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Curated
Simple Crosstabs

Advanced Cognitive Training for Independent and Vital Elderly (ACTIVE), United States, 1999-2008 (ICPSR 36036)

Released/updated on: 2015-07-29
Geographic coverage: Detroit, Baltimore, Indiana, United States, State College, Alabama, Maryland, Birmingham, Michigan, Pennsylvania, Boston, Indianapolis
Time period: 1999-01-01--2008-01-01

The data producers have recompiled the ACTIVE data into a new study which is available as of December 2023, ICPSR 38821; data users should plan to use study 38821 instead.

ACTIVE (Advanced Cognitive Training for Independent and Vital Elderly), 1999-2008 was a multisite randomized controlled trial conducted at six field sites with New England Research Institutes (NERI) as the coordinating center. The field sites included the University of Alabama at Birmingham, Hebrew Senior Life (formerly Hebrew Rehabilitation Center for the Aged) in Boston, Indiana University, Johns Hopkins University in Baltimore, Pennsylvania State University, and Wayne State University (Detroit). Data in this study are drawn from measures of cognitively demanding daily activities performed by participants who received a variety of cognitive interventions. Measures included both cognitive functioning (memory, inductive reasoning, speed processing, and general knowledge) and daily functioning (everyday problem solving, observations of daily living, complex reaction time, and general functional ability). Secondary to these measures, the study also includes data on health care and service utilization, driving habits, and mobility. Data were collected at the start of the study (baseline) as well as one, two, three, five, and ten years into the study. This collection includes the data from the tenth year of the study as well as a comprehensive analytical dataset, incorporating data from the previous collections (data from previous waves of the study as well as participant demographic data can be found in ICPSR 4248). A total of 2,832 older adults were enrolled in the trial, and 2,802 were included in the analytical sample. Twenty-six percent of the participants were African American.

Curated
Simple Crosstabs

Advanced Cognitive Training for Independent and Vital Elderly (ACTIVE), United States, 1999-2019 (ICPSR 38821)

Released/updated on: 2023-12-11
Geographic coverage: Detroit, Indiana, United States, Alabama, Birmingham, Michigan, Pennsylvania, Baltimore, Massachusetts, State College, Maryland, Boston, Indianapolis
Time period: 1999-01-01--2019-12-31

ACTIVE (Advanced Cognitive Training for Independent and Vital Elderly) was a multisite randomized controlled trial conducted at six field sites with New England Research Institutes (NERI) as the coordinating center. The field sites included the University of Alabama at Birmingham, Hebrew Senior Life (formerly Hebrew Rehabilitation Center for the Aged) in Boston, Indiana University, Johns Hopkins University in Baltimore, Pennsylvania State University, and Wayne State University (Detroit). Data in this study are drawn from measures of cognitively demanding daily activities performed by participants who received a variety of cognitive interventions. Measures included both cognitive functioning (memory, inductive reasoning, speed processing, and general knowledge) and daily functioning (everyday problem solving, observations of daily living, complex reaction time, and general functional ability). Secondary to these measures, the study also includes data on health care and service utilization, driving habits, and mobility. Data were collected at the start of the study (baseline) as well as one, two, three, five, and ten years into the study.

This collection integrates data from two previous collections (ICPSR 4248 and ICPSR 36036) and fills in gaps that existed in these two collections. In addition, this collection features composite scores for constructs like memory, reasoning speed, Short Form Health Survey (SF-36), Social Determinants of Health (SDOH), as well as data from the National Death Index and state driving records.

Please read the collection notes for important analysis details.

Curated

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

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

Black Rural and Urban Caregivers Mental Health/Functioning, Missouri, 1999-2002 (ICPSR 36349)

Released/updated on: 2019-01-28
Geographic coverage: United States, Missouri
Time period: 1999-01-01--2002-01-01

The Black Rural and Urban Caregivers Mental Health/Functioning data collection includes survey data collected in 2000-2002 from African American females age 65 and older, who provide unpaid care for older African American adults in the St. Louis Metropolitan area and seven rural Missouri counties (Butler, Dunklin, Mississippi, New Madrid, Pemiscot, Scott, and Stoddard).

