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Behavioral Risk Factor Surveillance System (BRFSS), 2003 (ICPSR 34085)

Released/updated on: 2013-08-05
Geographic coverage: Oregon, Vermont, Puerto Rico, Indiana, United States, Oklahoma, Maine, Utah, Nebraska, West Virginia, Massachusetts, North Dakota, Wisconsin, Arizona, Nevada, District of Columbia, Rhode Island, Montana, Hawaii, Kansas, New York (state), New Jersey, Michigan, Iowa, New Mexico, Illinois, Texas, Connecticut, New Hampshire, Louisiana, Ohio, Georgia, Virginia, Maryland
Time period: 2003-01-01--2003-12-31
The Behavioral Risk Factor Surveillance System (BRFSS) is a state-based system of health surveys that collects information on health risk behaviors, preventive health practices, and health care access primarily related to chronic disease and injury. For many states, the BRFSS is the only available source of timely, accurate data on health-related behaviors. BRFSS was established in 1984 by the Centers for Disease Control and Prevention (CDC); currently data are collected monthly in all 50 states, the District of Columbia, Puerto Rico, the United States Virgin Islands, and Guam. More than 350,000 adults are interviewed each year, making the BRFSS the largest telephone health survey in the world. States use BRFSS data to identify emerging health problems, establish and track health objectives, and develop and evaluate public health policies and programs. The BRFSS is a cross-sectional telephone survey conducted by state health departments with technical and methodologic assistance provided by CDC. States conduct monthly telephone surveillance using a standardized questionnaire to determine the distribution of risk behaviors and health practices among adults. Responses are forwarded to CDC, where the monthly data are aggregated for each state, returned with standard tabulations, and published at the year's end by each state. The BRFSS questionnaire was developed jointly by CDC's Behavioral Surveillance Branch (BSB) and the states. When combined with mortality and morbidity statistics, these data enable public health officials to establish policies and priorities and to initiate and assess health promotion strategies.
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Bicol Community Survey (BCS), 1981: [Philippines] (ICPSR 6888)

Released/updated on: 2006-03-30
Geographic coverage: Philippines, Global
Time period: 1981-01-01--1981-12-31
During 1981, the Bicol Community Survey gathered data from 100 barangays located in the same provinces of the Philippines that were sampled by the BICOL MULTIPURPOSE SURVEY (BMS), 1978: [PHILIPPINES] (ICPSR 6878): Albay, Camarines Sur, and Sorsogon. Barangays are political subdivisions equivalent to villages in rural areas and to neighborhoods in urban areas. Data were gathered at the community level from barangay heads, health care providers (both public and private), traditional birth practitioners (hilots), traditional healers (herbolario), and barangay residents using a questionnaire divided into six different sections, each with its own particular focus. The six sections correspond to the six data files in this collection. Part 1, Infant Food Prices, contains information from one store in each barangay on content, availability, and price information of infant foods. Part 2, Health Services: Availability and Distance, contains one observation for each barangay from either barangay captains, barangay officials, or housewives regarding the time and cost of travel to health providers, both public and private. Part 3, Health Services: Prices and Quality, provides information from 518 heads of health care facilities, private health care professionals, traditional birth practitioners, and traditional healers about travel costs, costs per visit, and costs for prescribed medication. Part 4, Promotional Practices of Infant Food Companies, offers responses from hilots, heads of health facilities, and private professionals about brands of infant formula available, whether free samples and pamphlets were provided, and whether supplies such as pads, pencils, equipment, or posters were donated. Part 5, Environmental Sanitation, provides data from sanitary inspectors on water availability, water conditions, and garbage disposal within the barangay. For Part 6, Health Professionals Survey Data, heads of facilities and private professionals were given a self-administered survey regarding the demographic, educational, and employment characteristics of workers, along with their knowledge of and attitude toward breast-feeding. Interviews conducted with hilots by field workers using the same questionnaire are also included.
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Border Contraceptive Access Study, El Paso, Texas 2005-2008 (ICPSR 32561)

Released/updated on: 2011-11-07
Geographic coverage: El Paso, Ciudad Juarez, United States, Texas, Mexico, Chihuahua
Time period: 2005-01-01--2008-12-31

Oral contraceptive (OC) users living in El Paso, Texas were interviewed to assess motivations for patronizing a United States clinic or a Mexican pharmacy with over-the-counter (OTC) pills and to determine which women were likely to use the OTC option. The experiences of OC users who obtained their contraception from Mexican pharmacies were compared with those of women who obtained their pills from family planning clinics in El Paso, Texas, where eligible low-income women often pay nothing. 532 clinic users and 514 pharmacy users were surveyed about background characteristics, motivations for choosing their oral contraception source, and satisfaction with this source. For more information, please see the Border Contraceptive Access Study website.

