ABC News Clinton Statement #2 Poll, August 1998 (ICPSR 2633)
ABC News Media Poll, January 1997 (ICPSR 2171)
ABC News Mini-Monthly Poll, December 1995 (ICPSR 6687)
ABC News "Nightline" GOP Strategy Poll, May 1998 (ICPSR 2490)
ABC News "Nightline" Newt Gingrich and Ethics Poll, January 1997 (ICPSR 2172)
ABC News "Nightline" Starr Report Poll #4, September 1998 (ICPSR 2641)
ABC News/Washington Post Clinton Scandal/Iraq Poll, February 1998 (ICPSR 2510)
ABC News/Washington Post Libby Indictment Two-Nighter Poll, October 2005 (ICPSR 4523)
ABC News/Washington Post Poll, May 1987 (ICPSR 8843)
ABC News/Washington Post Poll, September 1999 (ICPSR 2807)
Afrobarometer Round 5: The Quality of Democracy and Governance in Ghana, 2012 (ICPSR 35548)
Afrobarometer Round 5: The Quality of Democracy and Governance in Lesotho, 2012 (ICPSR 35551)
Afrobarometer Round 5: The Quality of Democracy and Governance in Liberia, 2012 (ICPSR 35552)
CBS News/60 Minutes/Vanity Fair National Survey, March #3, 2013 (ICPSR 34998)
CBS News Lying Poll, May 1997 (ICPSR 4494)
CBS News Monthly Poll #2, February 1998 (ICPSR 2459)
Center for Research on Social Reality [Spain] Survey, December 1990: Religious Beliefs and Practices (ICPSR 6978)
Center for Research on Social Reality [Spain] Survey, November 1991: Religiosity and Social Ethics (ICPSR 9898)
Center for Research on Social Reality [Spain] Survey, November 1992: Social Ethics (ICPSR 6058)
Focus Groups on Public Attitudes about Genomic Expansion Study (PAGES), United States, 2017 (ICPSR 38458)
Industry Partnership Views Survey, United States, 2016 (ICPSR 37033)
The contained collection was designed to assess potential perceptions of two hypothetical health science research collaborations. The studies were also designed to test the utility of using procedural justice concepts to assess perceptions of research legitimacy as a theoretical way to determine public opinions on conflicts of interest.
The researchers performed three experimental studies to examine how different combinations of partners in a research collaboration influence subjects' perceived procedural fairness and legitimacy based on collaborative partnerships.
Datafiles:
Experience 1: 1000 cases, 92 variables
Experience 2: 1058 cases, 88 variables
Experience 3: 2107 cases, 76 variables
For more information about this study, please visit the study publication here.
Interdisciplinary National Study Investigating Genetics and Health Testing at Work (INSIGHT@Work): Employer Perspectives, United States, 2020-2025 (ICPSR 39645)
This research was supported by a grant from the National Human Genome Research Institute of the National Institutes of Health (R01HG010679). This project was conducted as part of the multi-aim R01 and led by Charles Lee and J. Scott Roberts. The project explores stakeholders' perspectives on key characteristics for implementation of workplace genetic testing (wGT).
The project had three specific aims and a supplementary aim:
- Aim 1: Examine employers' perspectives through a landscape analysis to ascertain the prevalence and distribution of wGT among US companies
- Aim 2: Investigate employees' views and perceptions of the benefits, risks, and limitations of wGT through (a) a national survey of working adults and (b) a survey of individuals working at a large US healthcare system who were offered wGT by their employer
- Aim 3: Conduct a modified Delphi process with multiple surveys and a deliberative workshop among key stakeholders and distill the finding of Aims 1 and 2 to inform a normative assessment of wGT.
- Supplement: Examine genetic counselors' perspectives on and experiences with wGT using semi-structured interviews and a national survey
This study, led by Co-Investigators Debra Mathews and Kayte Spector-Bagdady, examined Aim 1 and the employer perspectives towards workplace genetic testing.
Interdisciplinary National Study Investigating Genetics and Health Testing at Work (INSIGHT@Work): Genetic Counselor Perspectives, United States, 2020-2025 (ICPSR 39648)
This research was supported by a grant from the National Human Genome Research Institute of the National Institutes of Health (R01HG010679). This project was conducted as part of the multi-aim R01 and led by Charles Lee and J. Scott Roberts. The project explores stakeholders' perspectives on key characteristics for implementation of workplace genetic testing (wGT).
The project had three specific aims and a supplementary aim:
- Aim 1: Examine employers' perspectives through a landscape analysis to ascertain the prevalence and distribution of wGT among US companies
- Aim 2: Investigate employees' views and perceptions of the benefits, risks, and limitations of wGT through (a) a national survey of working adults and (b) a survey of individuals working at a large US healthcare system who were offered wGT by their employer
- Aim 3: Conduct a modified Delphi process with multiple surveys and a deliberative workshop among key stakeholders and distill the finding of Aims 1 and 2 to inform a normative assessment of wGT.
