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Consumers in North America rely more and more on information gleaned from the Internet to inform their health-related decisions. The quality of this information may be a subject of concern, especially given the growing emphasis on shared decision-making between patient and health care professionals (Makoul & Clayman, 2006; Wong et al., 2000). Shared decision-making can improve the planning and carrying out of therapies (Brett et al., 2014; Brown, Brown, & Sharma, 2000), facilitate adaptation of new knowledge to specific patient communities (Brett et al., 2014; Collier, 2011; Fagerlin, Zikmund-Fisher, & Ubel; Frank, Basch, & Selby, 2014) and make information more accessible to patients by making it more user-friendly (Brett et al., 2014). There are a variety of tools to evaluate web resources, with a different scope, whose validity is not yet confirmed.
In order to make good health care decisions, people need to fully understand the risks and benefits of each treatment or therapy. Researchers have long stated that there is a gap between the evidence presented in the information, and the decisions people take, or between the creation of knowledge and its intended use (Bero et al., 1998; Dopson, Locock, Gabbay, Ferlie, & Fitzgerald, 2003; Lang, Wyer, & Haynes, 2007). If we consider knowledge translation as a two-step process, the first step would be filtering and distilling the evidence (Cohen et al., 2008; Grimshaw et al., 2006), while the second step would be the adoption or implementation of evidence. This second step is the most difficult to understand. Looking for an explanation, many researchers considered behaviour-change factors (Ajzen & Albarracen, 2007; Ajzen, Czasch, & Flood, 2009; S. Michie, Johnston, Abraham, & Walker, 2005; Susan Michie, van Stralen, & West, 2011). But the tipping point, between the presentation of the evidence, and its adoption, remains unexplained. The “packaging of information”, warrants further attention as it may not adequately reflect the intended knowledge or effectively reach the intended audience.
In this study, we present a relatively new tool, the Communication AssessmenT Checklist in Health (CATCH). We use CATCH to evaluate the quality of health information on HON approved health websites intended for prostate cancer patients. We chose to focus on web resources for prostate cancer because it is the most common cancer in men (Collin et al., 2008), and it is also one of the most difficult cancers for patients to comprehend and formulate health decisions because of the variety of treatment options available (Clark, Wray, & Ashton, 2001; Stamey, McNeal, Yemoto, Sigal, & Johnstone, 1999). The results will allow us to draw a parallel between the websites with the highest overall CATCH score and the websites contained in the 2015 list of “Top health websites you can trust” published by CAPHIS.