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Curated

ABC News/Washington Post Poll of Public Opinion on Health, September 1982 (ICPSR 9048)

Released/updated on: 2005-11-04
Geographic coverage: United States
This special-topic poll is part of a continuing series of monthly surveys that solicit public opinion on the presidency and on a range of other political and social issues. Respondents were asked about their overall health and any illnesses they had ever had. They were also asked their views on health-related topics, especially venereal disease and herpes. Respondents were asked about sexually-transmitted diseases and about their own experiences with these diseases (if any). Demographic information about the respondent includes age, sex, race, marital status, employment status, income, educational background, and type of residence.
Curated

Army Study to Assess Risk and Resilience in Servicemembers (STARRS) (ICPSR 35197)

Released/updated on: 2025-10-01
Geographic coverage: United States
Time period: 2011-01-01--2024-01-01

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April 29, 2025: STARRS - Longitudinal Study Wave 4 (LSW4) data released

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The Army Study to Assess Risk and Resilience in Servicemembers (STARRS) is an extensive study of mental health risk and resilience among military personnel. Army STARRS consists of eight separate but integrated epidemiologic and neurobiologic studies. Survey data for three of the Army STARRS study components are available via Secure Dissemination or via the ICPSR Virtual Data Enclave: New Soldier Study (NSS); All Army Study (AAS) and Pre-Post Deployment Study (PPDS). Also available are data for the STARRS-Longitudinal Study (STARRS-LS), which are follow-up surveys conducted with Army STARRS participants from AAS, NSS and PPDS studies. Lastly, baseline administrative data from the Army/Department of Defense (DoD) and blood sample flags for Soldiers who had blood drawn as a part of their participation in NSS or PPDS are available.

The AAS component of Army STARRS assesses soldiers' psychological and physical health, events encountered during training, combat, and non-combat operations, and life and work experiences across all phases of Army service. The AAS data includes data on soldiers' psychological resilience, mental health, and risk for self-harm.

The NSS data are drawn from new soldiers who have just entered the Army. The data contain information on soldier health, personal characteristics, and prior experiences. Results from a series of neurocognitive tests are also included in the NSS data.

The PPDS data are drawn from active duty soldiers who were interviewed at four points in time: 3-4 months prior to deployment to Afghanistan; within 1-2 weeks after return from deployment; 1-3 months after return from deployment; and 9-12 months after return from deployment. The PPDS data contain information on soldiers' psychological resilience, mental health, deployment experiences, and risk for self-harm.

The STARRS-LS data are from multiple follow-up interviews with individuals who previously participated in the AAS, NSS and PPDS study components of Army STARRS. STARRS-LS data contain follow-up information on soldiers' and veterans' physical and mental health, resilience and risk for self-harm, military and employment status, deployment experience, and personal characteristics as they move through their Army careers and after they leave the Army.

Curated

Bruising as a Forensic Marker of Physical Elder Abuse in Orange County, California, 2006-2008 (ICPSR 28144)

Released/updated on: 2012-12-21
Geographic coverage: United States, California
Time period: 2006-07-01--2008-05-01
The purpose of the study was to describe bruising as a marker of physical elder abuse. Consenting older adults were examined to document location and size of bruises and assess whether they were inflicted during physical abuse. An expert panel confirmed physical abuse. A research nurse conducted study assessments on 67 adults aged 65 and older reported to Adult Protective Services for suspected physical elder abuse in Orange County, California between July 2006 and May 2008. The study contains a total of 142 variables including age, sex, ethnicity, functional status, medical conditions, cognitive status, history of falls, bruise size, bruise location and color, recall of cause, and responses to the Revised Conflicts Tactics Scales (CTS2) and to the Elder Abuse Inventory (EAI).
Curated

Comparing Two Ways to Manage Symptoms for Patients Who Have Chronic Migraine and Frequent Medication Use (The MOTS Trial), United States, 2017-2020 (ICPSR 38546)

Released/updated on: 2022-12-14
Geographic coverage: United States
Time period: 2017-02-20--2020-12-22
The Medication Overuse Treatment Strategy (MOTS) research trial sought to understand the relationship between individuals who suffer from chronic migraines and their use (or overuse) of medications to treat their migraines. A diagnosis of chronic migraines means that a person experiences headaches on 15 days or more per month with at least 8 of those days meeting the diagnostic criteria for migraine with or without aura. Of the nearly 7 million individuals in the United States who suffer from chronic migraines more than half of them overuse medication intended to relieve the symptoms. However, that overuse can bring about other medical issues. This research trial enrolled 720 chronic migraine sufferers from 34 clinics across the country. The subjects were randomized into two groups. A total of 361 patients were randomized to the treatment strategy that included migraine-preventive therapy with switching off the overused medication to an alternative used with a limited frequency, while 359 patients were randomized to migraine-preventive medication with continuation of the overused medication with no maximum limit.
Curated
Partially restricted

Database for Forensic Anthropology in the United States, 1962-1991 (ICPSR 2581)

Released/updated on: 2006-03-30
Geographic coverage: United States
Time period: 1962-01-01--1991-01-01
This project was undertaken to establish a computerized skeletal database composed of recent forensic cases to represent the present ethnic diversity and demographic structure of the United States population. The intent was to accumulate a forensic skeletal sample large and diverse enough to reflect different socioeconomic groups of the general population from different geographical regions of the country in order to enable researchers to revise the standards being used for forensic skeletal identification. The database is composed of eight data files, comprising four categories. The primary "biographical" or "identification" files (Part 1, Demographic Data, and Part 2, Geographic and Death Data) comprise the first category of information and pertain to the positive identification of each of the 1,514 data records in the database. Information in Part 1 includes sex, ethnic group affiliation, birth date, age at death, height (living and cadaver), and weight (living and cadaver). Variables in Part 2 pertain to the nature of the remains, means and sources of identification, city and state/country born, occupation, date missing/last seen, date of discovery, date of death, time since death, cause of death, manner of death, deposit/exposure of body, area found, city, county, and state/country found, handedness, and blood type. The Medical History File (Part 3) represents the second category of information and contains data on the documented medical history of the individual. Variables in Part 3 include general comments on medical history as well as comments on congenital malformations, dental notes, bone lesions, perimortem trauma, and other comments. The third category consists of an inventory file (Part 4, Skeletal Inventory Data) in which data pertaining to the specific contents of the database are maintained. This includes the inventory of skeletal material by element and side (left and right), indicating the condition of the bone as either partial or complete. The variables in Part 4 provide a skeletal inventory of the cranium, mandible, dentition, and postcranium elements and identify the element as complete, fragmentary, or absent. If absent, four categories record why it is missing. The last part of the database is composed of three skeletal data files, covering quantitative observations of age-related changes in the skeleton (Part 5), cranial measurements (Part 6), and postcranial measurements (Part 7). Variables in Part 5 provide assessments of epiphyseal closure and cranial suture closure (left and right), rib end changes (left and right), Todd Pubic Symphysis, Suchey-Brooks Pubic Symphysis, McKern & Steward--Phases I, II, and III, Gilbert & McKern--Phases I, II, and III, auricular surface, and dorsal pubic pitting (all for left and right). Variables in Part 6 include cranial measurements (length, breadth, height) and mandibular measurements (height, thickness, diameter, breadth, length, and angle) of various skeletal elements. Part 7 provides postcranial measurements (length, diameter, breadth, circumference, and left and right, where appropriate) of the clavicle, scapula, humerus, radius, ulna, scarum, innominate, femur, tibia, fibula, and calcaneus. A small file of noted problems for a few cases is also included (Part 8).
Curated

Established Populations for Epidemiologic Studies of the Elderly, 1981-1993: [East Boston, Massachusetts, Iowa and Washington Counties, Iowa, New Haven, Connecticut, and North Central North Carolina] (ICPSR 9915)

