Abstract

Plain English summaryResearchers carrying out research in the NHS in England have to obtain approval for their study from an NHS Research Ethics Committee (REC). Involving the public in research helps to ensure studies are ethically acceptable to the people taking part, and therefore supports the REC review. The form used by RECs asks researchers to describe any involvement that has taken place before the review or any planned for the future. We analysed researchers’ reports of involvement in 2748 applications to RECs in 2014, to assess how well their approaches to involvement are informing the review process. We found that researchers rarely describe involvement in enough detail to help REC members. It is difficult to judge whether previous involvement has shaped the research design in any way, and whether plans for future involvement are meaningful. It also seems that some researchers remain unclear about involvement and its purpose at different stages. This may be severely limiting its impact.So that public involvement can usefully inform REC reviews in future, the Health Research Authority, which oversees RECs, will carry out further work to find out what information RECS need about involvement. This information will be used to change the application form and to develop guidance and training for REC members and the wider research community. Researchers may also benefit from clearer guidance on the value and purpose of involvement at key research stages: early design, data collection and the dissemination of results.Background Researchers conducting research in the NHS in England are required to submit their study for approval by an NHS Research Ethics Committee (REC). Public involvement in research prior to REC review helps to ensure studies are ethically acceptable to participants, thus informing the review process. The Integrated Research Application System (IRAS) used by RECs, asks researchers to describe any involvement in the development of their project, and in its delivery and dissemination. We analysed researchers’ reports of involvement to assess how well current approaches to involvement are supporting REC review.Methods We used a mixed methods approach. The anonymised free-text data from all 2748 non-educational applications submitted to RECs in 2014 were analysed using NVivo. Themes were developed from the data and used to summarise and categorise the different types of reports of involvement. The frequency of common types of report was analysed using simple statistics.Results In general, researchers rarely describe any prior involvement in sufficient detail to know what was done and what difference this made. This makes it difficult to judge whether the involvement shaped the research design in any way to make it more ethically acceptable. Similarly, researchers’ plans for future involvement are not clear enough to enable RECs to make a proper assessment of whether this involvement will be meaningful, or whether potential ethical concerns raised by involvement have been addressed. This analysis also shows there is still considerable misunderstanding amongst researchers around what involvement means, and its purpose at different stages of a project. This may be severely limiting the potential for impact.Conclusions So that public involvement can usefully inform REC review in future, the HRA is undertaking a collaborative exercise to understand what information RECS need about involvement, and what changes need to be made to the IRAS form. At the same time it will develop guidance and training for REC members and the wider research community about how public involvement can support ethical review. Researchers may also benefit from guidance on the value and purpose of involvement at the research stages: design, data collection and dissemination of results.

Highlights

  • Background Researchers conducting research in theNHS in England are required to submit their study for approval by an NHS Research Ethics Committee (REC)

  • So that public involvement can usefully inform REC review in future, the Health Research Authority (HRA) is undertaking a collaborative exercise to understand what information RECS need about involvement, and what changes need to be made to the Integrated Research Application System (IRAS) form

  • Researchers conducting most types of research in the NHS in England are required to submit their study for ethical review by an NHS Research Ethics Committee (REC) within the Health Research Authority’s Research Ethics Service (RES) [1]

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Summary

Introduction

Background Researchers conducting research in theNHS in England are required to submit their study for approval by an NHS Research Ethics Committee (REC). In recognition of the importance of public involvement in helping to ensure the ethical acceptability of research, the Integrated Research Application System (IRAS) application form includes a question (QA14-1) about public involvement (see Fig. 1). This question asks researchers to describe how the public have contributed to the planning and design of the proposed research and how they will continue to be involved in its conduct and management. It contains a series of tick-boxes for researchers to identify which stages of the research cycle they have involved or plan to involve the public (design, management, undertaking, analysis and/or dissemination), plus a free-text box where they can describe the involvement in detail, or justify their decision to have no involvement in their research.

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