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Showing 1 – 50 of 120 results.
Curated

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Charleston Heart Study, Charleston, South Carolina, 1960-2000 (ICPSR 4050)

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

Children and Neighborhoods: Randomized Study of Mobility (Continuation-Revised) (ICPSR 36000)

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

China Health and Nutrition Survey (CHNS) (ICPSR 176)

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

Cleveland Study of the Elderly: a Follow-Up, 1984-1988 (ICPSR 6985)

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

Community Hospital Program (CHP) Access Impact Evaluation Surveys, 1978-1979, 1981 (ICPSR 8245)

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

Cross-National Equivalent File (CNEF), 1970-2009 (ICPSR 145)

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

Daily Experience in Adolescence and Biomarkers of Early Risk for Adult Health (ICPSR 35952)

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

Danish 1905 Cohort Study, 1998 (ICPSR 3960)

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

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

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

Elucidating Biopsychosocial Mediators of HIV Progression (ICPSR 35912)

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

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

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

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

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

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

Curated

Epidemiology of Depression and Help-Seeking Behavior, 1979-1983, Los Angeles, California (ICPSR 24761)

Released/updated on: 2010-03-15
Geographic coverage: Los Angeles, California
Time period: 1979-01-01--1983-01-01
This project examined the epidemiological distribution of depression in a large metropolitan area. It employed structural equation models to examine the role of stress and social support systems in the occurrence of the condition. Other analysis focused on the antecedents of help-seeking. Using a multistage cluster sample, a probability sample of 1,003 adults (aged 18 and older), a representative sample of the Los Angeles County population, was interviewed in 1979. Three follow-up interviews were conducted over the next year, with an additional fifth interview in 1983. The study has been divided into five parts identified as: Time1, Time2, Time3, Time4, and Time5. Time1 focuses on demographic information, such as marital status, employment status, education, family relationships, household information, sex, and ethnicity. The other main focus of Time1 was on respondents' general health condition and their health insurance. Time2, Time3, Time4, and Time5 focus on diagnostic aspects of depression, social support, the role of stress, in addition to asking respondents questions regarding their behavior and mood, environmental and employment changes, and major life events.
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.
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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.
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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.
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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.
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Human Aging: A Biological and Behavioral Longitudinal Study of Healthy Aged Males, 1957-1968 (ICPSR 7678)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1957-01-01--1968-01-01
This data collection contains data gathered in a longitudinal study of a sample of men aged 65 to 92 who were in good health during the first wave of the study in 1957. The chief aim of the study was to focus on the nature of the normal aging process in individuals of advanced age. The 47 study participants had not suffered from accidents, illnesses, severe emotional or personality problems, or environmental difficulties that might have led to premature aging, but 20 participants showed evidence of asymptomatic subclinical disease. This group represented the typical or "average" healthy aged individual with minimal degrees of physical pathology. Five years later, in 1962, a follow-up study was conducted with 29 of the 39 men still alive. The second follow-up, done in 1968, involved 19 of the surviving 23 men. The data are arranged in files by year: 1957, 1962, and 1968. Included are psychiatric data and medical evaluative data as well as various psychological and medical test scores (e.g., psychometric data, electroencephalographic data, audiological test data, responses to the Minnesota Multiphasic Personality Inventory (MMPI), Rorschach test results, personality test results, Inflund Selective Recall Test results, audiometric conduction findings, clinical psychology ratings, cerebral blood flow, and metabolism studies), and biographical and demographic data.
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Impact of Intimate Partner Violence on Women's Labor Force Participation in Illinois, 1999-2002 (ICPSR 4126)

Released/updated on: 2012-05-23
Geographic coverage: United States, Illinois
Time period: 1999-01-01--2000-01-01

The first goal of this study was to identify the incidence of partner violence among Temporary Assistance for Needy Families (TANF) recipients over a three-year period. The second goal of this study was to examine the impact of partner violence on women's labor force participation over time. A final goal of this research was to explore the short and longer-term consequences of victimization on women's employment and economic well-being, as well as their physical and mental health.

