This study investigated what web users share on a health website and how the demographic characteristics of users reflect health information sharing behavior. By using a content analysis method, this study analyzed 1,042 randomly chosen messages in the discussion board of a health website. The results revealed that the health website users emotionally supported other users, provided health information, and built relationships between them. Two third of the health website users shared his/her thoughts or feelings about ALS (Lou Gehrig’s Disease) on the health website and one fourth of the health website users connected with others who had ALS. A half of the users actively provided information as a direct response to a question. No significant differences were discerned with regard to total posting frequency by age and gender effect. However, the male users in the 50s answered questions to others more actively and tried to manage their life better than the other age groups.
Ayers, S. L.. (2007). Chronic illness and health-seeking information on the Internet. Health, 11(3), 327-347.
Benigeri, M.. (2003). Shortcomings of health information on the Internet. Health Promotion International, 18(4), 381-386.
Buckland, M. K.. (1991). Information as thing. Journal of the American Society for Information Science, 42(5), 351-360.
Cotton, S. R.. (2001). Implications of Internet technology for medical sociology in the new millennium. Sociological Spectrum : Mid-South Sociological Association, 21(3), 319-340.
Czaja, S. J.. (2006). Factors predicting the use of technology : Findings from the center for research and education on aging and technology enhancement(create). Psychology and Aging, 21(2), 333-352.
Detlefsen, E. G.. (2004). Where am I to go? Use of the Internet for consumer health information by two vulnerable communities. Library Trends, 53(2), 283-300.
Dervin, B.. (1983). Information as a user construct: The relevance of perceived information needs to synthesis and interpretation, In Knowledge structure and use: Implications for synthesis and interpretation:Temple University Press.
Dickey, M. H.. (2007). Do you read me? : Perspective making and perspective taking in chat communications. Journal of the Association for Information Systems, 8, 47-70.
Dryburgh, H.. (2001). Changing our ways: Why and how Canadians use the Internet. http://www.statcan.ca/cgibin/downpub/listpub.cgi?catno=56F0006XIE.
Fox, S.. (2002). Vital decisions : How internet users decide what information to trust when they or their loved ones are sick:Pew Internet & American Life Project.
Fox, S.. (2012). Pew internet: Health. http://www.pewinternet.org/Commentary/2011/November/Pew-Internet-Health.aspx.
Goldsmith, J.. (2000). How will the Internet change our health system?. Health Affairs, 19(1), 148-156.
Huber, J. T.. (2000). Information needs and information-seeking of HIV positive men and women. Medical Reference Services Quarterly, 19(1), 39-48.
Keith, J. H.. (2009). Using the Internet to provide care for persons living with HIV. Aids Patient Care and STDs, 23(12), 1033-1041.
김여라. (2010). 인터넷 의료정보의 사회적·법적 쟁점에 관한 탐색적 연구. 언론과학연구, 10(2), 179-220.
Kremer, H.. (2007). People living with HIV : Sources of information on antiretroviral treatment and preferences for involvement in treatment decision-making. European Journal of Medical Research, 12(1), 34-42.
Leckie, G. J.. (1996). Modeling the information seeking of professionals : A general model derived from research on engineers, health care professionals, and lawyers. Library Quarterly, 66(2), 161-193.
이동숙. (2007). 개인의 성별, 정보추구성향 및 불건강 행위 간 관계 연구. 성인간호학회지, 19(2), 219-227.
McCreadie, M.. (1999). Trends in analyzing access to information. Part I : Crossdisciplinary conceptualizations of access. Information Processing and Management, 35(1), 45-76.
Mayer, D. K.. (2007). Cancer survivors’ information seeking behaviors: A comparison of survivors who do and do not seek information about cancer. Patient Education and Counseling, 65(3), 342-350.
Miller, L. M.. (2012). Online health information seeking : The influence of age, information trustworthiness, and search challenges. Journal of Aging and Health, 24(3), 525-541.
(2012). PatientsLikeMe. http://www.patientslikeme.com/.
Rutten, L. J. F.. (2005). Information needs and sources of information among cancer patients : A systematic review of research(1980-2003). Patient Education and Counseling, 57(3), 250-261.
Sabel, M. S.. (2005). Patterns of Internet use and impact on patients with melanoma. Journal of the American Academy of Dermatology, 52(5), 779-785.
Saracevic, T.. (1999). Information science. Journal of the American Society for Information Science, 50(12), 1051-1063.
Salander, P.. (2002). Bad news from the patient’s perspective : An analysis of the written narratives of newly diagnosed cancer patients. Social Science and Medicine, 55(5), 721-732.
Sonnenberg, F. A.. (1997). Health information on the Internet : Opportunities and pitfalls. Archives of Internal Medicine, 157, 151-152.
Veinot, T. C.. (2009). Interactive acquisition and sharing : Understanding the dynamics of HIV/AIDS information networks. Journal of the American Society for Information Science and Technology, 60(11), 2313-2332.
Volk, R. M.. (2007). Expert searching in consumer health : an important role for librarians in the age of the Internet and the web. Journal of the Medical Library Association, 92(2), 203-207.
Webster, F.. (2002). The idea of an information society, In Theories of the information society:Routledge.
Wicks, P.. (2010). Sharing health data for better outcomes on PatientsLikeMe. Journal of Medical Internet Research, 12(2), 9-.
우영운. (2007). 국내 건강정보 웹사이트의 신뢰성과 만족도 현황 분석. 한국콘텐츠학회 논문지, 7(3), 110-117.
Wright, J. B.. (1998). Quality connection on the internet. Healthcare Executive, 13(1), 44-45.
Ybarra, M.. (2008). Reasons, assessments, and actions taken: Sex and age differences in uses of Internet health information. Health Education Research, 23(3), 512-521.