Released/updated on: 2006-01-18
Geographic coverage: North Carolina, Iowa, New Haven, United States, Massachusetts, Connecticut, Boston
Time period: 1981-01-01--1993-01-01
The goals of the Established Populations for Epidemiologic Studies of the Elderly (EPESE) project were to describe and identify predictors of mortality, hospitalization, and placement in long-term care facilities and to investigate risk factors for chronic diseases and loss of functioning. The survey elicited information from persons 65 years of age and older in four geographic locations: East Boston, Massachusetts, New Haven, Connecticut, Iowa and Washington Counties, Iowa, and five counties in north central North Carolina. The public use baseline data (Part 1) cover demographic characteristics (age, sex, race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Data from six follow-up surveys conducted in all four of the sites are also provided (Parts 2-4 and 6-8), along with information from death certificates for deaths occurring in the first six years of follow-up for all four sites (Part 5).
Curated

Euro-Barometer 37.2: Elderly Europeans, April-May 1992 (ICPSR 9958)

Released/updated on: 2008-06-04
Geographic coverage: United Kingdom, Portugal, Global, Spain, Greece, Netherlands, Belgium, Luxembourg, Ireland, Denmark, Italy, France, Germany
Time period: 1992-04-20--1992-05-19
This round of Euro-Barometer surveys queried respondents on standard Euro-Barometer measures such as public awareness of and attitudes toward the Common Market and the European Community (EC), and also focused on the elderly and their activities, finances, and health care. Respondents were asked what sorts of things in life were of interest to them, whether they were treated with more respect as they grew older, the extent to which they agreed with several popular conceptions about being older, and whether they felt as though they were treated as second-class citizens by public institutions, certain professions, service providers, or their families. Other questions queried respondents about the amount of free time they had in their daily routines, what activities they had pursued during the past week, how often they saw their families, how much contact they had with young people and whether they would like to have more, and how often they felt lonely. Respondents were also asked whether they were members of voluntary organizations or charity groups and whether they would join a political party formed to further the interests of the elderly. Financial questions included whether the respondent preferred a pension for the elderly to spend as they wished or reduced prices and concessions for the elderly, how they would describe their current financial situation, whether their financial situation was secure, and what made them feel financially secure or insecure. Respondents were also asked a series of health-related questions, including whether they had any long-standing illness, disability, or infirmity that limited their activities in any way, whether anyone gave them regular help or assistance with personal care or household tasks, who gave this care, and whom they would turn to should they need extra help or assistance. Demographic and other background information was gathered on life satisfaction, number of people residing in the home, size of locality, home ownership, and region of residence, as well as the respondent's age, sex, marital status, number of children, education, employment status, occupation, work sector, age of retirement or expected age of retirement, religiosity, subjective social class, and left-right political self-placement.
Curated

Evaluation of Regionalized Networks of High-Risk Pregnancy Care, 1970-1979 (ICPSR 8469)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1970-01-01--1979-01-01
Data provided in this collection were gathered to evaluate the effectiveness of a five-year program demonstrating regionalization of perinatal health care for mothers and infants. There are three distinct types of data in the collection. The first consists of records of live births in eight program regions and eight comparison regions. Included in these records are data on the size and type of institution of birth, birthweight, number of previous births and pregnancies, gestational age, and method of delivery. Also provided are demographic data such as age, race, educational level, and marital status of the mother. The unit of analysis is the live birth. The second type of data in the collection consists of matched birth and death data for infants, using the same geographical coverage as the live birth data. Each record contains the data provided in the live birth data, plus information such as the place of death, age at death, and cause of death. The unit of analysis is infant deaths for which birth data are available. The third type of data are derived from a survey of infant health at one year of age. Included in this are data on employment, education, and previous pregnancies of the mother, plus information on pre- and post-natal hospitalization, medical care, and infant health. Additional data are provided for a test, administered to each infant, of adaptive, gross and fine motor, and receptive language development.
Curated
Restricted

Forensic Markers of Physical Elder Abuse, Los Angeles, California, 2014-2017 (ICPSR 37050)

Released/updated on: 2018-08-07
Geographic coverage: United States, Los Angeles, California
Time period: 2014-09-01--2017-02-01

These data are part of NACJD's Fast Track Release and are distributed as they were received from the data depositor. The files have been zipped by NACJD for release, but not checked or processed except for the removal of direct identifiers. Users should refer to the accompanying readme file for a brief description of the files available with this collection and consult the investigator(s) if further information is needed.

This study sought to: (1) document the spectrum of injuries and injury characteristics observed among physically-abused older adults reported to Adult Protective Services (APS) and compare those findings to injuries found among non-abused older adults, (2) identify observable injury characteristics and abuse circumstances that healthcare providers, law enforcement and prosecutors consider to be key forensic markers of physical abuse, (3) document information and evidence integral for achieving successful criminal prosecution, and (4) describe approaches that community-based frontline workers can employ to better document evidence of physical abuse.

The data included in this collection were collected under a National Institute of Justice-funded project that sought to document the spectrum and characteristics of injuries observed among physically abused, community-dwelling APS clients.

The collection includes two SAS datasets: injury.sas7bdat (with 47 variables and 403 cases) and subjectleveldata.sas7bdat (with 122 variables and 165 cases); and three SAS System Program Files: analysis-code-v1.sas, cleaned-injury-datasets-v1.sas, and formats.sas. Demographic variables in the collection are in the subjectleveldata.sas7bdat dataset, and include age, year of birth, gender, race, language, and level of education.

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Hispanic Established Populations for the Epidemiologic Study of the Elderly (HEPESE) Wave 9, 2016 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 39038)

Released/updated on: 2024-06-05
Geographic coverage: United States, New Mexico, Texas, Colorado, California, Arizona
Time period: 2016-01-26--2016-11-10

The Hispanic EPESE provides data on risk factors for mortality and morbidity in older Mexican Americans in order to contrast how these factors operate differently than in non-Hispanic Whites, African Americans, and other major ethnic groups.

The Wave 9 dataset comprises the eighth follow-up of the baseline Hispanic Established Populations for the Epidemiologic Studies of the Elderly, 1993-1994: [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 2851). The baseline Hispanic EPESE collected data on a representative sample of community-dwelling Mexican Americans, aged 65 years and older, residing in the five Southwestern states of Arizona, California, Colorado, New Mexico, and Texas.

The public-use data covers demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health behaviors, self-reported use of dental, hospital, and nursing home services, and depression. Subsequent follow-ups allow examination of the predictors of mortality, changes in health outcomes, institutionalization, changes in living arrangements, as well as changes in life situations and quality of life.

During this 9th Wave (Dataset 1), 2016, 480 re-interviews were conducted either in person or by proxy, with 283 of the original respondents interviewed in 1993-1994. This Wave also includes 197 re-interviews from the 902 new respondents added at Wave 5 in 2004-2005. All respondents were aged 85 and over at Wave 9.

The Wave 9 Informant Interviews dataset (Dataset 2) includes data from interviews with 460 respondents who provided information on themselves as well as the older respondents. The older respondents were asked to provide the name and contact information of the person they are "closer to" or they "depend on the most for help." These INFORMANTS, many of whom provide caregiving support to the older respondents, were contacted, and interviewed regarding the health, function, social situation, finances, and general well-being of the older Hispanic EPESE respondents. Information was also collected on the informant's health, function, and caregiver responsibilities and burden. This dataset includes information from the 460 informants, more than two-thirds of whom were children of the respective respondents. Thus, there are 460 respondent-informant dyads that provide opportunities for caregiving research.

