Evidence map›Paper›PMID 42894246›Full record

ArticleTrials2026

Intracluster correlation coefficients for neonatal trials: an analysis of national population level clinical data.

S Jawad, A T Prevost, C Gale

Abstract read
In one paragraph

Article in Trials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

S JawadNeonatal Medicine, School of Public Health, Faculty of Medicine, Imperial College London, Chelsea and Westminster Hospital Campus, 369 Fulham Road, London, SW10 9NH, UK.
A T PrevostMoorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.
C GaleNeonatal Medicine, School of Public Health, Faculty of Medicine, Imperial College London, Chelsea and Westminster Hospital Campus, 369 Fulham Road, London, SW10 9NH, UK. christopher.gale@imperial.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClustering of outcomes occurs naturally in neonatal data due to multiple births clustered by mother and infants clustered within the neonatal unit administering their care. Estimating these cluster effects is important for neonatal study design and impacts upon sample sizes for neonatal trials.

methodsWe analysed retrospective data from all neonatal admissions in England and Wales between January 2016 and January 2020 held in the National Neonatal Research Database. Intracluster correlation coefficients (ICCs) and their 95% confidence intervals were calculated for core neonatal outcomes and those commonly used in trials, at the level of both the neonatal unit and mother. Results were stratified by gestational age and neonatal unit level of birth. To illustrate the impact of clustering, the design effect was estimated for a theoretical cluster trial.

resultsIntracluster correlation coefficients varied between outcomes and gestational age groups. Neonatal unit level intracluster correlation coefficients were low for mortality (0.0054, 95% CI 0.0039, 0.0068) and other core outcomes (severe necrotising enterocolitis 0.0042, 95% CI 0.0020, 0.0063) and were higher for outcomes related to care delivery (duration of intensive care 0.0237, 95% CI 0.0177, 0.0298; duration receiving parenteral nutrition 0.0265, 95% CI 0.0197, 0.0332). Gestation at birth was inversely correlated with neonatal unit ICC estimates. At the level of the mother, ICC estimates were generally larger, especially for preterm infants.

conclusionsWe have estimated ICCs for key neonatal outcomes at the level of both neonatal unit and mother with high precision using national, population-level routinely recorded data. These ICC estimates can be used to inform future neonatal studies and sample size calculations for neonatal trials.

Indexed as

Clinical Trials as TopicIntensive Care Units, NeonatalResearch DesignCluster AnalysisDatabases, FactualEnglandFemaleGestational AgeHumansInfant MortalityInfant, NewbornRetrospective StudiesSample SizeWalesClusterDesign effectIntracluster correlation coefficientNeonatalNeonatal trial designPretermRandomised controlled trial

Identifiers

PMID42894246
PMCPMC13679098

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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.