Showing 1 – 14 of 14 results.
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Bicol Multipurpose Survey (BMS), 1994: [Philippines] (ICPSR 6890)
Released/updated on: 2013-05-15
Geographic coverage: Philippines, Global
The objectives of the 1994 Bicol Multipurpose Survey, which were similar to those of the BICOL MULTIPURPOSE SURVEY (BMS), 1978: [PHILIPPINES] (ICPSR 6878) and the 1983 BMS (ICPSR 6889), were to gather information on income, earnings, mobility, fertility, farm production, and health from the residents of the Bicol Region in the Philippines. Households in the province of Camarines Sur were surveyed, with a primary focus on household characteristics, adult and child health, value and income of assets or properties, expenditures on education and liabilities, income such as cash and in-kind transfers, and income from household members not residing in the household, along with agricultural production of rice and other crops. Information about the barangay (a barangay is a political subdivision equivalent to a village in rural areas and to a neighborhood in urban areas) in which the household was located includes environmental sanitation, availability of community services, and cost for community services or family planning. Data regarding successor households (households where the children had taken over the management and supervision of family assets) were examined, along with intergenerational income mobility data (the impact of parental income and investments on children).
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Community Hospital Program (CHP) Access Impact Evaluation Surveys, 1978-1979, 1981 (ICPSR 8245)
Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1978-01-01--1979-01-01
This data collection evaluates group medical practices and the ways in which they affect both access to and use of medical services. Group practices, sponsored by the Robert Wood Johnson Foundation Community Hospital Program (CHP), were selected for use in this assessment. The data were collected by the Center for Health Administration Studies at the University of Chicago, with the assistance of Chilton Research Services. Two surveys were conducted for the study: a baseline survey in 1978-1979 and a follow-up in 1981. Community residents and CHP patients in 12 communities were interviewed. Demographic and medical care data were collected for selected individuals and families in the survey areas. Data on regular sources of medical care for individuals include the type of organization used, type of practice, accessibility, frequency of visits, types of health care professionals seen, cost, and satisfaction. Also in the collection are data on perceived health, episodes of illness (including symptoms, duration, disability days, and doctors consulted), use of preventive health care services, and insurance coverage. Demographic data for individuals and families include age, sex, race, educational attainment, employment, and income. Of the 198 files in this collection, 88 are "raw" data files and 110 are frequencies. The data files consist of four types. The first type are Sample Person files. These contain the responses of group practice patients and community members. The second type are Doctor Episode files, which record doctors and episodes of illness. Family files make up the third type of file, and consist of family members' responses to the survey. Analysis files, linking patient and doctor data, are the fourth type of file. The SPSS frequency files correspond to the data files: two per file for the Sample Person files, and one per file for the remaining three types of files.
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Community Tracking Study Household Survey, 1996-1997, and Followback Survey, 1997-1998: [United States] (ICPSR 2524)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-07-01--1997-07-01, 1997-10-01--1998-08-01
This data collection comprises two components of the Community Tracking Study (CTS), the Household Survey and the Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. At the beginning of each interview, a household informant was identified and queried about the composition of the household. With this information, individuals in the household were grouped into family insurance units (FIU). An FIU reflects family groupings typically used by insurance carriers. It includes an adult household member, his or her spouse, if any, and any dependent children 0-17 years of age (or 18-22 years of age if a full-time student). Family informants, selected from each FIU in the household, provided information on health insurance coverage, health care use, usual source of care, and the general health of all persons in the FIU. These informants also provided information on family income and out-of-pocket expenses for health care, as well as employment, race, and Hispanic origin for all adult FIU members. Each adult in the household, including the FIU informants, responded through a self-response module to questions regarding unmet health care needs, patient trust, satisfaction with physician choice, limitations in daily activities, smoking behaviors, and last doctor visit. In FIUs with more than one child under 18, only one child was randomly selected for inclusion in the survey. The family informant responded on behalf of the child regarding unmet needs and satisfaction with physician choice. The adult family member who took this child to his or her last doctor visit responded to questions about the visit. The Followback Survey was designed to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to health plans and other organizations that offered or administered the comprehensive private health insurance policies covering Household Survey respondents in the 60 CTS sites. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
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Community Tracking Study Household Survey, 1998-1999, and Followback Survey, 1998-2000: [United States] (ICPSR 3199)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1998-01-01--2000-01-01
This collection comprises the second round of the Community Tracking Study (CTS) Household Survey and the second round of the CTS Followback Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and their effects on care delivery and individuals. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first round of the Household Survey (COMMUNITY TRACKING STUDY HOUSEHOLD SURVEY, 1996-1997, AND FOLLOWBACK SURVEY, 1997-1998: [UNITED STATES] (ICPSR 2524)), the second round of the Household Survey was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. The purpose of the Followback Survey was to obtain detailed information on private health insurance coverage reported in the Household Survey. It was administered to the health plans and other organizations (managed care organizations, third-party administrators, employer or union plans, and employers) that offered or administered the respondents' comprehensive private health insurance policies. Information on private health insurance policies collected by the Followback Survey includes product type, gatekeeping, consumer cost sharing, provider payment methods, and coverage of mental health and/or substance abuse services.