This study used the first three years of data from the Illinois Families Study (IFS). The first of the annual surveys was administered between November 1999 and September 2000, the second between February 2001 and September 2001, and the third between February 2002 and September 2002.

The three data files contain very similar information including such items as a household roster, housing and neighborhood characteristics, employment, literacy and skills, parenting, and children. There is also information related to the respondent's history, health, self-efficacy, life events, experiences with domestic violence, civic participation and social support, income resources, and experiences with welfare.

The Part 1 (Wave 1 Data) data file contains 1,323 cases and 942 variables. The Part 2 (Wave 2 Data) data file contains 1,183 cases and 763 variables. The Part 3 (Wave 3 Data) data file contains 1,072 cases and 778 variables.

Additional information about the Illinois Families Study (IFS) is available on the IFS Web site.

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Infant Health and Development Program (IHDP): Enhancing the Outcomes of Low Birth Weight, Premature Infants in the United States, 1985-1988 (ICPSR 9795)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1985-01-01--1988-01-01
The Infant Health and Development Program was a collaborative, randomized, longitudinal, multisite clinical trial designed to evaluate the efficacy of comprehensive early intervention in reducing the developmental and health problems of low birth weight, premature infants. An intensive intervention extending from hospital discharge to 36 months corrected age was administered between 1985 and 1988 at eight different sites. The study sample of infants was stratified by birth weight (2,000 grams or less, 2,001-2,500 grams) and randomized to the Intervention Group or the Follow-Up Group. The Intervention Group received home visits, attendance at a special child development center, and pediatric follow-up. The Follow-Up Group received only the pediatric follow-up component of the program. Measures of cognitive development, behavioral status, health status, and other variables were collected from both groups at predetermined time points. Cognitive development was assessed by the Stanford-Binet Intelligence Scale, the Bayley Mental and Motor Scales, the Peabody Picture Vocabulary Test--Revised, and the Beery-Buktenica Developmental Test of Visual Motor Integration. Behavior problems were measured using the Richman-Graham Behavior Checklist and Achenbach's Child Behavior Checklist. Health status was evaluated through the dimensions of morbidity (defined as the presence or absence of health conditions), functional status (defined by limitations in activities of daily living due to health problems), changes in physical growth, and maternal perception of the child's health. The many other variables and indices in the data collection include site, pregnancy complications, child's birth weight and gestation age, birth order, child's gender, household composition, day care arrangements, source of health care, quality of the home environment, parents' race and ethnicity, and maternal age, education, IQ, and employment.
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The Irish Longitudinal Study on Ageing (TILDA), COVID-19 Study, 2020 (ICPSR 38681)

Released/updated on: 2025-05-12
Geographic coverage: Ireland

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

The Irish Longitudinal Study on Ageing (TILDA) collects information on all aspects of health, economic and social circumstances from adults aged 50 years and over who reside in Ireland. Waves of data collection take place every two years. TILDA provides a comprehensive and accurate picture of the characteristics, needs and contributions of older persons in Ireland to inform and support improvements in policy and practice; advancements in technology and innovation; tailored education and training through an enhanced ageing research infrastructure; harmonisation with leading international research to ensure adoption of best policy and practice and comparability of results. TILDA is necessary to act as the foundation on which we can plan appropriate health, medical, social and economic policies for our older adults.

Participants were invited to complete the COVID Self Completion Questionnaire to capture their experiences during the COVID-19 pandemic. This data collection was planned in response to the pandemic and took place during the time when Wave 6 fieldwork was originally scheduled to take place.

The TILDA COVID-19 Study covers a range of aspects of the lives of adults aged 60 years and older during the first few months of the pandemic. As well as information on changes to normal day activities due to social-distancing and other restrictions on social interactions, we examine how these alterations to peoples' lives have impacted on their physical and mental wellbeing. The study also records peoples' exposure to the virus as well as that of their families and friends.

