Showing 1 – 16 of 16 results.
Curated
Cost of Providing Transportation and In-home Services to the Elderly, 1982-1983 (ICPSR 8309)
Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1982-01-01--1983-01-01
This data collection contains the results of a survey conducted to examine the costs of providing (1) transportation and (2) in-home services to the elderly in the United States in 1982-1983. Both parts of the study examined the costs of administrative, professional, and clerical staff, including wages paid, number of full- and part-time staff, and fringe benefits, and office expenses, such as the cost of office machines, equipment, supplies, and furniture. Insurance and taxes paid were also investigated, as were accounting, advertising, and legal counsel costs. The transportation services section of the study classified agencies providing the services studied by type, e.g., private for-profit, private non-profit, public, and other. This portion of the study also determined vehicle descriptions, revenue by source, and hours that service was provided. The in-home services section of the study examined several types of services offered, e.g., nursing care, therapy, personal care, housekeeping, physician visits, nutrition and social service counseling, and companionship. This section also classified agencies providing services by type, e.g., government-based public health, government-based social services, private non-profit, and private for-profit.
Curated
Danish 1905 Cohort Study, 1998 (ICPSR 3960)
Released/updated on: 2016-08-22
Geographic coverage: Denmark, Global
Time period: 1905-01-01--1998-01-01
This data collection provides information on individuals born in Denmark in 1905 and who were still living in Denmark in 1998. The overall goal of the study was to establish a genetic-epidemiological database to shed light on the aging process among the extremely old. The data focus on their physical and cognitive functioning. Respondents were asked if they had been previously diagnosed with diseases such as diabetes, arthritis, asthma, migraine, cancer, stroke, heart attack, or depression, and if they were experiencing such ailments as cough, body pains, and bone fracture and were taking medication for them. Questions probed respondents' feelings about their health, life, and future. To assess respondents' general health and functioning, they were asked if they needed assistance with toileting, bathing, dressing, and mobility around the house; how often they needed to use the bathroom during the night; and if they used physical aids such as wheelchairs, eyeglasses, crutches, catheters, or diapers. They were also tested for memory and cognition, mobility, vision, speech, hearing, and lung functioning. Information was also elicited on respondents' mental state and awareness, energy level, menopause, frequency of visits with children and family, visits from a nurse, use of home care services, sleeping patterns, smoking and drinking habits, weight gain or loss, exercises, social activities, hobbies, reading habits, television viewing, and recent deaths in the family. Demographic information includes age, education, and marital status.
Curated
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.
Curated
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.
Curated
Longitudinal Study of Aging Danish Twins, 1995 (ICPSR 21041)
Released/updated on: 2009-06-09
Geographic coverage: Denmark, Global
Time period: 1995-02-01--1995-04-01
The focus of the "Longitudinal Study of Aging Danish Twins (LSADT)" was on elucidating the causes of variation in survival, health, diseases, loss of abilities, and cognitive functions among the elderly and oldest-old. The LSADT was conducted every two years between 1995 and 2005 and consists of six waves. The study is comprised of interviews of elderly Danish twins aged 75 years and older (later 70 years and older). At each interview wave, the interview assessment was based on the interview used in the previous waves, which covers health, physical functioning, cognitive functioning, depression symptomatology, social factors, lifestyle characteristics, and quality of life. The self-report interview assessments were supplemented with objective indicators of physical strength and agility, behavioral speed, and pulmonary peak-flow. Biological material was also collected from the participants for future DNA analysis.
Curated
National Health Interview Survey, 1979 (ICPSR 8049)
Released/updated on: 2011-02-16
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 kind of health services people receive. There are five core files within the 1979 survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, region, condition list assigned, and type of PSU. The Person File (Part 2) includes information on sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. 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 a seventh data set have been added to the core files. The Home Care Supplement 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. Also in the Person file are the Home Care Supplement variables which were used to define the need for personal (individual) home care as a result of a chronic health condition, as well as the use of eyeglasses and contact lenses and hearing aids. The Residential Mobility Supplement File (Part 7) includes basic demographic variables and length of hospital stay, amount of time one has lived at the same residence, and reasons for moving.
