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Alameda County [California] Health and Ways of Living Study, 1974 Panel (ICPSR 6838)

Released/updated on: 2008-01-31
Geographic coverage: United States, California
These data constitute the second wave of a survey designed to study the influence of health practices and social relationships on the physical and mental health of a typical sample of the population. The first wave (HEALTH AND WAYS OF LIVING STUDY, 1965 PANEL [ALAMEDA COUNTY, CALIFORNIA] [ICPSR 6688]) collected information for 6,928 respondents (including approximately 500 women aged 65 years and older) on chronic health conditions, health behaviors, social involvements, and psychological characteristics. The 1974 questionnaire was sent to 6,246 living subjects who had responded in 1965, and were able to be located. A total of 4,864 individuals responded in 1974. Questions were asked on marital and life satisfaction, parenting, physical activities, employment, and childhood experiences. Demographic information on age, race, height, weight, education, income, and religion was also collected. Included with this dataset is a separate file (Part 2) containing mortality data for respondents who died between the 1965 and 1974 panels, and information on nonrespondents.
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Simple Crosstabs

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

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

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

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

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

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

Curated

Americans View Their Mental Health, 1957 (ICPSR 3503)

Released/updated on: 1992-02-16
Geographic coverage: United States
In 1957, the United States Congress established the Joint Commission on Mental Illness and Health to evaluate the nation's resources for coping with both the psychological and economic problems of mental illness. The Commission sponsored a nationwide survey, which was conducted by the Survey Research Center at the University of Michigan, to assess the subjective mental health of "normal" American adults and to determine in detail how they coped with problems of adjustment. During the spring of 1957, a sample of American adults was interviewed on various areas in which problems might arise, including marriage, parenthood, employment, and general social relationships. Information about leisure time, past and present physical and mental health, and motives for affiliation, achievement, and power were also sought. Three questionnaire forms were employed, each addressed to a randomly selected third of the sample.
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Americans View Their Mental Health, 1957 and 1976: Selected Variables (ICPSR 7949)

Released/updated on: 2005-11-04
Geographic coverage: United States
This data collection contains 262 comparable variables from AMERICANS VIEW THEIR MENTAL HEALTH, 1957 (ICPSR 3503) and AMERICANS VIEW THEIR MENTAL HEALTH, 1976 (ICPSR 7948). Investigators were interested in determining whether the 1957 descriptive findings remained stable or had changed by 1976, and whether relationships established between sex, age, education, marital status, well-being, role experience, problems, and methods of dealing with stress were replicated or altered in the 1976 results. Variables focus on various areas in which problems might arise, including marriage, parenthood, employment, and general social relationships. Information about leisure time, past and present physical and mental health, and motives for affiliation, achievement, and power were also sought.
Curated

Americans View Their Mental Health, 1976 (ICPSR 7948)

Released/updated on: 2005-11-04
Geographic coverage: United States
Funded in 1975 by the National Institute of Mental Health, this data collection proposed to assess the quality of American life and to influence national policy aimed at enhancing mental health resources. This collection contains 262 variables that were also included in AMERICANS VIEW THEIR MENTAL HEALTH, 1957 (ICPSR 3503). The survey queried American adults on various areas in which problems might arise, including marriage, parenthood, employment, and general social relationships. Information about leisure time, past and present physical and mental health, and motives for affiliation, achievement, and power were also sought. In addition, extensive information was collected concerning help-seeking, the readiness of people to use professional help for mental health problems, the particular helpers they used, referral mechanisms, and evaluation of help received.
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Changing Lives of Older Couples (CLOC): A Study of Spousal Bereavement in the Detroit Area, 1987-1993 (ICPSR 3370)

Released/updated on: 2006-01-18
Geographic coverage: Detroit, United States, Michigan
Time period: 1987-01-01--1993-01-01
Changing Lives of Older Couples (CLOC) is a large multi-wave prospective study of spousal bereavement. Face-to-face baseline interviews with married older adults in the Detroit, Michigan standardized metropolitan statistical area (SMSA) were conducted between June 1987 and April 1988, and follow-up interviews were conducted at six months (Wave 1), 18 months (Wave 2), and 48 months (Wave 3) after a spouse's death. Each widowed person was assigned a same-age, same-sex, same-race matched control from the baseline sample. Controls were interviewed again at each of the three follow-ups as well. Spousal loss was monitored using state-provided monthly death records and through daily obituaries from local area newspapers. The National Death Index (NDI) and direct ascertainment of death certificates were used to confirm all deaths. The primary strength of the CLOC study is its ability to measure spousal bereavement quantitatively. For this purpose a global grief scale and six grief subscales, unique to the CLOC study, were prepared. Depression was measured for all respondents with conceptualizations of depression at each wave, as well as major depressive episodes according to DSM-III-R criteria. Other survey questions focused on the social, psychological, and physical functioning of older adults (e.g., demographic, financial, housing, life events, social support, work and activities, marriage and family, religion, health and well-being). For a portion of the respondents (n = 432) in what was referred to as the MacBat study, various biomedical indicators (motor and cognitive, physiological, endocrinological and biochemical) were measured as well. The CLOC study has been subset into four primary datasets. The core, or Complete, dataset (Part 1) contains all available variables from all four waves of the study (Baseline, W1, W2, W3) for the entire sample of 1,532 persons (excluding clones, the 13 individuals who initially participated in a follow-up interview as control subjects, but who subsequently experienced spousal loss, and then entered the study as bereaved subjects). The Baseline Only dataset (Part 2) contains all variables collected at the baseline interview (V1-V957) for the entire sample of 1,532 persons (excluding clones). It also contains the baseline physiological variables (V20001-V20991) from the subsample of 432 persons who also participated in the baseline MacBat portion of the study. The Widowed-Controls Only datasets (Parts 3 and 4) contain all available data from anyone who participated as either a widowed person or a control subject in at least one of the three CLOC follow-up surveys (W1, W2, W3). This dataset is available with or without clones (n = 558 subjects including clones, and n= 545 excluding clones). The Couples Only dataset (Part 5) contains data collected from both the husband and the wife of 423 couples (n = 846) and includes all available data from all four waves of data collection (baseline, W1, W2, W3). Each record contains data for the wife (the "V" variables) and data for the husband (the "S" variables). A Clones Only dataset (Part 6) is also included for the advanced user and contains data for the 13 individuals identified as clones. A case-control matched design is recommended for analysis of the Clones Only data.
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Charleston Heart Study, Charleston, South Carolina, 1960-2000 (ICPSR 4050)