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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--1979-12-31, 1981-01-01--1981-12-31
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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Partially restricted

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--2000-12-31
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.
Curated
Partially restricted

Health Tracking Household Survey, 2007 [United States] (ICPSR 26001)

Released/updated on: 2011-04-15
Geographic coverage: United States
Time period: 2007-01-01--2007-12-31

The 2007 Health Tracking Household Survey (HTHS) is the successor to the Community Tracking Study (CTS) Household Surveys which were conducted in 1996-1997 (ICPSR 2524), 1998-1999 (ICPSR 3199), 2000-2001 (ICPSR 3764), and 2003 (ICPSR 4216). Although the HTHS questionnaires are similar to the CTS Household Survey questionnaires, the HTHS sampling design does not have the community focus intrinsic to CTS. Whereas the CTS design focused on 60 nationally representative communities with sample sizes large enough to draw conclusions about health system change in 12 communities, the HTHS design is a national sample not aimed at measuring change within communities. Hence, "Community" was dropped from the study title. Like the CTS Household Surveys, HTHS collected information on health insurance coverage, use of health services, health expenses, satisfaction with health care and physician choice, unmet health care needs, usual source of care and patient trust, health status, adult chronic conditions, height and weight, and smoking behavior. In addition, the survey inquired about perceptions of care delivery and quality, problems with paying medical bills, use of in-store retail and onsite workplace health clinics, patient engagement with health care, sources of health information, and shopping for health care.

At the beginning of the interview, a household informant provided information about the composition of the household which was used to group the household members into family insurance units (FIU). Each FIU comprised an adult household member, his or her spouse or domestic partner (same sex and other unmarried partners), if any, and any dependent children 0-17 years of age or 18-22 years of age if a full-time student (even if living outside the household). In each FIU in the household, a FIU informant provided information on insurance coverage, health care use, usual source of care, and general health status of all FIU members. This informant also provided information on family income as well as employment, earnings, employer-offered insurance plans, and race/ethnicity for all adult FIU members. Moreover, every adult in each FIU (including the FIU informant) responded through a self-response module to questions that could not be answered reliably by proxy respondents, such as questions about unmet needs, assessments of the quality of care, consumer engagement, satisfaction with physician choice, use of health information, health care shopping, and detailed health questions. The FIU informants responded on behalf of children regarding unmet needs, satisfaction with physician choice, and use of health care information.

Curated

Indonesian Family Life Survey, 1993 (ICPSR 6706)

Released/updated on: 2006-01-12
Geographic coverage: Kalimantan, Java, Bali, Sumatra, West Nusa Tenggara, Global, Indonesia, Sulawesi
Time period: 1993-01-01--1993-12-31

This release of the 1993 Indonesian Family Life Survey (IFLS-1-PR) is a revised and restructured version of the Wave 1 data. This data collection provides a broad range of economic, demographic, and health information at both the household and community levels across 13 provinces on the islands of Java, Sumatra, Bali, West Nusa Tenggara, Kalimantan, and Sulawesi. A sample of 7,224 households was interviewed during August 1993 through January 1994. Household-level data cover topics such as household characteristics, income, education of both adults and children, marriage histories, inter-household transfers, pregnancy history, and knowledge and use of contraceptives. At the community-facility level, information was gathered from village leaders and heads of village women's groups in each of the 321 enumeration areas (EAs) where the households were located. Questions were asked regarding community characteristics (transportation, water and sanitation, history of schools, and availability of health facilities), nurses, midwives, and paramedics (facility management and family planning history, vignettes on types of care), and traditional health practitioners (buying or making herbal medicines or using services of traditional practitioners, rituals, and incantations). When the household data are combined with the community-facility data, the 1993 Indonesian Family Life Survey provides a unique look at areas of fertility, family planning, infant and child health, education, migration, employment, and the social, economic, and health status of over 7,000 households in a diverse setting during a period of rapid demographic and socioeconomic change.

As of June 2015, there are four waves of data for the IFLS. However, a fifth wave of data collection has begun. Please see the IFLS Web site for more information on how to obtain these data.