Curated
National Health Interview Survey, 1994: Second Supplement on Aging (ICPSR 2563)
Released/updated on: 2007-02-12
Geographic coverage: United States
The National Health Interview Survey, 1994: Second Supplement on Aging (SOA II), conducted approximately 10 years after the original SOA (see NATIONAL HEALTH INTERVIEW SURVEY, 1984 [ICPSR 8659], Parts 6 and 7), had four specific aims. The first was to provide a replication of the first SOA to determine whether changes had occurred in the level of disability among older persons between 1984 and the mid-1990s. The second aim was to elicit information on the causes and correlates of changes in health and functioning in older Americans, including background demographic characteristics, health behaviors, and attitudes, pre-existing illness, and social and environmental support. The third was to describe the sequence and consequences of health events, including utilization of health care and services for assisted community living, on the physiological consequences of disability such as pain and fatigue, on social consequences such as changes in social activities, living arrangements, social support, and use of community services, and on the deployment of assisted living strategies and accessibility of technological and environmental adaptations. The final aim was to serve as the baseline for another national longitudinal study focusing on older Americans, the SECOND LONGITUDINAL STUDY OF AGING (LSOA II) (for the first LSOA see NATIONAL HEALTH INTERVIEW SURVEY: LONGITUDINAL STUDY OF AGING, 70 YEARS AND OVER, 1984-1990 [ICPSR 8719]).
Curated
National Home and Hospice Care Survey, 1992 (ICPSR 6536)
Released/updated on: 2006-01-12
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 1992 is the first annual survey of home health agencies and hospices and their patients and discharges. The survey was designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff personnel, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff people most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes service provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, race, Hispanic origin, and marital status.
Curated
National Home and Hospice Care Survey, 1993 (ICPSR 6664)
Released/updated on: 2006-01-12
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 1993 is the second annual survey of home health agencies and hospices and their current patients and discharges. This survey was designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with the agency administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff personnel, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff persons most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes service provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, Hispanic origin, race, and marital status.
Curated
National Home and Hospice Care Survey, 1994 (ICPSR 6733)
Released/updated on: 2006-01-12
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 1994 is the third annual survey of home health agencies and hospices and their current patients and discharges. These surveys were designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with the agency administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff personnel, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff persons most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes services provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, race, Hispanic origin, and marital status.
Curated
National Home and Hospice Care Survey, 1996 (ICPSR 2707)
Released/updated on: 2006-01-18
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 1996 is the fourth survey of home health agencies and hospices and their current patients and discharges. These surveys were designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with the agency administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff personnel, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff persons most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes services provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, race, Hispanic origin, and marital status.
Curated
National Home and Hospice Care Survey, 1998 (ICPSR 3763)
Released/updated on: 2006-01-18
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 1998 examines home health agencies and hospices and their current patients and discharges. These surveys were designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with the agency administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff persons most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes services provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, race, Hispanic origin, and marital status.
Curated
National Home and Hospice Care Survey, 2000 (ICPSR 3791)
Released/updated on: 2006-06-22
Geographic coverage: United States
The National Home and Hospice Care Survey (NHHCS) for 2000 examines home health agencies and hospices and their current patients and discharges. These surveys were designed to provide information for those who establish standards for, plan, provide, and assess long-term care services, both in the home and in inpatient settings. Data on agency characteristics were obtained through personal interviews with the agency administrators and include the number of home health and hospice patients served in the last 12 months, type of facility ownership (i.e., profit, nonprofit, government, other), Medicare and Medicaid certification, number and type of staff, and the hours they worked. Data on a sample of patients currently receiving home health and hospice care as well as a sample of discharges were obtained by interviewing staff persons most familiar with the care provided to these patients. Respondents were requested to refer to medical or other records whenever necessary. No patient was interviewed directly. Information for patients currently receiving services and discharged patients includes services provided and provider type, type of residence, referral source, medical diagnosis, type of care (home health or hospice), type of aids used (eyeglasses, dentures, walker, cane, oxygen, hospital bed, etc.), daily living activities that required assistance, and billing charges and expected payment source(s). The discharge diagnosis for discharged patients was also recorded. Demographic variables for both types of patients include sex, age, race, Hispanic origin, and marital status.
