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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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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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Integrated Public Health Surveys, 2010-2011 (ICPSR 33822)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2010-01-01--2011-12-31

This collection comprises a single data file which was produced as part of the data harmonization efforts of the Robert Wood Johnson Foundation and the United States Centers for Disease Control and Prevention. The file contains merged data from five sources:

  1. 2010 National Profile of Local Health Departments, a survey of local health departments conducted by the National Association of County and City Health Officials (NACCHO).

  2. 2011 National Profile Survey of Local Boards of Health, a survey of local boards of health conducted by the National Association of Local Boards of Health (NALBOH).

  3. 2010 State and Territorial Public Health Survey, a survey of state and United States territory health departments conducted by the Association of State and Territorial Health Officials (ASTHO).

  4. 2011 County Health Rankings, a compilation of county-level health measures and within-state county health rankings produced by the University of Wisconsin Population Health Institute.

  5. 2010 Census Demographic Profile Summary File, a series of tables with housing and population data from the 2010 Census.

Produced by matching data from the last four sources to the NACCHO data, the data file contains one case for each of the 2,107 local health departments (LHD) that responded to the NACCHO survey. Each LHD's record in the file includes the ASTHO data for its state health department and the NALBOH data for its local board of health (LBH), if it had a LBH and the LBH responded to the NALBOH survey. (If a LHD had multiple LBHs, then the first one in the NALBOH data was matched to the LHD). In addition, county (or county equivalent)-level data from the County Health Rankings and Census Demographic Profile Summary File were matched to the records of the 1,535 LHDs represented in the data file with a jurisdiction covering a single county or county equivalent.

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National Health and Nutrition Examination Survey I: Epidemiologic Followup Study, 1986 (ICPSR 9466)

Released/updated on: 1992-02-17
Geographic coverage: United States
Time period: 1986-01-01--1986-12-31
The NHANES I Epidemiologic Followup Study (NHEFS) is a longitudinal study of adults originally examined, measured, and interviewed in 1971-1975 as part of the first National Health and Nutrition Examination Survey (NHANES I). The NHEFS was jointly initiated by the National Center for Health Statistics (NCHS), the National Institute on Aging, and other components of the National Institutes of Health and Public Health Service. The primary purpose of the followup study is to investigate longitudinal relationships between the extensive data on physiological, nutritional, behavioral, and demographic characteristics collected during NHANES I and subsequent morbidity or mortality from specific diseases and conditions. The 1982-1984 wave of data collection for NHEFS followed all medically examined respondents who had been 25 to 74 years in 1971-1975. The 1986 NHEFS wave focused on older members of the NHANES I NHEFS cohorts, those who had been 55-74 years of age at their baseline examinations in 1971-1975 and were not known to be deceased at the time of the 1982-1984 NHEFS. In the 1986 NHEFS, the surviving respondents were 65-89 years of age. Data were collected on changes in vital, health, and functional status and use of health care services that had occurred since the last contact, whether the contact was in 1982-1984 or 1971-1975. The vital and tracing status file documents efforts to trace all subjects who had been 55 years of age and over at NHANES I (N = 5,677) and ascertain their vital status and demographic data. Further data collection was aimed at the 3,980 subjects who were not known to be deceased by 1982-1984. Thirty-minute telephone interviews were conducted with either sample members (N = 2,558) or with proxies for the incapacitated (N = 469) and deceased (N = 581) subjects. Questions were asked on household composition, self-reports of physician-diagnosed medical conditions (with detail on reports of cancer, bone fractures, and non-hospital health facility stays), death if applicable, functional limitations, use of health care facilities, and interviewer observations about the respondent. Items on coronary bypass surgery, pacemaker procedures, and community services utilization were 1986 additions to the NHEFS questionnaire. For those respondents who had not been interviewed in 1982-1984, questions were included on smoking and alcohol use, vision and hearing, exercise and weight, and pregnancy and menstrual history. Health care facility records were abstracted to provide diagnostic and summary information on single or multiple overnight stays in hospitals and nursing homes for 2,021 subjects reporting such stays. Death certificate data, including International Classification of Diseases, 9th Revision codes for multiple causes of death, were added for 661 decedents reported since the 1982-1984 wave, for a total of 2,266 decedents.
External data

