National Archive of Computerized Data on Aging

National Survey of Access to Medical Care, 1975-1976 (ICPSR 7730) RSS

Principal Investigator(s):

Summary:

This study was undertaken for the purpose of providing baseline national indicators of access to health care for an evaluation of a program of hospital-based primary care group practices funded by the Robert Wood Johnson Foundation. The main objective of that large-scale social experiment was to improve access to medical care for the population in areas served by the groups. The access framework and questionnaires designed for the study were developed to provide empirical indicators of the concept that could be used to monitor progress toward this objective. Five data collection instruments were used by the study: the Household Enumeration Folder, the Main Questionnaire, the Health Opinions Questionnaire, the Physician Supplement, and the Hospital/Extended Care Supplement. The Household Enumeration Folder collected basic demographic information on all household members and served as a screener for the episode of illness and minority oversamples. The Main Questionnaire collected information on disability, symptoms of illness, episodes of illness, socioeconomic and demographic characteristics, and access to health care: sources of medical care utilized, problems associated with access to sources of care (e.g., transportation, parking, waiting time for an appointment), satisfaction with medical services received, utilization of medical diagnostic procedures, dental care, and eye care, and insurance coverage and out-of-pocket expenditures for health care. Respondents' opinions concerning the medical care that they received were gauged by the Health Opinions Questionnaire. The Physician Supplement and the Hospital/Extended Care Supplement collected information on physicians contacted and facilities utilized in connection with reported episodes of illness. File 1, File 2, and File 3 constitute the data files for this collection. File 1 comprises data from the Household Enumeration Folder, the Main Questionnaire, and the Health Opinions Questionnaire, plus variables from secondary sources, such as characteristics, derived from the American Medical Association Physician Masterfile, of physicians named as caregivers by respondents, and medical shortage data, from various sources, for the respondent's county of residence. File 2 contains the data from the Physician Supplement, while File 3 provides the data collected by the Hospital/Extended Care Supplement.

Access Notes

Dataset(s)

DS0:  Study-Level Files
Documentation:
DS1:  File 1: Data From Main Questionnaire and Other Sources - Download All Files (37.4 MB)
Documentation:
Data:
DS2:  File 2: Physician Supplement Data - Download All Files (18.3 MB)
Documentation:
Data:
DS3:  File 3: Hospital/Extended Care Supplement Data - Download All Files (17.8 MB)
Documentation:
Data:

Study Description

Citation

Andersen, Ronald, and Lu Ann Aday. National Survey of Access to Medical Care, 1975-1976. ICPSR07730-v2. Ann Arbor, MI: Inter-university Consortium for Political and Social Research[distributor], 2013-05-31. http://doi.org/10.3886/ICPSR07730.v2

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Funding

This study was funded by:

  • Robert Wood Johnson Foundation (RWJ 4550)
  • National Center for Health Services Research (NCHSR 230-76-0096)

Scope of Study

Subject Terms:   health, hospitals, issues, physicians, public health

Geographic Coverage:   United States

Time Period:  

  • 1975--1976

Date of Collection:  

  • 1975--1976

Universe:   Noninstitutionalized population of the United States.

Data Types:   administrative records data, survey data

Data Collection Notes:

The weight variable V805 is a character (string) variable written in scientific notation with nine significant digits. Variable V857 is a numeric version of V805 that is rounded to six significant digits.

Methodology

Sample:   A self-weighting probability sample was selected using the National Opinion Research Center master sample. In addition, special oversamples were selected for three groups: persons experiencing episodes of illness, southern non-SMSA Blacks, and southwestern Spanish-heritage persons.

Data Source:

personal interviews, county-level data from published sources, and the American Medical Association Physician Masterfile

Extent of Processing:  ICPSR data undergo a confidentiality review and are altered when necessary to limit the risk of disclosure. ICPSR also routinely creates ready-to-go data files along with setups in the major statistical software formats as well as standard codebooks to accompany the data. In addition to these procedures, ICPSR performed the following processing steps for this data collection:

  • Performed recodes and/or calculated derived variables.
  • Checked for undocumented or out-of-range codes.

Version(s)

Original ICPSR Release:  

Version History:

  • 2013-05-31 ICPSR converted the OSIRIS dictionaries to SPSS setups, replaced the OSIRIS data maps with record layout files, and added SPSS versions of the data files to the collection. In addition, ICPSR corrected variable V857 (weight variable rounded to six significant digits) in File 1: Data From Main Questionnaire and Other Sources.
  • 2006-01-18 File CB7730.ALL.PDF was removed from any previous datasets and flagged as a study-level file, so that it will accompany all downloads.
  • 1998-06-30 The codebook and data maps are now available as PDF files.

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