|
Sign In to gain access to subscriptions and/or personal tools.
|
Qualitative Health Research, Vol. 15, No. 3,
325-345 (2005)
DOI: 10.1177/1049732304272916
© 2005 SAGE Publications
Virtually He@lthy: The Impact of Internet Use on Disease Experience and the Doctor-Patient Relationship
Alex Broom
School of Healthcare, University of Leeds, United Kingdom
In the current study, the author explores the complex effects and contradictory roles of the Internet as a source of empowerment and control, and as a site of "risk management." Drawing on a study of the Internet usage of Australian men with prostate cancer, the author investigates how access to information and online support affects mens experiences of disease and, in particular, the possible implications of Internet-informed patients for the doctor-patient relationship. The data reveal that accessing information and/or support online can have a profound effect on mens experiences of prostate cancer, providing a method of taking some control over their disease and limiting inhibitions experienced in face-to-face encounters. However, it is also clear that some medical specialists view Internet-informed patients as a challenge to their power within medical encounters and, as a result, employ disciplinary strategies that reinforce traditional patient roles and alienate patients who use the Internet.
Key Words: Internet prostate cancer online support risk empowerment

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. L. Oliffe
Book Review: Robertson, S. (2007). Understanding men and health: Masculinities, identity and well-being. Berkshire, UK: Open University Press
American Journal of Men's Health,
June 1, 2008;
2(2):
190 - 191.
[PDF]
|
 |
|

|
 |

|
 |
 
A. Broom and P. Tovey
The role of the Internet in cancer patients' engagement with complementary and alternative treatments
Health (London) ,
April 1, 2008;
12(2):
139 - 155.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
C. F. van Uden-Kraan, C. H. C. Drossaert, E. Taal, B. R. Shaw, E. R. Seydel, and M. A. F. J. van de Laar
Empowering Processes and Outcomes of Participation in Online Support Groups for Patients With Breast Cancer, Arthritis, or Fibromyalgia
Qual Health Res,
March 1, 2008;
18(3):
405 - 417.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
M. A. Martinez, T. Kind, E. Pezo, and K. L. Pomerantz
An Evaluation of Community Health Center Adoption of Online Health Information
Health Promot Pract,
January 1, 2008;
9(1):
59 - 67.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
C. N. Wathen and R. M. Harris
"I Try to Take Care of It Myself." How Rural Women Search for Health Information
Qual Health Res,
May 1, 2007;
17(5):
639 - 651.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Oliffe and S. Thorne
Men, Masculinities, and Prostate Cancer: Australian and Canadian Patient Perspectives of Communication With Male Physicians
Qual Health Res,
February 1, 2007;
17(2):
149 - 161.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
K. L. Schwartz, T. Roe, J. Northrup, J. Meza, R. Seifeldin, and A. V. Neale
Family Medicine Patients' Use of the Internet for Health Information: A MetroNet Study
J Am Board Fam Med,
January 1, 2006;
19(1):
39 - 45.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Broom
Medical specialists' accounts of the impact of the Internet on the doctor/patient relationship
Health (London) ,
July 1, 2005;
9(3):
319 - 338.
[Abstract]
[PDF]
|
 |
|
|