Evidence Summary
Frequent Internet Users May Prefer More Health Care Information and
Participation in Decision-Making
A Review of:
Xie, B., Wang, M., Feldman, R., & Zhou, L. (2013). Internet use frequency and patient-centered care: Measuring patient
preferences for participation using the Health Information Wants Questionnaire.
Journal of Medical Internet Research,
15(7), e132. doi:10.2196/jmir.2615
Reviewed by:
Eamon C. Tewell
Reference & Instruction Librarian
Long Island University, Brooklyn Campus
Brooklyn, New York, United States of America
Email: eamon.tewell@liu.edu
Received: 15 Sep. 2013 Accepted: 17 Feb.
2014
2014 Tewell.
This is an Open Access article distributed under the terms of the Creative
Commons‐Attribution‐Noncommercial‐Share Alike License 2.5 Canada (http://creativecommons.org/licenses/by‐nc‐sa/2.5/ca/),
which permits unrestricted use, distribution, and reproduction in any medium,
provided the original work is properly attributed, not used for commercial
purposes, and, if transformed, the resulting work is redistributed under the
same or similar license to this one.
Abstract
Objective – To determine whether there is a significant
relationship between patients’ frequency of Internet use and their health care
information and decision-making preferences.
Design – Cross-sectional questionnaire survey.
Settings – Undergraduate classes at a large state
university and senior-oriented computer classes at public libraries and senior
centers.
Subjects – 438 respondents, including 226 undergraduates (mean
age 20) and 212 community-dwelling older adults (mean age 72).
Methods – Respondents were administered the Health
Information Wants Questionnaire (HIWQ), a 21-item instrument designed to
measure preferences for 7 types of health information and decision-making, in
group settings.
Main Results – The younger age group spent significantly more time
online compared to the older age group. Frequent Internet users in both
populations expressed an overall preference for more information regarding
diagnosis, but less information for psychosocial and health care provider
concerns. Internet use was positively correlated to the overall preference
rating, leading the researchers to suggest that, as a whole, regular Internet
users prefer more information and independence in decision-making.
Conclusions – The study concludes that Internet use frequency is
associated with an overall preference for obtaining health information and
participating in decision making. Internet use as related to different types of
preferences is inconsistent. Age was not found to be associated with the
overall preference rating, and time spent online is proposed to be a stronger
indicator of respondents’ health information preferences. The authors suggest
that future studies utilizing the HIWQ take a longitudinal approach in order to
better track how patient preferences for information may evolve over time.
Commentary
The Internet has
revolutionized the ways in which patients seek and obtain health information.
Due to the decentralization of information that traditionally required the
consult of a medical specialist, patients have the ability to select their
level of participation in personal health care decisions. The Internet
introduced two primary challenges to the medical profession, as noted by
Blumenthal (2002): those that are cognitive (creating unmediated access to
medical information), and those that are collegial (allowing users to make
decisions regarding the health care professional they choose). This
democratization of access has led to a conceivable shift in patient preferences
and involvement regarding one’s health care. While a considerable body of
research addresses the health information seeking behavior of various
populations, the authors of this study attempt to compare the Internet use of
two age groups and their preferences for health information. By finding a
marginal correlation between online activity and patient participation, this
paper’s contribution to the literature is that it provides some degree of
support for the significance of Internet use as it relates to the provision of
patient-centered health care.
The study’s strengths
lie in its description of both methodology and process for data collection,
which with the exception of the survey instrument’s omission, are presented
adequately. The discussion of the results is grounded in the literature on
changes brought to the medical profession by online information. Statistical
significance of the results was tested and verified, and appropriate tables and
graphs visualizing the data accompany the text. While these factors contribute
favorably to the strength of the evidence presented, shortcomings in the
sampling technique, data collection, and data analysis significantly reduce the
validity of the findings.
Limitations of the
study include two that are common to research relying upon survey data: the use
of a convenience sample and biases inherent in self-reported responses. The
convenience sample, which the authors acknowledge as an issue for external
validity, can lead to unrepresentative results and the inability to generalize
findings. Because one population selected was older adults in computer
workshops, this group is likely to have a greater interest in improving their
computer skills and may not reflect the attitudes of adults their age not in computer
workshops. Additionally, the study notes that a survey respondent’s stated
preference may not reflect actual practice, given that the survey can measure
only how subjects state they would act in a hypothetical situation. More
intrinsically problematic for the study at hand is the authors’ selection of
independent variables, as the sampling is based on the single demographic
variable of age. Selecting two age groups at each extreme of Internet use not
only ignores other age groups that use the Internet, but fails to account for a
host of other factors that have been shown to be more robust predictors of
online health information seeking, including socioeconomic status, gender, and
Internet use experience.
The slightly unusual
method for data collection presents additional issues. Surveys are frequently
conducted online, or if in print, distributed through postal mail, yet the
authors opted to collect survey responses in group settings. This potentially
introduces issues of respondent anonymity and confidentiality, as well as
researcher conflict or bias if involved in the survey distribution and
collection process. The data analysis would be strengthened by the use of
regression analysis instead of analysis of variance, as the former allows for
the proper investigation of the relationships between the myriad variables that
should be accounted for. The researchers’ conclusions and recommendations do
not account for several factors, including the omission of suitable predictors;
the assumption that individuals rely solely on the Internet when seeking health
information; the fact that the Internet represents a variety of information
sources in itself, each of varying quality and type; and the fact that
information source characteristics, such as reliability, have a considerable
impact on its use.
The significance of
this research lies less in its findings than in the usefulness of the survey
instrument for further research. In terms of recommendations for health care
professionals, the researchers suggest that Internet use can be an advantageous
way to consider the dimensions of patient interest in participating in their
own care process. To the benefit of researchers, this study contributes to the
further validation of HIWQ, a survey that expands upon previous instruments
used for measuring patient preferences and that would be of use in future work
conducted on the topic. At its best, the Internet’s impact on
how the general public accesses health information is one of democratization
and empowerment, as the authors of this study propose. While the
evidence is modest due to the limitations of the survey methodology, sampling
technique, and data analysis reported, it represents a step towards considering
patient involvement with and confidence in the medical decision-making process.
References
Blumenthal, D. (2002). Doctors in a wired world: Can professionalism
survive connectivity? Milbank Quarterly,
80(3), 525-546. doi:10.1111/1468-0009.00021