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向参与者传播试验结果时信息项目和首选传递方式的相对重要性:一项混合方法研究。

The relative importance of information items and preferred mode of delivery when disseminating results from trials to participants: A mixed-methods study.

机构信息

Health Services Research Unit, University of Aberdeen, Aberdeen, UK.

出版信息

Health Expect. 2022 Feb;25(1):419-429. doi: 10.1111/hex.13402. Epub 2021 Dec 8.

Abstract

BACKGROUND

Participants want to receive the results of trials that they have participated in. Dissemination practices are disparate, and there is limited guidance available on what information to provide to participants and how to deliver it.

OBJECTIVES

This study aimed to establish what trial participants believe should be included in a results summary and how this information should be delivered.

METHODS

A mixed-methods design was used with focus groups and interviews involving women convenience-sampled from two host randomized-controlled trials. Participants ranked information items in order of their importance for inclusion in a trial results summary and potential modes of delivery by preference. All participants provided written informed consent.

RESULTS

Sixteen women (mean age [SD] = 71.6 [9.7] years) participated. Participants ranked 'individual results from the study' and 'summary of overall trial results' as most important. Themes such as reassurance and setting results in context were identified as contributing to participants' decisions around ranking. 'A thank you for your contribution to the study' was ranked the least important. Delivery by post was the preferred mode of receiving results, with receiving a hard copy of results cited as helpful to refer back to.

CONCLUSION

Our findings provide insight into what information trial participants deem as important when receiving trial results and how they would like results delivered. Involving patients during development of trial results to be communicated to participants could help to ensure that the right information is delivered in the right way.

PATIENT OR PUBLIC CONTRIBUTION

Public partners were involved in focussed aspects of study conduct.

摘要

背景

参与者希望收到他们参与的试验的结果。传播实践存在差异,对于向参与者提供哪些信息以及如何提供这些信息,目前提供的指导有限。

目的

本研究旨在确定试验参与者认为应包含在结果摘要中的内容,以及应如何提供这些信息。

方法

采用混合方法设计,对从两项随机对照试验中方便抽样的女性进行焦点小组和访谈。参与者根据重要性对信息项进行排序,以将其纳入试验结果摘要,并按偏好选择潜在的传递方式。所有参与者均提供了书面知情同意书。

结果

16 名女性(平均年龄[标准差] = 71.6 [9.7]岁)参与了研究。参与者将“研究的个人结果”和“总体试验结果摘要”列为最重要的信息。诸如“获得研究结果时感到安心”和“为试验结果提供背景信息”等主题被确定为参与者对排名的决定因素。“感谢您对研究的贡献”被列为最不重要的信息。通过邮寄传递结果是首选的方式,收到试验结果的硬拷贝被认为有助于参考。

结论

我们的研究结果提供了有关参与者在收到试验结果时认为哪些信息重要以及他们希望如何传递结果的见解。在向参与者传达试验结果的开发过程中让患者参与,有助于确保以正确的方式传递正确的信息。

患者或公众参与

公众合作伙伴参与了研究的重点方面。

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Health research participants' preferences for receiving research results.健康研究参与者对接收研究结果的偏好。
Clin Trials. 2016 Dec;13(6):582-591. doi: 10.1177/1740774516665598. Epub 2016 Aug 24.

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