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Sexual assault is the most common violent crime committed on college campuses today. One in five women have experienced a completed or attempted sexual assault as an undergraduate. In one study, 28% of first-year college women experienced unwanted sexual contact and 7% experienced sexual assault or attempted sexual assault in the first semester of their first year of college, while 7% of college men reported an attempted or completed assault during their college experience. Growing evidence suggests the effectiveness of using online tools and video games for public health intervention and education.

Because of the positive impact of these digital strategies, researchers saw a need to bring this research to sexual violence prevention, where there has been limited use of digital applications. The goal of this project was to design and evaluate the pedagogical effectiveness and cost effectiveness of a video game to reduce sexual and relationship violence. It was hypothesized that the video game could enhance the self-confidence of male and female late adolescents (ages 18-24) to practice safe, appropriate, and effective approaches for intervening in situations where sexual and/or relationship violence (including stalking) is occurring, has the potential to occur, or recently occurred.

The Forces of Change Survey is an annual survey completed by the state and territorial health agencies that comprise the membership of the Association of State and Territorial Health Officials (ASTHO). ASTHO is the national nonprofit organization representing public health agencies in the United States, the U.S. territories and freely associated states, and the District of Columbia, and the over 100,000 public health professionals these agencies employ. The Forces of Change Survey primarily focuses on emergent and rapidly changing trends. The data collected sought to determine the current climate at state and territorial health agencies as it related to budget, workforce, accreditation, and special interest topics. The 2017 Forces of Change Survey examined the following topics:

• Health agency resources
• Activities related to the Zika virus
• Opioid epidemic response
• Communicating the value of public health
• Efforts to advance health equity

The web-based survey, fielded by ASTHO in May of 2017, was administered to state and territorial health agencies through their senior deputies. A total of 52 health agencies responded (from 46 states, Washington, D.C., and five territories and freely associated states). Data included as part of this collection includes one dataset with 122 variables for 52 cases.

The 2012 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The 121-question instrument was disseminated electronically in October 2012 and completed by senior deputies at each S/THA. The survey closed in May 2013; the response rate was 96 percent among the 50 states and D.C., and 92 percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

The 2016 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The 129-question instrument was disseminated electronically in April 2016 and completed by senior deputies at each S/THA. The survey closed in September 2016; the response rate was 98 percent among the 50 states and D.C., and 97 percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

The 2019 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The instrument was disseminated electronically in April 2019 and completed by state and territorial health agency staff at each S/THA including senior deputies, chief financial officers, and human resource directors. The survey closed in January 2020; the response rate was 100% percent among the 50 states and D.C., and 98% percent among all states, territories, and freely associated states.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

The 2020 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The survey aims to define the scope of state and territorial public health services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The instrument was significantly shortened for this data collection and separated into three separate surveys. The surveys were administered in December 2020 and completed by state and territorial health agency staff at each S/THA including senior deputies, chief financial officers, and human resource directors. The survey closed in March 2021; 80% of states and DC responded to at least one survey, of which 40% of states and DC responded to all three surveys; 38% of territories responded to at least one survey, of which 11% responded to all three surveys.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

The 2022 ASTHO Profile Survey is a survey conducted by the Association of State and Territorial Health Officials (ASTHO) to gather information on state, territorial, and freely associated state public health agencies (S/THAs) and their activities, structure, and resources. The Profile aims to define the scope of S/THA services, identify variations in practice among public health agencies, and contribute to the development of best practices in governmental public health. The Profile began in 2007 and was fielded on average every three years between 2007 and 2022. The data collected through the Profile represent the breadth of work overseen by health agencies and shows how the public health field has shifted in response to societal changes and emergent needs. Data also reflect the structural nuances and limitations in which agencies conduct their work.

Changes may be made to the dataset after it is archived. Please contact [email protected] to request the most updated datasets. Additional information on the study can be found by visiting the ASTHO Profile Survey website.

