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. 2022 Jul 27;78(10):1647–1655. doi: 10.1007/s00228-022-03366-3

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Concern about the potential consequences of sharing personal information. Shown is the response distribution to a question worded as, “During your participation in clinical trials, you have consented to the disclosure of your personal data to third parties in anonymized form. How concerned are you about the following possible consequences of sharing anonymous clinical trial data?”