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The Irish Longitudinal Study on Ageing (TILDA), Wave 1, 2009-2011 (ICPSR 34315)

Released/updated on: 2025-05-07
Geographic coverage: Ireland
Time period: 2009-01-01--2011-01-01

This catalog record includes detailed variable-level descriptions, enabling data discovery and comparison. The TILDA Series data files, including studies 34315, 38681, 37105, 37106, 38670, 38674, are no longer available from ICPSR and NACDA at the request of the data producer due to concerns related to EU and Irish data privacy and data sharing rules. Individuals interested in obtaining TILDA data access at this time should reach out to the TILDA project directly (https://tilda.tcd.ie/data/accessing-data/).

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

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Simple Crosstabs

The Irish Longitudinal Study on Ageing (TILDA), Wave 3, 2014-2015 (ICPSR 37106)

Released/updated on: 2025-05-12
Geographic coverage: Ireland
Time period: 2014-01-01--2015-01-01

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

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

The third wave of TILDA interviews were undertaken between March 2014 and October 2015. Of the 7,445 interviewed in Wave 2, a third interview was obtained for 6,874 respondents. These consisted of the self, proxy and end-of-life interviews types. In addition to the returning respondents, 28 interviews were obtained from eligible household members who had chosen not to take part in Wave 1 or the new spouses/partners of existing respondents.

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

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Simple Crosstabs

The Irish Longitudinal Study on Ageing (TILDA), Wave 4, 2016 (ICPSR 38670)

Released/updated on: 2025-05-12
Geographic coverage: Ireland

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

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

The fourth wave of TILDA interviews were undertaken between January and December 2016. A total of 5,713 participants completed the self-interview.

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

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The Irish Longitudinal Study on Ageing (TILDA), Wave 5, 2018 (ICPSR 38674)

Released/updated on: 2025-05-12
Geographic coverage: Ireland

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

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

The fifth wave of TILDA interviews were undertaken between January and December 2018. A total of 4,978 participants completed the self-interview.

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

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Japanese General Social Survey (JGSS), 2006 (ICPSR 25181)

Released/updated on: 2010-05-06
Geographic coverage: Japan, Global
This survey was designed to solicit political, sociological, and economic information from people living in Japan. The data were collected between October 3 and November 3, 2006, using face-to-face interviews and self-administered questionnaires. Respondents were asked to give employment information for themselves and their spouses, including industry, size of employer, number of hours worked, level of job satisfaction, and time spent commuting. Respondents were also queried regarding employment information and education level of their parents when the respondent was aged 15. Several questions were asked about household composition, the type of residence, the state of respondents' finances during the last few years and compared to other Japanese families both past and present, sources of financial support, the ease of improving one's standard of living in Japan, and the use of credit cards and consumer financing. Views were also sought on divorce, the roles of each spouse, issues involving children, the responsibility of the government, and taxation issues. In terms of health, questions were asked regarding the physical and mental health of respondents and their household members, the frequency of smoking and alcohol consumption, and their views on genetically modified foods. Quality of life questions addressed the amount of satisfaction respondents received from life, and how often they participated in sports, leisure, and volunteer activities. Additional topics covered were euthanasia, the use of technology, juvenile delinquency, car ownership and usage, their level of trust in various institutions, and whether respondents belonged to religious, trade, or social service organizations. Demographic variables include age, sex, education level, employment status, occupation, labor union membership, marital status, type of residential area (e.g., urban or rural), household income, perceived social status, political orientation, political party affiliation, and religious affiliation.
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Japanese General Social Survey (JGSS), 2008 (ICPSR 30661)

Released/updated on: 2015-07-21
Geographic coverage: Asia, Japan, Global
The Japanese General Social Surveys (JGSS) Project is a Japanese version of the General Social Survey (GSS) project closely replicating the original GSS of the National Opinion Research Center at the University of Chicago. It provides data for analyses of Japanese society, attitudes and behaviors which make international comparisons possible. The objectives of the JGSS project are three-fold: (1) to collect and build cumulative data on general social surveys in Japan in a regular and consistent manner, thus enabling a time-series analysis; (2) to provide data for secondary analyses to researchers and university students in various social science fields; and (3) to provide data in a format useful for international comparative studies, research, and reports.
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Longitudinal Study of Aging Danish Twins, 1995 (ICPSR 21041)

