Showing 1 – 18 of 18 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
Geriatric Home Care Utilization: San Francisco, 1968-1975 (ICPSR 7853)
Released/updated on: 2006-03-30
Geographic coverage: San Francisco, United States, California
Time period: 1968-01-01--1975-01-01
This data collection reported on geriatric clients served by San Francisco Home Health Services, Inc. (SFHHS) between 1968 and 1975. The study was designed to document and analyze the natural history of home care service use from entry to exit, noting what types of users were in a home care agency's program and how intensively services were utilized. The study also identified outcome categories useful for response to public policy questions on the effectiveness of various service types in meeting geriatric needs. Also examined was the relationship of home care use to nursing home entry, and to the need for other services. In Part 1, data for 2,435 clients were gathered from case records at SFHHS. Variables used in the analysis include entry characteristics (e.g, age, sex, condition, living arrangement, and contextual variables such as referral source, prior source of care, and payment type), duration, intensity, and type of service utilization, as well as discharge or exit status. Some of these are calculated variables derived from each case's accumulated monthly service records (found in their raw form in Part 2). Part 2 contains 35,729 client monthly service records, which are distributed as raw data as received from SFHHS. Variables include billing date, pay plan, and frequency and intensity of assistance.
Curated
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.
Curated
National Health Interview Survey, 1994: Second Longitudinal Study on Aging, Wave 2, 1997 (ICPSR 3526)
Released/updated on: 2007-03-01
Geographic coverage: United States
The Second Longitudinal Study of Aging (LSOA II) is a collaborative effort of the National Center for Health Statistics (NCHS) and the National Institute on Aging (NIA). The NATIONAL HEALTH INTERVIEW SURVEY, 1994: SECOND SUPPLEMENT ON AGING (ICPSR 2563), serves as the baseline for this study. LSOA II Wave 2 interviews were conducted with a total of 7,998 respondents who were interviewed at baseline and consists of 7,060 survivor interviews and 998 decedent interviews. LSOA II Wave 2 is comprised of two data files, the Survivor Data (Part 1) and the Decedent Data (Part 2). The Survivor Data contains one record for each sample person (N = 9,447) interviewed at baseline and includes information drawn from several additional sources, including NATIONAL HEALTH INTERVIEW SURVEY, 1994 (ICPSR 6724) core questionnaire, NATIONAL HEALTH INTERVIEW SURVEY, 1994: FAMILY RESOURCES INCOME AND ASSETS SUPPLEMENT (ICPSR 2656), and NATIONAL HEALTH INTERVIEW SURVEY ON DISABILITY, 1994: PHASE I, DISABILITY OUTCOME SUPPLEMENT (ICPSR 2539). Wave 2 questions examined migration, convalescent home utilization, persistent symptomatic conditions such as pain in legs, swelling in feet, etc., nutrition, influenza immunization, mammogram, prostate, and cholesterol screenings, routine use of vitamins and aspirin, and detailed questions on home health care utilization. In addition a random one-quarter sample of the follow-up respondents were chosen to complete the Childhood Health and Family Longevity Module. This section is similar to that administered during the 1996 Health and Retirement Survey (HRS). Variable SF3462 indicates whether the sample person answered the childhood module. For the Decedent Data (Part 2) information was gathered from a family member or close relative regarding sample persons (N = 938) who were deceased at the time of Wave 2 interviews. Questions focused on housing, long-term care, assistance with key activities, chronic conditions, cognitive functioning, and health care use and health insurance.
