Cervical Ripening at Home or In-Hospital – prospective cohort study and process evaluation Our aim is to compare home versus in-hospital cervical ripening to determine whether home cervical ripening is within an acceptable margin of in-hospital cervical ripening for the safety outcome of neonatal unit (NNU) admission, whether it is more acceptable to women and whether it is cost-effective from both NHS and patient perspectives. Chief Investigator: Dr Sarah Stock Image Number and location of participating sites / geographical scope (by region/ country): Expected 30 sites (18 sites open, 5 in set up)EudraCT number: N/AISRCTN number: 32652461 Funder: NIHR HTA Start and End dateOf grant award: 01/12/2019 - 30/11/2022Of recruitment: Ongoing Current status: In recruitmentWebsite: https://choicestudy.co.uk/Email: CHOICE.Study@ed.ac.uk UK GDPR Privacy Statement: If you have participated in this study and would like to read how it complies with UK GDPR, please read this document. Document qCHOICE Data Protection Information Sheet (205.25 KB / PDF) Chief Investigator: Dr Sarah Stock, Usher Institute of Population Health Sciences and Informatics, NINE Edinburgh BioQuarter, 9 Little France Road, Edinburgh, EH16 4UX Trial Manager: CHOICE.Study@ed.ac.uk ECTU Involvement: Trial Management, Statistics, Data Management This article was published on 2024-09-24