Asthma is one of the nation's most common and costly chronic conditions, affecting over 38 million Americans at some time in their lives. Managing asthma requires a long term, multifaceted approach, including patient education, behavior changes, asthma trigger avoidance, pharmacological therapy, and frequent medical follow-up. This study provides asthma data available at the state and local level to direct and evaluate interventions undertaken by asthma control programs located in the state health departments. Improved tracking for asthma is critical for planning and evaluating efforts to reduce the health burden from the disease.

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 methodological 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. Data derived from the questionnaire provide health departments, public health officials, and policymakers with necessary behavioral information. 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. Demographic variables include race, age, sex, education level, marital status, employment status, and income level.

The Behavioral Risk Factor Surveillance System (BRFSS) is a system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. Established in 1984 with 15 states, BRFSS now collects data in all 50 states as well as the District of Columbia and three U.S. territories. BRFSS completes more than 400,000 adult interviews each year.

These data come from surveillance activities conducted by the Guttmacher Institute over several decades, collecting or compiling data for the period 1994 through 2016. These activities track the numbers of women who have a potential demand for contraceptive care (because they are of reproductive age, sexually active and not seeking to become pregnant), the subset of these women who likely need public support for care (because of their family income level or their age), the numbers of women who receive contraceptive services from publicly funded clinics, and the numbers of clinics providing publicly supported contraceptive services. These efforts have been conducted periodically, typically about every five years, but at times the intervals between efforts were shorter or longer than five years. The most recent data were collected or compiled for 2015 (women served) and 2016 (women with potential demand for services).

This release includes two separate datasets. Dataset 1, "Need for contraceptive services," provides county-level aggregate data for 6 different years (1995, 2000, 2002, 2006, 2010, and 2016). For each county, the data represent estimates of the number of women who have a potential demand for contraceptive services and the number who likely need public support for care, both in total, and according to key socio-demographic characteristics. Dataset 2, "Clinics providing contraceptive services and women served," provides county-level aggregate data for six different years (1994, 1997, 2001, 2006, 2010, and 2015). For each county, the data represent the number of publicly funded clinics according to clinic type and funding status and the number of female contraceptive patients served at those clinics.

This data collection contains the TrainingFinder Real-time Affiliate Integrated Network (TRAIN) database dictionary and three data files derived from the TRAIN database. A project of the Public Health Foundation, TRAIN (www.train.org) is a comprehensive learning resource for public health professionals, such as epidemiologists, public health officials, health educators, environmental health professionals, social workers, nurses, physicians, emergency responders, and mental health providers. Learners can use TRAIN to search for on-site and distance learning courses, register on-line for courses, provide and view feedback about courses, and create a personal training record of competency-based training and continuing education requirements. Course providers can use TRAIN to publicize courses, manage online registration and student rosters, collect feedback from learners, and post course materials and discussion topics.

Core Competencies for Public Health Professionals is a set of skills, knowledge, and attitudes necessary for the broad practice of public health. Adopted by the Council on Linkages Between Academia and Public Health Practice, this list of competencies was incorporated into TRAIN.

Comprising a small subset of the information in the TRAIN database, the three data files were tailored to facilitate public health systems and services research. The first data file contains demographic information about every registered TRAIN learner: street address, county, city, state, ZIP code, country, education level, gender, race, Hispanic origin, birth date, primary language, and secondary language. The second data file is a tabulation which shows the core competencies covered by each course offered through TRAIN, together with the course titles, expiration dates, and the organizations offering the courses. The last data file is a tabulation which shows the number of TRAIN courses and learners by core competency and professional role.

The TRAIN database dictionary describes all of the variables in the TRAIN database, including those not provided with this data collection.

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation have partnered to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low-to moderate-income backgrounds.

Questions in this COVID-19 survey focused specifically on experiences related to the pandemic (e.g., financial, physical, emotional), how respondents viewed the disproportionate impacts of the pandemic, whether and how respondents' views and priorities regarding health actions and investments are changing (including the roles of government and the private sector), and how general values about such issues as freedom and racism may be related to pandemic views and response expectations.