Because of inadequate recruitment knowledge about rural African American caregivers and persistent reports of challenges when involving African Americans elders in research, this study focused on the involvement of African American rural elders and recruitment of their female informal caregivers in a study of caregivers' well-being and service use. African Americans comprise the largest group of ethnic and racial minority elders aged 65 and older in the U.S. population thus making up one half of all ethnic and racial minority elders. Numerical changes in population size and increasing longevity of older African Americans direct attention to African American informal female caregivers- persons most likely to assist African American elderly with daily living tasks, personal needs, and long-term care. More disabled and chronically ill African American elders portend continuing need from informal or unpaid caregivers for dependent care.

There are two datasets associated with this study, a public-use (da36349-0001) and restricted-use (da36349-0002) version of the same survey data. Both data files contain 521 cases and 1438 variables. However, the restricted file contains continuous as opposed to categorical values for age variables rounded to the nearest whole number.

Curated

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

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

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

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

Curated

Chronic Illness and Caregiving, 2000: [United States] (ICPSR 3402)

Released/updated on: 2024-02-14
Geographic coverage: United States
The objective of this survey, which interviewed individuals from the general public, chronically ill persons, and informal caregivers, was threefold: (1) to assess public awareness of chronic care issues and the level of support for chronic care policy initiatives, (2) to examine experiences and needs of chronically ill Americans concerning health care and other assistance, and (3) to evaluate experiences and needs of informal caregivers. Questions to the general public addressed awareness of the availability of supportive and housing services for the chronically ill, knowledge about coverage for long-term care, concerns about the future of the chronic care delivery system, support for policy initiatives such as tax credits for the chronically ill and caregivers, and support for a policy that would ensure pharmaceutical coverage in Medicare. Chronically ill interviewees responded to questions about access to and experience with chronic care and other health care services, experiences with and needs for clinical services coordination, experiences with and needs for social supports and interventions, and adjustment skills and knowledge (e.g., what were their needs for learning how to live with chronic conditions). Questions for informal caregivers focused on experiences with caregiving (e.g., for whom they provided care, how many hours they devoted to caregiving per week, and living arrangements), balance between caregiving and other areas of their lives, experiences with and needs for respite care, and availability of social supports for caregivers.
Curated
Partially restricted

Community Tracking Study Household Survey, 1996-1997, and Followback Survey, 1997-1998: [United States] (ICPSR 2524)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-07-01--1997-07-01, 1997-10-01--1998-08-01
This data collection comprises two components of the Community Tracking Study (CTS), the Household Survey and the Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. At the beginning of each interview, a household informant was identified and queried about the composition of the household. With this information, individuals in the household were grouped into family insurance units (FIU). An FIU reflects family groupings typically used by insurance carriers. It includes an adult household member, his or her spouse, if any, and any dependent children 0-17 years of age (or 18-22 years of age if a full-time student). Family informants, selected from each FIU in the household, provided information on health insurance coverage, health care use, usual source of care, and the general health of all persons in the FIU. These informants also provided information on family income and out-of-pocket expenses for health care, as well as employment, race, and Hispanic origin for all adult FIU members. Each adult in the household, including the FIU informants, responded through a self-response module to questions regarding unmet health care needs, patient trust, satisfaction with physician choice, limitations in daily activities, smoking behaviors, and last doctor visit. In FIUs with more than one child under 18, only one child was randomly selected for inclusion in the survey. The family informant responded on behalf of the child regarding unmet needs and satisfaction with physician choice. The adult family member who took this child to his or her last doctor visit responded to questions about the visit. The Followback Survey was designed to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to health plans and other organizations that offered or administered the comprehensive private health insurance policies covering Household Survey respondents in the 60 CTS sites. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
Curated
Partially restricted

Community Tracking Study Household Survey, 1998-1999, and Followback Survey, 1998-2000: [United States] (ICPSR 3199)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1998-01-01--2000-01-01
This collection comprises the second round of the Community Tracking Study (CTS) Household Survey and the second round of the CTS Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first round of the Household Survey (COMMUNITY TRACKING STUDY HOUSEHOLD SURVEY, 1996-1997, AND FOLLOWBACK SURVEY, 1997-1998: [UNITED STATES] (ICPSR 2524)), the second round of the Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. The purpose of the Followback Survey was to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to the health plans and other organizations (managed care organizations, third-party administrators, employer or union plans, and employers) that offered or administered the respondents' comprehensive private health insurance policies. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
Curated
Partially restricted

