Computer Measurements and Interpretations of Electrocardiograms (ICPSR 8065)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Dental (ICPSR 8066)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Dermatology (ICPSR 8063)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Dietary Frequency and Adequacy (ICPSR 8057)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Food Consumption Intake (ICPSR 8068)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: General Well-Being (ICPSR 8056)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Health Care Needs, General Medical History and Supplements on Respiratory and Cardiovascular Data (ICPSR 8061)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Medical Examination (ICPSR 8055)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Medical History (ICPSR 7987)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Near and Distant Vision (ICPSR 8062)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Ophthalmology (ICPSR 8059)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I, 1971-1975: Spirometry (ICPSR 8064)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
Curated

National Health and Nutrition Examination Survey I: Epidemiologic Follow-Up Study, 1982-1984 (ICPSR 8900)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1982-01-01--1984-01-01
The National Health and Nutrition Examination Survey I Epidemiologic Followup Study (NHEFS) originated as a joint project between the National Center for Health Statistics (NCHS) and the National Institute on Aging (NIA). The design of NHEFS, which contains follow-up data on the NHANES I cohort, 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 the obtaining of 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 respondent interview was designed to gather information on selected aspects of the subject's health history since the time of the NHANES I exam. This information included a history of the occurrence or recurrence of selected medical conditions, an assessment of behavioral, social, nutritional, and medical risk factors believed to be associated with these conditions, and an assessment of various aspects of functional status. Whenever possible, the questionnaire was designed to retain item comparability between NHANES I and NHEFS in order to measure change over time. However, questionnaire items were modified, added, or deleted when necessary to take advantage of recent improvements in questionnaire methodology. The Vital and Tracing Status file is a master file containing tracing, vital status, and demographic data for all NHEFS respondents. In addition, it provides users with information on the availability of different survey components for each respondent. For example, variables have been created to indicate whether a death certificate was received for a deceased subject, hospital records were received, or a follow-up interview was completed. The Health Care Facility Record file offers data on respondents who had reported an overnight stay in a health care facility after 1970. Information on the name and address of the facility, the date of the stay, and the reason for the stay was recorded. The Mortality Data file contains death certificate information for 1,935 NHEFS decedents. The death certificate information is for deaths occurring from 1971 to 1983.
Curated

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.