4 PROGRESS, CONCLUSIONS
AND FUTURE WORK
The paper has proposed an original conceptual model
connecting the online health information behavior
and health behavior of the patients and online users in
an increasingly online world. Therefore, it aims to
provide much-needed understanding and implications
for changing roles of patient and physician
engagement in the emergent healthcare delivery
model contexts.
A survey has been developed including several
measurement items from published sources (already
tested for construct validity) for each construct shown
in the research model. It is targeted to be circulated to
partner hospitals in South Korea and other countries
with an expected completion rate of around three
hundred surveys. The survey will be administered by
qualified physicians or their staff members. The
adherence data would be collected from the same
patients by the same doctors (or their staff). A due
approval has been acquired from the author’s
institutional ethics board for conducting research
involving human subjects.
Once the data collection would be completed
(approximately 3-6 months), both the measurement
model and the structural model would be tested using
PLS-SEM (partial least squares- structural equation
modelling) approach. Further analysis would lead to
acceptance or negation of the hypotheses and their
underlying explanations.
Future research could consider to test other health
behavioural outcomes than adherence such as those
covered by RAND 36-item survey (Hays et al., 1993).
Additionally moderating or mediating roles of
physicians’ attitudes, physician’s competencies,
cultural differences and gender differences would
greatly enhance the understanding of this model.
Social exchange perspective appears to be an
interesting alternate perspective which could shed
further light on the nature of patient-physical
relationship in this context.
REFERENCES
Ajzen, I. 1985. From intentions to actions: A theory of
planned behavior, Berlin, Heidelberg, Springer. doi:
10.1007/978-3-642-69746-3_2.
Assis-Hassid, S., Heart, T., Reychav, I. & Pliskin, J. S.
2016. Modelling Factors Affecting Patient-Doctor-
Computer Communication in Primary Care.
International Journal of Reliable and Quality E-
Healthcare (IJRQEH), 5, 1-17. doi: 10.4018/IJRQEH.
2016010101.
Ba, S. & Wang, L. 2013. Digital health communities: The
effect of their motivation mechanisms. Decision
Support Systems, 55, 941-947. doi: doi.org/10.1016/
j.dss.2013.01.003.
Charles, C., Gafni, A. & Whelan, T. 1999. Decision-making
in the physician–patient encounter: revisiting the shared
treatment decision-making model. Social science &
medicine, 49, 651-661. doi: 10.1016/S0277-9536(99)
00145-8.
Chung, J. E. 2013. Patient–provider discussion of online
health information: results from the 2007 Health
Information National Trends Survey (HINTS). Journal
of health communication, 18, 627-648. doi:
10.1080/10810730.2012.743628.
Clayman, M. L., Bylund, C. L., Chewning, B. & Makoul,
G. 2016. The impact of patient participation in health
decisions within medical encounters: a systematic
review. Medical Decision Making, 36, 427-452. doi:
10.1177/0272989X15613530.
Dedding, C., van Doorn, R., Winkler, L. & Reis, R. 2011.
How will e-health affect patient participation in the
clinic? A review of e-health studies and the current
evidence for changes in the relationship between
medical professionals and patients. Social science &
medicine, 72, 49-53. doi: 10.1016/j.socscimed.2010.
10.017.
Fishbein, M. & Ajzen, I. 1975. Belief, Attitude, Intention
and Behavior: An Introduction to Theory and Research,
Reading, MA, Addison-Wesley.
Fox, S. 2011. The social life of health information 2011,
Pew Internet & American Life Project Washington,
DC.
Fox, S. & Duggan, M. 2015. Pew Internet and American
Life Project [Online]. Pew Research Center
Washington, DC. Available: http://www.pewinternet.
org/2015].
Frost, J. H. & Massagli, M. P. 2008. Social uses of personal
health information within PatientsLikeMe, an online
patient community: what can happen when patients
have access to one another’s data. Journal of medical
Internet research, 10. doi: 10.2196/jmir.1053.
Glanz, K., Rimer, B. K. & Viswanath, K. 2008. Health
behavior and health education: theory, research, and
practice, John Wiley & Sons.
Hameed, T. & Swar, B. 2015. Social value and information
quality in online health information search.
Australasian Conference on Information Systems 2015
Adelaide. Australasian Conference on Information
Systems arXiv preprint arXiv:1606.03507
Hays, R. D., Sherbourne, C. D. & Mazel, R. M. 1993. The
rand 36‐item health survey 1.0. Health economics, 2,
217-227.
Hesse, B. W., Nelson, D. E., Kreps, G. L., Croyle, R. T.,
Arora, N. K., Rimer, B. K. & Viswanath, K. 2005. Trust
and sources of health information: the impact of the
Internet and its implications for health care providers:
findings from the first Health Information National
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