Community Tracking Study Household Survey, 2000-2001: [United States] (ICPSR 3764)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2000-01-01--2001-01-01
This collection comprises the third round of the Community Tracking Study (CTS) Household Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and the effects of those changes on people. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the Household Survey (ICPSR 2524 and 3199), the third round was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. A new set of sample design variables was added to the third round data for variance estimation by statistical software packages other than SUDAAN.
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Partially restricted

Community Tracking Study Household Survey, 2003: [United States] (ICPSR 4216)

Released/updated on: 2007-12-03
Geographic coverage: United States
Time period: 2003-01-01--2004-01-01
This collection contains data and documentation for the fourth round of the Community Tracking Study (CTS) Household Survey. Sponsored by the Robert Wood Johnson Foundation, the CTS is a national study designed to track changes in the United States' health care system and their effects. The fourth round was administered to households in the 60 CTS sites: 51 metropolitan areas and nine nonmetropolitan areas which were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The first round of the CTS Household Survey was conducted in 1996-1997 (ICPSR 2524), the second round in 1998-1999 (ICPSR 3199), and the third in 2000-2001 (ICPSR 3764). Respondents to the fourth round provided information about health insurance coverage, use of health services, unmet needs for health care, children's special health care needs, out-of-pocket medical costs, patient trust in physicians, sources of health information, attitudes about medical care, and satisfaction with health care and health plans. Health status, chronic conditions, and risk attitudes and smoking behavior were additional topics covered by the fourth round questionnaire. The data include variables on height and weight, employment, income, ethnicity, race, United States citizenship, household composition, and demographic characteristics.
Curated

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

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

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

Curated

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

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

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

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

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

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

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

Curated

Established Populations for Epidemiologic Studies of the Elderly, 1981-1993: [East Boston, Massachusetts, Iowa and Washington Counties, Iowa, New Haven, Connecticut, and North Central North Carolina] (ICPSR 9915)

Released/updated on: 2006-01-18
Geographic coverage: North Carolina, Iowa, New Haven, United States, Massachusetts, Connecticut, Boston
Time period: 1981-01-01--1993-01-01
The goals of the Established Populations for Epidemiologic Studies of the Elderly (EPESE) project were to describe and identify predictors of mortality, hospitalization, and placement in long-term care facilities and to investigate risk factors for chronic diseases and loss of functioning. The survey elicited information from persons 65 years of age and older in four geographic locations: East Boston, Massachusetts, New Haven, Connecticut, Iowa and Washington Counties, Iowa, and five counties in north central North Carolina. The public use baseline data (Part 1) cover demographic characteristics (age, sex, race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Data from six follow-up surveys conducted in all four of the sites are also provided (Parts 2-4 and 6-8), along with information from death certificates for deaths occurring in the first six years of follow-up for all four sites (Part 5).
Curated

Health Interview Survey, 1963 (ICPSR 28381)

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

Health Interview Survey, 1964 (ICPSR 28663)

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

Health Interview Survey, 1965 (ICPSR 28761)

Released/updated on: 2010-07-13
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in the 1965 survey, each in a separate data file. The Person file (Part 1) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and occupation. These variables are found in the Condition and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 2) contains information for each reported health condition, with specifics on injury and accident reports. The Prescribed Medicine file (Part 3) contains general demographic information, cost of medications, when medications were obtained, and conditions for which medications were prescribed. The Non-prescribed Medicine file (Part 4) contains general demographic information, where medications were obtained and purchased, as well as short-stay hospital episodes. The Diabetes file (Part 5) includes information regarding symptoms of diabetes, genetic variables, and treatment regimen variables. The Hospital Episode file (Part 6) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed.
Curated

Health Interview Survey, 1966 (ICPSR 28801)

Released/updated on: 2010-07-15
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this year's survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition file (Part 3) and the Hospital Episode file (Part 4) as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Medical Care Cost file (Part 5) includes information regarding short-stay hospital visits, family income, and total medical bill costs.
Curated