Released/updated on: 2009-06-09
Geographic coverage: Denmark, Global
Time period: 1995-02-01--1995-04-01
The focus of the "Longitudinal Study of Aging Danish Twins (LSADT)" was on elucidating the causes of variation in survival, health, diseases, loss of abilities, and cognitive functions among the elderly and oldest-old. The LSADT was conducted every two years between 1995 and 2005 and consists of six waves. The study is comprised of interviews of elderly Danish twins aged 75 years and older (later 70 years and older). At each interview wave, the interview assessment was based on the interview used in the previous waves, which covers health, physical functioning, cognitive functioning, depression symptomatology, social factors, lifestyle characteristics, and quality of life. The self-report interview assessments were supplemented with objective indicators of physical strength and agility, behavioral speed, and pulmonary peak-flow. Biological material was also collected from the participants for future DNA analysis.
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Malawi Longitudinal Study of Families and Health (MLSFH), 1998-2021 (ICPSR 20840)

Released/updated on: 2026-03-04
Geographic coverage: Malawi, Africa
Time period: 1998-01-01--2021-01-01

The Malawi Longitudinal Study of Families and Health (MLSFH) is one of very few long-standing longitudinal cohort studies in a poor Sub-Saharan African (SSA) context. It provides a record of more than 25 years of demographic, socioeconomic, and health conditions in one of the world's poorest countries. Initial data collection began in 1998 under the Malawi Diffusion and Ideational Change Project (MDICP) to examine social networks and fertility decisions among married women and their husbands. While this initial study population is still followed, the scope of the project and population expanded to a broader focus on social and contextual determinants of health across the lifecourse in Malawi.

This collection includes Rounds 1 through 9 of the MLSFH, as well as supplemental data collections from Sexual Diaries, Migration Follow-Ups (MHM), a Biomarker Survey, Adverse Childhood Experiences (ACE), and a Benefits of Knowledge Intervention Survey. The MLSFH Data web page contains additional information and cohort profiles for all MLSFH data collections, including those not made available through ICPSR-DSDR.

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Medicare Current Beneficiary Survey, Calendar Year 1991: [United States] (ICPSR 6118)

Released/updated on: 2006-01-12
Geographic coverage: United States
This data collection is the first in a series of data releases planned from the ongoing Medicare Current Beneficiary Survey (MCBS). The MCBS is a continuous, multipurpose survey of a representative sample of the Medicare population. Sample persons are interviewed three times a year over several years to form a continuous profile of their health care experience. Field work for Round 1 began in September of 1991 and was completed in December. New rounds, which involve reinterviewing the same sample persons (or other appropriate respondents), begin every four months. Interviews are conducted regardless of whether the sample person resides at home or in a long-term care facility, using the questionnaire version appropriate to the setting. This first-round interview captured baseline information about the Medicare population, including their demographic characteristics (date of birth, sex, race, education, military service, and marital status), health status and functioning, insurance coverage, financial resources, and family support. Round 1 of the community interview, which questioned respondents living at home, also included a topical supplement on access to medical care, sources of medical care, and satisfaction with medical care.
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Mexican Health and Aging Study (MHAS) (ICPSR 142)

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

The Mexican Health and Aging Study (MHAS) is a national longitudinal study of adults 50 years and older in Mexico. The study is a collaborative effort among researchers from the Universities of Pennsylvania, Maryland, and Wisconsin in the United States, and the Instituto Nacional de Estadistica, Geografia e Informatica (INEGI) in Mexico.

The baseline survey includes a nationally representative sample of Mexicans aged 50 and over and their spouse/partners regardless of their age. A direct interview was sought with each individual, and proxy interviews were obtained when poor health or temporary absence precluded a direct interview. Topics covered include: health behavior and health status, childhood and family background, migration history, sources and amounts of income, and housing environment.

The MHAS is partly supported by the National Institutes of Health/National Institute on Aging and the INEGI in Mexico. The MHAS was designed as a longitudinal study with protocols highly comparable to the Health and Retirement Study (HRS) of the United States.

