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June 27, 2017

Data Sharing Statements for Clinical Trials: A Requirement of the International Committee of Medical Journal Editors

Author Affiliations
  • 1Secretary, ICMJE, and Executive Deputy Editor, Annals of Internal Medicine
  • 2Representative and Past President, World Association of Medical Editors
  • 3Scientific Editor-in-Chief, Ugeskrift for Laeger (Danish Medical Journal)
  • 4Chief Editor, PLOS Medicine
  • 5Editor-in-Chief, Annals of Internal Medicine
  • 6Deputy Editor, The Lancet
  • 7Editor-in-Chief, Journal of Korean Medical Science
  • 8Editor-in-Chief, Ethiopian Journal of Health Sciences
  • 9Editor, Bulletin of the World Health Organization, and Coordinator, WHO Press
  • 10Editor-in-Chief, The BMJ (British Medical Journal)
  • 11Editor-in-Chief, New Zealand Medical Journal
  • 12Editor, Revista Médica de Chile (Medical Journal of Chile)
  • 13Editor-in-Chief, New England Journal of Medicine
  • 14Editor-in-Chief, JAMA and the JAMA Network
  • 15Chief Scientific Editor, Deutsches Ärzteblatt (German Medical Journal) and Deutsches Ärzteblatt International
  • 16Representative and Associate Director for Library Operations, National Library of Medicine
JAMA. 2017;317(24):2491-2492. doi:10.1001/jama.2017.6514

The International Committee of Medical Journal Editors (ICMJE) believes there is an ethical obligation to responsibly share data generated by interventional clinical trials because trial participants have put themselves at risk. In January 2016 we published a proposal aimed at helping to create an environment in which the sharing of deidentified individual participant data becomes the norm. In response to our request for feedback we received many comments from individuals and groups.1 Some applauded the proposal while others expressed disappointment it did not more quickly create a commitment to data sharing. Many raised valid concerns regarding the feasibility of the proposed requirements, the necessary resources, the real or perceived risks to trial participants, and the need to protect the interests of patients and researchers.

It is encouraging that data sharing is already occurring in some settings. Over the past year, however, we have learned that the challenges are substantial and the requisite mechanisms are not in place to mandate universal data sharing at this time. Although many issues must be addressed for data sharing to become the norm, we remain committed to this goal.

Therefore, ICMJE will require the following as conditions of consideration for publication of a clinical trial report in our member journals:

  1. As of July 1, 2018, manuscripts submitted to ICMJE journals that report the results of clinical trials must contain a data sharing statement as described below.

  2. Clinical trials that begin enrolling participants on or after January 1, 2019, must include a data sharing plan in the trial’s registration. The ICMJE’s policy regarding trial registration is explained at http://www.icmje.org/recommendations/browse/publishing-and-editorial-issues/clinical-trial-registration.html. If the data sharing plan changes after registration this should be reflected in the statement submitted and published with the manuscript and updated in the registry record.

Data sharing statements must indicate the following: whether individual deidentified participant data (including data dictionaries) will be shared; what data in particular will be shared; whether additional, related documents will be available (eg, study protocol, statistical analysis plan); when the data will become available and for how long; and by what access criteria data will be shared (including with whom, for what types of analyses, and by what mechanism). Illustrative examples of data sharing statements that would meet these requirements are in the Table.

Examples of Data Sharing Statements That Fulfill These ICMJE Requirementsa
Examples of Data Sharing Statements That Fulfill These ICMJE Requirementsa

These initial requirements do not yet mandate data sharing, but investigators should be aware that editors may take into consideration data sharing statements when making editorial decisions. These minimum requirements are intended to move the research enterprise closer to fulfilling our ethical obligation to participants. Some ICMJE member journals already maintain, or may choose to adopt, more stringent requirements for data sharing.

Sharing clinical trial data is one step in the process articulated by the World Health Organization (WHO) and other professional organizations as best practice for clinical trials: universal prospective registration; public disclosure of results from all clinical trials (including through journal publication); and data sharing. Although universal compliance with the requirement to prospectively register clinical trials has not yet been achieved and requires continued emphasis, we must work toward fulfilling the other steps of best practice as well—including data sharing.

As we move forward into this new norm where data are shared, greater understanding and collaboration among funders, ethics committees, journals, trialists, data analysts, participants, and others will be required. We are currently working with members of the research community to facilitate practical solutions to enable data sharing. The United States Office for Human Research Protections has indicated that provided the appropriate conditions are met by those receiving them, the sharing of deidentified individual participant data from clinical trials does not require separate consent from trial participants.2 Specific elements to enable data sharing statements that meet these requirements have been adopted at ClinicalTrials.gov (https://prsinfo.clinicaltrials.gov/definitions.html#shareData). The WHO also supports the addition of such elements at the primary registries of the International Clinical Trials Registry Platform. Unresolved issues remain, including appropriate scholarly credit to those who share data, and the resources needed for data access, the transparent processing of data requests, and data archiving. We welcome creative solutions to these problems at www.icmje.org.

We envision a global research community in which sharing deidentified data becomes the norm. Working toward this vision will help maximize the knowledge gained from the efforts and sacrifices of clinical trial participants.

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Article Information

Corresponding Author: Darren B. Taichman, MD, PhD, Annals of Internal Medicine (dtaichman@acponline.org).

Published Online: June 5, 2017. doi:10.1001/jama.2017.6514

Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Peiperl reported receiving travel reimbursement to speak on data sharing from WHO and the Association of Healthcare Journalists. No other disclosures were reported.

Note: This article is being published simultaneously in Annals of Internal Medicine, BMJ (British Medical Journal), Bulletin of the World Health Organization, Deutsches Ärzteblatt (German Medical Journal), Ethiopian Journal of Health Sciences, JAMA, Journal of Korean Medical Science, New England Journal of Medicine, New Zealand Medical Journal, PLOS Medicine, The Lancet, Revista Médica de Chile (Medical Journal of Chile), and Ugeskrift for Laeger (Danish Medical Journal).

Disclaimer: Dr Sahni’s affiliation as representative and past president of the World Association of Medical Editors (WAME) does not imply endorsement by WAME member journals that are not part of the ICMJE.

Taichman  DB, Backus  J, Baethge  C,  et al.  Sharing clinical trial data: a proposal from the International Committee of Medical Journal Editors.  Ann Intern Med. 2016;164(7):505-506. doi:10.7326/M15-2928PubMedGoogle ScholarCrossref
Menikoff  J. Letter from Jerry Menikoff, MD, JD, Director, Office for Human Research Protections, to ICMJE Secretariat. March 7, 2017. http://icmje.org/news-and-editorials/menikoff_icmje_questions_20170307.pdf.