This study includes the results for Wave 1 for the general population.

Demographic information includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation have partnered to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low-to moderate-income backgrounds.

In the context of COVID-19, RAND and the Robert Wood Johnson Foundation partnered again to build from the National Survey of Health Attitudes to implement a longitudinal survey to understand how health views and values have been affected by the experience of the pandemic, with particular focus on populations deemed vulnerable or underserved, including people of color and those from low- to moderate-income backgrounds.

The study is a longitudinal study, collecting data in four waves. The study also included 2 populations: A sample of populations at greater risk, and a general population sample. This study includes the results for Wave 2 for populations at greater risk.

One previous wave and two future waves were conducted. The questions in the surveys were largely similar across all four waves. All respondents who participated in Wave 1 were invited to participate in the future waves.

Demographic info includes sex, marital status, household size, race and ethnicity, family income, employment status, age, and census region.

The COVID-19 Trends and Impact Survey (CTIS) was conducted by the Delphi Group at Carnegie Mellon University (CMU) in the United States (US) and by the University of Maryland (UMD) Social Data Science Center (SoDa) globally, in partnership with Meta. CTIS was a daily repeated cross-sectional survey that ran continuously starting April 6, 2020 in the US and starting April 23, 2020 globally. Both surveys concluded data collection on June 25, 2022. CTIS collected data in 200+ countries and territories, including 114 where Meta provided survey weights. The sampling frame was Facebook users aged 18 years or older who have been active on the platform in the last month. Sampled Facebook users saw the invitation at the top of their Feed, but the surveys were collected by the universities using Qualtrics. Meta neither collected nor received survey responses. The sample was stratified by subnational regions. Respondents were sampled as frequently as every month and as infrequently as every six months, depending on the population density of the subnational region in which they lived. Due to the minimum sampling frequency, pooled analyses should not combine more than a month of data. There were 12 versions of the survey questionnaires. The Delphi US CTIS was translated into 8 languages. The UMD Global CTIS was translated into 66 languages.

This collection is comprised of three categories of data:

a. Individual-level microdata files, which will be available to eligible academic and nonprofit researchers with fully executed Data Use Agreements (DUAs).

b. Daily aggregate estimates at the country and subnational region levels disseminated via public APIs at CMU and UMD.

c. Weekly and monthly aggregate estimates broken out by respondent characteristics (e.g., age, gender, vaccination status) at the country and subnational administrative level-1 region-level disseminated via publicly available CSV-formatted contingency tables.

This collection currently only contains the aggregate data, contingency tables and associated documentation. The microdata are forthcoming.

The United States COVID-19 Trends and Impact Survey (CTIS) was a voluntary survey of Facebook users in the United States conducted from April 2020 to June 2022. CTIS was intended to aid in pandemic forecasting and response at fine spatiotemporal detail. Through collaboration with Meta, it randomly sampled Facebook active users at a rate sufficient to provide roughly 35,000 responses per day, on average. Survey questions covered topics including COVID-like symptoms, behavior (such as social distancing), COVID testing, mental health, health-related beliefs, trust in officials and information sources, schooling, vaccination acceptance and hesitancy, and related subjects. Respondents provided their ZIP code. Demographic variables include age, gender, education, race/ethnicity, and occupation. Meta generated survey weights to correct for non-response and to match the US adult population age and gender distribution.

The 27 datasets make up the microdata. Users should see the Microdata User Guide for documentation on the use and interpretation of the microdata files.

Two zip files are available for public download: a monthly data zip file and a weekly data zip file. These include the aggregate data. To access these files, go to the "Download" tab and select "Other." Ensure you have enough storage space before proceeding, as the files are large.

Wave 3 of the Detroit Metro Area Community Study was conducted in collaboration with the Detroit Health Department in the summer of 2018 as part of the City's Community Health Assessment. Topics covered include healthcare access and utilization; neighborhood satisfaction and cohesion; community assets; and participants' priorities for change. Demographic information includes race, age, gender, education, household size, employment status, political ideology, and LGBTQIA affiliation.

