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They concluded that, considering the length and nature of the questionnaires, the obligation to fulfil the specific requirements of the Dutch law for Medical Research Involving Human Subjects was waived (reference: METC17.0652). Local approval was obtained from participating hospitals. All participating patients signed an informed consent form. This study was conducted in accordance with local laws and regulations.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"No details, images, or videos of patients are presented in the manuscript. The people depicted in Fig.\u00a01 are co-authors and a colleague who have consented to the use of their image for the purpose of this study.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"R. The is co-founder and CEO of ZorgKeuzeLab. K. Karssen is co-founder and technical director of ZorgKeuzeLab. After trial completion, ZorgKeuzeLab will request user fees from hospitals to implement the decision aid. Under certain conditions, the NKI-AVL will receive a percentage of these user fees. None of the other authors have competing interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"62"}}