National Officer-Involved Homicide Database (NOIHD), United States, 2000-2017 (ICPSR 38315)

Released/updated on: 2021-12-16
Geographic coverage: United States
Time period: 2000-01-01--2017-12-31
The National Officer-Involved Homicides Database (NOIHD) is a law-enforcement-wide database combining information on homicides resulting from all police actions (prior to booking) merged with crosswalks to law-enforcement agency- , demographic- , crime- , emergency department- , and gun-data. The database is aggregated at the level of law-enforcement agencies with annual measurement (2000-2017; n=641,821) suited for analysis of extant policy and/or policy changes that may be related to police-involved homicides in the United States. Interested data users will be required to complete the NOIHD Data Agreement form prior to receiving the data. The NOIHD Data Agreement is also available through the Fatal Encounters website. See Fatal Encounters Database, United States, 2000-present (ICPSR 38118) for additional information.
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National Profile of Local Health Departments, 2008 (ICPSR 26962)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2008-01-01--2008-12-31
Conducted by the National Association of County and City Health Officials (NACCHO), the purpose of this survey of local health departments (LHDs) was to advance and support the development of a database for LHDs to describe and understand their structure, function, and capacities. Each LHD in the United States received a questionnaire with a set of core questions. In addition, some of the LHDs received one of three randomly assigned modules of supplemental questions. The core questions covered jurisdictional information, governance, funding, workforce (staffing levels, occupations employed, top executive education and licensure, and percentages of staff by gender, race, and Hispanic origin), LHD activities, health disparities, and community health assessment and planning. The surveyed LHD activities include immunization, screening for diseases and conditions, treatment for communicable diseases, maternal and child health, epidemiology and surveillance activities, and regulation, inspection and/or licensing activities. Topics covered by Module 1 include awareness and use of NACCHO's operational definition of a functional local health department, familiarity with a voluntary national accreditation program (VNAP) for state and local health departments, LHD promotional activities, use of the logo and tagline that NACCHO developed for local governmental public health, and characteristics of LHD Web sites. Module 2 examined human resources, awareness and use of core competencies related to public health, interaction with academic institutions, internal agency strategic planning, sharing of resources with other LHDs, and information technology. Finally, Module 3 asked about community health assessment and health improvement planning, essential services and activities, land use planning, policy-making and advocacy, partnership and collaboration with other organizations, and access to health care services.
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National Profile of Local Health Departments, 2010 (ICPSR 32922)

Released/updated on: 2024-02-14
Geographic coverage: United States
Time period: 2010-01-01--2010-12-31
Conducted by the National Association of County and City Health Officials (NACCHO), the purpose of this survey of local health departments (LHDs) was to advance and support the development of a database for LHDs to describe and understand their structure, function, and capacities. A core set of questions was submitted to every LHD. In addition, some LHDs received one of two randomly assigned modules of supplemental questions. The core questions covered governance, funding, workforce (staffing levels, occupations employed, top executive education and licensure, and percentages of staff by race and Hispanic origin), LHD activities, and community health assessment and health improvement planning. The surveyed LHD activities include immunization, screening for diseases and conditions, treatment for communicable diseases, maternal and child health, epidemiology and surveillance activities, population-based primary prevention activities, and regulation, inspection and/or licensing activities. Topics covered by Module 1 included quality improvement, familiarity with a voluntary national accreditation program for state and local health departments, sharing of resources with other LHDs, emergency preparedness, and information technology. Module 2 examined human resources, policy-making and advocacy, access to health care services, practice-based research, health impact assessments, public health and law, and use of public health reports.
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Puerto Rican Elder: Health Conditions (PREHCO) Project, 2021-2024 (ICPSR 39091)

Released/updated on: 2026-03-31
Geographic coverage: Puerto Rico, United States
Time period: 2021-03-01--2024-07-31

These are the third and fourth waves of the PREHCO project (Puerto Rican Elder Health Conditions study) and have been developed between 2021 and 2024 as a collaboration between the University of Alabama at Birmingham and the University of Puerto Rico. The project began as a cross-sectional study of the non-institutionalized population aged 60 years or older in Puerto Rico. These waves followed the survivors of the original participants at the beginning of the fieldwork and aimed to examine the predictors of cognitive decline, disability, and mortality. The fourth wave of this study extends the follow-up of PREHCO to between 21 and 22 years after the initial data collection and aims to examine the predictors of cognitive decline, disability, and mortality.