Released/updated on: 2021-06-03
Geographic coverage: Charleston (South Carolina), United States, South Carolina
Time period: 1960-01-01--2000-01-01
The Charleston Heart Study (CHS) represents data collected over a 41-year period (1960-2000) in order to provide an understanding of the natural progression of aging in a community-based cohort. In 1960 the CHS began enrolling a random selection of community residents who were 35 years of age and older -- including men and women, Black and White. The primary hypothesis of the original study was to investigate racial differences in the manifestation and risk factors for coronary disease. Over the ensuing 40+ years, a variety of outcome measurements were incorporated into the re-examination of the participants, including psychosocial, behavioral, aging, and functional measures. As a longitudinal study, the CHS allows for the study of the risk factors, correlates, and consequences of aging, while simultaneously allowing for exploration of racial disparity in the manifestation of putative risk factors and outcomes. The CHS began with baseline data and added a special cohort of Black men. In subsequent years three separate follow-ups were conducted. The data include death information for respondents and background characteristics (age, race, sex, occupation, education, and marital status).
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CRELES-3: Costa Rican Longevity and Healthy Aging Study - Wave 3, 2009 (Costa Rica Estudio de Longevidad y Envejecimiento Saludable, Ronda 3) (ICPSR 35250)

Released/updated on: 2025-04-29
Geographic coverage: Central America, Global, Costa Rica, Latin America
Time period: 2009-02-01--2010-01-01
The Costa Rican Longevity and Healthy Aging Study (CRELES, or Costa Rica Estudio de Longevidad y Envejecimiento Saludable) is a nationally representative longitudinal survey of health and lifecourse experiences. CRELES-3 refers to the third wave of visits in this longitudinal study. The first two waves are available as ICPSR 26681 and ICPSR 31263. The original sample (Wave 1) was drawn from Costa Rican residents in the 2000 population census who were born in 1945 or before, with an over-sample of the oldest age range (ages 95 and over). A total of 2,827 Costa Ricans ages 60 and over participated in 2005. The second wave revisited the same participant group. The data presented here represent the third wave of fieldwork that was conducted from February 2009 to January 2010, with 1,855 surviving and contacted participants. CRELES data include factors contributing to older adults' length and quality of life. Among these data are self-reported physical health, psychological health, living conditions, health behaviors, health care utilization, social support, and socioeconomic status. Objective health indicators typically included in this series are anthropometrics, observed mobility, and biomarkers from fasting blood (such as cholesterol, glycosylated hemoglobin, and C-reactive protein). However, the third wave did not collect blood. Data regarding participants' deaths and conditions surrounding death were collected from interviews of surviving family members and are included in Wave 2 and Wave 3 data files. The collection includes a tracking file (Dataset 13) which links participants across the three waves and includes sampling weights. Demographic data included in the study include age during each wave, sex, marital status, education, number of children, type of housing, and geographic region in Costa Rica. Some elements of the demographic data are found only in Wave 1 and require linking the CRELES-3 data files with ICPSR 26681.
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Health and Ways of Living Study, 1965 Panel: [Alameda County, California] (ICPSR 6688)

Released/updated on: 2013-12-04
Geographic coverage: United States, California
The purpose of this survey was to explore the influence of health practices and social relationships on the physical and mental health of a typical sample of the population in Alameda County, California. The information obtained for the 6,928 respondents (including approximately 500 women aged 65 years and older) covers chronic health conditions, health behaviors, social involvements, and psychological characteristics. Questions were asked about marital and life satisfaction, parenting, physical activities, employment, and childhood experiences. Demographic variables include data on respondetns' age, race, height, weight, education, income, and religion.
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Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE) Disabling Process Study: 2001-2002 (ICPSR 36203)

Released/updated on: 2015-11-13
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2001-01-01--2002-01-01
This collection sought to examine relationships among components of the Enabling-Disabling Model as presented in the 1997 Institute of Medicine report, Enabling America: Assessing the Role of Rehabilitation Sciences. The Enabling-Disabling Model includes the following primary components: pathology, impairment, functional limitation, disability, and quality of life. In this model, disability is proposed to be influenced by pathology, impairment, and functional limitation. Disability is also seen as a function of the interaction between the person and the environment. This investigation examined relationships within the Enabling-Disabling Model in a random sample of Mexican American older adults. The specific aims were to: (1) examine the interrelationships among the components of the Enabling-Disabling Model over time in older Mexican-American adults, and (2) use components of the Enabling-Disabling Model to expand our understanding of the natural history of aging and to predict health related quality of life in older Mexican American adults. Data were collected from 621 older adults who were participating in the Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE). Only subjects who were physically capable of safely completing the muscle strength measures were included in the study. Baseline interviews were collected on this subsample in 2001 during Wave 4 (ICPSR 4314) of the larger Hispanic EPESE study. Follow-up data were collected in 2002 from 551 participants. Data were collected on information such as respondents' health status, activities of daily living and ability to perform tasks. Demographic and background information include age, relationship status, gender, marital status and household composition.
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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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The Longitudinal Study of Older People in Anhui Province, China, 2001-2003 (ICPSR 36388)

Released/updated on: 2016-05-16
Geographic coverage: China (Peoples Republic), Global
Time period: 2001-01-01--2003-01-01

The Longitudinal Study of Older People in Anhui Province, China, 2001-2003 examined the physical and psychological well-being of older adults (aged 60 and above) living in rural Anhui Province, China. The original purpose of the study was to study the impact of rural-to-urban migration on the physical and psychological well-being of older adults left behind in rural villages by their adult children.

This collection contains two parts; Part 1: 2001 Survey and Part 2: 2003 Follow-up Survey. Similar Questions were asked in the two surveys to assess intergenerational transfers and relations of the respondents, including social support, caregiving, emotional cohesion, remittances, grandchild care, and filial piety. Respondents were also asked about their health status (physical, emotional, and cognitive). Demographic information includes age, sex, marriage status, and education.

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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): Biomarker Project, 2004-2009 (ICPSR 29282)

Released/updated on: 2025-06-18
Geographic coverage: United States
Time period: 2004-07-30--2009-05-31

The Biomarker study is Project 4 of the Midlife in the United States (MIDUS) longitudinal study, a national survey of more than 7,000 Americans (aged 25 to 74) begun 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 (NIA), 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 website.

