Abstract

BackgroundIn an evidence-informed patient choice the patient has access to research-based information about the effectiveness of health care options and is encouraged to use this information in treatment decisions. This concept has seen growing popularity in recent years. However, we still know relatively little about users' attitudes to the use of research-based information, possibly because people have been unexposed to this type of information. After developing the BackInfo website where the results of Cochrane systematic reviews on the effects of low back pain were adapted and presented to lay users we evaluated how users responded to this information.MethodsFocus group meetings were held with 18 chronic back pain sufferers, after they had been sent a link to the website before the meetings.ResultsThe focus groups suggest that the most important challenges to the use of BackInfo's research-based information are not primarily tied to the comprehension or presentation of the information, but are mainly associated with participants' attitudes towards the credibility of research and researchers, and the applicability of research results to themselves as individuals. Possible explanations for participants' lack of trust in research and their apparent difficulties in applying this research to their own situations include aspects that may be typical for the general public including the media's presentation of research, and a lack of familiarity with and feelings of distance to research evidence. Other aspects may be typical for patient groups with chronic and unclear medical conditions, such as a lack of trust in the health care establishment in general.ConclusionIn order to enhance the credibility and applicability of research evidence, providers of research-based information could explore a number of possibilities including the use of including personal stories to illustrate the research outcomes.

Highlights

  • In an evidence-informed patient choice the patient has access to research-based information about the effectiveness of health care options and is encouraged to use this information in treatment decisions

  • In order to enhance the credibility and applicability of research evidence, providers of research-based information could explore a number of possibilities including the use of including personal stories to illustrate the research outcomes

  • As the preliminary study emphasised the need for information about the emotional, financial and social aspects of back pain as well as its clinical aspects, we developed information about welfare benefits and patient rights; and included back pain sufferers' personal stories collected and presented by a journalist

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Summary

Introduction

In an evidence-informed patient choice the patient has access to research-based information about the effectiveness of health care options and is encouraged to use this information in treatment decisions. This concept has seen growing popularity in recent years. Evidence-informed patient choice Evidence-informed patient choice "involves providing people with research-based information about the effectiveness of health care options and promoting their involvement in decisions about their treatment" [1]. In order to make an evidence-informed choice, the patient needs to have access to reliable information about the likely benefits and risks of at least two alternative interventions, which may include the option of no intervention [1] This information should be presented quantitatively and without recommendations. Researchers evaluating the effect of decision aids providing information about available treatments and their outcomes conclude that they may "improve knowledge and realistic expectations; enhance active participation in decision making; lower decisional conflict; decrease the proportion of people remaining undecided, and improve agreement between values and choice." [5]

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