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Community Tracking Study Household Survey, 2000-2001: [United States] (ICPSR 3764)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2000-01-01--2001-01-01
This collection comprises the third round of the Community Tracking Study (CTS) Household Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and the effects of those changes on people. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the Household Survey (ICPSR 2524 and 3199), the third round was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. A new set of sample design variables was added to the third round data for variance estimation by statistical software packages other than SUDAAN.
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Community Tracking Study Household Survey, 2003: [United States] (ICPSR 4216)
Released/updated on: 2007-12-03
Geographic coverage: United States
Time period: 2003-01-01--2004-01-01
This collection contains data and documentation for the fourth round of the Community Tracking Study (CTS) Household Survey. Sponsored by the Robert Wood Johnson Foundation, the CTS is a national study designed to track changes in the United States' health care system and their effects. The fourth round was administered to households in the 60 CTS sites: 51 metropolitan areas and nine nonmetropolitan areas which were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The first round of the CTS Household Survey was conducted in 1996-1997 (ICPSR 2524), the second round in 1998-1999 (ICPSR 3199), and the third in 2000-2001 (ICPSR 3764). Respondents to the fourth round provided information about health insurance coverage, use of health services, unmet needs for health care, children's special health care needs, out-of-pocket medical costs, patient trust in physicians, sources of health information, attitudes about medical care, and satisfaction with health care and health plans. Health status, chronic conditions, and risk attitudes and smoking behavior were additional topics covered by the fourth round questionnaire. The data include variables on height and weight, employment, income, ethnicity, race, United States citizenship, household composition, and demographic characteristics.
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Community Tracking Study Physician Survey, 1996-1997: [United States] (ICPSR 2597)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-08-01--1997-08-01
Sponsored by the Robert Wood Johnson Foundation, this survey is one component of the Community Tracking Study (CTS), a national study designed to track changes in the health care system and the effects of the changes on care delivery and on individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. The Physician Survey was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. Information gathered by the survey instrument includes physician supply and specialty distribution, practice arrangements and physician ownership of practices, sources of practice revenue, level and determinants of physician compensation, effects of care management strategies, and physicians' allocation of time, provision of charity care, career satisfaction, and perceptions of their ability to deliver care. For primary care physicians, the survey instrument also provided vignettes of various clinical presentations for which there was no prescribed method of treatment. These physicians were asked to indicate the percentage of patients for whom they would recommend the course of action specified in each particular vignette. Part 3, the Site and County Crosswalk Data File, describes which counties constitute each site. Part 4, the Physician Survey Summary File, contains site-level averages and percentages and standard errors of these estimates for selected attributes, e.g., the percentage of physicians who were foreign medical school graduates, average age of physicians, average percentage of patient care practice revenue from Medicaid, etc.
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Community Tracking Study Physician Survey, 1998-1999: [United States] (ICPSR 3267)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1998-01-01--1999-01-01
This study comprises the second round of the physician survey component of the Community Tracking Study (CTS) sponsored by the Robert Wood Johnson Foundation. The CTS is a national study designed to track changes in the American health care system and the effects of the changes on care delivery and on individuals. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first round of the physician survey (COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1996-1997: [UNITED STATES] (ICPSR 2597)), the second round was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. The survey instrument collected information on physician supply and specialty distribution, practice arrangements and physician ownership of practices, physician time allocation, sources of practice revenue, level and determinants of physician compensation, provision of charity care, career satisfaction, physicians' perceptions of their ability to deliver care, views on care management strategies, and various other aspects of physicians' practice of medicine. In addition, primary care physicians (PCPs) were asked to recommend courses of action in response to some vignettes of clinical presentations for which there was no prescribed method of treatment.
Dataset 3, the Site and County Crosswalk Data File, identifies the counties that constitute each CTS site.