The Biomarker Project (Project 4) of MIDUS 2 contains data from 1,255 respondents. These respondents include two distinct subsamples, all of whom completed the Project 1 Survey: (1) longitudinal survey sample (n = 1,054) and (2) Milwaukee sample (n = 201). The Milwaukee group contained individuals who participated in the baseline MIDUS Milwaukee study, initiated in 2005. The purpose of the Biomarker Project (Project 4) was to add comprehensive biological assessments on a subsample of MIDUS respondents, thus facilitating analyses that integrate behavioral and psychosocial factors with biology. The broad aim is to identify biopsychosocial pathways that contribute to diverse health outcomes. A further theme is to investigate protective roles that behavioral and psychosocial factors have in delaying morbidity and mortality, or in fostering resilience and recovery from health challenges once they occur. The research was not disease-specific, given that psychosocial factors have relevance across multiple health endpoints.

Biomarker data collection was carried out at three General Clinical Research Centers (at UCLA, University of Wisconsin, and Georgetown University). The biomarkers reflect functioning of the hypothalamic-pituitary-adrenal axis, the autonomic nervous system, the immune system, cardiovascular system, musculoskeletal system, antioxidants, and metabolic processes. Our specimens (fasting blood draw, 12-hour urine, saliva) allow for assessment of multiple indicators within these major systems. The protocol also included assessments by clinicians or trained staff, including vital signs, morphology, functional capacities, bone densitometry, medication usage, and a physical exam. Project staff obtained indicators of heart-rate variability, beat to beat blood pressure, respiration, and salivary cortisol assessments during an experimental protocol that included both a cognitive and orthostatic challenge. Finally, to augment the self-reported data collected in Project 1, participants completed a medical history, self-administered questionnaire, and self-reported sleep assessments. For respondents at one site (UW-Madison), objective sleep assessments were also obtained with an Actiwatch(R) activity monitor.

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

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

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

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

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

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

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Midlife in the United States (MIDUS 3): Biomarker Project, 2017-2022 (ICPSR 38837)

Released/updated on: 2023-11-14
Time period: 2017-04-01--2022-05-01

The Biomarker Project is one of multiple projects that comprise the MIDUS 3 (M3) "Integrative Pathways to Health and Illness" study. For the past two decades, the overarching objective of MIDUS has been to investigate linkages between sociodemographic, psychosocial, behavioral, and neurobiological variables to account for unfolding profiles of morbidity and mortality across the decades of adult life as well as the maintenance of good health and functional capacities. The study has facilitated analyses that pay attention simultaneously to age, gender, race, and socioeconomic variation in how psychosocial and neurobiological variables are linked. In addition, the M3 data permit longitudinal assessment of the impact of ongoing historical events, such as the 2008 economic recession, on the health of diverse-aged adults, which was also included in the MIDUS Refresher 1 (MR1) assessments. M3 included recruitment of additional twins to facilitate genomic analysis.

The M3 Biomarker Project (P4) includes assessment of multiple indicators of physiological regulation/dysregulation and health according to the basic protocol implemented in the MR1 study, which repeated and expanded the M2 biomarker protocol. The M3 protocol included bone density and body composition assessments at all sites and expansion of Actigraphy, Ankle Brachial Index (ABI) and Gait assessments to all three sites. Data were collected during a 24-hour stay at one of three Clinical Research Units (CRU).

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Midlife in the United States (MIDUS 3): Daily Diary Project, 2017-2019 (ICPSR 38529)

Released/updated on: 2022-09-22
Geographic coverage: United States
Time period: 2017-01-01--2019-12-31
The National Study of Daily Experiences (NSDE) is one of the in-depth studies that are part of the Midlife in the United States (MIDUS) longitudinal study of health and well-being. Known within the MIDUS study as the Daily Diary Project (2), the purpose of the NSDE is to examine the day-to-day lives, particularly the daily stressful experiences, of a subsample of MIDUS respondents. The primary aims of the MIDUS 3 Daily Diary project 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. During 2017-2019, the Daily Diary project collected data on a subsample of the MIDUS 3 survey sample, including cases from the MIDUS Milwaukee sample. A total of 1,236 respondents completed Daily Diary interviews. A subset of these respondents provided 4-days worth of saliva samples that provided data on cortisol and alpha amylase.
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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.

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Midlife in the United States (MIDUS 3): Neuroscience Project, 2017-2022 (ICPSR 38862)

Released/updated on: 2025-04-15
Geographic coverage: United States
Time period: 2017-01-01--2022-01-01

From 2004-2009, an initial follow-up of the original Midlife Development in the United States samples (MIDUS 2) was conducted with expansion of the protocol to include Neuroscience Project data collection and a sample of Black Americans from Milwaukee, WI. The MIDUS Neuroscience Project performed a second follow-up from 2017-2022 of the MIDUS Main and Milwaukee samples (MIDUS 3) on a subsample of those who completed the MIDUS 3 Survey and Biomarker Projects.

The goal was to examine indices of brain aging, function, and structure with a focus on the brain circuitry associated with individual differences in affective style, and to characterize the peripheral consequences of these central profiles for biological systems that may be relevant to health. The primary aims were to: (1) characterize individual differences in emotional reactivity, recovery, and sustaining processes using corrugator and zygomatic electromyography and eyeblink startle magnitude, (2) characterize individual differences in brain morphology and connectivity using structural magnetic resonance imaging (MRI) and diffusion weighted imaging (DWI) (3) characterize individual differences in functional activity within the neural circuitry of emotion using task and resting state fMRI, (4) calculate brain age, and (5) test the ability of these indices to predict the comprehensive array of health, wellbeing, cognitive, psychological, social, and life challenge factors assessed in other MIDUS projects. To probe individual differences in emotional processes, psychophysiological and fMRI measures of emotional responses to the presentation of negative, positive, and neutral pictures, and these same measures during a post-picture period were examined.

Emotion-influenced memory was assessed at both the psychophysiological and imaging sessions: (1) Free recall of the presented affective pictures at the end of the psychophysiological session. (2) Memory and likeability ratings for neutral faces paired with the affective pictures in the imaging task. Finally, selected tasks from the CANTAB assessed affective biases and cognitive processes important for emotion regulation.

