Literature DB >> 21505861

Health-related Internet use among cancer survivors: data from the Health Information National Trends Survey, 2003-2008.

Wen-Ying Sylvia Chou1, Benmei Liu, Samantha Post, Bradford Hesse.   

Abstract

INTRODUCTION: Increasing prevalence of Internet and new technologies are changing the communication pattern for patients and caregivers across the cancer care continuum. To date, little is known on how cancer survivors in the USA utilize the Internet for health-related purposes. This knowledge is crucial in developing effective communication programs to achieve quality and equitable cancer care.
METHODS: Data from 2003, 2005, and 2008 iterations of the NCI-sponsored Health Information National Trends Survey(HINTS) were analyzed to: (1) compare health-related Internet use (hereafter HRIU) between individuals with and without a cancer diagnosis, (2) report trends, prevalence, and user profiles of HRIU, including support group participation, e-mailing provider, buying medicine online, and cancer information seeking on the Internet. Descriptive analyses and weighted multivariate logistic regression analyses were performed.
RESULTS: While Internet penetration is growing over the years across the USA, cancer survivors access the Internet at a lower rate than general population (49.4% to 56.4% vs. 63.1% to 66.3%). Once on the Internet, they are more likely to use it for health-related purposes. Disparities in Internet access persists, as higher likelihood of Internet access is associated with younger age, higher education, non-Hispanic White race/ethnicity, metropolitan residence, and better self-rated health. On the other hand, among Internet-accessing survivors, socio-demographic, and health factors do not play a significant role in determining the pattern of HRIU.
CONCLUSIONS: The study identifies an increasing trend in HRIU among survivors, though the digital divide remains in Internet access. The findings also point to opportunities for narrowing the divide and using Internet to better serve survivors' needs, as individuals from wide-ranging backgrounds and experiences are equally engaging in health-related activities on the Internet. IMPLICATIONS FOR SURVIVORS: To increase equity and effectiveness in communication and cancer care, Internet access, functions, and technology literacy are important factors to be considered.

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Year:  2011        PMID: 21505861     DOI: 10.1007/s11764-011-0179-5

Source DB:  PubMed          Journal:  J Cancer Surviv        ISSN: 1932-2259            Impact factor:   4.442


  23 in total

1.  It's good to talk: comparison of a telephone helpline and website for cancer information.

Authors:  Rachel Hardyman; Pollyanna Hardy; Judith Brodie; Richard Stephens
Journal:  Patient Educ Couns       Date:  2005-06

2.  Internet usage among women with breast cancer: an exploratory study.

Authors:  J L Pereira; S Koski; J Hanson; E D Bruera; J R Mackey
Journal:  Clin Breast Cancer       Date:  2000-07       Impact factor: 3.225

3.  The Health Information National Trends Survey (HINTS): development, design, and dissemination.

Authors:  David E Nelson; Gary L Kreps; Bradford W Hesse; Robert T Croyle; Gordon Willis; Neeraj K Arora; Barbara K Rimer; K V Viswanath; Neil Weinstein; Sara Alden
Journal:  J Health Commun       Date:  2004 Sep-Oct

4.  Complementary therapies for cancer patients: assessing information use and needs.

Authors:  M J Verhoef; L Trojan; G D Armitage; L Carlson; R J Hilsden
Journal:  Chronic Dis Can       Date:  2009

5.  The importance of being expert: the quest for cancer information on the Internet.

Authors:  Sue Ziebland
Journal:  Soc Sci Med       Date:  2004-11       Impact factor: 4.634

6.  How the internet affects patients' experience of cancer: a qualitative study.

Authors:  Sue Ziebland; Alison Chapple; Carol Dumelow; Julie Evans; Suman Prinjha; Linda Rozmovits
Journal:  BMJ       Date:  2004-03-06

