Chronic Illness and Caregiving, 2000: [United States] (ICPSR 3402)
Principal Investigator(s): Thamer, Mae, Johns Hopkins University. School of Public Health
Summary: 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 awarenes... (more info)
This data is freely available.
Thamer, Mae. CHRONIC ILLNESS AND CAREGIVING, 2000: [UNITED STATES]. ICPSR03402-v1. Youngstown, OH, Binghamton, NY, and New York, NY: Harris Interactive, Inc. [producers], 2000. Ann Arbor, MI: Inter-university Consortium for Political and Social Research [distributor], 2006-05-04. doi:10.3886/ICPSR03402.v1
Persistent URL: http://dx.doi.org/10.3886/ICPSR03402.v1
This survey was funded by:
- Robert Wood Johnson Foundation (37084)
Scope of Study
Summary: 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.
Geographic Coverage: United States
Date of Collection:
Universe: Persons aged 18 and older in the United States.
Data Types: survey data
Data Collection Notes:
The data map is provided by ICPSR as an ASCII text file and the codebook and frequencies are provided by ICPSR as a Portable Document Format (PDF) file.
Sample: A national cross-section of adults was selected. Persons with a chronic illness and adults who provided informal caregiving services were oversampled. In all, interviews were conducted with 1,663 subjects, of which 680 were neither chronically ill nor caregivers, 189 were caregivers but not chronically ill, 559 were chronically ill but not caregivers, and 235 were chronically ill caregivers.
Original ICPSR Release: 2002-05-14
- 2006-05-04 An ICPSR Processing Note was added to the codebook concerning variable Q410 (Caregiver/Chronically Ill) and errors in the methodology section of the codebook. The study description was revised accordingly.
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