Evidence map›Paper›PMID 30798306›Full record

ArticleBMJ open2019

Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England.

Emily H Emmott, Matthew A Jay, Jenny Woodman

Abstract read
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
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  7. Article
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  9. Observational
  10. Data Resource: the National Pupil Database (NPD).International journal of population data science · 2019
    Article
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

3 authors.

Emily H EmmottDepartment of Anthropology, University College London, London, UK.ORCID 0000-0003-4862-179X
Matthew A JayUCL Legal Epidemiology Group, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.ORCID 0000-0003-2481-7755
Jenny WoodmanThomas Coram Research Unit, Department of Social Science, UCL Institute of Education, University College London, London, UK.ORCID 0000-0002-9403-4177

Funding

Medical Research Council MR/R502248/1Wellcome TrustWellcome Trust HOP001\1021
6 · The paper itself

Abstract

purposeThe Children in Need Census (CIN) is a case-based administrative dataset on children referred to social care services in England. CIN includes information on the 'needs' of children, and whether they received social care support. Local and national government bodies in England currently use CIN for evaluation purposes. Data are accessible to researchers under certain conditions, allowing researchers to investigate the health implications of adverse childhood experiences. However, CIN suffers from lack of metadata, meaning it can be challenging for researchers to process and interpret data, particularly if researchers are unfamiliar with the English children's social care system. To address this issue, we provide the background to CIN and describe the available data from 2008 to 2016.

participantsCIN is derived from case records held by English local authorities on all children referred to children's social care for a 'needs assessment', regardless of whether they are eventually assessed as 'in need of social care support'. Local authorities submit these case records to the UK Department for Education for collation. CIN holds information on an estimated 2.76 million children from October 2008 to March 2016. Since 2013/2014, just under 900 000 children have been recorded in the CIN annually, equivalent to around 8% of children in England (annual prevalence). Approximately, 650 000 children enter or renter the dataset each year, equivalent to 5% of children in England (annual incidence). DATA SUMMARY: Of the estimated 2.76 million children in the data, 50% are male and 47% female. 45% are referred to children's social care services due to abuse or neglect. 10.7% of children in CIN went onto a child protection plan, meaning they were judged to be (at risk of) suffering significant harm. FUTURE PLANS: CIN data collection is annual and ongoing. Data from the most recent census period typically become available for researchers in the following Spring.

Indexed as

CensusesDatasets as TopicSocial SupportAdolescentAdverse Childhood ExperiencesChildChild AbuseChild Health ServicesChild, PreschoolChild Protective ServicesCohort StudiesData CollectionEnglandFemaleHumansInfantchild protectionsocial medicine

Identifiers

PMID30798306
PMCPMC6398790

What OpenQuestion holds

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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.