Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England
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 C...
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description | 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 summaryOf 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 plansCIN data collection is annual and ongoing. Data from the most recent census period typically become available for researchers in the following Spring. |
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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 summaryOf 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 plansCIN data collection is annual and ongoing. Data from the most recent census period typically become available for researchers in the following Spring.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2018-023771</identifier><identifier>PMID: 30798306</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject><![CDATA[Adolescent ; Adverse childhood experiences ; Adverse Childhood Experiences - statistics & numerical data ; At risk youth ; Censuses ; Child ; Child Abuse - statistics & numerical data ; Child Health Services - statistics & numerical data ; Child Protective Services - statistics & numerical data ; Child, Preschool ; Children & youth ; Children with disabilities ; Cohort Studies ; Data Collection - methods ; Datasets ; Datasets as Topic ; Disability ; Education ; England ; Families & family life ; Female ; Humans ; Infant ; Infant, Newborn ; Local government ; Male ; Paediatrics ; Researchers ; Social Support]]></subject><ispartof>BMJ open, 2019-02, Vol.9 (2), p.e023771-e023771</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.</rights><rights>2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b472t-23427eaac2cda576e322a12fa198a4ac8949414600b3d1a2558cffaf152a10fb3</citedby><cites>FETCH-LOGICAL-b472t-23427eaac2cda576e322a12fa198a4ac8949414600b3d1a2558cffaf152a10fb3</cites><orcidid>0000-0002-9403-4177 ; 0000-0003-2481-7755 ; 0000-0003-4862-179X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bmjopen.bmj.com/content/9/2/e023771.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://bmjopen.bmj.com/content/9/2/e023771.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27549,27550,27924,27925,53791,53793,77601,77632</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30798306$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Emmott, Emily H</creatorcontrib><creatorcontrib>Jay, Matthew A</creatorcontrib><creatorcontrib>Woodman, Jenny</creatorcontrib><title>Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><description>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 summaryOf 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 plansCIN data collection is annual and ongoing. Data from the most recent census period typically become available for researchers in the following Spring.</description><subject>Adolescent</subject><subject>Adverse childhood experiences</subject><subject>Adverse Childhood Experiences - statistics & numerical data</subject><subject>At risk youth</subject><subject>Censuses</subject><subject>Child</subject><subject>Child Abuse - statistics & numerical data</subject><subject>Child Health Services - statistics & numerical data</subject><subject>Child Protective Services - statistics & numerical data</subject><subject>Child, Preschool</subject><subject>Children & youth</subject><subject>Children with disabilities</subject><subject>Cohort Studies</subject><subject>Data Collection - methods</subject><subject>Datasets</subject><subject>Datasets as Topic</subject><subject>Disability</subject><subject>Education</subject><subject>England</subject><subject>Families & family life</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Local government</subject><subject>Male</subject><subject>Paediatrics</subject><subject>Researchers</subject><subject>Social Support</subject><issn>2044-6055</issn><issn>2044-6055</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>ACMMV</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkc1q3DAUhUVJaUKaJygUQTfpwqn-ZWcRKCZ_ENJNuxayfJXxYEuONA707avJTELaVbWRQN_90NFB6BMlZ5Ry9a2b1nGGUDFC64owrjV9h44YEaJSRMqDN-dDdJLzmpQlZCMl-4AOOdFNzYk6QlMbVzFt8JyiH0Y4x-1qGPsEAQ8B3wP0uIWQl4xP29v7rziBi6nPOHrsXsAEHlIqpI8J5-gGO2JnE-C8zPPWXUyX4WG0of-I3ns7ZjjZ78fo19Xlz_amuvtxfdt-v6s6odmmYlwwDdY65nortQLOmKXMW9rUVlhXN6IRVChCOt5Ty6SsnffWU1kw4jt-jC523nnpJugdhE2yo5nTMNn020Q7mL9vwrAyD_HJKN7UuiFFcLoXpPi4QN6YacgOxhIC4pINo7WstZJcFfTLP-g6LimUeM-UUFooWii-o1yKOZcve30MJWbbqNk3araNml2jZerz2xyvMy_9FeBsB5Tp_zL-AfzKrOs</recordid><startdate>20190222</startdate><enddate>20190222</enddate><creator>Emmott, Emily H</creator><creator>Jay, Matthew A</creator><creator>Woodman, Jenny</creator><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9403-4177</orcidid><orcidid>https://orcid.org/0000-0003-2481-7755</orcidid><orcidid>https://orcid.org/0000-0003-4862-179X</orcidid></search><sort><creationdate>20190222</creationdate><title>Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England</title><author>Emmott, Emily H ; Jay, Matthew A ; Woodman, Jenny</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b472t-23427eaac2cda576e322a12fa198a4ac8949414600b3d1a2558cffaf152a10fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adverse childhood experiences</topic><topic>Adverse Childhood Experiences - statistics & numerical data</topic><topic>At risk youth</topic><topic>Censuses</topic><topic>Child</topic><topic>Child Abuse - statistics & numerical data</topic><topic>Child Health Services - statistics & numerical data</topic><topic>Child Protective Services - statistics & numerical data</topic><topic>Child, Preschool</topic><topic>Children & youth</topic><topic>Children with disabilities</topic><topic>Cohort Studies</topic><topic>Data Collection - methods</topic><topic>Datasets</topic><topic>Datasets as Topic</topic><topic>Disability</topic><topic>Education</topic><topic>England</topic><topic>Families & family life</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Local government</topic><topic>Male</topic><topic>Paediatrics</topic><topic>Researchers</topic><topic>Social Support</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Emmott, Emily H</creatorcontrib><creatorcontrib>Jay, Matthew A</creatorcontrib><creatorcontrib>Woodman, Jenny</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Emmott, Emily H</au><au>Jay, Matthew A</au><au>Woodman, Jenny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England</atitle><jtitle>BMJ open</jtitle><addtitle>BMJ Open</addtitle><date>2019-02-22</date><risdate>2019</risdate><volume>9</volume><issue>2</issue><spage>e023771</spage><epage>e023771</epage><pages>e023771-e023771</pages><issn>2044-6055</issn><eissn>2044-6055</eissn><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 summaryOf 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 plansCIN data collection is annual and ongoing. Data from the most recent census period typically become available for researchers in the following Spring.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>30798306</pmid><doi>10.1136/bmjopen-2018-023771</doi><orcidid>https://orcid.org/0000-0002-9403-4177</orcidid><orcidid>https://orcid.org/0000-0003-2481-7755</orcidid><orcidid>https://orcid.org/0000-0003-4862-179X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adverse childhood experiences Adverse Childhood Experiences - statistics & numerical data At risk youth Censuses Child Child Abuse - statistics & numerical data Child Health Services - statistics & numerical data Child Protective Services - statistics & numerical data Child, Preschool Children & youth Children with disabilities Cohort Studies Data Collection - methods Datasets Datasets as Topic Disability Education England Families & family life Female Humans Infant Infant, Newborn Local government Male Paediatrics Researchers Social Support |
title | Cohort profile: Children in Need Census (CIN) records of children referred for social care support in England |
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