7.  Cancer patients' decisions about discussing Internet information with their doctors.

Authors:  Carma L Bylund; Jennifer A Gueguen; Thomas A D'Agostino; Rebecca S Imes; Ellen Sonet
Journal:  Psychooncology       Date:  2009-11       Impact factor: 3.894

8.  Using the internet for health-related activities: findings from a national probability sample.

Authors:  Nancy L Atkinson; Sandra L Saperstein; John Pleis
Journal:  J Med Internet Res       Date:  2009-02-20       Impact factor: 5.428

9.  Social media use in the United States: implications for health communication.

Authors:  Wen-ying Sylvia Chou; Yvonne M Hunt; Ellen Burke Beckjord; Richard P Moser; Bradford W Hesse
Journal:  J Med Internet Res       Date:  2009-11-27       Impact factor: 5.428

10.  Use of the internet to communicate with health care providers in the United States: estimates from the 2003 and 2005 Health Information National Trends Surveys (HINTS).

Authors:  Ellen Burke Beckjord; Lila J Finney Rutten; Linda Squiers; Neeraj K Arora; Lindsey Volckmann; Richard P Moser; Bradford W Hesse
Journal:  J Med Internet Res       Date:  2007-07-12       Impact factor: 5.428

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  75 in total

Review 1.  Telemedicine and prostate cancer survivorship: a narrative review.

Authors:  Nnenaya Q Agochukwu; Ted A Skolarus; Daniela Wittmann
Journal:  Mhealth       Date:  2018-10-08

2.  Commitment of Newcomers and Old-timers to Online Health Support Communities.

Authors:  Diyi Yang; Robert Kraut; John M Levine
Journal:  Proc SIGCHI Conf Hum Factor Comput Syst       Date:  2017-05

3.  Self-disclosure and Channel Difference in Online Health Support Groups.

Authors:  Diyi Yang; Zheng Yao; Robert Kraut
Journal:  Proc Int AAAI Conf Weblogs Soc Media       Date:  2017-05

4.  Breast cancer prevention knowledge, beliefs, and information sources between non-Hispanic and Hispanic college women for risk reduction focus.

Authors:  Cynthia Kratzke; Anup Amatya; Hugo Vilchis
Journal:  J Community Health       Date:  2015-02

5.  Trends of online patient-provider communication among cancer survivors from 2008 to 2017: a digital divide perspective.

Authors:  Shaohai Jiang; Y Alicia Hong; Piper Liping Liu
Journal:  J Cancer Surviv       Date:  2019-02-12       Impact factor: 4.442

6.  Assessment of eHealth behaviors in national surveys: a systematic review of instruments.

Authors:  Y Alicia Hong; Jinmyoung Cho
Journal:  J Am Med Inform Assoc       Date:  2018-12-01       Impact factor: 4.497

7.  Immigrants' Use of eHealth Services in the United States, National Health Interview Survey, 2011-2015.

Authors:  Yang Wang; D Phuong Do; Fernando A Wilson
Journal:  Public Health Rep       Date:  2018-09-17       Impact factor: 2.792

8.  Cancer-related internet information communication between oncologists and patients with breast cancer: a qualitative study.

Authors:  Megan Johnson Shen; Robert C Dyson; Thomas A D'Agostino; Jamie S Ostroff; Maura N Dickler; Alexandra S Heerdt; Carma L Bylund
Journal:  Psychooncology       Date:  2015-01-28       Impact factor: 3.894

9.  Survivorship Challenges and Information Needs after Radiotherapy for Oral Cancer.

Authors:  Hoda Badr; Daniella Lipnick; Vishal Gupta; Brett Miles
Journal:  J Cancer Educ       Date:  2017-12       Impact factor: 2.037

10.  Preventing infections during cancer treatment: development of an interactive patient education website.

Authors:  Angela Dunbar; Eric Tai; Danielle Beauchesne Nielsen; Sonya Shropshire; Lisa C Richardson
Journal:  Clin J Oncol Nurs       Date:  2014-08       Impact factor: 1.027

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