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

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

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

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

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

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

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

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

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

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

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

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

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Midlife in the United States (MIDUS 1) National Study of Daily Experiences (NSDE), 1996-1997 (ICPSR 3725)

Released/updated on: 2023-01-25
Geographic coverage: United States
Time period: 1996-03-01--1997-03-01
The National Study of Daily Experiences (NSDE) is one of the in-depth studies that are part of the MacAuthur Foundation National Survey of Midlife in the United States (MIDUS). The purpose of the NSDE is to examine the day-to-day lives, particularly the daily stressful experiences, of a subsample of MIDUS respondents. Although previous daily diary research has advanced understanding of daily stress processes, there are important limitations in these studies that are addressed in the NSDE. First, previous studies in this area have relied on small and often unrepresentative samples that limit the ability to generalize findings. For this reason, the NSDE uses a large national sample of adults in the United States. Second, previous studies of individual differences in exposure and reactivity to daily events have typically examined only one source of variability, such as personality, to the exclusion of others. The NSDE corrects this problem by utilizing the data collected in the larger MIDUS survey on a wide array of sociodemographic and psychosocial variables to study the determinants of exposure and reactivity to daily stress. Third, previous studies have failed to investigate the role of genetics in both exposure and reactivity to daily stressors. The NSDE has a subsample of identical and fraternal same-sex twin pairs in order to explore this issue. The twins were selected if twin pairs had high self-reported certainty of zygosity, had completed the MIDUS interview and questionnaires, and had mailed in their cheek cell samples. A wide range of information was obtained using the daily telephone interview. Conducting interviews for an entire year provided information about seasonal variation in daily experiences. Respondents completed an average of 7.2 of the 8 interviews resulting in a total of 10,397 days of interviews. Data collection consisted of 40 separate "flights" of interviews with each flight representing the eight-day sequence of interviews from approximately 33 respondents. The entire interview was CATI programmed, which enabled researchers to incorporate skip patterns and open ended probe questions as well as to keypunch data during the interview, allowing data cleaning throughout the data collection. Demographic information includes gender and age.
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Midlife in the United States (MIDUS 2), 2004-2006 (ICPSR 4652)

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

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

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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.

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Midlife in the United States (MIDUS 2): Daily Stress Project, 2004-2009 (ICPSR 26841)

Released/updated on: 2017-11-20
Geographic coverage: United States
Time period: 2004-01-01--2009-01-01
The Daily Stress Project of MIDUS II contains data from 2,022 respondents. These respondents include three distinct groups, all of whom completed the Project 1 Survey: (1) longitudinal (n = 794), (2) expanded (n = 1,048), and (3) Milwaukee (n = 180). The longitudinal group included individuals who participated in the Daily Stress Project at Time 1, the expanded group consisted of Time 2 participants from all MIDUS subsamples (RDD, twins, siblings) who did not participate in the Daily Stress Project at Time 1, and the Milwaukee group contained individuals who participated in the baseline MIDUS Milwaukee study, initiated in 2005. The purpose of the Daily Stress Project was to examine how sociodemographic factors, health status, personality characteristics, and genetic endowment modify patterns of change in exposure to day-to-day life stressors as well as physical and emotional reactivity to these stressors. The primary aims were to: (1) describe how the links between multiple aspects of daily stressors (e.g., frequency, content, severity) and daily physical and emotional well-being change over ten years during adulthood; (2) examine how sociodemographic factors and personality characteristics influence change in both exposure to as well as changes in physical and emotional reactivity to daily stressors; (3) investigate how exposure and reactivity to daily stressors correlate with physiological indicators of physical health and predict changes in global health reports; and (4) explore the relative genetic and environmental influences mediating change in exposure and physical and emotional reactivity to daily stressors throughout adulthood. Respondents in the NSDE are a representative subsample of the MIDUS (Midlife in the United States) survey. The Daily Stress study is Project 2 of the MIDUS longitudinal study, a national survey of more than 7,000 Americans (aged 25 to 74) began in 1994. The purpose of the larger study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. 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). A description of the study and findings from it are available on the MIDUS Web site.
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