Literature DB >> 16537289

Relationship of Internet health information use with patient behavior and self-efficacy: experiences of newly diagnosed cancer patients who contact the National Cancer Institute's Cancer Information Service.

Sarah Bauerle Bass1, Sheryl Burt Ruzek, Thomas F Gordon, Linda Fleisher, Nancy McKeown-Conn, Dirk Moore.   

Abstract

This study examines the relationship of Internet health information use with patient behavior and self-efficacy among 498 newly diagnosed cancer patients. Subjects were classified by types of Internet use: direct use (used Internet health information themselves), indirect use (used information accessed by friends or family), and non-use (never accessing Internet information). Subjects were recruited from callers of the National Cancer Institute's (NCI's) Cancer Information Service, Atlantic Region. They were classified by type of Internet use at enrollment and interviewed by telephone after 8 weeks. There were significant relationships among Internet use and key study variables: subject characteristics, patient task behavior, and self-efficacy. Subjects' Internet use changed significantly from enrollment to 8 week follow-up; 19% of nonusers and indirect users moved to a higher level of Internet use. Significant relationships also were found among Internet use and perceived patient-provider relationship, question asking, and treatment compliance. Finally, Internet use was also significantly associated with self-efficacy variables (confidence in actively participating in treatment decisions, asking physicians questions, and sharing feelings of concern). The results of this study show that patients who are newly diagnosed with cancer perceive the Internet as a powerful tool, both for acquiring information and for enhancing confidence to make informed decisions.

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Mesh:

Year:  2006        PMID: 16537289     DOI: 10.1080/10810730500526794

Source DB:  PubMed          Journal:  J Health Commun        ISSN: 1081-0730


  48 in total

1.  Parental information seeking following a positive newborn screening for cystic fibrosis.

Authors:  James Price Dillard; Lijiang Shen; Jeffrey D Robinson; Phillip M Farrell
Journal:  J Health Commun       Date:  2010-12

2.  Differences in information seeking among breast, prostate, and colorectal cancer patients: results from a population-based survey.

Authors:  Rebekah H Nagler; Stacy W Gray; Anca Romantan; Bridget J Kelly; Angela DeMichele; Katrina Armstrong; J Sanford Schwartz; Robert C Hornik
Journal:  Patient Educ Couns       Date:  2010-10-08

3.  Effects of using online narrative and didactic information on healthcare participation for breast cancer patients.

Authors:  Meg Wise; Jeong Yeob Han; Bret Shaw; Fiona McTavish; David H Gustafson
Journal:  Patient Educ Couns       Date:  2008-01-16

4.  How do cancer patients navigate the public information environment? Understanding patterns and motivations for movement among information sources.

Authors:  Rebekah H Nagler; Anca Romantan; Bridget J Kelly; Robin S Stevens; Stacy W Gray; Shawnika J Hull; A Susana Ramirez; Robert C Hornik
Journal:  J Cancer Educ       Date:  2010-03-05       Impact factor: 2.037

5.  Colon cancer patient information seeking and the adoption of targeted therapy for on-label and off-label indications.

Authors:  Stacy W Gray; Katrina Armstrong; Angela Demichele; J Sanford Schwartz; Robert C Hornik
Journal:  Cancer       Date:  2009-04-01       Impact factor: 6.860

6.  The International Cancer Information Service: a worldwide resource.

Authors:  Marion E Morra; Chris Thomsen; Anne Vezina; Doreen Akkerman; Mary Anne Bright; Catherine Dickens; David J Hill; Michael Jefford
Journal:  J Cancer Educ       Date:  2007       Impact factor: 2.037

7.  The NCI's Cancer Information Service's Research Continuum Framework: integrating research into cancer education practice (1999-2004).

Authors:  Linda Fleisher; Julie Kornfeld; Sharon Davis; Marion E Morra; Linda Squiers
Journal:  J Cancer Educ       Date:  2007       Impact factor: 2.037

8.  The National Cancer Institute's Cancer Information Service: a premiere cancer information and education resource for the nation.

Authors:  Mary Anne Bright
Journal:  J Cancer Educ       Date:  2007       Impact factor: 2.037

9.  Cancer and the computerized family: towards a clinical ethics of "indirect" Internet use.

Authors:  Christian Simon; Sarah Schramm
Journal:  Med Health Care Philos       Date:  2008-02-19

10.  Experiences and attitudes of Dutch rheumatologists and oncologists with regard to their patients' health-related Internet use.

Authors:  Cornelia F van Uden-Kraan; Constance H C Drossaert; Erik Taal; Wim M Smit; Erwin R Seydel; Mart A F J van de Laar
Journal:  Clin Rheumatol       Date:  2010-04-11       Impact factor: 2.980

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