A survey of experts to identify methods to detect problematic studies: Stage 1 of the INSPECT-SR Project

Abstract

Background Randomised controlled trials (RCTs) inform healthcare decisions. Unfortunately, some published RCTs contain false data, and some appear to have been entirely fabricated. Systematic reviews are performed to identify and synthesise all RCTs which have been conducted on a given topic. This means that any of these 'problematic studies' are likely to be included, but there are no agreed methods for identifying them. The INSPECT-SR project is developing a tool to identify problematic RCTs in systematic reviews of healthcare-related interventions. The tool will guide the user through a series of `checks' to determine a study's authenticity. The first objective in the development process is to assemble a comprehensive list of checks to consider for inclusion. Methods We assembled an initial list of checks for assessing the authenticity of research studies, with no restriction to RCTs, and categorised these into five domains: Inspecting results in the paper; Inspecting the research team; Inspecting conduct, governance, and transparency; Inspecting text and publication details; Inspecting the individual participant data. We implemented this list as an online survey, and invited people with expertise and experience of assessing potentially problematic studies to participate through professional networks and online forums. Participants were invited to provide feedback on the checks on the list, and were asked to describe any additional checks they knew of, which were not featured in the list. Results Extensive feedback on an initial list of 102 checks was provided by 71 participants based in 16 countries across five continents. Fourteen new checks were proposed across the five domains, and suggestions were made to reword checks on the initial list. An updated list of checks was constructed, comprising 116 checks. Many participants expressed a lack of familiarity with statistical checks, and emphasized the importance of feasibility of the tool. Conclusions A comprehensive list of trustworthiness checks has been produced. The checks will be evaluated to determine which should be included in the INSPECT-SR tool.

Competing Interest Statement

JW, CH, GAA, LB, JJK declare funding from NIHR (NIHR203568) in relation to the current project. JW additionally declares Stats or Methodological Editor roles for BJOG, Fertility and Sterility, Reproduction and Fertility, Journal of Hypertension, and for Cochrane Gynaecology and Fertility. CH declares a Statistical Editor role for Cochrane Colorectal. LB additionally declares a role as Academic Meta-Research Editor for PLoS Biology, and that The University of Colorado receives remuneration for service as Senior Research Integrity Editor, Cochrane. JJK additionally declares a Statistical Editor role for The BMJ. AA declares that The Health Services Research Unit, University of Aberdeen, is funded by the Health and Social Care Directorates of the Scottish Government. VB is EiC of the Medical Journal of Australia and on the Editorial Board of Research Integrity and Peer Review. NJLB declares roles as Editorial Board member for International Review of Social Pyschology/ Revue Internationale de Psychologie Sociale, Statistical Advisory Board member for Mental Health Science, and Advisory Board member for Meta-Psychology. MC declares that he is Co-ordinating Editor for the Cochrane Methodology Review Group, Editor in Chief, Journal of Evidence-Based Medicine, and Coordinating Editor, James Lind Library. EF and TLa declare employment by Cochrane. EF additionally declares a role as Editorial Board member for Cochrane Synthesis and Methods. TLa additionally declares authorship of a chapter in the Cochrane Handbook for Systematic Reviews of Interventions and that he is a developer of standards for Cochrane intervention reviews (MECIR). TLi is funded by the National Eye Institute, National Institutes of Health (Grant #UG1 EY020522). SL is funded by NHMRC (APP1195189), and holds general or methodological editor positions for Cochrane Gynaecology and Fertility, Fertility and Sterility, and Human Reproduction. AL is on the editorial board of BMC Medical Ethics. BWM declares roles as Editor for Cochrane Gynaecology and Fertility and Sexually Transmitted Infections and for Fertility and Sterility. SL declares roles as Associate Editor for Human Reproduction, Methodological Editor for Fertility and Sterility, and Editor for Cochrane Gynaecology and Fertility. NOC is a member of the Cochrane Editoruial Board and holds an ERA-NET Neuron Co-Fund grant for a separate project. ALS declares funding from Australian National Health and Medical Research Council Investigator Grants (GNT2009432). ES is a Sign-off Editor for the Cochrane Library. MvW is coordinating editor of Cochrane Gynaecology and Fertility and Cochrane Sexually Transmitted Infections, Methodological Editor of Human Reproduction Update and editorial Editor of Fertility and Sterility. All other authors have nothing to declare.

Clinical Protocols

https://osf.io/6pmx5/

https://bmjopen.bmj.com/content/14/3/e084164.info

Funding Statement

This study/project is funded by the NIHR Research for Patient Benefit programme (NIHR203568). The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The University of Manchester ethics decision tool was used on 30/09/22. Ethical approval was not required for this study, since it involved asking experts for their professional opinion. This was confirmed with the Ethics Signatory.

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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