Involving patients and the public in e-health research

Patient-Centered E-Health

Volumn , Issue , 2008, Pages 115-125

  Powell, John ^a   Armstrong, Natalie ^b  

^a UNIVERSITY OF WARWICK   (United Kingdom)

^b UNIVERSITY OF LEICESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84899231973     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.4018/978-1-60566-016-5.ch009     Document Type: Chapter

References (16)

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2. Armstrong, N., Powell, J., Hearnshaw, H., & Dale, J. (2007). Design of a trial of internet-based selfmanagement for diabetes. Journal of Telemedicine and Telecare, 13(Supplement 1), 1-2.
3. Arnstein, S.R. (1969). A ladder of citizen participation in the USA. Journal of the American Institute of Planners, 35(4), 216-224.
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10. Hanley, B., Bradburn, J., Barnes, M., Evans, C., Goodare, H., Kelson, M., Kent, A., Oliver, S., Thomas, S. & Wallcraft, J. (2004). Involving the public in NHS, public health, and social care research: Briefing notes for researchers (second edition). Hampshire, UK: INVOLVE.
11. Hardey, M. (2001). E-health: The Internet and transformation of patients into consumers and producers of health knowledge. Information, Communication and Society, 4(3), 388-405.
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13. Herxheimer, A., & Goodare, H. (1999). Who are you, and who are we? Looking through some key words. Health Expectations, 2(1), 3-6.
14. Norman, C.D., & Skinner, H.A. (2006). E-health literacy: Essential skills for consumer health in a networked world. Journal of Medical Internet Research, 8(2), e9. Retrieved May 26, 2008, from at http://www.jmir.org/2006/2/e9/
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