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Early Experiences with Journal Data Sharing Policies: A Survey of Clinical Trial Investigators

Title
Early Experiences with Journal Data Sharing Policies: A Survey of Clinical Trial Investigators [electronic resource].
ISBN
9781085596954
Published
Ann Arbor : ProQuest Dissertations & Theses, 2019.
Physical Description
1 online resource (47 p.)
Local Notes
Access is available to the Yale community.
Notes
Source: Dissertations Abstracts International, Volume: 81-02, Section: B.
Includes supplementary digital materials.
Advisor: Gross, Cary.
Access and use
Access restricted by licensing agreement.
This item is not available from ProQuest Dissertations & Theses.
Summary
While some have advocated for medical journals to require sharing of clinical trial data, others have raised concerns regarding feasibility, ethical issues, and investigator willingness. We aimed to examine the opinions and experiences of corresponding authors of clinical trial articles who published in high-impact general medical journals that have explicit data sharing policies. We conducted a self-administered online survey of authors of clinical trials published January 1, 2012 through March 1, 2016 in three high-impact journals with policies either requiring all clinical trial authors to share data (PLOS Medicine) or publish a statement in the manuscript specifying whether they were willing to share (The BMJ, Annals of Internal Medicine). We surveyed authors about data sharing plans, responses to actual sharing requests, and willingness to share in response to hypothetical requests. Of 154 eligible trial authors, 90 (58%) responded. Among all respondents, 29% indicated that they had written a data sharing plan, and 52% had addressed data sharing in consent forms. 31 (of 89, 35%) respondents had received at least one data sharing request. Of the 68 requests received, 59 (87%) were granted. In response to scenarios depicting hypothetical requests, 87 (of 90, 97%) indicated they would be willing to share data for a meta-analysis, 66 (73%) would share their data for an analysis focused on replicating their primary study outcome, while only 15 (17%) would share their data for a secondary outcomes analysis if they had planned a similar analysis. In conclusion, about one third of surveyed authors had received at least one data-sharing request. However, many authors indicated a lack of preparation for data sharing and that their willingness to share was dependent on intent to publish a similar analysis.
Variant and related titles
Dissertations & Theses @ Yale University.
Format
Books / Online / Dissertations & Theses
Language
English
Added to Catalog
January 17, 2020
Thesis note
Thesis (M.D.)--Yale University, 2019.
Subjects
Also listed under
Yale University. School of Medicine.
Citation

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