Health Interview Survey, 1967 (ICPSR 28862)

Released/updated on: 2010-07-16
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are six types of records in the 1967 survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and occupation. These variables are found in the Condition file (Part 3) and the Hospital Episode file (Part 4) as well. The Person file (Part 2) also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit file (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. The Home Care file (Part 6) documents basic demographic information, eating habits, in-home mobility, hospital visits, and the extent that basic living activities and needs are performed with or without aid.
Curated

Health Interview Survey, 1968 (ICPSR 28881)

Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. This 1968 study was a transition for the National Health Interview Survey (NHIS) from fiscal year (July 1 to June 30) to calendar year. The 1968 files include both fiscal year files and calendar year files, with some overlap between corresponding fiscal year and calendar year files. During the fiscal year, the NHIS sample was split and two types of questionnaires were administered to approximately half of the overall sample: the "condition approach" questionnaire and the "person approach" questionnaire. During the second half of calendar year 1968, the entire NHIS sample was interviewed using the person approach questionnaire. During this time period, five NHIS files are referred to as "core" files because they were administered each year (through 1996). The five core files are Household, Person, Condition, Doctor Visit, and Hospital. No evidence of a fiscal year Household file was found, and the existing calendar year Household file had too many anomalies to be included in this release. Thus, this release consists of fiscal year and calendar year versions of four out of the five core files, and three supplement files, for a total of eleven files. The eleven types of records in this year's survey are each in a separate data file. The Person Calendar and Fiscal Year files (Part 1 and Part 6) include information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. The Person files also supply data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition Calendar and Fiscal Year files (Part 2 and Part 7) contain information for each reported health condition, with specifics on injury and accident reports. The Hospital Calendar and Fiscal Year files (Part 3 and Part 8) provide information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit Calendar and Fiscal Year files (Part 4 and Part 8) document doctor visits within the time period and identify acute or chronic conditions. The Motor Vehicle Person Accident Calendar and Fiscal Year files (Part 5 and Part 10) contain information regarding types of motor accidents, how many vehicles were involved in a given accident, injuries acquired from a given accident, time of day the accident occurred, and treatments given as a result of a given accident. The Home Care Fiscal Year file (Part 11) documents basic demographic information, eating habits, in-home mobility, hospital visits, and the extent to which basic living activities and needs are performed with or without aid.
Curated

Health Interview Survey, 1970 (ICPSR 7838)

Released/updated on: 2010-09-21
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode files as well. The Person file also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit file (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. The Health Insurance file (Part 6) includes information on education level, family income, hospital visits and length of stay, and also data on medical coverage, hospital coverage, medicare coverage, and doctor visit coverage. The Medical Care Cost file (Part 7) includes information on hospital bill expenses, doctor and dental bill expenses, optical bill expenses, and total personal and family expenses. The X-Ray file (Part 8) includes information on x-ray records, doctor visits, height, weight, and total medical x-ray visits.
Curated

Health Interview Survey, 1971 (ICPSR 8336)

Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The variables in the Household File (Part 2) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been added, along with the five core files. The Person Supplement File (Part 6) provides information on health conditions, hearing quality, doctor visits, and hospital stay information.
Curated

Health Interview Survey, 1972 (ICPSR 8337)

Released/updated on: 2010-09-30
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been added, along with the five core files. The Health Insurance File (Part 6) documents basic demographic information along with medical coverage and health insurance plans, as well as differentiates between hospital, doctor visit, and surgical insurance coverage.
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Health Interview Survey, 1973 (ICPSR 8338)

Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth and seventh file have been added, along with the five core files. The Condition Supplement File (Part 6) documents past bed days, duration of limitation of the condition, whether or not a doctor was seen, the type of injury incurred, satisfaction with treatment, whether or not a prescription was given or filled, and if applicable, the reason why medical attention was not sought. The Pregnancy File (Part 7) documents activity restriction, bed disability, work or school loss days, doctor and dental visits within the last two weeks to twelve months, number of chronic conditions, time since routine physical exams have been completed, and the number of times pregnancies have been terminated in the past twelve months, as well as how many live births have occurred over one's lifetime, and routine pregnancy related doctor visits.
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Health Interview Survey, 1974 (ICPSR 8339)

Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth and seventh file have been added along with the five core files. The Condition Supplement File (Part 6) provides further information regarding injuries, health status, medical advice received, travel time and waiting time for care, and satisfaction with health services provided. The Health Insurance File (Part 7) provides general demographic information as well as type of care obtained through insurance plans, work loss because of current conditions, and whether or not the patient has any type of insurance or no insurance coverage at all.
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Health Interview Survey, 1975 (ICPSR 7672)

Released/updated on: 2010-11-15
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode File as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions.
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Health Interview Survey, 1976 (ICPSR 8340)

Released/updated on: 2010-12-03
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions.
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Health Interview Survey, 1977 (ICPSR 7839)

Released/updated on: 2010-12-14
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, and geographic region. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, occupation, and limits on activity. The Condition File (Part 3) contains variables on the incidence of illness or injury within the past year. The Hospital Episode File (Part 4) contains variables on the incidence of hospitalizations and presence of chronic conditions. The Doctor Visit File (Part 5) includes variables regarding frequency of doctor visits, type of doctor seen, and reasons for each visit. A sixth, seventh, eighth, and ninth file have been provided. The Disability Supplement File (Part 6) contains variables on the need for help, services, and environment modifications. The H1 Supplement File (Part 7) includes basic demographic variables, medical information, health variables, doctor visits, medical insurance, work days lost, and activity level variables. The Special Aids Supplement File (Part 8)includes basic demographic variables, special aids onset and amount needed, medical information, health variables, and doctor visits. The Influenza Supplement File (Part 9) includes basic demographic variables, flu, grippe, or fever onset, work and school days lost, hospital visits, length of stay, and cost of care.
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Health Interview Survey, 1978 (ICPSR 8044)

Released/updated on: 2011-01-05
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, and geographic region. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, occupation, and limits on activity. The Condition File (Part 3) contains variables on the incidence of illness or injury within the past year. The Hospital Episode File (Part 4) contains variables on the incidence of hospitalizations and presence of chronic conditions. The Doctor Visit File (Part 5) includes variables regarding frequency of doctor visits, type of doctor seen, and reasons for each visit. A sixth and seventh file have been provided. The Family Medical Expenses File (Part 6) provides variables including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. Other variables include amounts paid for personal, family, and outside family dental bills, doctor bills, hospital bills, optical bills, prescription medicine, health insurance, and other medical expenses. Other questions include total personal, family, and outside family medical expenses, including and excluding health insurance, and the sex and race of the family head. The Immunization File (Part 7) includes basic demographic variables, hospital stay length, doctor visit periods, types of immunizations received, and when they were obtained.
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Health Interview Survey, 1981 (ICPSR 8319)

Released/updated on: 2011-04-25
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person File (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and industry and occupation. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition File (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode File (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit File (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. A sixth file has been provided. The Child Health Supplement File (Part 6) provides detailed data on child health and development. This supplement offers information on age of child, sex, birth-date, physical and social development, family relationships, prenatal care, hospitalization and illness, behavior, schooling, and seat-belt usage.
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Health Interview Survey, 1982 (ICPSR 8460)

Released/updated on: 2011-04-06
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in the 1982 core survey, each in a separate data file. The variables in the Household File (Part 1) in this collection include type of living quarters, size of family, region, condition list assigned, and type of PSU. The Person File (Part 2) variables include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. The Condition File (Part 3), Doctor Visit File (Part 4), and Hospital Episode File (Part 5) contain information on each reported condition, two-week doctor visit, or hospitalization (twelve-month recall), respectively. A sixth and seventh file have been provided. The Health Insurance Supplement File (Part 6) contains questions about health insurance plans pertaining to the type of plan, including private, Medicare, Medicaid, military and other plans, and coverage or reasons for lack of coverage are provided. The Preventive Care Supplement File (Part 7) contains variables that chronicle when routine tests, physicals, and preventative examinations have last been performed.
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Health Interview Survey, 1983 (ICPSR 8603)