Curated

Hispanic Health and Nutrition Examination Survey, 1982-1984 (ICPSR 8535)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1982-07-01--1984-12-01
Sixteen components focusing on nutritional practices and physical health comprise this survey of Hispanic Americans. The Body Measurements file includes anthropometric data on individuals such as skeletal and skin fold measurements, body circumferences, height, and weight. The Dental Health data provide dental history information, including the frequency of and reasons for visits to a dental hygienist, fluoride treatments, and the results of a clinical examination. The Blood and Urine Assessments component of the study contains clinical data such as red and white blood cell counts, serum iron and vitamin levels, amount of lead, and other assays. The Physician's Examination file provides the results of a basic physical exam, and the Dietary Practices/Food Frequency component includes information on food recall, special diets, frequency of meals, and consumption of various types of foods. The Adolescent and Adult History Questionnaire file supplies information on health care and problems getting care, dental care, health status, conditions, medical treatment, pesticide exposure, smoking, acculturation, meal programs for school-age children, reproductive history, and health status of children. Measures of Depression provides data on feelings of depression, how depression affected everyday life, help sought during depression, and weight changes and sleep loss due to depression. The Alcohol Consumption Data section includes information on the amount and kind of alcohol consumed, reasons for drinking, and self-perception of drinking habits. The Drug Abuse file offers information on the use of barbiturates and other sedatives, marijuana and hash, inhalants, and cocaine. The Hearing data were collected during the physical examination and provide information on respondents' ability to hear and the condition of their hearing organs. The Gallbladder Ultrasound data include information on disease, history of symptoms, findings of ultrasounds, and physical examinations of the gallbladder. Diabetes and OGTT (oral glucose tolerance test) data were also collected. Respondents were asked whether they had diabetes and were also questioned about age of onset, medication taken, diet, and if the OGTT had been administered. The file also contains detailed information on the OGTT, diet before the testing, time intervals between blood drawings, and plasma glucose values in milligrams and deciliters. The Vision section furnishes information on the respondent's eyesight, whether he or she had a problem seeing, appliances worn, age when corrective lenses were first worn, if a doctor had been visited for sight problems, and findings from a physician's examination. Measurements of the respondent's visual acuity with and without correction are also included in the data. The Child History section includes information on health status, health care utilization, infant feeding practices, participation in meal programs, school attendance, and language use. The 24-Hour Recall lists amounts of calories, protein, total fat, fatty acids, cholesterol, carbohydrates, dietary fiber, alcohol, vitamins, and minerals for each food item consumed by each person. It also contains a description of the food, ingestion period, approximate time of consumption, and food source. The data from the Measurement and Interpretation of Electrocardiograms file give an objective measure of the cardiac health status of individuals examined in the survey. Despite the limitations of such data, the electrocardiographic variables are carefully and completely defined. Also, an extensive process was used to ensure the accuracy of the findings. In addition, each part of this collection provides sociodemographic data, such as age, race, national origin, birthplace, education, employment, insurance, and use of public assistance. Also included are family data including number of people in the family, family income, poverty index, use of food stamps, and size of residence.
Curated

Intimate Partner Violence, Stalking and Sexual Violence Among Non-College-Attending Emerging Adults, United States, 2010 (ICPSR 36993)

Released/updated on: 2018-05-02
Geographic coverage: United States
Time period: 2010-01-22--2010-12-31

These data are part of NACJD's Fast Track Release and are distributed as they were received from the data depositor. The files have been zipped by NACJD for release, but not checked or processed except for the removal of direct identifiers. Users should refer to the accompanying readme file for a brief description of the files available with this collection and consult the investigator(s) if further information is needed.

This study sought to:

  1. Identify the prevalence of intimate partner violence, stalking and sexual violence among non-college-attending emerging adults.
  2. Explore the use of formal and informal help seeking and formal services among these victims.

The analysis in this study focused on non-college-attending emerging adults, with particular concern for the effect of their positive and negative encounters with sources of support - both in their immediate needs as well as future decisions to utilize victim services. This project also compared male and female victims because of variations in their respective use of services.

To address these research concerns, this project utilizes the data in the 2010 National Intimate Partner and Sexual Violence Survey (ICPSR #36140).

There are no data files available with this study. Only syntax files used by the researchers are provided.

Curated

The Iowa Adoption Studies, 1975-2008 (ICPSR 34369)

Released/updated on: 2020-11-09
Geographic coverage: Iowa, United States
Time period: 1975-01-01--2008-01-01

The Iowa Adoption Studies were conducted between 1975 and 2008. The group of studies consist of 5 independent waves of data collection each of which examined genetic (biological) and environmental influences on psychopathology. The adoption paradigm allowed separation of genetic and environmental influences on behavior, as well as joint influences due to gene x environment interaction. Adoptees were interviewed about lifetime psychopathology including substance abuse and dependence, antisocial personality, and mood disorders. A follow-up study was conducted from 2000-2004 that recruited all previous participants and natural offspring of the adoptive parents when available. Standardized psychiatric assessments were administered along with measures of personality disorders and traits, retrospective reports on childhood experiences with adoptive parents, and current symptomatology. An extensive neurocognitive assessment was conducted on a subset of participants who had standardized school achievement scores. The goal of this last wave of assessment was to evaluate the influence of substance use on mid-life cognition and health.

The respondents were assessed using a number of different surveys over the study period. The following describes the notable variables as well as descriptions of the surveys included in the dataset.

The first variables in the dataset identify sibling pairs and provides data on whether the respondents' biological parents suffered from mental health or substance abuse issues. Next birth records are provided that give basic information about the health of the person when he or she was born. This information is followed by the survey results of "The Schedule for Nonadaptive and Adaptive Personality" (SNAP) as well as variables that reflect the diagnosis of personality disorders and nonadaptive personality traits based on the SNAP survey responses.

The next section includes responses from "The Iowa Personality Disorder Screen," a quick personality disorder screen developed in 1999 intended for use in clinical and research settings.

Next, responses to Pearson Assessments "Brief symptoms inventory" are included as well as the scores calculated based on these survey responses. The results of this survey assess the mental state of the patient including scales on Somatization, Obsessive-Compulsive, Interpersonal Sensitivity, Depression, Anxiety, Hostility, Phobic Anxiety, Paranoid Ideation and Psychoticism.

The respondents also completed the "Buss-Durkee Hostility Questionnaire" and were assessed on measure regarding the following hostility traits: negativism, resentment, indirect hostility, assault, suspicion, irritability and verbal hostility.

Reponses to the "The Social Provisions Scale" survey are also included. The purpose of this survey is to assess the relationship the respondents have to other people. The 6 social provisions assessed include: guidance, reliable alliance, reassurance of worth, attachment, social integration, and opportunity for nurturance.

"The Parental Bonding Instrument" instrument was utilized to assess the respondents' relationships to their mothers and fathers.

A series of cognitive tests were administered to respondents. ICPSR is unable to provide the survey instruments used in the cognitive test due to copy write issues. These tests include:

Controlled Oral Word Association Test (COWAT)

North American Adult Reading Test (NAART)

Rey Figure and Rey Complex Figure Test and Recognition Trial (RCFT)

Shipley Institute of Living Scale (SILS)

Stroop Color and Word Test (SCWT)

Tower of Hanoi (TofH)

Comprehensive Trailmaking Test (CTMT)

Weschler Adult Intelligence Test (WAIS)

Weschler Memory Test (WMS)

The dataset also includes respondents' results of the Comprehensive Performance Test (CPT) and the Iowa Gambling Task (IGT)

Scores from the "Iowa Test of Basic Skills," a test of academic achievement that evaluates students knowledge in subjects including, mathematics, reading comprehension, and science, are included in the dataset. Respondents are evaluated in grades 4, 8 and 11.

The final section of the dataset includes two waves of the "Semi Structured Assessment for the Genetics of Alcoholism," a survey intended to assess the physical, psychological, and social manifestations of alcohol abuse. These survey responses make up the bulk of the dataset and include variables on a variety of topics including: demographics, medical history, substance use, eating disorders, depression, dysthymia, mania, ASP, suicide, PTSD, generalized anxiety disorder, OCD, social phobia, agoraphobia, panic disorder, home environment, gambling, and ADHD. Substances use investigated includes alcohol, tobacco, marijuana, sedatives, stimulants, cocaine, opiates, solvents, hallucinogens, and other drugs.

This dataset includes 934 cases and 9,370 variables.