Curated
National Health Interview Survey, 1994: Second Longitudinal Study on Aging, Wave 3, 2000 (ICPSR 3807)
Released/updated on: 2008-02-05
Geographic coverage: United States
The Second Longitudinal Study of Aging (LSOA II) is a collaborative effort of the National Center for Health Statistics (NCHS) and the National Institute on Aging (NIA). The NATIONAL HEALTH INTERVIEW SURVEY, 1994: SECOND SUPPLEMENT ON AGING (SOA II) (ICPSR 2563) serves as the baseline for this study. LSOA II, Wave 3 consists of 7,936 survivor interviews and 906 decedent interviews in two data files: the Survivor File (Part 1) and the Decedent File (Part 2). The Survivor File contains one record for each sample person (N = 9,447) interviewed at baseline and includes information drawn from several additional sources, including the 1994 National Health Interview Survey (ICPSR 6724) core questionnaire, the 1994 National Health Interview Survey: Family Resources Supplement (ICPSR 2656), Phase I of the 1994 National Health Interview Survey on Disability (ICPSR 2539), and the SOA II baseline interview (ICPSR 2563). Wave 3 questions (beginning at variable SF3664) examined migration, convalescent home utilization, nutrition, influenza immunization, mammogram, prostate, and cholesterol screenings, routine use of vitamins, aspirin, calcium supplements, and antioxidants, and detailed questions on home health care utilization. In addition, a random one-quarter sample of the follow-up respondents were chosen to complete the Childhood Health and Family Longevity Module. This section is similar to that administered during the 1996 Health and Retirement Survey (HRS). Variable SF3462 indicates whether the sample person answered the childhood module. For the Decedent File (Part 2), information was gathered from a family member or close relative regarding sample persons (N = 906) who were deceased at the time of Wave 3 interviews. Questions focused on housing, long-term care, assistance with key activities, chronic conditions, cognitive functioning, health care use, and health insurance.
Curated
National Long Term Care Channeling Evaluation, 1982-1984 (ICPSR 8683)
Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1982-01-01--1984-01-01
The United States Department of Health and Human Services initiated this survey to demonstrate and evaluate the cost savings and effectiveness of applying a case management approach to community-based long term care services for the frail elderly. The goal of case management is to coordinate and direct community, medical, and informal long term care services to the frail elderly as an alternative to institutionalization. The four main areas of evaluation are: 1) the use of hospitals, nursing homes, and other formal medical services, 2) public and private expenditures on formal community services including case-management, housing, and income transfers, 3) informal care by family and friends, and 4) individual outcomes, including quality of life, physical functioning, unmet service needs, and mortality of the elderly sample members.
Curated
National Medical Expenditure Survey, 1987: Household Survey, Care Giver and Care Receiver Supplements [Research File 31R] (ICPSR 6649)
Released/updated on: 2006-03-30
Geographic coverage: United States
The National Medical Expenditure Survey (NMES) series provides information on health expenditures by or on behalf of families and individuals, the financing of these expenditures, and each person's use of services. The Household Survey was fielded over four rounds of personal and telephone interviews at four-month intervals. Baseline data on household composition, employment, and insurance characteristics were updated each quarter, and information on all uses of and expenditures for health care services and sources of payment was obtained. Research File 31R provides information collected from two supplements administered as part of the Household Survey: the Care Receiver Supplement and the Care Giver Supplement. The Care Receiver Supplement (Part 2) was given to those Round 2 persons who answered positively to receiving help in at least one of three areas: assistance with Activities of Daily Living (ADL), assistance with Instrumental ADL (IADL), or financial assistance. This supplement asked for information on the care receiver's living situation, and amounts and types of assistance. The Care Giver Supplement (Parts 3 and 4) was administered in Rounds 2 and 5 to persons identified in the Long-Term Care Supplement (see ICPSR 9675) as being the main care-givers for other members of the dwelling unit who had difficulty with one or more ADLs or IADLs. This supplement obtained information on the impact of a caregiver's responsibilities on his or her employment, income, and physical and mental health, as well as the extent of the impaired person's psychological and social disabilities. Part 1, Person-Level Summary Data, supplies information such as age, sex, race, marital status, and education of the respondents.
Curated
National Medical Expenditure Survey, 1987: Household Survey Data on Home Health Care and Medical Equipment Purchases and Rentals [Public Use Tape 14.2] (ICPSR 9944)
Released/updated on: 2006-03-30
Geographic coverage: United States
The 1987 NMES provides information on health expenditures by or on behalf of families and individuals, the financing of these expenditures, and each person's use of services. The Household Survey is one of the three major components of the 1987 National Medical Expenditure Survey (NMES). (The other two components are the Survey of American Indians and Alaska Natives [SAIAN] and the Institutional Population Component.) The Household Survey was fielded over four rounds of personal and telephone interviews at four-month intervals. Baseline data on household composition, employment, and insurance characteristics were updated each quarter, and information on all uses of and expenditures for health care services and sources of payment was obtained. Public Use Tape 14.2 provides two data files containing information on expenditures for formal home health care and the purchase or rental of medical equipment, supplies, and other medical items. The Home Health Care file contains information on each person in the Household Survey using these services in 1987. Each record is restricted to the set of formal services provided during the year by each type of provider sent by each unique agency furnishing home health care. This file provides person-level demographic information such as age, sex, and race, and information on household-reported medical conditions associated with the use of home health care. The Medical Equipment and Supplies file contains one record per type of medical item for each eligible person in the Household Survey who reported having purchased, rented, or otherwise obtained such items. This file also provides person-level demographic information, and medical condition and date of purchase variables.