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Midlife in the United States (MIDUS): Boston Longitudinal Study (BOLOS) of Cognition in Midlife, 1995-2008 (ICPSR 3596)

Released/updated on: 2017-10-13
Geographic coverage: United States, Massachusetts, Boston
Time period: 1995-10-01--1997-07-01, 2004-12-01--2008-07-01

This survey of adult management tasks began in 1995 as part of a larger national project (MIDUS) to investigate the patterns, predictors, and consequences of midlife development in the areas of physical health, psychological well-being, and social responsibility. Conducted in Boston, the survey was designed to examine how adults manage tasks in three domains of life -- work, family, and health. Further goals were to describe the subjective experience of goal attainment in midlife and to link it with objective measures of short-term longitudinal changes and cognitive functioning. During the national study, the Boston area was intentionally oversampled in order to create a subset to be used for in-depth study of management processes in midlife.

The Boston study began six months after the national study, and consisted of three interviews: a 30-minute phone interview followed by a 20-minute mail questionnaire (Time 1), a 90-minute in-person combination of cognitive tests, cortisol testing, photograph taking, and interview (Time 2), and a 30-minute phone interview (Time 3), conducted at six-month intervals. The focus was on projects related to family, work, and health that participants were working on during the period of the study. Each successive interview investigated participants' assessments of their progress in the present, recollection of six months in the past, and prediction six months into the future. Two waves of data collection were completed for this study. There were 151 respondents who participated in the first wave, 151 respondents who participated in both waves, and 26 additional respondents who participated in the second wave of data collection.

At Time 1, participants generated a list of two important family, work, and health tasks, then chose one of each as the most important in that domain. For each of the most important tasks, questions were asked about deadlines, whether participants were doing tasks because they had to do them, felt that they should do them, or chose to do them, and whether participants were doing tasks for themselves, others, or both. All six projects were ranked according to importance, and participants divided all their time into percentages spent on family, work, and health. The majority of questions on the mail questionnaire at Time 1 were taken from the Midlife Development Inventory (MIDI), the instrument created for the national study.

Respondents were asked to rate their control over health, to make assessments about present, past, and future health, to list any serious illnesses, and to indicate their physical health status. Study participants also rated their mental health, and discussed stressful life events in the last six months for self, spouse/significant other, parents, and children. Other questions focused on depression, mastery and constraints, community involvement, family, work, and life satisfaction. Scales used included the Ryff Well-Being Scales, the Eysenck Personality Inventory, the Staudinger and Baltes Wisdom Scale (1995), and the Ways of Coping Scale.

Time 2 was done in-person, and included a 50-minute series of cognitive tests followed by a 40-minute interview. The cognitive testing consisted of nine measures of cognitive ability completed in the following order: WAIS Forward Digit Span, WAIS Backward Digit Span, WAIS Vocabulary, counting backwards test, letter comparison test, dual-task test involving the counting backwards and letter comparison tests, WAIS Digit Symbol, Schaie-Thurston Letter Series, and Raven's Advanced Progressive Ma Matrices.

The Time 2 interview began with a series of questions asking about each of the family, work, and health tasks elicited from the participants in Time 1. Many questions were repeated from the MIDI including rating physical health, family life, work situation, and life overall, rating physical and mental health from poor to excellent, and a measure of stressful life events in the last six months for self, spouse/significant other, parents, and children. Participants were asked to rate how old they felt and how old they looked and to indicate their total yearly household income. Lastly, a series of open-ended questions asked about best and worst aspects of family, work, and health, how participants managed their daily life, the most challenging aspect of life and how it was managed, and what participants found most helpful in carrying out their daily life. Photographs were taken of participants at the conclusion of the interview.

Time 3 asked again about each of the most important family, work, and health tasks elicited from the participants in Time 1. Newly developed questions asked participants about ideas related to middle age, including when the participant believed middle age begins and ends, whether the participant was younger than, in, or older than middle age, the biggest changes in middle age, the best and worst aspects of middle age, whether the participant knew anyone who had had a "midlife crisis," and whether he or she would have or had had a midlife crisis. Participants were asked to rate how often they had problems and how often things went well with respect to a list of 26 domains, and how much stress and how much control they had in these domains. Lastly, participants were asked whether they had ever returned to a degree-oriented educational program after being out of school for five or more years, whether they were presently taking classes to further their education, and whether being a participant in the study had influenced the ways they thought about their family, work, and health projects.

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Midlife in the United States (MIDUS): Psychological Experiences Follow-Up Study, 1998 (ICPSR 2911)

Released/updated on: 2018-03-23
Geographic coverage: United States
Time period: 1998-03-01--1998-09-01
The Midlife in the United States (MIDUS) data collection was a collaborative, interdisciplinary investigation of patterns, predictors, and consequences of midlife development in the areas of physical health, psychological well-being, and social responsibility. This component of the first MIDUS data collection was designed to understand popular metaphors of personal turmoil and change, such as the "midlife crisis," the "change of life," the "empty nest syndrome," and more. The primary objective of the Psychological Experiences Study was to explore how adults perceive psychological change in their lives. The study used questions derived from John Clausen's definition of "turning points" and other sources to collect data on self-perceived psychological changes involving work, important relationships, views about the self and dreams, beliefs about the midlife crisis, and recent major life events and transitions. This study was a random telephone follow-up of 724 respondents of the original MIDUS random-digit-dial sample. Part 1 of this collection consists of the quantitative data obtained from the telephone interviews. Part 2 includes the open-ended responses to selected questions from the telephone interviews.
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Midlife in the United States (MIDUS Refresher 1), 2011-2014 (ICPSR 36532)

Released/updated on: 2025-09-17
Geographic coverage: United States
Time period: 2008-01-01--2009-01-01, 2011-01-01--2014-01-01

In 2011-2014, the MIDUS Refresher study recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the five decadal age groups of the MIDUS 1 baseline survey [ICPSR 2760]. The MIDUS Refresher survey employed the same comprehensive assessments as those assembled on the existing MIDUS sample, but with additional questions about the effect of the economic recession of 2008-09.