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Los Angeles Metropolitan Area Surveys [LAMAS] 3, 1971 (ICPSR 36611)

Released/updated on: 2017-01-31
Geographic coverage: Los Angeles, California

The Los Angeles Metropolitan Area Surveys [LAMAS] 3, 1971 collection reflects data gathered in 1973 as part of the Los Angeles Metropolitan Area Surveys (LAMAS). The LAMAS, beginning in the spring of 1970, are a shared-time omnibus survey of Los Angeles County community members, usually repeated twice annually. The LAMAS were conducted ten times between 1970 and 1976 in an effort to develop a set of standard community profile measures appropriate for use in the planning and evaluation of public policy.

The LAMAS instruments, indexes, and scales were used to track the development and course of social indicators (including social, psychological, health, and economic variables) and the impact of public policy on the community. Questions in this survey cover respondents' attitudes toward the following topics: the concept of a model neighborhood, air pollution, medical problems and health care services in the community, local government politics, police relations, crime, the Mexican-American protests, and public transportation. A sub-sample of households in the San Fernando Area were asked questions about the 1970 earthquake, rating the effectiveness of local government response and the respondents' feelings about possible future disasters.

Demographic variables included in this dataset include age, marital status, religion, sex, education, income, geographic origin, and race.

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Midlife in the United States (MIDUS 3): Biomarker Project, 2017-2022 (ICPSR 38837)

Released/updated on: 2023-11-14
Time period: 2017-04-01--2022-05-01

The Biomarker Project is one of multiple projects that comprise the MIDUS 3 (M3) "Integrative Pathways to Health and Illness" study. For the past two decades, the overarching objective of MIDUS has been to investigate linkages between sociodemographic, psychosocial, behavioral, and neurobiological variables to account for unfolding profiles of morbidity and mortality across the decades of adult life as well as the maintenance of good health and functional capacities. The study has facilitated analyses that pay attention simultaneously to age, gender, race, and socioeconomic variation in how psychosocial and neurobiological variables are linked. In addition, the M3 data permit longitudinal assessment of the impact of ongoing historical events, such as the 2008 economic recession, on the health of diverse-aged adults, which was also included in the MIDUS Refresher 1 (MR1) assessments. M3 included recruitment of additional twins to facilitate genomic analysis.

The M3 Biomarker Project (P4) includes assessment of multiple indicators of physiological regulation/dysregulation and health according to the basic protocol implemented in the MR1 study, which repeated and expanded the M2 biomarker protocol. The M3 protocol included bone density and body composition assessments at all sites and expansion of Actigraphy, Ankle Brachial Index (ABI) and Gait assessments to all three sites. Data were collected during a 24-hour stay at one of three Clinical Research Units (CRU).

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Natality Detail File, 2007 [United States] (ICPSR 36521)

Released/updated on: 2016-08-26
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during the calendar year 2007. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Part 1 contains data on births occurring within the United States, while Part 2 contains data on births occurring in the United States territories of Puerto Rico, the U.S. Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates and other statistics related to this study can be found in the User Guide, under Detailed Technical Notes.

Demographic variables include the child's sex and year of birth, parents' ages, races, ethnicities, education levels, as well as mother's marital status and residency status.

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Natality Detail File, 2008 [United States] (ICPSR 36513)

Released/updated on: 2016-10-31
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during the calendar year 2008. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while Dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the U.S. Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as method of delivery, prenatal care, tobacco and alcohol use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates and other statistics related to this study can be found in the User Guide, under Detailed Technical Notes.

Demographic variables include the child's sex, and month and year of birth, and the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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Natality Detail File, 2009 [United States] (ICPSR 36501)

Released/updated on: 2016-08-12
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during calendar year 2009. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while Dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco and alcohol use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates, and other statistics related to this study can be found in an Appendix to the User Guide, under Detailed Technical Notes.

Demographic variables include the child's sex and month and year of birth, and the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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Natality Detail File, 2010 [United States] (ICPSR 36500)

Released/updated on: 2016-12-14
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during calendar year 2010. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates, and other statistics related to this study can be found in an Appendix to the User Guide under Detailed Technical Notes.

Demographic variables include the child's sex and month and year of birth and the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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Simple Crosstabs

Natality Detail File, 2011 [United States] (ICPSR 36490)

Released/updated on: 2016-12-02
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during the calendar year 2011. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while Dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the U.S. Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth rates, fertility rates, and other aggregate statistics can be found in the Detailed Technical Notes section of the ICPSR User Guide.

Demographic information includes the child's sex and month and year of birth, the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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Simple Crosstabs

Natality Detail File, 2012 [United States] (ICPSR 36469)

Released/updated on: 2016-09-16
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

The Natality Detail File, 2012 [United States] provides information on live births in the United States during the calendar year 2012. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while Dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the U.S. Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco and alcohol use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates and other statistics related to this study can be found in an Appendix to the User Guide, under Detailed Technical Notes.

Demographic variables include the child's sex and month and year of birth and the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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Simple Crosstabs

Natality Detail File, 2014 [United States] (ICPSR 36461)

Released/updated on: 2016-10-07
Geographic coverage: Puerto Rico, United States, Guam, Virgin Islands of the United States, American Samoa, Northern Mariana Islands

This collection provides information on live births in the United States during the calendar year 2014. The natality data in these files are a component of the vital statistics collection effort maintained by the federal government. Birth data is limited to births occurring in the United States to United States residents and nonresidents. Births occurring to United States citizens outside of the United States are not included in this data collection.

Dataset 1 contains data on births occurring within the United States, while Dataset 2 contains data on births occurring in the United States territories of Puerto Rico, the U.S. Virgin Islands, Guam, American Samoa, and the Commonwealth of the Northern Mariana Islands. Variables describe the place of delivery, who was in attendance, and medical and health data such as the method of delivery, prenatal care, tobacco and alcohol use during pregnancy, pregnancy history, medical risk factors, and infant health characteristics.

Birth and fertility rates and other statistics related to this study can be found in an Appendix to the User Guide, under Detailed Technical Notes.

Demographic variables include the child's sex and month and year of birth and the parents' ages, races, ethnicities, education levels, as well as the mother's marital status and residency status.

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National Crime Surveys Extract: Personal Crime Longitudinal Files, 1976-1982 (ICPSR 8315)

Released/updated on: 2005-11-04
Geographic coverage: United States
Time period: 1976-01-01--1982-01-01
The National Crime Survey (NCS) collects data on personal and household victimization through an ongoing national survey of households and household members. Only data for robbery and assaults are included in this dataset. There are two data files: Assault Victim Experiences, and Victim and Non-Victim Responses. Items included are time and place of occurrence, injuries suffered, medical expenses incurred, number, age, race, and sex of offender(s), relationship of offender(s) to victim, marital status, employment, military experience, and residency.
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National Crime Surveys: Redesign Data: Peoria Record Check Study (ICPSR 8669)

Released/updated on: 2006-03-30
Geographic coverage: United States
The purpose of this study was to measure criminal activity in the United States based on survey reports of crime victims. In the study two different questionnaire forms were used in order to assess which provided better responses. One form was very lengthy and asked detailed questions about each household, person, and incident. The second form was much shorter and asked very generalized questions. The data collection was an attempt to find alternative methods of sampling, interviewing, designing questionnaires, managing data, and reporting results. Detailed information is provided on household characteristics and other characteristics of the respondents, as well as on crime incidents, including burglary, vandalism, assault, and rape.
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National Health and Nutrition Examination Survey I, 1971-1975: Health Care Needs, General Medical History and Supplements on Respiratory and Cardiovascular Data (ICPSR 8061)