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International Data Base, February 1990 (ICPSR 8490)

Released/updated on: 1992-02-16
Geographic coverage: Global
This dataset contains information from tables of demographic, economic and social data for the countries of the world. Information presented includes population, health, nutrition, mortality, fertility, family planning and contraceptive use, literacy, housing, and economic activity data. Tabular data are broken down by such variables as age, sex, and urban/rural residence.
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National Hospital Discharge Survey, 1979-2006: Multi-Year Public Use File (ICPSR 24281)

Released/updated on: 2009-01-28
Geographic coverage: United States
Time period: 1979-01-01--2006-12-31
The National Hospital Discharge Survey (NHDS) collects medical and demographic information annually from a sample of hospital discharge records. Variables include patients' demographic characteristics (sex, age, race, marital status), dates of admission and discharge, source and type of admission, status at discharge, final diagnoses, surgical and nonsurgical procedures, dates of surgeries, and sources of payment. Information on hospital characteristics such as bed size, ownership, and region of the country is also included. This collection includes data for non-newborns for 1979-1989 (Dataset 1), non-newborns for 1990-2006 (Dataset 2) and newborns for 1979-2006 (Dataset 3). The medical information is coded using the INTERNATIONAL CLASSIFICATION OF DISEASES, 9TH REVISION, CLINICAL MODIFICATION (ICD-9-CM). In addition, there are several Excel files that contain information needed to calculate relative standard errors (RSEs) and to compute utilization rates based on Census population estimates (POPs).
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National Hospital Discharge Survey, 2005 (ICPSR 20380)

Released/updated on: 2007-12-13
Geographic coverage: United States
Time period: 2005-01-01--2005-12-31
The 2005 National Hospital Discharge Survey (NHDS) collects medical and demographic information annually from a sample of hospital discharge records. Variables include patients' demographic characteristics (sex, age, race, marital status), dates of admission and discharge, source and type of admission, status at discharge, final diagnoses, surgical and nonsurgical procedures, dates of surgeries, and sources of payment. Information on hospital characteristics such as bedsize, ownership, and region of the country is also included. The medical information is coded using the INTERNATIONAL CLASSIFICATION OF DISEASES, 9TH REVISION, CLINICAL MODIFICATION (ICD-9-CM).
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National School Health Services Program Evaluation, 1981-1982 (ICPSR 8302)

Released/updated on: 2008-06-03
Geographic coverage: United States
Time period: 1981-01-01--1982-12-31
The National School Health Services Program Evaluation documents the nature and scope of a wide range of health services provided to school-age children by by nurse practitioners, school health nurses, physicians, and health aides. The information provided by this collection includes: (1) records of communications between educators, health professionals, and parents, (2) the type, severity, and disposition of problems treated at schools (plus referral sources and the types of health care professionals involved), (3) nurse practitioners' findings from medical histories and physical examinations of students, and (4) data on individual health care episodes at the schools, including unresolved problems. Information supplied by a survey of parents of children in participating schools includes data on health care sources and expenses for the child, plus data on specific medical problems and treatment. Basic demographic characteristics such as the sex and race of the child, parents' educational background, and family income are also provided.
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National Survey of Adolescents, 2004: Burkina Faso (ICPSR 22408)

Released/updated on: 2008-07-24
Geographic coverage: Burkina Faso, Africa, Sub-Saharan Africa
Time period: 2004-04-01--2004-06-30
The National Survey Adolescents was launched in 2004 in four Sub-Saharan African countries--Burkina Faso, Ghana, Malawi, and Uganda--to provide detailed information on adolescent risk-taking and health-seeking behavior as related to HIV, STDs and unintended pregnancy. The study examined a range of factors (e.g., behavioral, sociocultural, economic) that could lead to increased vulnerability to risk. The study also encompassed knowledge of means of prevention, sources of trusted information and health care, and impediments to adolescents' abilities to apply their knowledge and take preventive action. The survey in Burkina Faso was administered between April and June 2004. Using a two-stage stratified sample design that selected households from rural and urban clusters, 5,400 households were listed for initial screening. After an initial interview in each household, individual surveys were administered in person to adolescents between the ages of 12 and 19 who were de facto or de jure members of the household. This process collected 6,489 individual interviews with adolescents. Because of the sensitive nature of questions administered in the survey, informed consent forms were obtained from both parents/guardians and the respondents, and in all possible instances interviewers and respondents were paired by gender.
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National Survey of Adolescents, 2004: Ghana (ICPSR 22409)

