Patient and public involvement in a study of multimedia clinical trial information for children, young people and families

Rebecca Sheridan, J. Preston, S. Stones, S. Ainsworth, Danielle H Taylor, Robyn Challinor, S. Ainsworth, J. Martin-Kerry, L. Brady, P. Knapp
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引用次数: 6

Abstract

There is increasing recognition of the need to involve the public in health research, but accounts of how best to achieve this are scarce. This article describes public involvement in the TRials Engagement in Children and Adolescents (TRECA) study, which is developing and evaluating multimedia information resources to inform children, young people and their familes about clinical trials. A dedicated group of young people with long-term health conditions and their parents met regularly throughout the study; further involvement was sought when specific input was required. Review of formal impact records and informal discussions highlighted how public involvement can positively influence research practice and the people involved. By detailing the methods of involvement used, this work also provides guidance for successfully implementing public involvement in research, and highlights challenges that should be considered in future research projects.
患者和公众参与研究多媒体临床试验信息为儿童,青少年和家庭
人们越来越认识到公众参与卫生研究的必要性,但关于如何最好地实现这一目标的叙述却很少。本文描述了公众对儿童和青少年试验参与(TRECA)研究的参与情况,该研究正在开发和评估多媒体信息资源,以便向儿童、青少年及其家人介绍临床试验。一组有长期健康问题的年轻人和他们的父母在研究过程中定期会面;当需要具体投入时,寻求进一步参与。对正式影响记录的审查和非正式讨论强调了公众参与如何对研究实践和参与人员产生积极影响。通过详细介绍所使用的参与方法,这项工作还为成功实施公众参与研究提供了指导,并强调了未来研究项目中应考虑的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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