Released/updated on: 1992-02-16
Geographic coverage: United States
The National Health and Nutrition Examination Surveys (Cycle I) were designed to measure the nutritional status and health of the U.S. population aged 1-74 years and to obtain more detailed information on the health status and medical care needs of adults aged 25-74 years in the civilian noninstitutionalized population.
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National Health and Nutrition Examination Survey I, 1971-1975: Model Gram File Composition (ICPSR 8070)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1971-01-01--1975-01-01
Consists of 3,500 food items with food groups, food codes, alpha-numeric descriptions, and preferred food model codes and gram conversion factors. The Nutrient Composition file is the actual nutrient analysis in 100 gram edible portions of all foods listed in the Model Gram file.
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National Health and Nutrition Examination Survey I: Epidemiologic Follow-Up Study, 1982-1984 (ICPSR 8900)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1982-01-01--1984-01-01
The National Health and Nutrition Examination Survey I Epidemiologic Followup Study (NHEFS) originated as a joint project between the National Center for Health Statistics (NCHS) and the National Institute on Aging (NIA). The design of NHEFS, which contains follow-up data on the NHANES I cohort, consisted of five steps. The first step focused on tracing and locating all subjects in the cohort or their proxies and determining their vital status. The second step involved the obtaining of death certificates for subjects who were deceased. Interviews with the participants or their proxies constituted the third phase of the follow-up. The fourth phase of the follow-up included measurements of pulse, blood pressure, and weight for interviewed respondents, and the fifth step was the acquisition of relevant hospital and nursing home records, including pathology reports and electrocardiograms. The respondent interview was designed to gather information on selected aspects of the subject's health history since the time of the NHANES I exam. This information included a history of the occurrence or recurrence of selected medical conditions, an assessment of behavioral, social, nutritional, and medical risk factors believed to be associated with these conditions, and an assessment of various aspects of functional status. Whenever possible, the questionnaire was designed to retain item comparability between NHANES I and NHEFS in order to measure change over time. However, questionnaire items were modified, added, or deleted when necessary to take advantage of recent improvements in questionnaire methodology. The Vital and Tracing Status file is a master file containing tracing, vital status, and demographic data for all NHEFS respondents. In addition, it provides users with information on the availability of different survey components for each respondent. For example, variables have been created to indicate whether a death certificate was received for a deceased subject, hospital records were received, or a follow-up interview was completed. The Health Care Facility Record file offers data on respondents who had reported an overnight stay in a health care facility after 1970. Information on the name and address of the facility, the date of the stay, and the reason for the stay was recorded. The Mortality Data file contains death certificate information for 1,935 NHEFS decedents. The death certificate information is for deaths occurring from 1971 to 1983.
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National Health and Nutrition Examination Survey I: Epidemiologic Follow-Up Study, 1987 (ICPSR 9854)

Released/updated on: 2006-01-12
Geographic coverage: United States
The National Health and Nutrition Examination Survey I Epidemiologic Follow-Up Study (NHEFS) is a longitudinal study which uses as its baseline those adult persons aged 25 to 74 years who were examined in the first National Health and Nutrition Examination Survey (NHANES I). The NHEFS surveys were designed to investigate the association between factors measured at the baseline and the development of specific health conditions. The NHEFS is comprised of a series of follow-up surveys, three of which have been completed. The first wave of data collection, the 1982-1984 NHEFS (ICPSR 8900), included all persons who were between 25 and 74 years of age at their NHANES I examination. The second wave of data collection, the 1986 NHEFS (ICPSR 9466), included the NHEFS cohort who were 55-74 years at their baseline examination and not known to be deceased at the time of the 1982-1984 NHEFS. The third wave, the 1987 NHEFS, was conducted for the entire nondeceased NHEFS cohort. The 1982-1984 NHEFS consisted of five steps. The first step focused on tracing and locating all subjects in the cohort or their proxies and determining their vital status. The second step involved obtaining death certificates for subjects who were deceased. Interviews with the participants or their proxies constituted the third phase of the follow-up. The fourth phase of the follow-up included measurements of pulse, blood pressure, and weight for interviewed respondents, and the fifth step was the acquisition of relevant hospital and nursing home records, including pathology reports and electrocardiograms. The 1986 NHEFS assessed changes to the health and functional status of the oldest members of the NHEFS cohort since the last contact period. The 1987 NHEFS also collected information on changes in the health and functional status of the NHEFS cohort since the last contact period. The Vital and Tracing Status file contains summary information about the status of the entire NHEFS cohort. The Health Care Facility Record file contains information on reports of stays in hospitals and nursing homes as well as information abstracted from facility medical records. The Mortality Data file contains data abstracted from the death certificates from all three NHEFS surveys. The Interview Data file contains information on selected aspects of the subject's health history since the time of the NHANES I exam.
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National Health and Nutrition Examination Survey I: Epidemiologic Follow-up Study, 1992 (ICPSR 6861)

Released/updated on: 2000-06-21
Geographic coverage: United States
The National Health and Nutrition Examination Survey I Epidemiologic Followup Study (NHEFS) is a longitudinal study that follows participants from the NHANES I who were aged 25-74 in 1971-1975. The NHEFS surveys were designed to investigate the association between factors measured at the baseline and the development of specific health conditions and functional limitations. Follow-up data were collected in 1982-1984 (ICPSR 8900), 1986 (ICPSR 9466), 1987 (ICPSR 9854), and 1992. The 1992 NHEFS collected information on changes in the health and functional status of the NHEFS cohort since the last contact period. The Vital and Tracing Status file (Part 1) provides summary information about the status of the NHEFS cohort. The Interview Data file (Part 2) covers selected aspects of the respondent's health history, including injuries, activities of daily living, vision and hearing, medical conditions, exercise, weight, family history of cancer, surgeries, smoking, alcohol use, and medical care utilization. The Health Care Facility Stay files (Parts 3 and 4) supply information about stays in hospitals, nursing homes, and mental health care facilities, as well as information abstracted from facility medical records. The Mortality Data file (Part 5) contains data abstracted from the death certificates for NHEFS decedents.
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National Health and Nutrition Examination Survey II, 1976-1980: Behavioral Questionnaire, Ages 25-74 Years (ICPSR 9552)

Released/updated on: 1992-02-17
Geographic coverage: United States
Time period: 1976-01-01--1980-01-01
This dataset from the National Health and Examination Survey II (NHANES II) features supplemental variables on personality and activity-level behaviors that may be related to coronary heart disease. Additionally, demographic variables and sampling weights are included in the file. The Demographic Section is divided into four parts: residence data, sample person data, household data, and head of household data. The residence data include information on where the respondent lives, size of place, and total number of persons in the household and/or family. Variables in the sample person data cover age, birth date, sex, race, state of birth, marital status, national origin or ancestry, educational status, and job- and work-related questions. Household data are concerned with characteristics such as total number of rooms in the residence, number of bedrooms, type of kitchen facilities, whether there are running water facilities in the household, and type of heating and cooling systems. Additional household variables offer information on transportation, the languages spoken in the household, and income for the past year. The head of household data include items such as head's age at interview, birth date, sex, race, state of birth, marital status, ancestry, education status, work status, and military service history. The Sample Weight Section provides appropriate adjustments to be used in making population estimates for the examined sample ages 25-74 as a whole, for the portion of the sample who had the medical history interview only, for those that had specific laboratory tests, for specific age/sex/race strata, and for poverty/nonpoverty status. The final section, variables from the Behavior Questionnaire, includes the 19-item Jenkins Activity Survey (1965 version), which elicits information on the sample respondent's perceptions of his or her own tendencies to be hard-driving, impatient, pressured by time, irritated, and competitive. Ten other questions were asked on amount and frequency of physical activity.
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National Health and Nutrition Examination Survey II, 1976-1980: Medical History Ages 12-74 Years (ICPSR 8183)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1976-01-01--1980-01-01
The Health and Nutrition Examination Survey II, 1976-1980: Medical History ages 12-74 years contains demographic characteristics and health histories of 18,447 interviewed persons 12-74 years of age. The medical histories include items on medication, hospital care, tuberculosis, a variety of acute and chronic diseases, tobacco usage, physical activity, weight, height, vision disability, exposure to pesticides, gastrointestinal problems, and, for females, a menstrual and pregnancy history. Data were also collected on anemia, diabetes, respiratory conditions, hearing and speech, liver and gallbladder conditions, kidney and bladder disease, allergies, hypertension, cardiovascular conditions, stroke, arthritis (stressing middle and upper back and neck problems), and participation in food programs.
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National Health and Nutrition Examination Survey II, 1976-1980: Medical History Ages 6 Months-11 Years (ICPSR 8182)