The MIDUS Refresher collection is split into two datasets: Aggregate Data and Coded Text Data. The Coded Text Dataset provides coded responses to open-ended question items in the Aggregate Dataset. The survey data collection (Project 1) [MIDUS, ICPSR 2760] consisted of a 30-minute phone interview followed by two 50-page mailed self-administered questionnaires. Survey data were collected on demographic, psycho-social, and physical and mental health information. This new crosssectional MIDUS sample allows the examination of period effects on health (mental and physical) related to the economic recession by comparing the pre-recession MIDUS 1 sample with the post-recession MIDUS Refresher sample. A further objective of the MIDUS Refresher sample was to strengthen cross-project analyses in MIDUS by increasing the sample sizes available for testing hypotheses dealing with the interplay of key factors (e.g., socioeconomic status, gender, psychosocial factors, biological factors) in mid- and laterlife health. To that end, the MIDUS Refresher sample followed the same multi-disciplinary protocol established in the main MIDUS sample, in that after completing the survey protocol respondents were asked to complete a cognitive assessment by phone (Project 3) [MIDUS 3, ICPSR 36346] and later became eligible to participate in daily diary assessments (Project 2) [MIDUS 2, ICPSR 4652] biomarker assessments (Project 4) [MIDUS 2: Biomarker Project, ICPSR 29282] and neuroscience assessments (Project 5) [MIDUS 2: Neuroscience Project, ICPSR 28683].

The MIDUS Refresher was funded by the National Institute on Aging as two separate but related efforts: The MIDUS Refresher younger decades (MRY), was fielded in November, 2011, and recruited over 2,100 new participants aged 25 to 54; Funding was later added for the MIDUS Refresher older decades (MRO), which was fielded in June, 2013 and recruited over 1,400 new participants aged 55 to 74.

Demographic variables include age, sex, gender, race, religion, and marital status.

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Midlife in the United States (MIDUS Refresher 1): Cognitive Project, 2011-2014 (ICPSR 37081)

Released/updated on: 2021-04-06
Geographic coverage: United States
Time period: 2011-01-01--2014-01-01

The Midlife in the United States (MIDUS Refresher): Cognitive Project, 2011-2014 collection includes data collected as part of the MIDUS Refresher study. The MIDUS Refresher study (2011-2014, ICPSR 36532) recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the five decadal age groups of the MIDUS 1 baseline survey (ICPSR 2760). Participants in the MIDUS Refresher survey were recruited for the Brief Test of Adult Cognition via Telephone (BTACT) interview. All recruited participants who completed the initial telephone interview were invited to complete the questionnaires, and, whether or not they returned the questionnaires, were invited to participate in the Cognitive Interview. In addition to the national MIDUS Refresher sample, respondents to the MIDUS Milwaukee Refresher sample (see ICPSR 36722) were also eligible to participate in the BTACT interview. From February, 2012, through September, 2014, respondents completed the cognitive interview. For the Cognitive Project MIDUS Refresher BTACT data were collected from 2,763 MIDUS Refresher participants.

The BTACT is 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. It includes seven subtests: word list recall immediate, word list recall delayed, backward digit span, number series, counting backward speed task, category fluency, and an attention switching reaction time task. The Refresher cognitive project provides a rich data set to examine individual differences in cognitive functioning with a diverse national sample in terms of age, sex, socioeconomic status (income, education) and geographical region.

Demographic variables in this collection include sex and age

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Midlife in the United States (MIDUS Refresher 1): Daily Diary Project, 2012-2014 (ICPSR 37083)

Released/updated on: 2020-12-14
Geographic coverage: United States
Time period: 2012-10-01--2014-11-01

The MIDUS Refresher Daily Diary Project (aka National Study of Daily Experiences or NSDE) contains data from 782 respondents. 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:

  1. To 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. To 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. To investigate how exposure and reactivity to daily stressors correlate with physiological indicators of physical health and predict changes in global health reports; and
  4. To explore the relative genetic and environmental influences mediating change in exposure and physical and emotional reactivity to daily stressors throughout adulthood.

The Daily Diary study is comprised of a subsample of the MIDUS (Midlife in the United States) Refresher, a national survey of nearly 3,600 Americans (aged 25 to 75) conducted during 2011-2014. The MIDUS Refresher survey was designed to replenish the original MIDUS 1 baseline cohort and allow the examination of period effects on health (mental and physical) related to the economic recession by comparing the pre-recession MIDUS 1 sample with the post-recession MIDUS Refresher sample. Guiding hypotheses, at the most general level, were that behavioral and psychosocial factors are consequential for health (physical and mental).

Demographic variables in this collection include sex and age.

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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.

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Midlife in the United States (MIDUS Refresher 2), 2022-2024 (ICPSR 39670)

Released/updated on: 2026-02-10
Geographic coverage: United States
Time period: 2022-01-01--2024-12-31

In 2011-2014, the MIDUS Refresher study recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the age groups of the MIDUS 1 baseline survey in 1995. The MIDUS Refresher survey employed the same comprehensive assessments as existing MIDUS sample, with additional questions about the effect of the Great Recession in 2008-09. Survey data were collected on demographic, psychosocial, and health and well-being information.

In 2022-2024, the second wave of survey data (MIDUS Refresher 2) was collected on longitudinal 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 data allow examination of period effects on health and well-being related to the COVID-19 pandemic by comparing the pre-pandemic MIDUS Refresher 1 data with the post-pandemic MIDUS Refresher 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 across various population groups in the U.S.

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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.

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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.
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National Longitudinal Study of Adolescent to Adult Health (Add Health), 1994-2008 [Restricted Use] (ICPSR 35249)

Released/updated on: 2014-06-24
Geographic coverage: United States
The National Longitudinal Study of Adolescent to Adult Health (Add Health) is a longitudinal study of a nationally representative sample of adolescents in grades 7-12 in the United States during the 1994-95 school year. The Add Health cohort has been followed into young adulthood with four in-home interviews, the most recent in 2008, when the sample was aged 24-32. Add Health combines longitudinal survey data on respondents' social, economic, psychological and physical well-being with contextual data on the family, neighborhood, community, school, friendships, peer groups, and romantic relationships, providing unique opportunities to study how social environments and behaviors in adolescence are linked to health and achievement outcomes in young adulthood. The fourth wave of interviews expanded the collection of biological data in Add Health to understand the social, behavioral, and biological linkages in health trajectories as the Add Health cohort ages through adulthood.
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National Survey of Black Americans, 1979-1980 (ICPSR 8512)