Curated
National Medical Expenditure Survey, 1987: Household Survey I, Population and Home Health Providers (ICPSR 9339)
Released/updated on: 2006-01-18
Geographic coverage: United States
This data collection contains two data files derived from information gathered in the initial screening and Round 1 interviews of the Household Survey component of the 1987 NATIONAL MEDICAL EXPENDITURE SURVEY (NMES). The Person File contains data on each person sampled in the first round of the Household Survey. Data are included on each sampled person's self-reported coverage under private health insurance and public programs such as Medicaid, Medicare, and CAMPUS/CAMPVA. In addition, data describe difficulties and help with activities of daily living such as bathing, dressing, eating, toileting, handling money, walking, shopping, preparation of meals, light housekeeping, and the use of telephones and transportation. For persons with difficulties in activities of daily living, there is also information on prior nursing home institutionalization and the use of special equipment, adult day care, senior centers, home-delivered and congregate meals, special transportation, and telephone assurance. The Person File covers a broad range of personal background variables: age, sex, race, ethnicity, Hispanic ancestry, marital status, family relationships, educational status, employment status, occupation, industry, wages and salary, length of time at work, characteristics of the workplace, union membership, and military service. The Home Health Provider File contains data (as reported by the Household Survey respondents) on each provider of formal or informal services who came to the home of a person in the Household Survey sample within a month of the Round 1 interview. Information in the Home Health Provider File includes date of the provider's last visit, length of stay in the home, type of services rendered, provider's place of work, provider's medical specialty, if any, and whether or not the provider was a relative of the person receiving help.
Curated
National Medical Expenditure Survey, 1987: Survey of American Indians and Alaska Natives, Population Data, Data from the Health Status Questionnaire and Access to Care Supplement, and Expenditures and Sources of Payment Data [Public Use Tape 37] (ICPSR 6490)
Released/updated on: 1995-06-05
Geographic coverage: United States
The National Medical Expenditure Survey (NMES) series provides information on health expenditures by or on behalf of families and individuals, the financing of these expenditures, and each person's use of services. The Survey of American Indians and Alaska Natives (SAIAN) was designed in collaboration with the Indian Health Service (IHS), and used the same data collection instruments, interview procedures, and time frame as the NMES Household Survey component. However, the SAIAN differed from the Household Survey in several respects. The SAIAN sample was interviewed only three times and was not given the supplements on long-term care, caregiving, and care-receiving. Also, SAIAN respondents were asked additional questions on topics such as use of IHS facilities and traditional medicine, and were given a modified self-administered questionnaire with separate versions for adults and children. Interviewers for the SAIAN were mainly American Indians or Alaska Natives, and about 20 percent of the interviews were not conducted entirely in English. Of these, approximately 40 percent were conducted entirely in the native language of the respondent. Public Use Tape 37 contains the final 1987 calendar year SAIAN data, and updates all previous releases of SAIAN data. Variables include population characteristics (demographic information, native language, household composition, employment, health insurance, eligibility status) health statistics (medical conditions, illnesses, limitations on activities, vaccinations), prescribed medicines (dates medication last taken, name of medication prescribed, number of medication purchases made during the year), home health care, medical items purchased, rented, or otherwise obtained, type of traditional medical practitioner seen by respondent, type of service obtained during dental visits, inpatient hospital stays (reason for entry, surgery performed, days and nights in hospital, date entered and discharged), ambulatory visits and telephone calls to physicians' offices, visits to hospital outpatient departments, and visits to hospital emergency rooms.