Released/updated on: 2011-04-13
Geographic coverage: United States
The basic purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in household, and geographic region. The variables in the Person File (Part 2) include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition (Part 3), Doctor Visit (Part 4), and Hospital Episode (Part 5) Files contain information on each reported condition, two-week doctor visit, or hospitalization (twelve-month recall), respectively. A sixth, seventh, eighth, and ninth file have been added, along with the five core files. The Alcohol/Health Practices Supplement File (Part 6) includes information on diet, smoking and drinking habits, and health problems. The Bed Days and Dental Care Supplement File (Part 7) contains information on the number of bed days, the number of and reason for dental visits, treatment(s) received, type of dentist seen, and travel time for visit. The Doctor Services Supplement File (Part 8) supplies data on visits to doctors or other health professionals, reasons for visits, health conditions, and operations performed. The Health Insurance Supplement File (Part 9) documents basic demographic information along with medical coverage and health insurance plans, as well as differentiates between hospital, doctor visit, and surgical insurance coverage.
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Hispanic Health and Nutrition Examination Survey, 1982-1984 (ICPSR 8535)

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

Home Health Agency Quality Improvement Strategies, United States, 2013-2018 (ICPSR 38652)

Released/updated on: 2023-02-16
Geographic coverage: United States
Time period: 2013-01-01--2018-12-31
The main objective of the study was to assess home health agency quality improvement strategies across the United States. A mail-based survey was administered to a national sample of directors of home health agencies. The survey asked about the technologies, health services, and quality measures used at each agency, and they had considered or adopted these in the time period between 2013 and 2018.
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Partially restricted

Hospitalized Older Persons Evaluation (HOPE) Study, 1991-1993: [California] (ICPSR 6560)

Released/updated on: 2006-01-12
Geographic coverage: United States, California
Time period: 1991-03-01--1993-05-31
The HOPE study was a multi-center randomized clinical trial mounted to determine the effects of hospital inpatient consultative comprehensive geriatric assessment (CGA) under typical practice conditions on selected patient health and health services utilization outcomes. The main outcome measures were functional status, health status, mortality, rehospitalization, and total use of health care services for hospital patients 65 years of age and older. Functional status was evaluated by questions about limitations in patients' activities of daily living due to health problems. Also included were items covering living arrangements (with whom and where), ethnicity, education, and marital status. Health status questions covered patients' perceptions of mental health and current physical health. The functional and health status of patients was measured prior to CGA treatment and randomization, again at 3 months post-randomization, and at 12 months post-randomization. Functional and health status data are included in Parts 3-8. Health services utilization data (Parts 9-15) cover patient use of medical services such as urgent care, emergency room, radiology, durable medical equipment, and medications (prescribed and over the counter). Mortality information (Part 17) includes date of lost contact or death, and data source of survival status. Hospitalization measures (Part 18) include date of admission and discharge, admittance source diagnoses and procedures, and inpatient/outpatient status.
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Simple Crosstabs

The Irish Longitudinal Study on Ageing (TILDA), COVID-19 Study, 2020 (ICPSR 38681)

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

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

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

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

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

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Simple Crosstabs

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

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

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

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

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Simple Crosstabs

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

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

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

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

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

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

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Simple Crosstabs

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

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

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

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

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

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

Curated
Simple Crosstabs

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

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

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

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

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

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

Curated

Kaiser Permanente Study of the Oldest Old, 1971-1979 and 1980-1988: [California] (ICPSR 4219)

Released/updated on: 2011-02-07
Geographic coverage: United States, California
Time period: 1971-01-01--1988-01-01
This data collection is an epidemiological study of chronic disease in the oldest old. It is based on information collected from Kaiser Permanente facilities in Northern California. Members of Kaiser Permanente Medical Care programs who were aged 65 or older at the time the data were being collected and who had taken a multiphasic health checkup examination within four to six years of the baseline date were included in the study. There are several components to the dataset. Part 1, Master Records, includes information from the morbidity review, in which over 35 chronic conditions or diagnoses were abstracted from the member charts, as well as detailed diagnostic criteria for the major conditions. A prevalence review was done, which included the four years prior to the baseline date for these same conditions. Recurrent disease is included for the following conditions: cancers, myocardial infarction, and various forms of strokes. A detailed account of outpatient health services use, and data from the multiphasic health checkup, which was administered to each participant during the nine yearly follow-ups, are also included in the Master Records file. Part 2, Hospitalization, contains records of causes and dates of hospitalizations and discharges and nursing home admissions. There is also a section on incomplete reviews and the reasons for them. Demographic information and some lifestyle information from the multiphasic health checkup (e.g., smoking, alcohol, and Body Mass Index) are also in this file.
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National Health and Nutrition Examination Survey (NHANES), 1999-2000 (ICPSR 25501)