Released/updated on: 2005-11-04
Geographic coverage: United States
Time period: 1979-01-01--1980-01-01
The purpose of this data collection is to provide an appropriate theoretical and empirical approach to concepts, measures, and methods in the study of Black Americans. The questionnaire was developed over two years, with input from social scientists, students, and a national advisory panel of Black scholars. The final instrument encompasses several broad areas related to Black American life. The study explores neighborhood-community integration, services, crime and community contact, the role of religion and the church, physical and mental health, and self-esteem. It also examines employment, the effects of chronic unemployment, the effects of race on the job, and interaction with family and friends. In addition, the survey provides information on racial attitudes, race identity, group stereotypes, and race ideology. Demographic variables include education, income, occupation, and political behavior and affiliation.
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National Survey of Black Americans, Waves 1-4, 1979-1980, 1987-1988, 1988-1989, 1992 (ICPSR 6668)

Released/updated on: 2005-11-04
Geographic coverage: United States
The purpose of this data collection was to provide an appropriate theoretical and empirical approach to concepts, measures, and methods in the study of Black Americans. Developed with input from social scientists, students, and a national advisory panel of Black scholars, the survey investigates neighborhood-community integration, services, crime and community contact, the role of religion and the church, physical and mental health, self-esteem, life satisfaction, employment, the effects of chronic unemployment, the effects of race on the job, interaction with family and friends, racial attitudes, race identity, group stereotypes, and race ideology. Demographic variables include education, marital status, income, employment status, occupation, and political behavior and affiliation.
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National Survey of Families and Households, Wave 2: 1992-1994, [United States] (ICPSR 6906)

Released/updated on: 2018-06-06
Geographic coverage: United States
Time period: 1992-07-01--1994-08-01

The National Survey of Families and Households (NSFH), Wave 2 1992-1994, a longitudinal population-based survey of families and households in the United States, investigates the causes and consequences of changes in American family and household structure. This is the second wave of a three part survey. The current study, NSFH Wave 2, is the second follow up and was conducted in 1992-1994. The sample included all NSFH Wave 1 main respondents and spouse/partner with focal children and all other NSFH Wave 1 main respondents ages 45 and over in 2000, as well as their NSFH Wave 1 spouse/partner.

The Wave 2 survey included the following components: (1) an interview of all surviving members of the original sample via face-to-face personal interview, (2) a personal interview with the current spouse or cohabiting partner almost identical to the interview with the main respondent, (3) a personal interview with the original spouse or partner of the primary respondent in cases where this relationship had ended, (4) a telephone interview with "focal children" who were originally aged 13-18 in Wave 1, (5) a short telephone interview with "focal children" who were originally aged 5-12 in Wave 1, (6) short proxy interviews with a surviving spouse or other relative in cases where the original respondent had died or was too ill to interview, and (7) a telephone interview with a randomly-selected parent of the main respondent. Demographic information collected includes sex, age, marital status, education, and employment

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National Survey of Families and Households, Wave 3: 2001-2003, [United States] (ICPSR 171)

Released/updated on: 2018-06-06
Geographic coverage: United States
Time period: 2001-01-01--2003-01-01
The National Survey of Families and Households (NSFH) is a longitudinal population-based survey series that seeks to examine the causes and consequences of change in American family and household structures. NSFH Wave 3 was conducted in 2001-2003 and represents the third follow-up survey. The Wave 3 sample included interviews with all NSFH Wave 1 main respondents and spouse/partner with a focal child eligible for the NSFH Wave 2 interviews, interviews with these focal children (now aged 18-34), and interviews with all other NSFH Wave 1 main respondents aged 45 and over in the year 2000, as well as their NSFH Wave 1 spouse/partner.
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National Survey of the Japanese Elderly, 1987 (ICPSR 6842)

Released/updated on: 2005-11-04
Geographic coverage: Japan, Global
This survey, which is partially comparable in content to AMERICANS' CHANGING LIVES: WAVES I, II, III, AND IV, 1986, 1989, 1994, AND 2006 (ICPSR 4690) and the NATIONAL HEALTH INTERVIEW SURVEY, 1984: SUPPLEMENT ON AGING (ICPSR 8659), was designed for use in cross-cultural analyses of aging in the United States and Japan. The survey has nine sections: demographics (age, sex, marital status, education, employment), social integration (interpersonal contacts, social supports), health status (attempts to measure limitations on daily life and activities, health conditions, level of physical activity), subjective well-being and mental health status (life satisfaction, morale), psychological indicators (life events, locus of control, self-esteem), financial situation (financial status), memory (measures of cognitive functioning), and interviewer observations (assessments of respondents).
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National Survey of the Japanese Elderly, 1990 (ICPSR 3407)

Released/updated on: 2005-11-04
Geographic coverage: Japan, Global
This survey, a follow-up to the original Wave I survey undertaken in 1987 (ICPSR 6842), was designed to create a panel dataset for use in cross-cultural analyses of aging in Japan and the United States. It was created to match as closely as possible with Wave I, while also allowing for growth in specific areas of interest. In addition, the survey was designed to be partially comparable in content with AMERICANS' CHANGING LIVES: WAVES I, II, III, AND IV, 1986, 1989, 1994, AND 2006 (ICPSR 4690) and the NATIONAL HEALTH INTERVIEW SURVEY, 1984: SUPPLEMENT ON AGING (ICPSR 8659). The survey has nine sections: demographics (age, sex, marital status, education, employment), social integration (interpersonal contacts, social supports), health status (limitations on daily life and activities, health conditions, level of physical activity), subjective well-being and mental health status (life satisfaction, morale), psychological indicators (life events, locus of control, self-esteem), financial situation (financial status), memory (measures of cognitive functioning), and interviewer observations (assessments of respondents).
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National Survey of the Japanese Elderly, 1993 (ICPSR 4145)

Released/updated on: 2005-03-15
Geographic coverage: Japan, Global
This survey, a follow-up to the original Wave I and Wave II surveys undertaken in 1987 (ICPSR 6842) and 1990 (ICPSR 3407), was designed to create a panel dataset for use in cross-cultural analyses of aging in Japan and the United States. It was created to match as closely as possible with Wave I, while also allowing for growth in specific areas of interest. In addition, the survey was designed to be partially comparable in content with AMERICANS' CHANGING LIVES: WAVES I, II, AND III, AND IV, 1986, 1989, 1994, AND 2006 (ICPSR 4690) and the NATIONAL HEALTH INTERVIEW SURVEY, 1984: SUPPLEMENT ON AGING (ICPSR 8659). The survey has nine sections: demographics (age, sex, marital status, education, employment), social integration (interpersonal contacts, social supports), health status (limitations on daily life and activities, health conditions, level of physical activity), subjective well-being and mental health status (life satisfaction, morale), psychological indicators (life events, locus of control, self-esteem), financial situation (financial status), memory (measures of cognitive functioning), and interviewer observations (assessments of respondents).
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National Survey of the Japanese Elderly, 1996 (ICPSR 26621)

