Institute of Medicine. To Err is Human: Building a Safer Health System. Washington, DC: National Academy Press; 2000.
Institute of Medicine. Crossing the Quality Chasm: A New Health System for the 21st Century. Washington, DC: National Academy Press; 2001.
Charles C, Gafni A, Whelan T. Shared decision-making in the medical encounter: what does it mean? (or it takes at least two to tango). Soc Sci Med. 1997;44:681–92.
Woolf SH, Chan EC, Harris R, et al. Promoting informed choice: transforming health care to dispense knowledge for decision making. Ann Intern Med. 2005;143:293–300.
Rimer BK, Briss PA, Zeller PK, Chan ECY, Woolf SH. Informed decision making: what is its role in cancer screening? Cancer. 2004;101(5 Suppl):1214–28.
Arora NK, McHorney CA. Patient preferences for medical decision making: who really wants to participate? Med Care. 2000;38:335–41.
Levinson W, Kao A, Kuby A, Thisted RA. Not all patients want to participate in decision making. a national study of public preferences. J Gen Intern Med. 2005;20:531–5.
Viswanath K. Science and society: the communications revolution and cancer control. Nat Rev Cancer. 2005;5:828–35.
Cline RJ, Haynes KM. Consumer health information seeking on the Internet: the state of the art. Health Educ Res. 2001;16:671–92.
Hesse BW, Nelson DE, Kreps GL, et al. 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. Arch Intern Med. 2005;165:2618–24.
Rutten LJ, Arora NK, Bakos AD, Aziz N, Rowland J. Information needs and sources of information among cancer patients: a systematic review of research (1980-2003). Patient Educ Couns. 2005;57:250–61.
Ayanian JZ, Zaslavsky AM, Guadagnoli E, et al. Patients’ perceptions of quality of care for colorectal cancer by race, ethnicity, and language. J Clin Oncol. 2005;23:6576–86.
Nelson DE, Kreps GL, Hesse BW, et al. The Health Information National Trends Survey (HINTS): development, design, and dissemination. J Health Commun. 2004;9:443–60; discussion 81–4.
Arora NK, Johnson P, Gustafson DH, McTavish F, Hawkins RP, Pingree S. Barriers to information access, perceived health competence, and psychosocial health outcomes: test of a mediation model in a breast cancer sample. Patient Educ Couns. 2002;47:37–46.
Fox S. Health information online. Technical report from the Pew Internet and American Life Project. Washington, DC: Pew Research Center; 2005.
Fox S, Rainie L. Vital decisions: how Internet users decide what information to trust when they or their loved ones are sick. Technical report from the Pew Internet and American Life Project. Washington, DC: Pew Research Center; 2002.
Fox S, Fallows D. Internet health resources. Technical Report from the Pew Internet and American Life Project. Washington, DC: Pew Research Center; 2003.
Squiers L, Finney Rutten LJ, Treiman K, Bright MA, Hesse B. Cancer patients’ information needs across the cancer care continuum: evidence from the Cancer Information Service. J Health Commun. 2005;10 (1 Suppl):15–34.
Tu HT, Hargraves JL. Seeking health care information: most consumers still on the sidelines. Issue Brief Cent Stud Health Syst Change. 2003;(61):1–4.
Jung HP, Baerveldt C, Olesen F, Grol R, Wensing M. Patient characteristics as predictors of primary health care preferences: a systematic literature analysis. Health Expect. 2003;6:160–81.
Berland GK, Elliott MN, Morales LS, et al. Health information on the Internet: accessibility, quality, and readability in English and Spanish. JAMA. 2001;285:2612–21.
Silberg WM, Lundberg GD, Musacchio RA. Assessing, controlling, and assuring the quality of medical information on the Internet: caveant lector et viewor—let the reader and viewer beware. JAMA. 1997;277:1244–5.
Kim P, Eng TR, Deering MJ, Maxfield A. Published criteria for evaluating health related web sites: review. BMJ. 1999;318:647–9.
Jadad AR, Gagliardi A. Rating health information on the Internet: navigating to knowledge or to Babel? JAMA. 1998;279:611–4.
Viswanath K, Breen N, Meissner H, et al. Cancer knowledge and disparities in the information age. J Health Commun. 2006;11(1 Suppl):1–17.
Curtin R, Presser S, Singer E. Changes in telephone survey nonresponse over the past quarter century. Public Opinion Quarterly. 2005;69:87–98.
Biener L, Garrett CA, Gilpin EA, et al. Consequences of declining survey response rates for smoking prevalence estimates. Am J Prev Med. 2004;27:254–7.