Released/updated on: 1992-02-16
Geographic coverage: United States
The Health and Nutrition Examination Survey II, 1976-1980: Medical History ages 6 months-11 years contains demographic characteristics and health histories of 6,839 interviewed persons 6 months-11 years of age. The medical histories obtained include items on birth weight, birth order, sitting and walking stages, infant feeding, congenital conditions, accidental poisoning, bad accidents, hospitalizations, activity limitation, pneumonia, colds, diarrhea, pica, vision problems, chronic conditions checklists, allergies, lead poisoning, medications, kidney, bladder, and urinary tract conditions, anemia, hearing and speech, lung and chest conditions, school meal programs, and parents' height and weight.
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National Health and Nutrition Examination Survey II, 1976-1980: Physician Examination, Ages 6 Months-74 Years (ICPSR 8686)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1976-01-01--1980-01-01
The NHANES II Physician Examination data collection contains two parts of the extensive data available from NHANES II: demographic information obtained during the household interview, and the results of the physician's examination. The demographic data include information on the type of residence and housing, composition of the household, vehicles, languages spoken, income sources and amounts, food stamps and commodity foods, employment, age, race and national ancestry, sex, education, marital status, veteran status, and region of country. The physical examination data include 1)measurements of systolic and diastolic blood pressure, 2)examination of head, eyes, ears, nose, and throat, 3)thyroid and chest evaluations, 4)heart, pulse, kidney and abdominal evaluations, 5)examinations of joints, 6)musculoskeletal evaluations, and 7)limited neurological and skin evaluation. The data also include a summary of diagnostic impressions coded by the standard International Classification of Diseases, Adapted (ICDA) codes.
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National Health Interview Survey, 1976: Diabetes Supplement (ICPSR 9705)

Released/updated on: 2010-12-06
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. The 1976 Diabetes Supplement provides variables from the core Person File (see HEALTH INTERVIEW SURVEY, 1976 [ICPSR 8340]) including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. The variables unique to this supplement include items on whether the respondent has diabetes, history of diabetes, type of diabetes, experience with insulin, insulin reaction, feelings about diabetes, medications used for diabetes, awareness of the disease, and conditions related to diabetes. Other questions include number of days spent in bed over a 12-month period, number of children, height, weight, eye conditions, and employment history.
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National Health Interview Survey, 1987: Cancer Risk Factor Supplement, Epidemiology Study (ICPSR 9341)

Released/updated on: 1992-02-17
Geographic coverage: United States
The National Health Interview Surveys (NHIS) continuously monitor illness and injury, disability and chronic impairments, and health services used by people in the United States. In 1987, additional interviews were conducted with two subsamples of NHIS respondents to gather data on cancer control and epidemiology. Like the Cancer Control supplement, this Cancer Epidemiology supplement included questions on acculturation (in terms of language, ethnicity, and place of birth), dietary knowledge, smoking and tobacco use, and occupational history. The Cancer Epidemiology supplement also included questions on frequency and portion sizes of food and drink items, vitamin and mineral intake, reproduction, hormone use, family's and respondent's history of cancer, height and weight, and participation in social activities. Approximately 90 demographic, health status, and health care variables from the core data files are included on the supplement file.
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National Health Interview Survey, 1989: Diabetes Supplement (ICPSR 6048)

Released/updated on: 1993-10-02
Geographic coverage: United States
The basic purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Each year, the National Center for Health Statistics conducts the NHIS, a personal interview household survey that uses a nationwide sample of the civilian, noninstitutionalized population of the United States. The NHIS includes a core set of questions that remains virtually unchanged across years on a variety of sociodemographic and health-related concerns. In addition, one or more current health topics is selected for special emphasis annually. In 1989, the NHIS included an extensive set of questions, asked of each identified and self-confirmed adult diabetic in an interviewed family, on dietary practices, health care usage, use of medication, and other related subjects. In addition, in half of the responding families, an adult sample person was randomly selected to respond to a series of questions on diabetes risk factors. If the selected sample person was a diabetic, the questions were asked within the context of the detailed questions on diabetes health practices and knowledge mentioned above. This collection also contains data from the basic questionnaire (see NATIONAL HEALTH INTERVIEW SURVEY, 1989 [ICPSR 9583]), including age, sex, race, marital status, education, veteran status, income, family relationship, self-reported health status, and activity limitations, and the number of bed days, doctor visits, and hospital stays in the previous year.
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National Health Interview Survey, 1992: Cancer Control Supplement (ICPSR 6344)

Released/updated on: 1994-10-19
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. The 1992 Cancer Control Supplement includes variables from the NHIS core Person File (see NATIONAL HEALTH INTERVIEW SURVEY, 1992 [ICPSR 6343]), including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. Variables unique to this supplement include items on acculturation (e.g., language, ethnic identification, place of birth of self and parents), medical care, food knowledge, cancer knowledge and attitudes, cancer screening knowledge and practice, smoking and other tobacco use, and occupational exposures to harmful substances.
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National Health Interview Survey, 1992: Cancer Epidemiology Supplement (ICPSR 6349)

Released/updated on: 1994-10-19
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. The 1992 Cancer Epidemiology Supplement includes variables from the NHIS core Person File (see NATIONAL HEALTH INTERVIEW SURVEY, 1992 [ICPSR 6343]), including sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. Variables unique to this supplement include information on acculturation (in terms of language, ethnicity, and place of birth), dietary knowledge, smoking and tobacco use, and occupational history. The supplement also covers frequency and portion sizes of food and drink items, vitamin and mineral intake, hormone use, family's and respondent's history of cancer, and respondent's height and weight.
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National Intimate Partner and Sexual Violence Survey (NISVS): General Population Survey Raw Data, 2010 (ICPSR 34305)

Released/updated on: 2016-06-09
Geographic coverage: United States
Time period: 2010-01-22--2010-12-31

The National Intimate Partner and Sexual Violence Survey (NISVS) is an ongoing nationally representative survey that assesses experiences of sexual violence, stalking, and intimate partner violence among adult women and men in the United States and for each individual state. The survey focused exclusively on violence and collects information about

  • Sexual violence by any perpetrator, including information related to rape, being made to penetrate someone else, sexual coercion, unwanted sexual contact, and non-contact unwanted sexual experiences
  • Stalking, including the use of technologies such as text messages, emails, monitoring devices (e.g., cameras and GPS, or global positioning system devices), by perpetrators known and unknown to the victim
  • Physical violence by an intimate partner
  • Psychological aggression by an intimate partner, including information on expressive forms of aggression and coercive control
  • Control of reproductive or sexual health by an intimate partner

In addition to collecting lifetime and 12 month prevalence data on sexual violence, stalking, and intimate partner violence, the survey collects information on the age at the time of the first victimization, demographic characteristics of respondents, demographic characteristics of perpetrators (age, sex, race/ethnicity) and detailed information about the context in which these types of violence occur.

The primary objectives of the survey are to describe the prevalence and characteristics of sexual violence, stalking, and intimate partner violence in the United States; who is most likely to experience these forms of violence; the context in which sexual violence, stalking, and intimate partner violence are experienced; and the consequences and impacts of these forms of violence.

The data file contains 18,957 cases and 26,114 variables.