Dataset 4, the Physician Survey Summary File, contains site-level estimates and standard errors of the estimates for selected physician characteristics, e.g., the percentage of physicians who were foreign medical school graduates, the mean age of physicians, and the mean percentage of patient care practice revenue from Medicaid.
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Community Tracking Study Physician Survey, 2000-2001: [United States] (ICPSR 3820)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2000-01-01--2001-01-01
This study comprises the third round of the physician survey component of the Community Tracking Study (CTS). Sponsored by the Robert Wood Johnson Foundation, the CTS is a large-scale investigation of changes in the health care system and their effects on people. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the physician survey, COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1996-1997: [UNITED STATES] (ICPSR 2597) and COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1998-1999: [UNITED STATES] (ICPSR 3267), the third round was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. The survey instrument collected information on physician supply and specialty distribution, practice arrangements and physician ownership of practices, physician time allocation, sources of practice revenue, level and determinants of physician compensation, provision of charity care, career satisfaction, physicians' perceptions of their ability to deliver care, effects of care management strategies, and various other aspects of physicians' practice of medicine. Part 3, the Site and County Crosswalk Data File, identifies the counties that constitute each CTS site. Part 4, Physician Survey Summary File, contains site-level estimates and standard errors for selected physician characteristics, e.g., the average age of physicians, the percentage of physicians who were either very or somewhat dissatisfied with their overall career in medicine, and the average percentage of patients with prescription coverage that included the use of a formulary.
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First Malaysian Family Life Survey, 1976-1977 (ICPSR 6170)
Released/updated on: 1998-12-23
Geographic coverage: Malaysia, Global
The First Malaysian Family Life Survey, 1976-1977 (MFLS-1), was conducted in Peninsular Malaysia as a retrospective life history survey of 1,262 households containing an ever-married woman aged 50 or younger. Full life histories were collected through personal interviews with these women and their husbands regarding fertility-related events, marriage, employment, migration, income and wealth, attitudes and expectations with respect to family size and composition, community characteristics, time allocation, and transfers of goods, help, and money between the respondents and others. The survey collected data in three separate rounds held at four-month intervals. The majority of the survey was administered in Round 1, while the second and third rounds collected data on new questions not asked in Round 1 and also updated some of the Round 1 data, most notably the work and pregnancy histories. In October 1981, the individual-level dataset (Part 142) was created, consisting of one fixed-length record per individual per household. Variables included at both the individual and household levels provide information on demographics, time allocation, and income and wealth. Due to processing constraints, most of the retrospective data have been omitted from the individual-level dataset.
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Guatemalan Survey of Family Health (EGSF), 1995 (ICPSR 2344)
Released/updated on: 2025-11-06
Geographic coverage: Guatemala, Global
Time period: 1995-05-01--1995-10-01
The Guatemalan Survey of Family Health (EGSF) was undertaken to investigate the health of children under the age of five and women during pregnancy and childbirth residing in 60 communities within the departments (geopolitical units) of Chimaltenango, Suchitepequez, Totonicapan, and Jalapa in Guatemala. Data were collected at the household, individual, and community levels to gain an in-depth understanding of the way residents in these rural populations think about their health, treatment, and family relations.
Data at the household level (Parts 1-5, 90-92) provide information on household members, relation to household head, age, education, and language used.
The individual-level data (Parts 6-37) describe the respondent's background, marital/relationship history, social ties and social support, and economic status, along with health beliefs, a complete birth history, knowledge and use of contraception, health problems and treatment during the last two pregnancies, and anthropometry on mothers and children. Extensive data were gathered regarding the health problems and treatment for each of the two youngest children born since January 1990, with particular focus on diarrhea and respiratory infections.
The community data (Parts 41-60) supply information gathered from three knowledgeable individuals called "key informants" about occupations in the community, crops grown, wages, utilities and community services, and the history of the community. Parts 61-89 contain information regarding Health Posts (health care centers) through interviews conducted with key informants, doctors (Parts 72-80), and other health service providers (Parts 81-89), including traditional providers such as curers, midwives, and bone setters, regarding their practices, patients, referrals, fees, payment, and the use of specific treatments.
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Robert Wood Johnson Foundation Employer Health Insurance Survey [Community Tracking Study and State Initiatives in Health Care Reform Program], 1997 (ICPSR 2935)
Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 1996-01-01--1997-01-01
The objectives of this study were to describe and understand employers' and employees' behavior with respect to employment-based health insurance, to track trends in health insurance provided by employers, and to evaluate selected policies to regulate or expand employment-based health insurance coverage. Sampling was designed to permit estimates for selected communities that are part of the Robert Wood Johnson Foundation (RWJF) Community Tracking Study (CTS) and for selected states of interest to the RWJF State Initiatives in Health Care Reform Program. Data were collected on employers' offers of health insurance coverage, employees' eligibility and enrollment in health plans, and, for each plan offered, the plan type (HMO, POS, PPO, conventional), premiums (employer and employee contributions), benefits, cost-sharing, and employer self-insurance status. The study also collected information on the characteristics of employers and workers, including the number of employees at the establishment, the number of employees statewide and nationwide, and the distribution of workers by hours worked, age, sex, and earnings.
