Abstract

BackgroundIncreasingly, evidence-based health information, in particular evidence from systematic reviews, is being made available to lay audiences, in addition to health professionals. Research efforts have focused on different formats for the lay presentation of health information. However, there is a paucity of data on how patients integrate evidence-based health information with other factors such as their preferences for information and experiences with information-seeking. The aim of this project is to explore how people with multiple sclerosis (MS) integrate health information with their needs, experiences, preferences and values and how these factors can be incorporated into an online resource of evidence-based health information provision for people with MS and their families.MethodsThis project is an Australian-Italian collaboration between researchers, MS societies and people with MS. Using a four-stage mixed methods design, a model will be developed for presenting evidence-based health information on the Internet for people with MS and their families. This evidence-based health information will draw upon systematic reviews of MS interventions from The Cochrane Library. Each stage of the project will build on the last. After conducting focus groups with people with MS and their family members (Stage 1), we will develop a model for summarising and presenting Cochrane MS reviews that is integrated with supporting information to aid understanding and decision making. This will be reviewed and finalised with people with MS, family members, health professionals and MS Society staff (Stage 2), before being uploaded to the Internet and evaluated (Stages 3 and 4).DiscussionThis project aims to produce accessible and meaningful evidence-based health information about MS for use in the varied decision making and management situations people encounter in everyday life. It is expected that the findings will be relevant to broader efforts to provide evidence-based health information for patients and the general public. The international collaboration also permits exploration of cultural differences that could inform international practice.

Highlights

  • Evidence-based health information, in particular evidence from systematic reviews, is being made available to lay audiences, in addition to health professionals

  • The evidencebased research information will be supported by documentation that is reflective of people’s needs, experiences, preferences and values, and will help people to integrate the research information into, and apply it to, their own circumstances

  • The lack of carefully grounded consultations when developing health information has been a major gap in this area in the past [36]

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Summary

Introduction

Evidence-based health information, in particular evidence from systematic reviews, is being made available to lay audiences, in addition to health professionals. Evidence-based health information for patients Systematic reviews represent the highest level of evidence of the effectiveness of health care interventions [1]. It has been clinicians who have used evidence from systematic reviews of controlled trials to. Cochrane systematic reviews summarise evidence from trials on the effects of treatments (medicines, surgery, rehabilitation), and behavioural and informational interventions. These reviews are the most rigorous summary of the evidence available. In Italy, Italian translations of selected plain language summaries of Cochrane reviews are available free to the public on the PartecipaSalute web site [6] and in the “SM Italia” journal of the Associazione Italiana Sclerosi Multipla (AISM)

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