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National Intimate Partner and Sexual Violence Survey (NISVS): General Population Survey Raw Data, 2011 (ICPSR 37520)

Released/updated on: 2020-09-08
Geographic coverage: District of Columbia, United States

The National Intimate Partner and Sexual Violence Survey (NISVS) is an ongoing nationally representative survey that assesses experiences of sexual violence, stalking, and intimate partner violence among adult women and men in the United States and for each individual state. The survey focused exclusively on violence and collects information about:

  • Sexual violence by any perpetrator, including information related to rape, being made to penetrate someone else, sexual coercion, unwanted sexual contact, and non-contact unwanted sexual experiences
  • Stalking, including the use of newer technologies such as text messages, emails, monitoring devices (e.g., cameras and GPS, or global positioning system devices), by perpetrators known and unknown to the victim
  • Physical violence by an intimate partner
  • Psychological aggression by an intimate partner, including information on expressive forms of aggression and coercive control
  • Control of reproductive or sexual health by an intimate partner

In addition to collecting lifetime and 12 month prevalence data on sexual violence, stalking, and intimate partner violence, the survey collects information on the age at the time of the first victimization, demographic characteristics of respondents, demographic characteristics of perpetrators (age, sex, race/ethnicity) and detailed information about the context in which these types of violence occur.

The primary objectives of the survey are to describe the prevalence and characteristics of sexual violence, stalking, and intimate partner violence in the United States; who is most likely to experience these forms of violence; the context in which sexual violence, stalking, and intimate partner violence are experienced; and the consequences and impacts of these forms of violence.

The data file contains 14,884 cases and 25,783 variables.

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National Intimate Partner and Sexual Violence Survey (NISVS): General Population Survey Raw Data, 2012 (ICPSR 37581)

Released/updated on: 2020-09-08
Geographic coverage: District of Columbia, United States

The National Intimate Partner and Sexual Violence Survey (NISVS) is an ongoing nationally representative survey that assesses experiences of sexual violence, stalking, and intimate partner violence among adult women and men in the United States and for each individual state. The survey focused exclusively on violence and collects information about

  • Sexual violence by any perpetrator, including information related to rape, being made to penetrate someone else, sexual coercion, unwanted sexual contact, and non-contact unwanted sexual experiences
  • Stalking, including the use of technologies such as text messages, emails, monitoring devices (e.g., cameras and GPS, or global positioning system devices), by perpetrators known and unknown to the victim
  • Physical violence by an intimate partner
  • Psychological aggression by an intimate partner, including information on expressive forms of aggression and coercive control
  • Control of reproductive or sexual health by an intimate partner

In addition to collecting lifetime and 12 month prevalence data on sexual violence, stalking, and intimate partner violence, the survey collects information on the age at the time of the first victimization, demographic characteristics of respondents, demographic characteristics of perpetrators (age, sex, race/ethnicity) and detailed information about the context in which these types of violence occur.

The primary objectives of the survey are to describe the prevalence and characteristics of sexual violence, stalking, and intimate partner violence in the United States; who is most likely to experience these forms of violence; the context in which sexual violence, stalking, and intimate partner violence are experienced; and the consequences and impacts of these forms of violence.

The data file contains 14,188 cases and 31,941 variables. Demographic variables include gender, race, marital status, age, and education level.

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National Intimate Partner and Sexual Violence Survey (NISVS): General Population Survey Raw Data, 2015 (ICPSR 37632)

Released/updated on: 2020-09-08
Geographic coverage: United States

The National Intimate Partner and Sexual Violence Survey is an ongoing, nationally representative survey that assesses experiences of sexual violence, stalking, and intimate partner violence among adult women and men in the United States and for each individual state. The survey is focused exclusively on violence and collects information about:

  • Sexual violence by any perpetrator, including information related to rape, being made to penetrate someone else, sexual coercion, unwanted sexual contact, and non-contact unwanted sexual experiences.
  • Stalking, including the use of technologies such as text messages, emails, monitoring devices (e.g., cameras and GPS, or global positioning system devices), by perpetrators known and unknown to the victim.
  • Physical violence by an intimate partner.
  • Psychological aggression by an intimate partner, including information on expressive forms of aggression and coercive control.
  • Control of reproductive or sexual health by an intimate partner.

In addition to collecting lifetime and 12-month prevalence data on sexual violence, stalking, and intimate partner violence, the survey collects information on the age at the time of the first victimization, demographic characteristics of respondents, demographic characteristics of perpetrators (age, sex, race/ethnicity) and detailed information about the context in which these types of violence occur.

The primary objectives of the survey are to describe the prevalence and characteristics of sexual violence, stalking, and intimate partner violence in the United States; who is most likely to experience these forms of violence; the context in which sexual violence, stalking, and intimate partner violence are experienced; and the consequences and impacts of these forms of violence.

The data file contains 10,917 cases and 14,963 variables.

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National Intimate Partner and Sexual Violence Survey (NISVS): General Population Survey Raw Data, 2016/2017 (ICPSR 38960)

Released/updated on: 2024-09-05
Geographic coverage: District of Columbia, United States
Time period: 2016-01-01--2017-01-01

The National Intimate Partner and Sexual Violence Survey is an ongoing, nationally representative survey that assesses experiences of sexual violence, stalking, and intimate partner violence among adult women and men in the United States. The survey is focused exclusively on violence and collects information about:

  • Sexual violence by any perpetrator, including information related to rape, being made to penetrate someone else, sexual coercion and unwanted sexual contact.
  • Stalking, including the use of technologies such as text messages, emails, monitoring devices (e.g., cameras and GPS, or global positioning system devices), by perpetrators known and unknown to the victim.
  • Psychological aggression by an intimate partner, including information on expressive forms of aggression and coercive control.
  • Physical violence by an intimate partner.

In addition to collecting lifetime and 12-month prevalence data on sexual violence, stalking, and intimate partner violence, the survey collects information on the age at the time of the first victimization, demographic characteristics of respondents, characteristics of perpetrators (age, sex, race/ethnicity, relationship to the respondent) and detailed information about the context in which these types of violence occur.

The primary objectives of the survey are to describe the prevalence and characteristics of sexual violence, stalking, and intimate partner violence in the United States; who is most likely to experience these forms of violence; the context in which sexual violence, stalking, and intimate partner violence are experienced; and the consequences and impacts of these forms of violence.

The survey was conducted in both English and Spanish, ensuring inclusivity and broader participation. The documentation package includes both the English and Spanish versions of the questionnaire.

The data file contains 30,947 observations and 428 variables.

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National Medical Expenditure Survey, 1987: Survey of American Indians and Alaska Natives, Population Data, Data from the Health Status Questionnaire and Access to Care Supplement, and Expenditures and Sources of Payment Data [Public Use Tape 37] (ICPSR 6490)

Released/updated on: 1995-06-05
Geographic coverage: United States
The National Medical Expenditure Survey (NMES) series provides information on health expenditures by or on behalf of families and individuals, the financing of these expenditures, and each person's use of services. The Survey of American Indians and Alaska Natives (SAIAN) was designed in collaboration with the Indian Health Service (IHS), and used the same data collection instruments, interview procedures, and time frame as the NMES Household Survey component. However, the SAIAN differed from the Household Survey in several respects. The SAIAN sample was interviewed only three times and was not given the supplements on long-term care, caregiving, and care-receiving. Also, SAIAN respondents were asked additional questions on topics such as use of IHS facilities and traditional medicine, and were given a modified self-administered questionnaire with separate versions for adults and children. Interviewers for the SAIAN were mainly American Indians or Alaska Natives, and about 20 percent of the interviews were not conducted entirely in English. Of these, approximately 40 percent were conducted entirely in the native language of the respondent. Public Use Tape 37 contains the final 1987 calendar year SAIAN data, and updates all previous releases of SAIAN data. Variables include population characteristics (demographic information, native language, household composition, employment, health insurance, eligibility status) health statistics (medical conditions, illnesses, limitations on activities, vaccinations), prescribed medicines (dates medication last taken, name of medication prescribed, number of medication purchases made during the year), home health care, medical items purchased, rented, or otherwise obtained, type of traditional medical practitioner seen by respondent, type of service obtained during dental visits, inpatient hospital stays (reason for entry, surgery performed, days and nights in hospital, date entered and discharged), ambulatory visits and telephone calls to physicians' offices, visits to hospital outpatient departments, and visits to hospital emergency rooms.
Curated