Released/updated on: 2012-02-22
Geographic coverage: United States
Time period: 1999-01-01--2000-01-01
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. The 1999-2000 NHANES contains data for 9,965 individuals (and MEC examined sample size of 9,282) of all ages. Many questions that were asked in NHANES II, 1976-1980, Hispanic HANES 1982-1984, and NHANES III, 1988-1994, were combined with new questions in the NHANES 1999-2000. The 1999-2000 NHANES collected data on the prevalence of selected chronic conditions and diseases in the population and estimates for previously undiagnosed conditions, as well as those known to and reported by respondents. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The interview includes demographic, socioeconomic, dietary, and health-related questions. The examination component consists of medical, dental, and physiological measurements, as well as laboratory tests. Demographic data file variables are grouped into three broad categories: (1) Status Variables: Provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 1999-2000 data). (2) Recoded Demographic Variables: The variables include age (age in months for persons through age 19 years, 11 months; age in years for 1-84 year olds, and a top-coded age group of 85+ years), gender, a race/ethnicity variable, an education variable (high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), and pregnancy status variable. Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: Sample weights are available for analyzing NHANES 1999-2000 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
Curated

National Health and Nutrition Examination Survey (NHANES), 2001-2002 (ICPSR 25502)

Released/updated on: 2012-02-22
Geographic coverage: United States
Time period: 2001-01-01--2002-01-01
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. The 2001-2002 NHANES contains data for 11,039 individuals (and MEC examined sample size of 10,477) of all ages. Many questions that were asked in NHANES II, 1976-1980, Hispanic HANES 1982-1984, and NHANES III, 1988-1994, were combined with new questions in the NHANES 2001-2002. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2001-2002 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable to come to the examination center may be given a less extensive examination in their homes. Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2001-2002 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1-84 year olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year data set. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2001-2002 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
Curated

National Health and Nutrition Examination Survey (NHANES), 2003-2004 (ICPSR 25503)

Released/updated on: 2016-07-11
Geographic coverage: United States
Time period: 2003-01-01--2004-01-01

The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year.

For NHANES 2003-2004, there were 12,761 persons selected for the sample, 10,122 of those were interviewed (79.3 percent) and 9,643 (75.6 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2003-2004 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2002. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2003-2004 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable or unwilling to come to the examination center may be given a less extensive examination in their homes.

Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2003-2004 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1- to 84-year-olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year data set. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2003-2004 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.

Curated

National Health and Nutrition Examination Survey (NHANES), 2005-2006 (ICPSR 25504)

Released/updated on: 2012-02-22
Geographic coverage: United States
Time period: 2005-01-01--2006-01-01
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. For NHANES 2005-2006, there were 10,348 persons selected for the sample, 10,122 of those were interviewed (79.3 percent) and 9,643 (75.6 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2005-2006 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2004. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2005-2006 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable or unwilling to come to the examination center may be given a less extensive examination in their homes. Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2005-2006 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1- to 84-year-olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2005-2006 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
Curated

National Health and Nutrition Examination Survey (NHANES), 2007-2008 (ICPSR 25505)

