Evidence map›Paper›PMID 39900413›Full record

ArticleBMJ open2025

Developing a core outcome set for assessing interventions and care for parents after neonatal death in high-income countries (iCHOOSE Neonatal study): protocol for a mixed-methods study.

Anna Davies, Charlotte Williams, Christy Burden, Sadie Mullin, Lucy Moy, Maggie Redshaw, Mehali Patel, Abigail Fraser, Lisa Hinton, Mary Lynch and 7 more

Abstract read
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Anna DaviesAcademic Women's Health Unit, Translational Health Sciences, University of Bristol, Bristol, UK Anna.davies@bristol.ac.uk.ORCID http://orcid.org/0000-0003-0743-6547
Charlotte WilliamsAcademic Women's Health Unit, Translational Health Sciences, University of Bristol, Bristol, UK.
Christy BurdenAcademic Women's Health Unit, Translational Health Sciences, University of Bristol, Bristol, UK.
Sadie MullinAcademic Women's Health Unit, Translational Health Sciences, University of Bristol, Bristol, UK.
Lucy MoyUniversity of Bristol, Bristol, UK.
Maggie RedshawIndependent Research Consultant, Bristol, UK.ORCID http://orcid.org/0000-0001-5506-3330
Mehali PatelStillbirth and Neonatal Death Society, London, UK.
Abigail FraserMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Lisa HintonUniversity of Oxford, Oxford, UK.
Mary LynchAcademic Women's Health Unit, Translational Health Sciences, University of Bristol, Bristol, UK.
Abi MerrielUniversity of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0003-0352-2106
Dimitris SiasakosEGA Institute for Women's Health, UCL, London, UK.
James WebbeSection of Neonatal Medicine, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-8546-3212
David OddCardiff University, Cardiff, UK.
Laura TimlinWomen & Children's Health, North Bristol NHS Trust, Bristol, UK.
Leanne WattsIndependent Parent Representative, London, UK.
Danya BakhbakhiAcademic Women's Health Unit, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0003-1906-5069

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeonatal death exerts long-lasting impact on parents' mental health, finances and relationships, and the wider family. There is national and international momentum to evaluate interventions to support parents after the death of a baby. Core Outcome Sets (COSs) provide a minimum set of outcomes, agreed by stakeholders to be important, which should be evaluated in all studies to support evidence syntheses and identification of the most effective interventions. We aim to develop a COS for assessing interventions and care after neonatal death in high-income countries, to support future evidence syntheses and enable the identification of effective interventions and care for parents. METHODS AND ANALYSIS: We will develop the COS in six phases. A parent involvement group and stakeholder steering committee have been established and have informed each planned phase: (1) systematic review of quantitative studies evaluating care and interventions provided after neonatal death, to describe interventions, outcomes and outcome measurement tools used to assess intervention effectiveness; (2) qualitative interviews with parents who have experienced neonatal death to identify outcomes important and relevant to them; (3) think-aloud interviews with stakeholders (bereaved parents, healthcare professionals and other stakeholders) to develop and refine an online survey; (4) real-time online international Delphi survey with bereaved parents, healthcare professionals and other stakeholders to shortlist outcomes for consideration in the COS; (5) adapted nominal group online consensus meetings with parents, healthcare professionals and other stakeholders to agree final COS and (6) identification of a preliminary set of measurement tools. ETHICS AND DISSEMINATION: Ethical approval has been granted for all activities to be undertaken by the University of Bristol Health Sciences Faculty Research Ethics Committee (reference: 15121). We will disseminate the findings via peer-reviewed publications and relevant academic and professional conferences. PROSPERO REGISTRATION NUMBER: CRD42020151365.

Indexed as

Outcome Assessment, Health CareParentsPerinatal DeathDelphi TechniqueDeveloped CountriesHumansInfant, NewbornQualitative ResearchResearch DesignSystematic Reviews as TopicMethodsNEONATOLOGYPatient Reported Outcome Measures

Identifiers

PMID39900413
PMCPMC11795395

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.