National Mortality Followback Survey, 1966-1968 (ICPSR 8370)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1966-01-01--1968-01-01
This survey was designed primarily to obtain information on the smoking habits of decedents by examining death certificates and questionnaires mailed to death record informants. Smoking variables in this data collection include number of cigarettes smoked when the decedent smoked most, number smoked the year before death, number smoked three years before death, and cigar and pipe smoking occurrence three years before death. Demographic variables include marital status, family type, number of children, living arrangements, size of family, birth and death of the decedent, family income and family debt, and cause of death.
Curated

National Mortality Followback Survey, 1986 (ICPSR 9410)

Released/updated on: 2006-01-18
Geographic coverage: United States
The 1986 National Mortality Followback Survey (NMFS) is the first National Center for Health Statistics (NCHS) mortality followback study since the 1966-1968 survey of the same name (ICPSR 8370). The 1986 NMFS supplements characteristics of mortality found in the routine vital statistics system by collecting information from death certificate informants or other knowledgeable relatives, and from health care facilities that were used by decedents in the last year of life. The death records provide demographic data on the decedent and information on the circumstances of death (location, time, underlying causes, and other health conditions at time of death) and use of medical facilities in the preceding year. Additional issues addressed in the informant questionnaire were health care sought and provided in the last year of life, risk factors associated with premature death, socioeconomic status and mortality, and reliability of selected items reported on the death certificate. Health care facilities provided information on diagnosis, diagnostic and surgical procedures performed on the decedent, and length of stay.
Curated

National Mortality Followback Survey, 1993 (ICPSR 2900)

Released/updated on: 2005-02-21
Geographic coverage: United States
The National Mortality Followback Survey (NMFS) Program, begun in the 1960s by the National Center for Health Statistics (NCHS), uses a sample of United States residents who die in a given year, supplementing information derived from the death certificate with information from the next of kin or another person familiar with the decedent's life history. This information, sometimes enhanced by administrative records, is collected in order to study the etiology of disease, demographic trends in mortality, and other health issues. The 1993 National Mortality Followback Survey (NMFS) sampled individuals aged 15 years and over who died in 1993. Forty-nine of the 50 state vital registration areas, as well as the independent vital registration areas of the District of Columbia and New York City, granted approval to sample their death certificates. (South Dakota declined to participate due to a state law restricting the use of death certificate information.) A sample of 22,957 death certificates from 1993 was then drawn. To obtain reliable numbers for important population subgroups, such as persons under age 35, women, and the Black population, death certificates from those subgroups were oversampled. The 1993 NMFS survey focused on five subject areas: (1) socioeconomic differentials in mortality, (2) associations between risk factors and cause of death (use of tobacco, alcohol, drugs, firearms, motor vehicles), (3) disability (medical condition and cognitive functioning during the last year of life), (4) access and utilization of health care facilities during the last year of life (number of doctor visits, days bedridden, nursing home experiences, use of assistive medical devices, availability of health insurance), and (5) reliability of certain items reported on the death certificate. Demographic variables include age, gender, race, marital status, birthplace, education, occupation and industry, and income and assets. The 1993 NMFS survey differed from the previous mortality followback surveys in several ways: First, it emphasized deaths due to homicide, suicide, and unintentional injury. Second, the subject areas were considerably broader (many previously-surveyed subject areas, however, are included for trend analysis). This survey was also the first to acquire national-level information from medical examiners and coroners. Finally, the complexity of the questionnaire necessitated telephone or in-person interviews. The 1993 NMFS was designed in collaboration with other agencies of the Public Health Service, Department of Health and Human Services, and the National Highway Traffic Safety Administration.
Curated

National Survey of the Aged [United States], 1957 (ICPSR 7686)

Released/updated on: 2006-03-30
Geographic coverage: United States
This survey, sponsored by the Health Information Foundation at the University of Chicago and conducted at the National Opinion Research Center, consists of three component parts. Part 1, the Health Needs of Older Persons, covers health, the use of medical facilities, the cost of medical care, the older person's sources of income, his/her social relationships, attitudes toward younger family members, work, religion, and a self-evaluation of health status for persons aged 60 and over. Part 2, Household Enumeration: Noninterviewed Individuals, contains information describing persons located during the enumeration process who were unable to complete an interview. For Part 3, Public Attitudes on Older People, a cross-section of adult Americans was surveyed. This survey was mainly concerned with the level of responsibility younger and middle-aged people assumed for older relatives, the kinds of plans they were making for their own maintenance in later years, and overall attitudes on the part of all age groups toward certain situations that are commmon in later life.
Curated

Oregon Youth Study Three Generational Study, Multi-Wave, 1995-2022 (ICPSR 39046)

Released/updated on: 2025-05-20
Geographic coverage: Oregon, United States
Time period: 1995-01-01--2022-01-01
This study is part of the Oregon Youth Study (OYS), which began in 1983 and has now become the Three Generational Study (3GS). The aim of the original study was to examine the etiology of antisocial behaviors in boys, with the longer-term goal of designing preventative interventions. The longitudinal study expanded to include data collection regarding the relationships between the original male respondents, their romantic partners, and their offspring. This particular study focuses on the biological mothers and fathers (original OYS respondents) of offspring in the Three Generational Study. Data is collected across multiple waves, spanning from 1995 to 2022. It provides supplemental information that supports the continuing aims of the various waves within the OYS and 3GS studies. It examines the familial and personal history of the adult respondents, examining intergenerational trends of social behavior, alcohol and substance use, criminal behavior, mental health, and medical history. In particular, it includes detailed information about the personal history of the biological mothers of 3GS offspring.
Curated
Partially restricted
Simple Crosstabs

Project Migrante: Health Status and Access to Health Care Among Migrants on Mexico's Northern Border, 2020-2021 (ICPSR 38601)

Released/updated on: 2023-06-07
Geographic coverage: Tijuana, Matamoros, Mexico, Ciudad Juárez
Time period: 2020-01-01--2021-01-01

The Migrante Project is a binational study that examines health status and access to health care among Mexican migrants. Since 2007, Migrante investigators have implemented a series of cross-sectional probability-based surveys on Mexico's northern border. The current phase of Migrante includes three survey waves (N=1,200 each), each focused on a specific topic area. Data for the Wave I survey focused on HIV and sexual/reproductive health. Wave II is focused on non-communicable disease. Data collection for this wave is ongoing. Wave III (data to be collected in 2023) will focus on mental health and substance use. All surveys contain additional questions on socio-demographics, health status, health care access, migration history, and contextual factors related to migration stage. All waves also include biometric testing (for example, rapid HIV testing). Participants are sampled from four different migrant flows:

  • Northbound flow: Migrants traveling north and arriving at the border from other regions in Mexico
  • Southbound flow - Border: Migrants traveling from the Mexico side of the Mexico-US border to points farther south
  • Southbound flow - U.S.: Migrants returning to Mexico from the U.S. voluntarily
  • Deported flow: Migrants returning to Mexico from the U.S via deportation

The data herein come from the Wave I survey and were collected in Tijuana, Matamoros, and Ciudad Juárez, Mexico between August 2020 and September 2021. The study employed a multistage sampling design, with a combination of geographic and temporal sampling units, modeled after the Encuesta sobre Migración en la Frontera Norte de México (EMIF Norte). Migrante sampling sites for Wave I included bus stations, airports, and deportation stations in each of the three cities.

Eligible individuals were at least 18 years old, born in Mexico or other Latin American countries, fluent in Spanish, not residents of the city where the survey is being conducted (except for deported migrants), and traveling for labor reasons or change of residence. In total, there were 1,398 observations (northbound flow N=347, southbound flow N=703, and deported flow N=348) in Wave I, with 1,257 individuals completing the Wave I survey. Three hundred and six of these individuals belonged to the deported flow, 306 to the northbound flow, 336 to the southbound border flow, and 309 to the southbound U.S. flow. Consent rates ranged from 13% to 98% depending on the flow and survey city. Migrante surveys can be used to produce population-level estimates of health outcomes and health care access, investigate variations across migration phases, and explore the impact of health care and immigration policies on migrants' health outcomes, healthcare access, and individual and environmental health determinants.