Curated
National Medical Expenditure Survey, 1987: Survey of American Indians and Alaska Natives, Preliminary Data on Home Health Care, Medical Equipment Purchases and Rentals, and Traditional Medicine [Public Use Tape 23.2P] (ICPSR 6251)
Released/updated on: 2006-03-30
Geographic coverage: United States
The National Medical Expenditure Survey (NMES) series provides information on health expenditures by or on behalf of families and individuals, the financing of these expenditures, and each person's use of services. The Survey of American Indians and Alaska Natives (SAIAN) was designed in collaboration with the Indian Health Service (IHS), and used the same data collection instruments, interview procedures, and time frame as the NMES Household Survey component. However, the SAIAN differed from the Household Survey in several respects. The SAIAN sample was interviewed only three times and was not given the supplements on long-term care, caregiving, and care-receiving. Also, SAIAN respondents were asked additional questions on topics such as use of IHS facilities and traditional medicine, and were given a modified self-administered questionnaire with separate versions for adults and children. Interviewers for the SAIAN were mainly American Indians or Alaska Natives, and about 20 percent of the interviews were not conducted entirely in English. Of these, approximately 40 percent were conducted entirely in the native language of the respondent. Part 1 of this collection contains information on formal home care providers for each eligible person in the SAIAN who reported receiving home health services, including date the provider was seen, provider's length of stay, type of agency the provider worked for, and kind of help performed by the provider. Demographic information on the recipient (race, age, and sex), and household-reported medical conditions associated with the use of home health care is also included. Part 2 contains information on medical items purchased, rented, or otherwise obtained. Demographic variables similar to those in Part 1 are provided, along with medical conditions and dates that items were obtained. Part 3 contains variables on the type of traditional practitioner seen by respondents, as well as demographic and medical condition variables.
Self-published
National Neighborhood Data Archive (NaNDA): Healthcare Services by Census Tract and ZCTA, United States, 1990-2022 (ICPSR 209050)
Released/updated on: 2026-03-31
Time period: 1990-01-01--2022-01-01
This dataset contains measures of the number and density of health care services per United States Census Tract or ZIP Code Tabulation Area (ZCTA) from 1990 through 2022. The dataset includes four separate files for four different geographic areas (GIS shapefiles from the United States Census Bureau).
Curated
Nihon University Japanese Longitudinal Study of Aging (NUJLSOA) (ICPSR 156)
Released/updated on: 2006-06-19
Geographic coverage: Japan, Global
The NUJLSOA is a longitudinal survey of a nationally representative sample of the population aged 65 and over in Japan. The first wave of data was collected in November 1999, the second in November 2001, and a third wave in November 2003. The study was designed primarily to investigate health status of the Japanese elderly and changes in health status over time. An additional aim was to investigate the impact of long-term care insurance system on the use of services by the Japanese elderly and to investigate the relationship between co-residence and the use of long term care. While the focus of the survey is health and health service utilization, other topics relevant to the aging experience are included such as intergenerational exchange, living arrangements, caregiving, and labor force participation.
Curated
Pediatric Home Care: Results of a National Evaluation of Programs for Ventilator-Assisted Children, 1974-1983 (ICPSR 8948)
Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1974-01-01--1983-01-01
This collection examines three programs designed to facilitate the discharge of ventilator-assisted children to the home or a homelike alternative. Program personnel, advisory board members, and the primary caregivers of the children were interviewed as part of the evaluation. This study is the first comprehensive and systematic effort of its kind to develop a conceptual and methodological approach to gathering data on this new population of technology-assisted children. The ultimate outcomes examined were the ventilator-assisted child's quality of life, the stress and adaptation experienced by the care- giver(s) and family unit, and the cost-effectiveness of the alternative home care arrangements relative to traditional inpatient care.
Curated
Restricted
Post-Acute Care Supplement (PACS) Research Files, 2000-2010 (ICPSR 34443)
Released/updated on: 2013-02-28
Geographic coverage: United States
Time period: 2000-01-01--2010-12-31
Overview. The Post-Acute Care Supplement (PACS) files were developed from two administrative data sets that capture assessments at multiple points in post-acute care: the Outcome and Assessment Information Set (OASIS) Summary File (OASF): 2000-2010, which covers home health care, and the Long-Term Care Annual Summary File (LTCASF): 2000-2010, which covers nursing homes. Annual files were developed for the period 2000 to 2010 that summarize health conditions, functional status, and care patterns into one observation per beneficiary per year.
