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Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE) Frailty Study: 2006-2009 (ICPSR 36321)

Released/updated on: 2016-03-29
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2006-01-01--2009-01-01
The Hispanic Established Populations for Epidemiologic Studies of the Elderly (EPESE) Frailty Study sought to apply a standard definition of frailty in a well-defined sample of Mexican American older adults and to examine the impact of frailty on disability, health related quality of life, institutionalization, and mortality in this population over time. This project is a continuation of a prior study (the Hispanic EPESE) examining the enabling-disabling process in this same population of aging Mexican Americans; data were collected from 1,031 older adults who were participating in the Hispanic EPESE. Only subjects who were physically capable of safely completing the muscle strength measures were included. Baseline interviews were collected for this subsample in 2006/2007 during Wave 6 (ICPSR 29654) of the Hispanic EPESE study. This collection includes data about respondents' health status, activities of daily living and their ability to perform tasks. Two-year follow-up data were collected in 2008/2009 from 731 participants in Wave 1. Demographic and background information include age, relationship status, gender, marital status and household composition.
Curated

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 Survey of Institutionalized Persons, 1976 (ICPSR 7866)

Released/updated on: 1992-02-16
Geographic coverage: United States
This data collection was designed to obtain information about the services and resources of the various types of long-term care facilities in the United States, i.e., chronic care institutions (providing care for people with chronic conditions, diseases, and handicaps), institutions that provide care for the mentally ill and mentally handicapped, nursing homes, homes for the aged, and residential schools and treatments centers. Six major areas of concern were examined in this study: (1) the appropriateness of placement/admission and discharge, plus possible alternatives, (2) the quality of life within the institutional environment, (3) the residents' rights and legal status, (4) the medical and non-medical services provided and needed, (5) the sources of financing such care, and (6) the impact of government programs and policies upon the costs and provision of certain types of service. This information was collected from 9,090 residents of 851 institutions and from 3,289 of their family members. Administrative staff at each resident's facility also provided information about that facility as well as the sampled resident. Data about the resident's institution include its basic characteristics, e.g., type of care provided, ownership, number of beds, occupancy rate, and services and programs offered. Resident data include basic social and demographic characteristics, reason for institutionalization, cost of care, current activities, type of treatment, and the physical limitations of the institutional population. Family data examine the next of kin's relationship to the resident, e.g., relative's proximity to the institution, frequency of visits, and monetary contributions to the resident, as well as the next of kin's demographic characteristics and views of the resident and his or her institutionalization.