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This research programme improved understanding of parent experiences of babies born before 32 weeks, developed a two-stage consent pathway for other intrapartum trials and has informed clinical guidelines and the research agenda.

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Lelia Duley 1,*, Jon Dorling 2, Susan Ayers 3, Sandy Oliver 4, Charles William Yoxall 5, Andrew Weeks 6, Chris Megone 7, Sam Oddie 8, Gill Gyte 9, Zoe Chivers 10, Jim Thornton 2, David Field 11, Alexandra Sawyer 12, William McGuire 8

1 Nottingham Clinical Trials Unit, University of Nottingham, Nottingham, UK
2 Department of Child Health, Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK
3 Centre for Maternal and Child Health Research, School of Health Sciences, City, University of London, London, UK
4 Social Science Research Unit and EPPI-Centre, Institute of Education, University of London, London, UK
5 Neonatal Unit, Liverpool Women’s Hospital, Liverpool, UK
6 University of Liverpool and Liverpool Women’s Hospital, Members of Liverpool Health Partners, UK
7 Inter Disciplinary Ethics Applied, University of Leeds, Leeds, UK
8 Centre for Reviews and Dissemination, University of York, York, UK
9 National Childbirth Trust, London, UK
10 Bliss, London, UK
11 Department of Health Sciences, University of Leicester, Leicester, UK
12 School of Health Sciences, University of Brighton, Brighton, UK
* Corresponding author Email: lelia.duley@nottingham.ac.uk

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