Different Approaches to requesting Consent for Routine data linkage in Neonatal follow-up (ACORN): protocol for a 2×2 factorial randomised trial

Introduction Routinely collected data can be linked to research data to create a rich dataset and inform practice. However, consent is normally required to link identifiable data. Reported rates of consent to data linkage for children ranged from 21% to 96%, but no studies have investigated differen...

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Библиографические подробности

Главные авторы:	Jane E Harding, Barry Milne, Jenny Rogers, Greg Gamble, Jane Marie Alsweiler, Christopher McKinlay, Gavin Brown, Aakash Bajirao Rajay, Caroline Anne Crowther, Nike Franke, Trecia Wouldes
Формат:	Artigo
Язык:	Inglês
Опубликовано:	BMJ Publishing Group 2022-07-01
Серии:	BMJ Open
Online-ссылка:	https://bmjopen.bmj.com/content/12/7/e060476.full
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