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Second Malaysian Family Life Survey: 1988 Interviews (ICPSR 9805)
Released/updated on: 2005-11-04
Geographic coverage: Malaysia, Global
This collection, the second wave of a panel survey, provides household-level retrospective and current data for Peninsular Malaysian women and their husbands and covers traditional topics of demographic research such as fertility, nuptiality, migration, and mortality as well as social and economic factors affecting family decision-making. The overall purpose of the data collection was to study household behavior in diverse settings during a period of rapid demographic and socioeconomic change. Eight survey instruments were used in this study. The tracking instrument, MFLS-2, was used for all households where an interview was attempted, and recorded information such as disposition of survey and questionnaires, number of eligibles, and respondent identifiers. The MF20 instrument, Household Members, was administered to all Panel sample households that were located. It solicited information on the status of the household members and included items such as location, marital status, education, and birthdate. The MF21 form, Household Roster, was used on all households interviewed in the survey. This form collected demographic information on current and very recent household members. The MF22 form, Female Life History, surveyed the Panel women and their selected daughters and daughters-in-law, and the New Sample women. Information collected by this form included pregnancy history and related events, marital, work, and migration histories, family background, and education. The MF23 form, Male Life History, collected data from husbands of the Panel women, selected sons and sons-in-law, and husbands of New Sample women. Data on marital, work, and migration histories, education, and family background were recorded. The MF24 form, Senior Life History, was administered to selected persons aged 50 or more and contained questions on marriages, children living elsewhere, literacy, work experience, migration history, health, and family background. The MF25 form, Household Economy, collected data on household economy from all households interviewed in this wave. Forms MF26 and MF27 were used to generate community-level data subfiles for this collection. Part 97 (MF26DIST--District-Level Data) contains one record for each of the 78 districts of Peninsular Malaysia. This file provides information (most of which pertains to 1988, but some of which dates back to 1970) on health services (e.g., number of hospitals, health centers, and doctors), family planning services (e.g., number of family planning clinics, contraceptive use), birth, death, and fertility rates, number of primary and secondary schools, ethnic distributions, and industrial and occupational distributions. Part 98 (MF26EB--Community-Level Data) contains one record for each of the 398 Enumeration Blocks selected for MFLS-2 and the 52 Primary Sampling Units used in MFLS-1. This file gives the current status of family planning services, general health services, schools, water and sanitation, housing costs, agriculture, transportation, population, urban/rural status, and government programs. Part 99 (MF27COMM--Community-Level Data) offers data for the same units as Part 98 and contains similar information, along with retrospective data on family planning services, health services, schools, and water treatment. Merged files (Parts 106-112) that contain one record per respondent were created by ICPSR using the variables CASE SPLIT PERSON for MF22, MF23, MF24, and MF25 on the New and Senior samples and the Panel and Children samples.
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Tecumseh Community Health Study, 1959-1969 (ICPSR 8969)
Released/updated on: 1992-02-16
Geographic coverage: United States, Tecumseh, Michigan
The Tecumseh Community Health Study is a longitudinal, ongoing prospective epidemiologic study of a natural community's health and disease status. Data have been collected on the Tecumseh population in southeast Michigan for over 30 years, beginning with a 1957 canvass of all households and adding all newcomers to the community until 1970, after which only previous residents have been followed. The Tecumseh project has conducted over 80 different studies, including both disease-specific investigations and studies concerned with the prevalence and incidence of disease in the community. The core data file for the years 1959-1969 contains data collected in Round I: 1959-1960, Round II: 1962-1965, and Round III: 1967-1969 (referred to as the Cardiovascular Studies I, II, and III, and the General Surveillance Study II). These data include information taken from baseline medical history interviews, medical examinations, clinical measurements, laboratory work, and electrocardiograms. Mortality status of all persons at the time of attempted or actual contact in Round III is also provided. The major variable groups include demographic information, family history of major diseases, systematic review of present and past symptoms and conditions, smoking and drinking habits, physical examinations, measurements and laboratory work, and electrocardiogram results.