Abstract

BackgroundPublication and outcome reporting bias is often caused by researchers selectively choosing which scientific results and outcomes to publish. This behaviour is ethically significant as it distorts the literature used for future scientific or clinical decision-making. This study investigates the practicalities of using ethics applications submitted to a UK National Health Service (NHS) research ethics committee to monitor both types of reporting bias.MethodsAs part of an internal audit we accessed research ethics database records for studies submitting an end of study declaration to the Hampshire A research ethics committee (formerly Southampton A) between 1st January 2010 and 31st December 2011. A literature search was used to establish the publication status of studies. Primary and secondary outcomes stated in application forms were compared with outcomes reported in publications.ResultsOut of 116 studies the literature search identified 57 publications for 37 studies giving a publication rate of 32 %. Original Research Ethics Committee (REC) applications could be obtained for 28 of the published studies. Outcome inconsistencies were found in 16 (57 %) of the published studies.ConclusionsThis study showed that the problem of publication and outcome reporting bias is still significant in the UK. The method described here demonstrates that UK NHS research ethics committees are in a good position to detect such bias due to their unique access to original research protocols. Data gathered in this way could be used by the Health Research Authority to encourage higher levels of transparency in UK research.

Highlights

  • Publication and outcome reporting bias is often caused by researchers selectively choosing which scientific results and outcomes to publish

  • Since the Health Research Authority (HRA) incorporates the National Research Ethics Service (NRES), whose research ethics committees (RECs) review and provide ethical opinions on all research using National Health Service (NHS) patients, it seemed logical that the HRA plays a greater role in monitoring publication outcomes

  • Cohort of studies As part of an internal audit we accessed Integrated Research Application System (IRAS) records of research projects that submitted an end of study notification to the South Central, Hampshire A research ethics committee between 1st January 2010 and 31st December 2011

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Summary

Introduction

Publication and outcome reporting bias is often caused by researchers selectively choosing which scientific results and outcomes to publish. Since the HRA incorporates the National Research Ethics Service (NRES), whose research ethics committees (RECs) review and provide ethical opinions on all research using NHS patients, it seemed logical that the HRA plays a greater role in monitoring publication outcomes. In recognition of this the HRA business plan for 2013–2014 contains the stated aim of “working with all the relevant partners to help create an environment where clinical trials are registered and research results get published” [8]

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