Released/updated on: 2010-10-04
Geographic coverage: Japan, Global
This survey is the fourth wave of a study conducted jointly by the Institute of Gerontology at the University of Michigan (IoG) and the Tokyo Metropolitan Institute of Gerontology (TMIG). Previous waves of data were collected in November of 1987 (ICPSR 6842), November of 1990 (ICPSR 3407), and November of 1993 (ICPSR 4145). The survey was designed to create a panel dataset for use in cross-cultural analyses of aging between the United States and Japan. This is the first, and to date only, panel study designed for cross-cultural analyses on aging. Therefore, this survey represents a unique contribution to the gerontological archives for cross-cultural aging. The survey was designed to match as closely as feasible the Wave I instrument, however it had to allow for dynamic growth in areas of interest. The Wave I instrument was designed to be at least partially comparable to many pre-existing surveys of the aged. Specifically it incorporates components from the American's Changing Lives surveys conducted by Jim House et al. of the Institute for Social Research (ISR) at the University of Michigan and the 1984 National Health Interview Survey Supplement on Aging.
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Quality of American Life, 1971 (ICPSR 3508)

Released/updated on: 1992-02-16
Geographic coverage: United States
The purpose of this study was to survey Americans about perceived quality of life by measuring perceptions of their socio-psychological condition, their needs and expectations from life, and the degree to which those needs were satisfied. The data were collected via personal interviews from a nationwide probability sample of 2,164 persons 18 years of age and older during the summer of 1971. Closed and open-ended questions were used to probe respondents' satisfactions, dissatisfactions, aspirations, and disappointments in a variety of life domains, such as dwelling/neighborhood, local services (e.g., police, roads, and schools), public transportation, present personal life, life in the United States, education, occupation, job history/expectation, work life, housework, leisure activities, organizational affiliations, religious affiliation, health problems, financial situation, marriage (including widowhood, divorce, and separation), children/family life, and relationships with family and friends. In addition to broad questions about satisfaction with each of these domains and their importance to the respondents, specific sources of gratification and frustration are explored. Other questions focused on life as a whole and the extent to which respondents felt they had control over their lives (e.g., rating of various aspects of life, (dis)satisfaction with life, personal efficacy, and social desirability measures). Personal data include sex, age, race, ethnic background, childhood family stability, military service, and father's occupation and education. Observational data are included on housing and neighborhood characteristics as well as respondents' appearance, intelligence, and sincerity. An instructional subset of this study is also available (see ICPSR INSTRUCTIONAL SUBSET: QUALITY OF AMERICAN LIFE, 1971 [ICPSR 7516], also prepared by Campbell, Converse, and Rodgers.) It includes questions representative of the major areas covered in the original, longer survey. A related dataset, QUALITY OF AMERICAN LIFE, 1978 (ICPSR 7762), continues the survey conducted in 1971.
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RAND Survey of Compensation for Accidental Injuries in the United States, August 1987-August 1988 (ICPSR 3084)

Released/updated on: 2012-07-12
Geographic coverage: United States
Time period: 1987-08-01--1988-08-01
This survey was conducted in 1989 to look at the consequences of injuries that had occurred within the past year. The main purpose was to examine medical treatment, activity restriction, loss reimbursement, and decisions regarding liability claims related to accidental injuries. Work-related stress and injuries that were fatal, resulted in institutionalization, or were caused by pharmaceutical products were not included. Questions were posed regarding treatment following the accident, resulting impairment, rehabilitation expenditures, tort liability payment, insurance benefits, expected claims, and legal assistance, along with psychological and social consequences from making the claims. While many features of this study are comparable to both the Current Population Survey (CPS) and the National Health Interview Survey (NHIS), the RAND survey is different in that questions regarding liability-claiming behaviors were asked over the course of a year, and questions about visits to care providers were included. Demographic information on respondents consists of sex, age, and education.
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Religion, Aging, and Health Survey, 2001, 2004 [United States] (ICPSR 3255)

Released/updated on: 2006-04-17
Geographic coverage: United States
This data collection looks at religion, self-rated health, depression, and psychological well-being in a sample of older Blacks and older Whites (aged 65 and over) within the United States. Questions were asked regarding religious status, activities, and beliefs among those who currently practice the Christian faith, those who used to be Christian but are not now, and those who have never been associated with any religion during their lifetimes. Demographic variables include age, race, sex, education, and income. Wave II was collected in 2004 and reinterviewed 1,024 respondents. There were 75 respondents who refused to participate, 112 who could not be located, 70 that were too ill for participation, 11 who had moved to nursing homes and 208 were deceased.
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Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001 (ICPSR 3253)

Released/updated on: 2006-03-30
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-01
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Data were collected through randomized clinical trials at six sites: University of Alabama--Birmingham, the Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee--Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions studied included psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services. Although interventions varied by site, all sites collected the same data at the same time intervals. The impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization was assessed. Parts 1 through 5 contain screening data and a short mental status questionnaire. Parts 6 through 24 contain baseline data and cover activities of daily living, anxiety, and caregiver health and behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 25 and 26 contain tracking data and also include an examination of interventions.
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Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001, Baseline and Follow-Up Data (ICPSR 3678)

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

Released/updated on: 2006-10-27
Geographic coverage: Palo Alto, United States, Tennessee, Memphis, California, Alabama, Florida, Birmingham, Philadelphia, Pennsylvania, Miami
Time period: 2001-01-01--2004-01-01
Built upon the findings of RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH, 1996-2001, BASELINE AND FOLLOW-UP DATA [ICPSR 3678], REACH II designed and tested a single multi-component intervention among family caregivers of persons with Alzheimer's disease or related disorders. The overall objectives were (1) to identify and reduce modifiable risk factors among diverse family caregivers of patients with Alzheimer's Disease or a related disorder, (2) to enhance the quality of care provided to the care recipients, and (3) to enhance the well-being of the caregivers. REACH II is the first project to simultaneously test a comprehensive caregiver intervention in three distinct racial/ethnic groups: Hispanic/Latino, Black/African-American, and White/Caucasian. The intervention was based on a risk-appraisal approach in which five areas of risk--depression, burden, self-care, social support, and patient problem behaviors--that are central to caregiver well-being and quality of life were matched to corresponding intervention components. These components included education, skills to manage troublesome care-recipient behaviors, social support, cognitive strategies for reframing negative emotional responses, and strategies for enhancing healthy behaviors and managing stress. Consistent with this approach, the primary outcome was a multivariate quality of life indicator that assessed caregiver depression, burden, self-care, social support, and patient problem behaviors. Two hallmarks of caregiver intervention studies--caregiver clinical depression and patient institutionalization--were assessed as secondary outcomes. The dataset names listed in this collection include the shortened name of the form administered.
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Social Environment and Biomarkers of Aging Study (SEBAS) in Taiwan, 2000 and 2006 (ICPSR 3792)