Data Access. These data are not available from ICPSR. Because the data contain confidential CMS assessment data, researchers will need to secure a data use agreement from CMS. For researchers who secure a DUA, the files will be distributed to them through the Medicare/Medicaid Research Information Center (MedRIC) ([email protected]).
Curated
Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001, Baseline and Follow-Up Data (ICPSR 3678)
Released/updated on: 2006-09-26
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-01
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Baseline data (ICPSR 3253) were collected through randomized clinical trials at six sites: University of Alabama-Birmingham, The Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee-Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions such as psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services varied by site. This collection contains baseline data along with follow-up data at 6-, 12-, and 18-month intervals from each site with focus on the impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization. Also included are follow-up batteries, transition batteries (placement, bereavement, discontinued), and data reporting missed visits. Parts 1 through 5 contain screening data and responses to a short mental status questionnaire. Parts 6 through 34 contain baseline data along with follow-up data at 6, 12, and 18-month intervals and cover activities of daily living, anxiety, and caregiver health and health behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 35 through 40 contain tracking data and also include an examination of interventions.
Curated
Resources for Enhancing Alzheimer's Caregiver Health (REACH II), 2001-2004 (ICPSR 4354)
Released/updated on: 2006-10-27
Geographic coverage: Palo Alto, United States, Tennessee, Memphis, California, Alabama, Florida, Birmingham, Philadelphia, Pennsylvania, Miami
Time period: 2001-01-01--2004-01-01
Built upon the findings of RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH, 1996-2001, BASELINE AND FOLLOW-UP DATA [ICPSR 3678], REACH II designed and tested a single multi-component intervention among family caregivers of persons with Alzheimer's disease or related disorders. The overall objectives were (1) to identify and reduce modifiable risk factors among diverse family caregivers of patients with Alzheimer's Disease or a related disorder, (2) to enhance the quality of care provided to the care recipients, and (3) to enhance the well-being of the caregivers. REACH II is the first project to simultaneously test a comprehensive caregiver intervention in three distinct racial/ethnic groups: Hispanic/Latino, Black/African-American, and White/Caucasian. The intervention was based on a risk-appraisal approach in which five areas of risk--depression, burden, self-care, social support, and patient problem behaviors--that are central to caregiver well-being and quality of life were matched to corresponding intervention components. These components included education, skills to manage troublesome care-recipient behaviors, social support, cognitive strategies for reframing negative emotional responses, and strategies for enhancing healthy behaviors and managing stress. Consistent with this approach, the primary outcome was a multivariate quality of life indicator that assessed caregiver depression, burden, self-care, social support, and patient problem behaviors. Two hallmarks of caregiver intervention studies--caregiver clinical depression and patient institutionalization--were assessed as secondary outcomes. The dataset names listed in this collection include the shortened name of the form administered.
Curated
Robert Wood Johnson Foundation Supportive Services Program in Senior Housing, Tenant Characteristics and Service Use, 1990-1991: [United States] (ICPSR 6013)
Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1990-05-01--1991-10-01
These data describe tenants of subsidized elderly housing who used services provided by the Robert Wood Johnson Foundation Supportive Services Program in Senior Housing (RWJF SSPSH), and document use of these services. Services provided by the RWJF SSPSH program included housekeeping, transportation, meals, running errands, assistance with forms, personal care, and home health care. Three types of data comprise this collection: (1) participant information taken at first service delivery (Part 1), (2) administrative logs describing services delivered to each client (Parts 2-7), and (3) information on each site participating in the program (Part 8). Information about the participants includes age, gender, living arrangements, monthly income, health status, ability to do light and heavy tasks, and ability to do personal tasks. Information on service delivery includes the type and amount of each service delivered, whether the tenant paid for the service, how the service was funded, and the quarter in which the service was delivered. Site information includes subsidy type, building start date, type of location (urban, suburban, or rural), and whether the site had a full- or part-time service coordinator.