The Eurobarometer series is a unique cross-national and cross-temporal survey program conducted on behalf of the European Commission. These surveys regularly monitor public opinion in the European Union (EU) member countries and consist of standard modules and special topic modules. The standard modules address attitudes towards European unification, institutions and policies, measurements for general socio-political orientations, as well as respondent and household demographics. The special topic modules address such topics as agriculture, education, natural environment and resources, public health, public safety and crime, and science and technology.

This round of Eurobarometer surveys covers the special topic of public health and includes the following major areas of focus: (1) check-up and prevention, (2) oral health, (3) alcohol habits, (4) smoking habits, (5) organ and blood donation, and (6) sport and physical activity. Questions pertain to medical tests and health exams received in the past 12 months, eating a healthy diet, exercise, visits and access to a dentist, and food and drink consumption. Other questions addressed alcohol consumption within the past 12 months, smoking status and behavior, as well as the knowledge of human organ donation and transplant, and safety of blood transfusions compared to 10 years ago.

Demographic and other background information collected includes age, gender, nationality, marital status, occupation, age when stopped full-time education, household composition, ownership of a fixed or a mobile telephone and other durable goods, difficulties in paying bills, level in society, and Internet use. In addition, country-specific data includes type and size of locality, region of residence, and language of interview (select countries).

The Eurobarometer series is a unique cross-national and cross-temporal survey program conducted on behalf of the European Commission. These surveys regularly monitor public opinion in the European Union (EU) member countries and consist of standard modules and special topic modules. The standard modules address attitudes towards European unification, institutions and policies, measurements for general socio-political orientations, as well as respondent and household demographics. The special topic modules address such topics as agriculture, education, natural environment and resources, public health, public safety and crime, and science and technology.

This round of Eurobarometer surveys covers the special topics: national and European identity, and electromagnetic fields and health. Questions pertain to citizenship and origin of family, connections with other countries, knowledge of languages, mobility across countries in the next 10 years, attachment to other countries, regional identity, and belonging to majority and minority groups. Other questions address awareness of electromagnetic fields sources and their effects on health, as well as opinions about protection from these fields.

Demographic and other background information collected includes age, gender, nationality, marital status and parental relations, occupation, age when stopped full-time education, household composition, ownership of a fixed or mobile telephone and other goods, difficulties in paying bills, level in society, and Internet use. In addition, country-specific data includes type and size of locality, region of residence, and language of interview (select countries).

The Eurobarometer series is a unique cross-national and cross-temporal survey program conducted on behalf of the European Commission. These surveys regularly monitor public opinion in the European Union (EU) member countries and consist of standard modules and special topic modules. The standard modules address attitudes towards European unification, institutions and policies, measurements for general socio-political orientations, as well as respondent and household demographics. The special topic modules address such topics as agriculture, education, natural environment and resources, public health, public safety and crime, and science and technology.

This round of Eurobarometer surveys includes the standard indicators on living conditions and expectations and covers the following special topics: (1) the European Social Fund (ESF), (2) civil justice, (3) development aid, (4) Africa and the EU, and (5) food risk. Questions pertain to living conditions and expectations, opinions on the ESF, the civil justice and commercial legal proceedings in the member states and the EU, and attitudes towards assisting developing countries. Other questions address Africa's problems, image, and relation to the EU, as well as opinions on food-related hazards.

Demographic and other background information includes age, gender, nationality, marital status, occupation, age when stopped full-time education, household composition, ownership of a fixed or mobile telephone and other durable goods, difficulties in paying bills, level in society, and Internet use. In addition, country-specific data includes type and size of locality, region of residence, and language of interview (select countries).

