The DESiGN trial (DEtection of Small for Gestational age Neonate), evaluating the effect of the Growth Assessment Protocol (GAP): study protocol for a randomised controlled trial.


Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
04 Mar 2019
Historique:
received: 08 05 2018
accepted: 06 02 2019
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 27 6 2019
Statut: epublish

Résumé

Stillbirth rates in the United Kingdom (UK) are amongst the highest of all developed nations. The association between small-for-gestational-age (SGA) foetuses and stillbirth is well established, and observational studies suggest that improved antenatal detection of SGA babies may halve the stillbirth rate. The Growth Assessment Protocol (GAP) describes a complex intervention that includes risk assessment for SGA and screening using customised fundal-height growth charts. Increased detection of SGA from the use of GAP has been implicated in the reduction of stillbirth rates by 22%, in observational studies of UK regions where GAP uptake was high. This study will be the first randomised controlled trial examining the clinical efficacy, health economics and implementation of the GAP programme in the antenatal detection of SGA. In this randomised controlled trial, clusters comprising a maternity unit (or National Health Service Trust) were randomised to either implementation of the GAP programme, or standard care. The primary outcome is the rate of antenatal ultrasound detection of SGA in infants found to be SGA at birth by both population and customised standards, as this is recognised as being the group with highest risk for perinatal morbidity and mortality. Secondary outcomes include antenatal detection of SGA by population centiles, antenatal detection of SGA by customised centiles, short-term maternal and neonatal outcomes, resource use and economic consequences, and a process evaluation of GAP implementation. Qualitative interviews will be performed to assess facilitators and barriers to implementation of GAP. This study will be the first to provide data and outcomes from a randomised controlled trial investigating the potential difference between the GAP programme compared to standard care for antenatal ultrasound detection of SGA infants. Accurate information on the performance and service provision requirements of the GAP protocol has the potential to inform national policy decisions on methods to reduce the rate of stillbirth. Primary registry and trial identifying number: ISRCTN 67698474 . Registered on 2 November 2016.

Sections du résumé

BACKGROUND BACKGROUND
Stillbirth rates in the United Kingdom (UK) are amongst the highest of all developed nations. The association between small-for-gestational-age (SGA) foetuses and stillbirth is well established, and observational studies suggest that improved antenatal detection of SGA babies may halve the stillbirth rate. The Growth Assessment Protocol (GAP) describes a complex intervention that includes risk assessment for SGA and screening using customised fundal-height growth charts. Increased detection of SGA from the use of GAP has been implicated in the reduction of stillbirth rates by 22%, in observational studies of UK regions where GAP uptake was high. This study will be the first randomised controlled trial examining the clinical efficacy, health economics and implementation of the GAP programme in the antenatal detection of SGA.
METHODS/DESIGN METHODS
In this randomised controlled trial, clusters comprising a maternity unit (or National Health Service Trust) were randomised to either implementation of the GAP programme, or standard care. The primary outcome is the rate of antenatal ultrasound detection of SGA in infants found to be SGA at birth by both population and customised standards, as this is recognised as being the group with highest risk for perinatal morbidity and mortality. Secondary outcomes include antenatal detection of SGA by population centiles, antenatal detection of SGA by customised centiles, short-term maternal and neonatal outcomes, resource use and economic consequences, and a process evaluation of GAP implementation. Qualitative interviews will be performed to assess facilitators and barriers to implementation of GAP.
DISCUSSION CONCLUSIONS
This study will be the first to provide data and outcomes from a randomised controlled trial investigating the potential difference between the GAP programme compared to standard care for antenatal ultrasound detection of SGA infants. Accurate information on the performance and service provision requirements of the GAP protocol has the potential to inform national policy decisions on methods to reduce the rate of stillbirth.
TRIAL REGISTRATION BACKGROUND
Primary registry and trial identifying number: ISRCTN 67698474 . Registered on 2 November 2016.

Identifiants

pubmed: 30832739
doi: 10.1186/s13063-019-3242-6
pii: 10.1186/s13063-019-3242-6
pmc: PMC6398257
doi:

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

154

Subventions

Organisme : Tommy's Baby Charity
ID : MQATAVR
Organisme : Stillborn and Neonatal Death Charity (GB)
ID : RG1011/16
Organisme : Guy's and St Thomas' Charity (GB)
ID : MAJ150704
Organisme : NIDDK NIH HHS
ID : R01 DK103246
Pays : United States
Organisme : Department of Health
ID : NIHR-KMF-2012-01-29
Pays : United Kingdom

Investigateurs

Peter Brocklehurst (P)
Susan Tebbs (S)
Caroline Doré (C)
Paul Seed (P)
Louisa Delaney (L)
Janet Cresswell (J)
Sarah Petty (S)
Bini Ajay (B)
Beverley Wright (B)
Hannah O'Donnell (H)
Melissa Howard (M)
Emma Wayman (E)
Paula Galea (P)
Mandish Dhanjal (M)
Elisa Iaschi (E)
Vanessa Hodge (V)
Hiran Samarage (H)
Sunder Chita (S)
Raffaele Napolitano (R)
Iris Tsikimi (I)
Fiona Ghalustians (F)
Spyros Bakalis (S)
Simona Cicero (S)
Elisabeth Peregrine (E)
Lyndsey Smith (L)
Deepa Janga (D)
Renata Hutt (R)
Edwin Chandraharan (E)

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Auteurs

Matias C Vieira (MC)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Sophie Relph (S)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Andrew Copas (A)

Centre for Pragmatic Global Health Trials, Institute for Global Health, University College London, Gower Street, London, WC1E 6BT, UK.

Andrew Healey (A)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Kirstie Coxon (K)

Faculty of Health, Social Care and Education, Kingston and St. George's University, 6th Floor, Hunter Wing, Cranmer Terrace, London, SW17 0RE, UK.

Alessandro Alagna (A)

The Guy's and St Thomas' Charity, 9 King's Head Yard, London, SE1 1NA, UK.

Annette Briley (A)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Mark Johnson (M)

Department of Surgery and Cancer, Imperial College London, Kensington, London, SW7 2AZ, UK.

Deborah A Lawlor (DA)

Population Health Science, Bristol Medical School, University of Bristol, Bristol, BS8 2BL, UK.
Bristol NIHR Biomedical Research Centre, Bristol, BS8 2BL, UK.

Christoph Lees (C)

Department of Surgery and Cancer, Imperial College London, Kensington, London, SW7 2AZ, UK.

Neil Marlow (N)

UCL Institute for Women's Health, University College London, Gower Street, London, WC1E 6BT, UK.

Lesley McCowan (L)

Faculty of Medical and Health Sciences, University of Auckland, Victoria Street West, Auckland, 1142, New Zealand.

Louise Page (L)

West Middlesex University Hospital, Chelsea and Westminster Hospital NHS Foundation Trust, Twickenham Road, Isleworth, TW7 6AF, UK.

Donald Peebles (D)

UCL Institute for Women's Health, University College London, Gower Street, London, WC1E 6BT, UK.

Andrew Shennan (A)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Baskaran Thilaganathan (B)

Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, Blackshaw Road, London, SW17 0QT, UK.
Molecular and Clinical Sciences Research Institute, St George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.

Asma Khalil (A)

Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, Blackshaw Road, London, SW17 0QT, UK.
Molecular and Clinical Sciences Research Institute, St George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.

Jane Sandall (J)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Dharmintra Pasupathy (D)

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, Women's Health Academic Centre KHP, 10th Floor North Wing, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK. dharmintra.pasupathy@kcl.ac.uk.

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Classifications MeSH