...
首页> 外文期刊>Journal of medical Internet research >Communicating Uncertainty in Written Consumer Health Information to the Public: Parallel-Group, Web-Based Randomized Controlled Trial
【24h】

Communicating Uncertainty in Written Consumer Health Information to the Public: Parallel-Group, Web-Based Randomized Controlled Trial

机译:向公众提供书面消费者健康信息的不确定性:并行组,基于Web的随机对照试验

获取原文

摘要

Background Uncertainty is integral to evidence-informed decision making and is of particular importance for preference-sensitive decisions. Communicating uncertainty to patients and the public has long been identified as a goal in the informed and shared decision-making movement. Despite this, there is little quantitative research on how uncertainty in health information is perceived by readers. Objective The aim of this study was to examine the impact of different uncertainty descriptions regarding the evidence for a treatment effect in a written research summary for the public. Methods We developed 8 versions of a research summary on a fictitious drug for tinnitus with varying degrees (Q1), sources (Q2), and magnitudes of uncertainty (Q3). We recruited 2099 members of the German public from a web-based research panel. Of these, 1727 fulfilled the inclusion criteria and were randomly presented with one of these research summaries. Randomization was conducted by using a centralized computer with a random number generator. Web-based recruitment and data collection were fully automated. Participants were not aware of the purpose of the study and alternative presentations. We measured the following outcomes: perception of the treatment effectiveness (primary), certainty in the judgement of treatment effectiveness, perception of the body of evidence, text quality, and intended decision. The outcomes were self-assessed. Results For the primary outcome, we did not find a global effect for Q1 and Q2 ( P =.25 and P =.73), but we found a global effect for Q3 ( P =.048). Pairwise comparisons showed a weaker perception of treatment effectiveness for the research summary with 3 sources of uncertainty compared to the version with 2 sources of uncertainty ( P =.04). Specifically, the proportion of the participants in the group with 3 sources of uncertainty that perceived the drug as possibly beneficial was 9% lower than that of the participants in the group with 2 sources of uncertainty (92/195, 47.2% vs 111/197, 56.3%, respectively). The proportion of the participants in the group with 3 sources of uncertainty that considered the drug to be of unclear benefit was 8% higher than that of the participants in the group with 2 sources of uncertainty (72/195, 36.9% vs 57/197, 28.9%, respectively). However, there was no significant difference compared to the version with 1 source of uncertainty ( P =.31). We did not find any meaningful differences between the research summaries for the secondary outcomes. Conclusions Communicating even a large magnitude of uncertainty for a treatment effect had little impact on the perceived effectiveness. Efforts to improve public understanding of research are needed to improve the understanding of evidence-based health information. Trial Registration German Clinical Trials Register DRKS00015911, https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00015911 International Registered Report Identifier (IRRID) RR2-10.2196/13425
机译:背景技术不确定性与证据通知的决策是不可或缺的,对偏好敏感决策特别重要。向患者和公众沟通不确定性长期以来一直被确定为知情和共享决策运动的目标。尽管如此,关于读者感知健康信息的不确定性几乎没有定量研究。客观本研究的目的是研究不同不确定性描述对公众书面研究摘要中治疗效果的证据的影响。方法我们开发了关于具有不同程度(Q1),源(Q2)和不确定度(Q3)的耳鸣的虚拟药物的8个关于耳鸣的研究概要的研究摘要。我们从一家以Web的研究小组招募了2099名德国公众成员。其中,1727年履行了纳入标准,并随机与这些研究摘要中的一个随机呈现。通过使用具有随机数发生器的集中式计算机进行随机化。基于Web的招聘和数据收集是完全自动化的。参与者不了解研究和替代演示的目的。我们衡量了以下结果:对治疗效果(初级)的看法,治疗效率判断,证据核查,文本质量和预期决定的认识。结果是自我评估的。结果的主要结果,我们没有找到Q1和Q2的全局效果(p = .25和p = .73),但我们发现Q3的全局效果(p = .048)。成对比较显示对研究摘要的治疗效果较弱的看法,与具有2个不确定性源的版本相比,与3个不确定性相比(P = .04)。具体而言,本集团参与者的比例具有3种不确定性的不确定性,以至于可能有益的药物可能低于本集团的参与者的9%,具有2个不确定性来源(92/195,47.2%VS 111/197分别为56.3%)。本集团参与者的比例与3个不确定性的来源,认为该药物具有不明确的益处的不确定程度是本集团的参与者的8%,具有2个不确定性来源(72/195,36.9%VS 57/197分别为28.9%)。然而,与具有1个不确定性的版本相比没有显着差异(p = .31)。我们没有发现二次结果的研究摘要之间存在有意义的差异。结论甚至对治疗效果的巨大不确定性沟通甚至对感知的有效性很小。需要改善对研究的公众了解的努力,以改善对基于证据的健康信息的理解。试用注册德语临床试验寄存器DRKS00015911,https://www.drks.de/drks_web/navigate.do? navigationId=trial.html&trial_id=drks00015911 International注册报告标识符(Inshrid)RR2-10.2196 / 13425

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号