Curated
National Home and Hospice Care Survey, 2007 (ICPSR 28961)
Released/updated on: 2010-09-01
Geographic coverage: United States
Time period: 2007-08-01--2008-02-01, 2007-09-01--2008-04-01
The National Home and Hospice Care Survey (NHHCS) was reintroduced into the field in 2007 after a 7-year break. During that time, the survey was redesigned and expanded to include a computer-assisted personal interviewing (CAPI) system, many new data items, and larger sample sizes of current home health patients and hospice discharges. All agencies that participated in the survey were either certified by Medicare and/or Medicaid or were licensed by a state to provide home health and/or hospice services and currently or recently served home health and/or hospice patients. Agencies that provided only homemaker services or housekeeping services, assistance with instrumental activities of daily living (IADLs), or durable medical equipment and supplies were excluded from the survey. The 2007 NHHCS included a supplemental survey of home health aides employed by home health and/or hospice agencies, called the National Home Health Aide Survey (NHHAS). The 2007 NHHCS data were collected through in-person interviews with agency directors and their designated staffs; no interviews were conducted directly with patients or their families and/or friends. Agency data collected, available in agency administrative records, included information on the year an agency was established, the types of services an agency provided, referral sources, specialty programs, and staffing characteristics. Data collected on home health patients and hospice discharges, available in medical records, included age, sex, race and ethnicity, services received, length of time since admission, diagnoses, medications taken, advance directives, and many other items.
The National Home Health Aide Survey (NHHAS), the first national probability survey of home health aides, was designed to provide national estimates of home health aides employed by agencies that provide home health and/or hospice care. The NHHAS survey instrument included sections on recruitment, training, job history, family life, management and supervision, client relations, organizational commitment and job satisfaction, workplace environment, work-related injuries, and demographics.
Curated
Simple Crosstabs
Swedish Adoption/Twin Study on Aging (SATSA), 1984, 1987, 1990, 1993, 2004, 2007, and 2010 (ICPSR 3843)
Released/updated on: 2015-05-13
Geographic coverage: Sweden, Global
Time period: 1984-01-01--2010-01-01
The Swedish Adoption/Twin Study on Aging (SATSA) was designed to study the origins of individual differences in aging and the environmental and genetic factors that are involved. SATSA began in 1984, and six additional waves were conducted in 1987, 1990, 1993, 2004, 2007, and 2010. The questionnaire was initially sent to all twins from the Swedish Twin Registry who were separated at an early age and raised apart; the survey was also administered to a control sample of twins who were raised together. The respondents were surveyed on items that included health status, how they were raised, work environment, alcohol consumption, and dietary and smoking habits, as well as questions about personality and attitudes; this information comprised the first component. The second component was collected from a subsample composed of 150 pairs of twins raised apart and 150 pairs of twins raised together. This subsample participated in seven waves of in-person testing, which included a health examination, structured interviews, and tests on functional capacity, cognitive abilities, and memory. The data are represented according to questionnaire and time number, and correspond to each wave/year: Questionnaire 1 and In-Person Testing Time 1 were in 1984; Questionnaire 2 and In-Person Testing Time 2 were in 1987; Questionnaire 3 and In-Person Testing Time 3 were in 1990; Questionnaire 4 and In-Person Testing Time 4 were in 1993; Questionnaire 5 was in 2003; In-Person Testing Time 5 was in 2004; Questionnaire 6 and In-Person Testing Time 6 were in 2007; In-Person Testing Time 7 was in 2010. The Administrative and Cognitive datasets include data from all years/waves. The Smell Survey dataset only includes data from 1990. No years were specified for the Contact measures and Separation measures datasets. Demographic and background information includes age, sex, education, family history, household composition and employment.
Curated
Title XX Planning by Area Agencies on Aging: United States, 1975-1977 (ICPSR 9012)
Released/updated on: 2005-11-04
Geographic coverage: United States
Time period: 1975-01-01--1977-01-01
This data collection contains information on United States Area Agencies on Aging and the social services they make available to the elderly through Title XX funding. The units of analysis are the agencies. Variables include agency programs supported by Title XX funding, amount of agency's 1975-1976 and 1976-1977 Title XX allocations, and the agency's involvement with city, county, state, and federal officials. Other items include percent of budget for self-care, in-home, out-of-home, health-related, and institutional services, source of budget, date of establishment, and number of professional positions.