The Eurobarometer series is a unique cross-national and cross-temporal survey program conducted on behalf of the European Commission. These surveys regularly monitor public opinion in the European Union (EU) member countries and consist of standard modules and special topic modules. The standard modules address attitudes towards European unification, institutions and policies, measurements for general socio-political orientations, as well as respondent and household demographics. The special topic modules address such topics as agriculture, education, natural environment and resources, public health, public safety and crime, and science and technology.

This round of Eurobarometer surveys diverged from the Standard Eurobarometer measures and queried respondents on the following major areas of focus: (1) the European Parliament (EP), (2) energy supply, (3) data protection and electronic identity, (4) chemical labeling, and (5) rare diseases. For the first major area of focus, the European Parliament, respondents were asked about their knowledge and opinion of the EP, whether the EP should play a more important or less important role, which policies should be given priority by the EP, and which values should be defended by the EP. For the second major area of focus, energy supply, respondents were queried about what goals should be prioritized in energy policies, what energy policies should be adopted, and whether or not there should be a communal European Union (EU) energy policy. Additionally, respondents were asked whether they believed it was in their country's energy security interest to assist other EU member states facing energy supply problems, as well as whether they believed it was desirable that their country provide assistance to other EU member states in the name of European solidarity. For the third major area of focus, questions address activities one performs on the Internet, opinions about types of information and data considered to be personal, types of information disclosed on social networking and online shopping sites and the risks, and measures taken to protect one's identity. Opinions were also collected on how personal information and data are acquired, treated, stored and protected by public and private organizations. For the fourth major area of focus, chemical labeling, respondents were asked about their use and perception of chemical products in various circumstances, how they determine whether or not a chemical product is hazardous, what the proper handling of chemical products is, where respondents find information about the potential dangers of chemical products, who to trust for information about chemical product safety, and whether or not they could correctly identify chemical product warning labels. For the fifth major area of focus, rare diseases, respondents were interviewed about what they believe rare diseases are, whether or not they knew or heard of someone with a rare disease, what society should do about rare diseases, what specific policy responses to rare diseases should be implemented by national health services and the EU as a whole, as well as whether or not they had heard of certain rare diseases.

Demographic and other background information collected includes age, gender, nationality, marital status and parental relations, left-right political self-placement, occupation, age when stopped full-time education, household composition, ownership of a fixed or a mobile telephone, difficulties in paying bills, level in society, and Internet use. In addition, country-specific data includes type and size of locality, region of residence, and language of interview (select countries).

The Eurobarometer series is a unique cross-national and cross-temporal survey program conducted on behalf of the European Commission. These surveys regularly monitor public opinion in the European Union (EU) member countries and consist of standard modules and special topic modules. The standard modules address attitudes towards European unification, institutions and policies, measurements for general socio-political orientations, as well as respondent and household demographics. The special topic modules address such topics as agriculture, education, natural environment and resources, public health, public safety and crime, and science and technology. This round of Eurobarometer surveys covers the following special topics:(1) Quality of Transport, (2) Cyber Security, (3) Value Added Tax, and (4) Public Health.

Respondents' opinions were collected regarding common forms of transportation, status of infrastructure in the respondent's country, reasons for using various forms of transportation, the use of autonomous vehicles, frequency and purpose of travel, and issues affecting rail, air, sea, and road transportation. Additional questions were asked regarding risks of cyber crime, respondents' use of the internet, how cyber security concerns have altered respondents' online behavior, prevention of online harassment of household children, and concern about and experience with being victimized in cyber crime. Respondents were also asked about the Value Added Tax (VAT) and how often they purchased goods from other EU member states. Further questions include knowledge of information regarding reimbursement for healthcare, and respondents' willingness to and opinions of policies related to blood, tissue, and organ donation.

Demographic and other background information collected includes age, gender, nationality, marital status, occupation, left-right political self-placement, age when stopped full-time education, household composition, ownership of a fixed or mobile telephone and other durable goods, difficulties in paying bills, self-assessed level in society, self-assessed social class, and Internet use. In addition, country-specific data includes type and size of locality, region of residence, and language of interview.