Released/updated on: 2012-02-22
Geographic coverage: United States
Time period: 2007-01-01--2008-01-01
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. For NHANES 2007-2008, there were 12,946 persons selected for the sample, 10,149 of those were interviewed (78.4 percent) and 9,762 (75.4 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2007-2008 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2006. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. The NHANES target population is the civilian, noninstitutionalized United States population. Beginning in 2007, some changes were made to the domains being oversampled. The primary change is the oversampling of the entire Hispanic population instead of just the Mexican American (MA) population, which has been oversampled since 1988. Sufficient numbers of MAs were retained in the sample design so that trends in the health of MAs can continue to be monitored. Persons 60 years of age and older, Blacks, and low income persons were also oversampled. In addition, for each of the race/ethnicity domains, the 12-15 and 16-19 year age domains were combined and the 40-59 year age minority domains were split into 10-year age domains of 40-49 and 50-59. This has led to an increase in the number of participants aged 40 and older and a decrease in 12- to 19-year-olds from previous cycles. The oversample of pregnant women and adolescents in the survey from 1999-2006 was discontinued to allow for the oversampling of the Hispanic population. NCHS is working with public health agencies to increase knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Demographic data file variables are grouped into three broad categories: (1) Status Variables: Provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number [SEQN] is a unique ID number assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2007-2008 data.) (2) Recoded Demographic Variables: The variables include age (age in months for persons under age 80, age in years for 1 to 80-year-olds, and a top-coded age group of 80 years and older), gender, a race/ethnicity variable, an current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), ratio of family income to poverty threshold, income, and a pregnancy status variable (adjudicated from various pregnancy-related variables). Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: Sample weights are available for analyzing NHANES 2007-2008 data. Most data analyses require either the interviewed sample weight (variable name: WTINT2YR) or examined sample weight (variable name: WTMEC2YR). The two-year sample weights (WTINT2YR, WTMEC2YR) should be used for NHANES 2007-2008 analyses.
Curated

National Health Interview Survey, 1969 (ICPSR 9800)

Released/updated on: 2010-09-16
Geographic coverage: United States
The purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are seven types of records in the 1969 survey, each in a separate data file. The variables in the Household file (Part 1) include type of living quarters, size of family, number of families in the household, presence of a telephone, number of unrelated individuals, and region. The Person file (Part 2) includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, employment status, and occupation. These variables are found in the Condition file (Part 3) and the Hospital Episode file (Part 4) as well. The Person file (Part 2) also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition file (Part 3) contains information for each reported health condition, with specifics on injury and accident reports. The Hospital Episode file (Part 4) provides information on medical conditions, hospital episodes, type of service, type of hospital ownership, date of admission and discharge, number of nights in hospital, and operations performed. The Doctor Visit file (Part 5) documents doctor visits within the time period and identifies acute or chronic conditions. The Special Aids file (Part 6) provides data on chronic conditions, the number of aids used, length of hospital stays, and information regarding doctor visits. The Arthritis file (Part 7) includes information on chronic conditions, length of hospital stays, restricted activities, and bed days.
Curated

National Health Interview Survey, 1973: Prescribed Medicine Supplement (ICPSR 9799)

Released/updated on: 2010-11-29
Geographic coverage: United States
The basic purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Provided with this Prescribed Medication Supplement are variables from the 1973 core Person File (see HEALTH INTERVIEW SURVEY, 1973 [ICPSR 8338]) including items such as sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. This Prescribed Medicine Supplement features information on when, how, and the number of times prescriptions were obtained, and the cost and payment source of prescriptions. The Prescribed Medicine File (Part 1) documents activity restriction, bed disability, work or school loss days, hospitalization days, the number of chronic conditions obtained, and source of payment for medication and care.
Curated

National Health Interview Survey, 1974: Currently Employed Supplement (ICPSR 9798)

Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. The Currently Employed Supplement File provides variables from the core Person File (see HEALTH INTERVIEW SURVEY, 1974 [ICPSR 8339]) including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. The variables unique to this Currently Employed Supplement (Part 1) include items on employment history, health insurance coverage, time away from work due to illness, days worked in a week, hours worked in a week, income earned per week, income lost per week due to illness, and reimbursement for time away from work.
Curated

National Health Interview Survey, 1974: Hypertension Supplement (ICPSR 9796)

Released/updated on: 2010-11-29
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Provided with this Hypertension Supplement are variables from the 1974 core Person File (see HEALTH INTERVIEW SURVEY, 1974 [ICPSR 8339]) including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. The variables unique to the Hypertension Supplement File (Part 1) include items on blood pressure history, weight control issues, doctor visits, salt use, medicines prescribed and/or used, side effects of medicine, number of bed days in the last year, whether the respondent's condition was covered by insurance, the last time the respondent had an electrocardiogram, chest x-ray, or diabetes check, and smoking, stroke, and cardiac histories.