- Supplement: Examine genetic counselors' perspectives on and experiences with wGT using semi-structured interviews and a national survey
This study, led by Wendy Uhlmann, examined the supplementary aim.
Interdisciplinary National Study Investigating Genetics and Health Testing at Work (INSIGHT@Work): Modified Delphi Process, United States, 2020-2025 (ICPSR 39647)
This research was supported by a grant from the National Human Genome Research Institute of the National Institutes of Health (R01HG010679). This project was conducted as part of the multi-aim R01 and led by Charles Lee and J. Scott Roberts. The project explores stakeholders' perspectives on key characteristics for implementation of workplace genetic testing (wGT).
The project had three specific aims and a supplementary aim:
- Aim 1: Examine employers' perspectives through a landscape analysis to ascertain the prevalence and distribution of wGT among US companies
- Aim 2: Investigate employees' views and perceptions of the benefits, risks, and limitations of wGT through (a) a national survey of working adults and (b) a survey of individuals working at a large US healthcare system who were offered wGT by their employer
- Aim 3: Conduct a modified Delphi process with multiple surveys and a deliberative workshop among key stakeholders and distill the finding of Aims 1 and 2 to inform a normative assessment of wGT.
- Supplement: Examine genetic counselors' perspectives on and experiences with wGT using semi-structured interviews and a national survey
This study, led by Co-Investigators Greg Feero and Anya E.R. Prince, examined Aim 3.
Los Angeles County Social Survey, 1995 (LACSS) (ICPSR 36563)
The Los Angeles County Social Survey (LACSS) continues the Los Angeles Metropolitan Area Studies (LAMAS) and the Southern California Social Surveys (SCSS). The Los Angeles County Social Survey (LACSS) is part of a continuing annual research project supported by the Institute for Social Science Research at the University of California, Los Angeles (UCLA).
The LACSS 1995 was conducted between April and July 1995. Los Angeles County residents were asked questions concerning ethnic relations, social dominance, social distance, immigration, affirmative action, employment, and government. A split ballot methodology was utilized concerning the topics of immigration and affirmative action. Respondents were randomly selected to answer a series of questions from one of three ballots. In addition, a different series of social distance questions were asked depending on the respondent's ethnicity. Questionnaires were provided in both English and Spanish languages.
Demographic information collected includes race, gender, religion, age, education level, occupation, birth place, political party affiliation and ideology, and origin of ancestry.
National Public Radio/Robert Wood Johnson Foundation/Harvard School of Public Health Poll: Health Education Survey, United States, 2013 (ICPSR 38381)
This catalog record includes detailed variable-level descriptions, enabling data discovery and comparison. The data are not archived at ICPSR. Users should consult the data owners (via the Roper Center for Public Opinion Research) directly for details on obtaining the data.
This collection includes variable-level metadata of the 2013 poll Health Education Survey, a survey from National Public Radio/Robert Wood Johnson Foundation/Harvard School of Public Health conducted by Social Science Research Solutions (SSRS). Topics covered in this survey include:
- Grade child enrolled in
- Location of child's school
- Enrollment total
- Giving grade to child's school
- Biggest problem at school
- Emphasis on various subjects
- School teaching same values as home values
- School obligations interfering with family time
- Knowledge about common core
- Common core improving education
- Method of learning about common core
- Success of common core
- School preparing students for careers
- Attending technical
- Vocational classes
- Preparing students for college
- Preparing students for job market
- Student plans after high school
- College or career planning services
- Healthiness of school lunches
- Foods available at school
- Length of school lunch
- Time of lunch period
- Vending machines at school
- Fast-food chains at school
- Physical education as mandatory
- Frequency of PE classes
- Length of PE classes
- PE classes for other purposes
- Rating PE school offerings
- Playgrounds available after school
- Recess as structured or free time
- School safety
- Security precautions at school
- Ways of preventing violence at school
- Increasing security after Newtown shooting
- Method of transport to school
- Time to get home from school
- Safety of travelling to school
- School related stress
- School counseling for stressed students
- Time of school day
The data and documentation files for this survey are available through the Roper Center for Public Opinion Research [Roper #31092359]. Frequencies and summary statistics for the 148 variables from this survey are available through the ICPSR social science variable database and can be accessed from the Variables tab.
Research Ethics in Patient-Centered Outcomes Research (PCOR) [Methods Study], United States, 2015-2019 (ICPSR 39567)
Patient-centered outcomes research, or PCOR, is a type of research that focuses on patient values and needs. PCOR includes patients in many parts of the research process, including helping to plan and conduct the study. Institutional Review Boards, or IRBs, oversee research studies to make sure patients participating in a study are protected from harm. But current IRB guidance may not address ethical issues that arise when patients are involved in other roles.
In this study, the research team created recommendations to guide IRB oversight of PCOR studies.