The Health Information National Trends Survey (HINTS): Development, Design, and Dissemination
By D. Nelson, Gary L. Kreps, B. Hesse, R. Croyle, G. Willis, Neeraj Arora, B. Rimer, K. Vish Viswanath, N. Weinstein, Sarah C. Alden. Journal of health communication, 2004
646 citations recorded by the source corpus.
Subfields: General Health Professions, Sociology and Political Science
View Paper: https://www.semanticscholar.org/paper/1617c97ed2584fd54988bc845cd0308209d74c76
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In General Health Professions
- Wura Jacobs
- Gary L. Kreps
- Nancy L. Atkinson
- Abby Prestin
- Neeraj Arora
- Richard P. Moser
- John R. Pleis
- Sandra L Saperstein
In Sociology and Political Science
Citations in the corpus
- Using the Internet for Health-Related Activities: Findings From a National Probability Sample (2009, background): “The HINTS survey collects nationally representative data about the US public’s cancer communication practices, information preferences, risk behaviors, attitudes, and cancer knowledge [20].”
- Social Media Use in the United States: Implications for Health Communication (2009, background): “Comprehensive reports on the conceptual framework and sample design of HINTS are published elsewhere [21,22].”
- Trust and sources of health information: the impact of the Internet and its implications for health care providers: findings from the first Health Information National Trends Survey. (2005, methodology): “Details of this survey are published elsewhere.(28) Briefly, HINTS is a nationally representative telephone survey of persons 18 years or older, scheduled to be conducted every 2 years.”
- Health information seeking in the digital age: An analysis of health information seeking behavior among US adults (2017, methodology): “More details on survey design, sampling strategies and methodology of the HINTS are published elsewhere (Finney et al., 2012; Nelson et al., 2004).”
- Predictors of eHealth Usage: Insights on The Digital Divide From the Health Information National Trends Survey 2012 (2014, background): “HINTS is a nationally representative survey of the US noninstitutionalized adult population that collects data on the American public’s need for, access to, and use of health-related information [39].”