Abstract
Background. We examined the main topics of inquiry (Subjects of Interaction—SOI) of calls made by the general public to the National Cancer Institute’s Cancer Information Service’s (CIS) 1-800-4-CANCER telephone information service.Methods. We analyzed data from 37,620 callers to the CIS between September 2002 and August 2003. We conducted frequencies, chi-squares, and logistic regressions to ascertain sample characteristics and sociodemographic correlates of each SOI.Results. We found differences in discussion of the 7 main SOI by age, sex, ethnicity, race, and education.Conclusions. Findings inform the CIS’ and other organizations’ efforts to develop and disseminate cancer information.
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Viswanath K. Science and society: the communications revolution and cancer control. Nat Rev Cancer. 2005;5:828–835.
Bowen D, Hickman KM, Powers D. Importance of psychological variables in understanding risk perceptions and breast cancer screening of African American women. Womens Health. 1997;3:227–242.
Breslow RA, Sorkin JD, Frey CM, Kessler LG. Americans’ knowledge of cancer risk and survival. Prev Med. 1997;26:170–177.
Buckland S. Unmet needs for health information: a literature review. Health Libr Rev. 1994;11:82–85.
Cotugna N, Subar AF, Heimendinger J, Kahle L. Nutrition and cancer prevention knowledge, beliefs, attitudes, and practices: the 1987 National Health Interview Survey. J Am Diet Assoc. 1992;92:963–968.
Finney 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;57:250–261.
Freimuth VS, Stein JA, Kean TJ. Searching for Health Information: The Cancer Information Service Model. Philadelphia, PA: University of Pennsylvania Press; 1989.
Johnson JD. Cancer-Related Information Seeking. Cresskill, NJ: Hampton; 1997.
Johnson JD, Case DO, Andrews JE, Allard SL. Genomics—the perfect information-seeking research problem. J Health Commun. 2005;10:323–329.
Johnson JD, Meischke H. Cancer information: women’s source and content preferences. J Health Care Mark. 1991;11:37–44.
Johnson JD, Meishcke H. Differences in evaluations of communication channels for cancer-related information. J Behav Med. 1992;15:429–445.
Johnson JD, Meischke H. Women’s preferences for cancer-related information from specific types of mass media. Health Care Women Int. 1994;15:23–30.
Lipkus IM, Iden D, Terrenoire J, Feaganes JR. Relationships among breast cancer concern, risk perceptions, and interest in genetic testing for breast cancer susceptibility among African-American women with and without a family history of breast cancer. Cancer Epidemiol Biomarkers Prev. 1999;8:533–539.
McDonald PA, Thorne DD, Pearson JC, Adams-Campbell LL. Perceptions and knowledge of breast cancer among African-American women residing in public housing. Ethn Dis. 1999;9:81–93.
Paul C, Tzelepis F, Walsh RA, Girgis A, King L, McKenzie J. Has the investment in public cancer education delivered observable changes in knowledge over the past 10 years? Cancer. 2003;97:2931–2939.
Venn MJ, Darling E, Dickens C, Quine L, Rutter DR, Slevin ML. The experience and impact of contacting a cancer information service. Eur J Cancer Care (Engl). 1996;5:38–42.
Darrow SL, Speyer J, Marcus AC, Ter Maat J, Krome D. Coping with cancer: the impact of the Cancer Information Service on patients and significant others. J Health Commun. 1998;3 (pt 6 suppl):86–96.
Davis SW, Fleisher L, Ter Maat J, Muha C, Laepke K. Treatment and clinical trials decision making: the impact of the Cancer Information Service. J Health Commun. 1998;3 (pt 5 suppl):71–85.
Finney Rutten LJ, Squiers L, Treiman K. Requests for information by family and friends of cancer patients calling the National Cancer Institute’s Cancer Information Service. Psychooncology [serial online]. November 2, 2005.
Maibach EW, Davis SW, Ter Maat J, Rivera N. Promoting cancer prevention and screening: the impact of the Cancer Information Service. J Health Commun. 1998;3 (pt 7 suppl) 97–108.
Manfredi C, Czaja R, Buis M, Derk D. Patient use of treatment-related information received from the Cancer Information Service. Cancer. 1993;71:1326–1337.
Muha C, Smith KS, Baum S, Ter Maat J, Ward JA. The use and selection of sources in information seeking: the Cancer Information Service experience. J Health Commun. 1998;3 (suppl pt 8):109–120.
Squiers LB, Finney Rutten LJ, Treiman K, Hesse B. Cancer patients’ information needs across the cancer care continuum: evidence from the Cancer Information Service. J Health Commun. 2005; (special issue): 15–34.
Thomsen CA, Ter Maat J. Evaluating the Cancer Information Service: a model for health communications. J Health Commun. 1998;3(suppl pt 1):1–13.
Ward JA, Baum S, Ter Maat J, Thomsen CA, Maibach EW. The value and impact of the Cancer Information Service telephone service. J Health Commun. 1998;3(suppl pt 4):50–70.
Squiers LB, Finney Rutten LJ, Atienza AA, Treiman, K, Moser RP, Hesse B. Awareness of the National Cancer Institute’s Cancer Information Service: results from the Health Information National Trends Survey (HINTS). J Health Commun. In press.
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Supported in whole or in part by federal funds from the National Cancer Institute, National Institutes of Health under contract N01-CO-124000. The content of this publication does not necessarily reflect the views of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government.
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Finney Rutten, L.J., Squiers, L. & Hesse, B. Cancer-related information sought by the general public: Evidence from the National Cancer Institute’s Cancer Information Service, 2002–2003. J Canc Educ 22, 91–98 (2007). https://doi.org/10.1007/BF03174355
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DOI: https://doi.org/10.1007/BF03174355