Released/updated on: 2014-06-17
Geographic coverage: Taiwan

The Social Environment and Biomarkers of Aging Study (SEBAS) in Taiwan, 2000 and 2006, provides information regarding the health and well-being of older persons in Taiwan. Taiwan has undergone rapid demographic, social, and economic changes, becoming a highly urbanized and industrial society with a growing population of persons age 65 or older. SEBAS explores the relationship between life challenges and mental and physical health, the impact of social environment on the health and well-being of the elderly, as well as biological markers of health and stress. The study collected self-reports of physical, psychological, and social well-being, plus extensive clinical data based on medical examinations and laboratory analyses. Examination of health outcomes included chronic illnesses, functional status, psychological well-being, and cognitive function. Questions regarding life challenges focused on perceived stress, economic difficulties, security and safety, and the consequences of a major earthquake. Biological markers were used to identify cardiovascular risk factors, metabolic process measures, immune-system activity, the hypothalamic-pituitary adrenal axis, and sympathetic nervous system activity. Two rounds of biomarker data collected in 2000 and 2006 were complemented by face-to-face interviews with the participants. Demographic and background variables included age, sex, education, ethnicity, occupation, and residency.

Additional information about the Social Environment and Biomarkers of Aging Study can be found at the Georgetown University Center for Populations and Health Web site.

A Webinar describing the Social Environment and Biomarkers of Aging Study (SEBAS) was presented June 20, 2016. All interested users can access the webinar here.

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Simple Crosstabs

Stroke Recovery in Underserved Populations 2005-2006 [United States] (ICPSR 36422)

Released/updated on: 2016-05-03
Geographic coverage: United States
Time period: 2005-01-01--2006-01-01

The Stroke Recovery in Underserved Populations 2005-2006 study was created to address the National Institute on Aging (NIA) Request For Application entitled "Research on Mind-Body Interactions and Health" (RFA OD-03-008). It addressed the NIA interest in "the impact of optimism, happiness, or a positive attitude on well-being and health; and social functioning and health." The study examined how positive emotion (e.g., joy, gratitude, love, contentment) and social networks independently and interactively contribute to recovery of functional status after stroke within two underserved groups. The specific study aims were to:

  1. Examine recovery of functional status (motor and cognitive function), for White, African American and Hispanic persons with stroke discharged from rehabilitation facilities
  2. Examine the contributions of positive emotion and social networks on recovery of functional status (motor and cognitive function), for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities; and
  3. Examine the interaction between positive emotion and social networks on recovery of functional status (motor and cognitive function) for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities.

The data were collected by the IT Health Track at four time points: at admission and discharge from rehabilitation facility, and 80-180 days and 365-425 days after discharge. These data emphasize recovery of motor and cognitive functional status, positive emotion, and social networks

The dataset contains 226 variables and 1219 cases from 11 rehabilitation facilities across the United States.

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Simple Crosstabs

Survey of Midlife in Japan (MIDJA 2), May-October 2012 (ICPSR 36427)

Released/updated on: 2018-02-19
Geographic coverage: Tokyo, Japan, Global
Time period: 2012-05-01--2012-10-01

In 2008, with funding from the National Institute on Aging (NIA), baseline survey data for the Survey of Midlife in Japan (MIDJA), April-September 2008 were collected from a probability sample of Japanese adults (N=1,027) aged 30 to 79 from the Tokyo metropolitan area (ICPSR 30822). In 2009-2010 biomarker data was obtained from a subset of these cases (ICPSR 34969).

The survey and biomarker measures obtained parallel those in a national longitudinal sample of Americans known as Midlife in the United States or MIDUS (ICPSR 2760: MIDUS 1 and ICPSR 4652: MIDUS 2). The central objective was to compare the Japanese sample (MIDJA) with the United States sample (MIDUS) to test hypotheses about the role of psychosocial factors in the health (broadly defined) of mid- and later-life adults in Japan and the United States.

In 2012, with additional support from NIA, a longitudinal follow-up of the MIDJA sample was completed. The data collection for this second wave (N=657) largely repeated the baseline assessments. The goal of the follow-up wave was to conduct comparisons of longitudinal data available from the Japanese sample (MIDJA) and the United States sample (MIDUS) to test the hypothesis about the role of psychosocial factors in predicting health changes (including biomarkers) in both cultural contexts. Cultural influences on age differences in health and well-being were also of interest.

Demographic and background information included gender, age, education, marital status, household composition, and income.

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Simple Crosstabs

Survey of Midlife in Japan (MIDJA), April-September 2008 (ICPSR 30822)

Released/updated on: 2018-03-09
Geographic coverage: Tokyo, Japan, Global
Time period: 2008-04-01--2008-09-30
The MIDJA study is a probability sample of Japanese adults (N = 1,027) aged 30 to 79 from the Tokyo metropolitan area. Survey data were collected on sociodemographic characteristics (age, gender, marital status, educational status), psychosocial characteristics (e.g., independence/interdependence, personality traits, sense of control, goal orientations, social support, family obligation, social responsibility), mental health (depression, anxiety, well-being, life satisfaction), and physical health (chronic conditions, health symptoms, functional limitations, health behaviors). These measures parallel those in a national longitudinal sample of midlife Americans known as MIDUS (ICPSR 4652: MIDUS II and ICPSR 2760: MIDUS I). The central objective is to compare the Japanese sample (MIDJA) with the United States sample (MIDUS) to test the hypothesis that the construct of interdependence predicts well-being and health in Japan, whereas the construct of independence predicts well-being and health in the United States. Cultural influences on age differences in health and well-being are also of interest.