PREHCO was designed as a study comparable to the Multicenter Project on Health and Well-being of Older Adults in Latin America and the Caribbean (SABE) developed by the Pan American Health Organization (PAHO) in several cities in Latin America, and with some studies carried out in the United States, mainly the Health and Retirement Study (HRS).

For this purpose, a questionnaire was designed that included sections on health conditions, physical and mental disability, functionality, use of medicines, health needs and social services, access to and use of health services, abuse, migration, housing conditions, patterns of help from family, community and public and government agencies, and others.

Since its inception, PREHCO has been funded with federal funds from the National Institute on Aging (NIA). Initially it was a project between the University of Wisconsin-Madison and the University of Puerto Rico from 2000-2009.

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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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Survey of HIV Status and Fertility Preferences in Sub-Saharan Africa, 2009-2010 (ICPSR 36718)

Released/updated on: 2017-04-10
Geographic coverage: Southern Province, Africa, Zambia, Lusaka, Northern Province, Sub-Saharan Africa
Time period: 2009-01-01--2010-12-31
The Survey of HIV Status and Fertility Preference in Sub-Saharan Africa 2009-2010 is one of eight community-based surveys conducted in Zambia and Nigeria exploring how HIV status relates to attitudinal and behavioral measures regarding HIV services and fertility preferences. Information was collected from 1,441 Zambian women aged 18-49 on topics such as fertility preferences, HIV status, pregnancy intention, current and previous pregnancies, attitudes toward and use of family planning, current and past sexual activity, past abortions, attitudes toward and knowledge about HIV, and attitudes toward and use of HIV services. Demographic variables include age, urban/rural location, native language, education, religion, and marital status.
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TAZAMA Health and Demographic Surveillance System, 1994-2012 (ICPSR 29541)

Released/updated on: 2014-11-18
Geographic coverage: Africa, Tanzania
Time period: 1994-01-01--2012-12-31

The TAZAMA Health and Demographic Surveillance System (HDSS) study site is located in the Kisesa and Bukandwe rural electoral wards in the Magu district of the Mwanza Region in Northern Tanzania. The two wards are comprised of six villages. There is one health center and five dispensaries (3 public and 2 private) in the study area. The two wards have eleven government primary schools (at least one in each village) and two secondary schools. Both Mwanza city and Magu town are accessible to residents; buses run along the main road and take about an hour and a half to get to Mwanza. Most of the residents are subsistence farmers; a lot of surplus agricultural produce is traded in Mwanza, which is Tanzania's second city. In the year 2012, the research study covered a population of about 30,000 people who live in the Kisesa and Bukandwe wards. The majority of the residents (about ninety five per cent) belong to the Sukuma ethnic group.

The DSS collects information on births and deaths and movements in and out of the households. It helps researchers to understand the population dynamics in the study area including fertility, mortality and migration patterns. It provides information on the structure of families that live together. The DSS study is also used to identify people who are eligible to participate in the serological surveys (the right age group, and continuously resident rather than just visiting). It provides the data for calculating the denominators for demographic rates.

The objectives of this study are as follows: (1) to improve understanding of the dynamics of the HIV epidemic; (2) to assess the demographic, social and economic impacts of the HIV/AIDS epidemic; (3) to evaluate the effects of national prevention, treatment and care interventions as implemented in Kisesa Ward; (4) to measure child and adult mortality and fertility in the general population and by HIV status; (5) to asses the leading causes of death through verbal autopsy; (6) to assess changes in the family structure due to HIV epidemic; and (7) to provide reliable data for district health planning.

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