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| Using Plain Language To Improve Patient Communications |
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| SciMed - Horizons | |||
| TS-Si News Service | |||
| Friday, 10 July 2009 15:00 | |||
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Seattle, WA, USA. Researchers can now access a toolkit based on plain language, a communication style centered on the audience's needs and abilities. Often, a trip to see the doctor means exposure to a storm of medicalese: like pyrosis, myocardial infarction, and more terms from a specialized vocabulary. If the doctor would say heartburn or heart attack, the patient might have a chance of learning what caused the chest pain. Jessica Ridpath observed health care researchers asking people to take part in clinical studies. She found that consent forms were to complex for people to understand and grant informed consent. A language lover, slam poet, and healthcare professional, Ridpath worried that unreadable consent forms were hindering informed decision making — and raising risks for participants and research institutions alike. So four years ago she created the Project to Review and Improve Study Materials (PRISM). Ridpath is the research communications coordinator at the Group Health Center for Health Studies (CHS) in Seattle, Washington. She has published an article in the American Journal of Health Promotion that presents findings from PRISM. Her article describes how PRISM evolved.
The Toolkit is based on plain language — a communication style centered on the audience's needs and abilities. Researchers can see how to use plain language in study materials through the Toolkit's many concrete examples, including an alternative word list.
PRISM swiftly drew interest from U.S. researchers and other health care professionals. They downloaded the Toolkit 2,000 times in its first year on the CHS web site. Ridpath and colleagues have presented PRISM resources at more than 10 professional conferences nationwide. [C.f. citation for download.] Ridpath led training workshops for external and non-research audiences, including Public Health — Seattle & King County. Her training of Group Health patient education writers led to an organization-wide plain language initiative, resulting in revisions to dozens of patient letters, brochures, and consent forms. Efforts to give health information a plain language makeover have been gaining steam across health care since the Institute of Medicine issued a report on the subject, Health Literacy: A Prescription to End Confusion (2004). The report concluded traditional health information is too complex for roughly 93 million Americans — half the adult population — to understand. Since then, the American Medical Association (AMA) and federal government have also focused on health literacy. Many plain language resources aimed at improving health literacy have sprung up online. Most focus on specific populations or illnesses. The PRISM Toolkit provides practical guidance addressing special challenges that researchers face when communicating with study participants. "The Toolkit is unique for its emphasis on research," said article co-author Sarah M. Greene, MPH, a CHS research associate. "But it can also be extended for use in health care and education." PRISM may help meet the Healthy People 2020 objectives: For the first time, they'll include health literacy targets and measures. "Centering research materials on patients is simply the right thing to do," said co-author Cheryl J. Wiese, MA, manager of the Survey Research Program. "Anecdotally, we think using plain language has helped us recruit study participants." As part of the PRISM editing service, Ridpath tracks readability improvements to study consent forms and other participant materials. To date, her readability editing has dropped reading level by an average of at least 2 grades, with most research materials now between 6th- and 8th-grade reading levels. And these scores don’t account for additional improvements from designing and reorganizing the documents. CitationLooking at Research Consent Forms Through a Participant-Centered Lens: The PRISM Readability Toolkit. Jessica R. Ridpath, Cheryl J. Wiese, Sarah M. Greene. American Journal of Health Promotion July/Aug 2009; 23(I6): 371
Download PDF Abstract Making consent forms understandable should be a goal of every institution and scientist involved in research. A well-written consent form explains in clear language such study aspects as randomization, the risks and benefits of participating in the study, and how data and privacy are protected. This paper describes the features of the Project to Review and Improve Study Materials (PRISM) Readability Toolkit, which is designed to help researchers develop consent forms that use familiar vocabulary, simple sentences and a plain layout of text.
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| Last Updated on Friday, 10 July 2009 13:29 |




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