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      User Experiences of the McMaster Optimal Aging Portal’s Evidence Summaries and Blog Posts: Usability Study

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          Abstract

          Background

          Evidence summaries and blogs can support evidence-informed healthy aging, by presenting high-quality health research evidence in plain language for a nonprofessional (citizen) audience.

          Objective

          Our objective was to explore citizens’ perceptions about the usability of evidence summaries and blog posts on the Web-based McMaster Optimal Aging Portal.

          Methods

          Twenty-two citizens (aged 50 years and older) and informal caregivers participated in a qualitative study using a think-aloud method and semistructured interviews. Eleven interviews were conducted in person, 7 over the telephone, and 4 by Skype.

          Results

          We identified themes that fell under 4 user-experience categories: (1) desirability: personal relevance, (2) understandability: language comprehension, grasping the message, dealing with uncertainty, (3) usability: volume of information, use of numbers, and (4) usefulness: intention to use, facility for sharing.

          Conclusions

          Participants recognized that high-quality evidence on aging was valuable. Their intended use of the information was influenced by how much it applied to their own health circumstances or those of a loved one. Some specific formatting features that were preferred included consistent layout, content organized by subheadings, catchy titles, numerical information summarized in a table, and inclusion of a glossary.

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          Most cited references35

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          Qualitative data analysis for applied policy research

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            Health promotion glossary.

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              Virtually he@lthy: the impact of internet use on disease experience and the doctor-patient relationship.

              Alex Broom (2005)
              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 men's 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 men's 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.
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                Author and article information

                Contributors
                Journal
                JMIR Hum Factors
                JMIR Hum Factors
                JMIR Human Factors
                JMIR Human Factors
                JMIR Publications (Toronto, Canada )
                2292-9495
                Jul-Dec 2016
                19 August 2016
                : 3
                : 2
                : e22
                Affiliations
                [1] 1Health Information Research Unit Department of Clinical Epidemiology and Biostatistics McMaster University Hamilton, ONCanada
                [2] 2School of Nursing McMaster University Hamilton, ONCanada
                [3] 3McMaster Health Forum, Centre for Health Economics and Policy Analysis Department of Clinical Epidemiology and Biostatistics McMaster University Hamilton, ONCanada
                [4] 4Division of e-Learning Innovation Faculty of Health Sciences McMaster University Hamilton, ONCanada
                Author notes
                Corresponding Author: Anthony J Levinson levinsa@ 123456mcmaster.ca
                Author information
                http://orcid.org/0000-0003-0449-0572
                http://orcid.org/0000-0002-1968-6765
                http://orcid.org/0000-0002-1453-3196
                http://orcid.org/0000-0002-3331-8766
                http://orcid.org/0000-0001-7917-3657
                http://orcid.org/0000-0001-5240-6449
                Article
                v3i2e22
                10.2196/humanfactors.6208
                5010647
                27542995
                afcbaf16-2a71-45a8-8faa-b803be1c514d
                ©Angela Barbara, Maureen Dobbins, R Brian Haynes, Alfonso Iorio, John N Lavis, Anthony J Levinson. Originally published in JMIR Human Factors (http://humanfactors.jmir.org), 19.08.2016.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Human Factors, is properly cited. The complete bibliographic information, a link to the original publication on http://humanfactors.jmir.org, as well as this copyright and license information must be included.

                History
                : 15 June 2016
                : 4 July 2016
                : 21 July 2016
                : 22 July 2016
                Categories
                Original Paper
                Original Paper

                web-based health information,consumer health information,usability testing,knowledge translation,aging

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