Released/updated on: 2008-07-24
Geographic coverage: Africa, Ghana, Sub-Saharan Africa
Time period: 2004-01-01--2004-05-31
The National Survey Adolescents was launched in 2004 in four Sub-Saharan African countries--Burkina Faso, Ghana, Malawi, and Uganda--to provide detailed information on adolescent risk-taking and health-seeking behavior as related to HIV, STDs and unintended pregnancy. The study examined a range of factors (e.g., behavioral, sociocultural, and economic) that could lead to increased vulnerability to risk. The study also encompassed knowledge of means of prevention, sources of trusted information and health care, and impediments to adolescents' abilities to apply their knowledge and take preventive action. The Ghanian portion was administered between January and May 2004. Using a two-stage stratified sample design that selected households from rural and urban clusters, 9,445 households were listed for initial screening. After an initial interview in each household, individual surveys were administered in person to adolescents between the ages of 12 and 19 who were de facto or de jure members of the household. This process collected 4,430 individual interviews with adolescents. Because of the sensitive nature of questions administered in the survey, informed consent forms were obtained from both parents/guardians and the respondents, and in all possible instances interviewers and respondents were paired up by gender.
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National Survey of Adolescents, 2004: Malawi (ICPSR 22410)

Released/updated on: 2008-07-24
Geographic coverage: Malawi, Africa, Sub-Saharan Africa
Time period: 2004-03-01--2004-08-31
The National Survey Adolescents was launched in 2004 in four Sub-Saharan African countries--Burkina Faso, Ghana, Malawi, and Uganda--to provide detailed information on adolescent risk-taking and health-seeking behavior as related to HIV, STDs and unintended pregnancy. The study examined a range of factors (e.g., behavioral, sociocultural, economic) that could lead to increased vulnerability to risk. The study also encompassed knowledge of means of prevention, sources of trusted information and health care, and impediments to adolescents' abilities to apply their knowledge and take preventive action. The survey in Malawi was administered between March and June 2004 and again in August 2004. Using a two-stage stratified sample design that selected households from rural and urban clusters, 7,750 households were listed for initial screening. After an initial interview in each household, individual surveys were administered in person to adolescents between the ages of 12 and 19 who were de facto or de jure members of the household. However, during the initial data collection period this process collected only 3,448 individual interviews with adolescents. Consequently, in August 2004, researchers extended the surveys to additional clusters excluded during the first round of surveys bringing the total number of individuals to 4,879. Because of the sensitive nature of questions administered in the survey, informed consent forms were obtained from both parents/guardians and the respondents, and in all possible instances interviewers and respondents were paired up by gender.
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Simple Crosstabs

National Survey of Adolescents, 2004: Uganda (ICPSR 22411)

Released/updated on: 2018-07-09
Geographic coverage: Africa, Uganda, Sub-Saharan Africa
Time period: 2004-02-01--2004-07-31
The National Survey Adolescents was launched in 2004 in four Sub-Saharan African countries--Burkina Faso, Ghana, Malawi, and Uganda--to provide detailed information on adolescent risk-taking and health-seeking behavior as related to HIV, STDs and unintended pregnancy. The study examined a range of factors (e.g., behavioral, sociocultural, economic) that could lead to increased vulnerability to risk. The study also encompassed knowledge of means of prevention, sources of trusted information and health care, and impediments to adolescents' abilities to apply their knowledge and take preventive action. The Ugandan portion was administered between February and July 2004. Using a two-stage stratified sample design that selected households from rural and urban clusters, 7,106 households were listed for initial screening. After an initial interview in each household, individual surveys were administered in person to adolescents between the ages of 12 and 19 who were de facto or de jure members of the household. This process collected 6,659 individual interviews with adolescents. Because of the sensitive nature of questions administered in the survey, informed consent forms were obtained from both parents/guardians and the respondents, and in all possible instances interviewers and respondents were paired up by gender.
Curated
Simple Crosstabs

Puerto Rican Elderly: Health Conditions (PREHCO) Project, 2002-2003, 2006-2007 (ICPSR 34596)

Released/updated on: 2013-09-13
Geographic coverage: Puerto Rico, United States
Time period: 2002-01-01--2007-12-31
The Puerto Rican Elderly: Health Conditions (PREHCO) study investigates issues affecting the elderly (individuals over 60 years of age) population in Puerto Rico: health status, housing arrangements, functional status, transfers, labor history, migration, income, childhood characteristics, health insurance, use of health services, marital history, mistreat, sexuality, etc. It is an island-wide, longitudinal sample survey of target individuals and their spouses with two waves of data collection: 2002-2003 and 2006-2007.
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Testing and Counseling for HIV: A Multi-site Study (ICPSR 35925)

Released/updated on: 2015-06-03
Geographic coverage: United States
This project collects data based on interviews with health providers, with clients of testing services, and with non-users of services towards testing and disclosure for HIV, as well as on observations at study sites. Data are collected at health facilities to investigate the factors that hinder or facilitate uptake testing and counseling (T&C) for HIV in different settings.
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