National Child Development Study: Biomedical Data, 2002-2004: Special Licence Access

The <i>National Child Development Study</i> (NCDS) is a continuing longitudinal study that seeks to follow the lives of all those living in Great Britain who were born in one particular week in 1958. The aim of the study is to improve understanding of the factors affecting human development over the whole lifespan.<br> <br> The NCDS has its origins in the <i>Perinatal Mortality Survey</i> (PMS) (the original PMS study is held at the UK Data Archive (UKDA) under SN 2137). This study was sponsored by the National Birthday Trust Fund and designed to examine the social and obstetric factors associated with stillbirth and death in early infancy among the 17,000 children born in England, Scotland and Wales in that one week. Selected data from the PMS form NCDS sweep 0, held alongside NCDS sweeps 1-3, under SN 5565.<br> <br> To date there have been seven attempts to trace all members of the birth cohort in order to monitor their physical, educational and social development. The first three sweeps were carried out by the National Children's Bureau, in 1965, when respondents were aged 7, in 1969, aged 11, in 1974, aged 16 (these sweeps form NCDS1-3, held together with NCDS0 under SN 5565). The fourth sweep, NCDS4, was conducted in 1981, when respondents were aged 23 (held under SN 5566). In 1985 the NCDS moved to the Social Statistics Research Unit (SSRU) - now known as the Centre for Longitudinal Studies (CLS) - and the fifth sweep was carried out in 1991, when respondents were aged 33, (NCDS5, held under SN 5567). For the sixth wave, conducted in 1999-2000, when respondents were aged 41-42 (NCDS6, held under SN 5578), fieldwork was combined with the 1999-2000 wave of the <i>1970 Birth Cohort Study</i> (BCS70), which is also conducted by CLS (and held at the UKDA under GN 33229). <br> <br> <i>Response datasets:</i><br> Two separate datasets covering response to NCDS over all nine waves are available. <i>National Child Development Deaths Dataset, 1958-2014: Special Licence Access</i> (SN 7717) covers deaths and <i>National Child Development Study Response Dataset, 1958-2005</i> (SN 5560) covers all other responses and outcomes. Users are advised to order these studies alongside the other waves of NCDS.<br> <br> <i>Additional studies:</i><br> In addition to the main NCDS sweeps, some further studies have also been conducted. In 1978, a postal survey was conducted of the schools attended by members of the birth cohort at the time of the third follow-up of 1974, in order to obtain details of public examination entry and performance. Similar details were also sought from sixth-form and further education colleges etc., where these were identified by schools. Also, a 37-year sample survey of the NCDS cohort, focusing on basic skills, is held under SN 4992.<br> <br> The UKDA also holds a number of NCDS-related files (for example, of data collected in the course of a special study of handicapped school-leavers, at age 18 (held under SN 2024) and the data from a 5% feasibility study, conducted at age 20 (held under SN 2025), which preceded NCDS4. A parent migration dataset, based on NCDS5, is held under SN 4324, and a study detailing partnership histories, compiled from NCDS sweeps 5 and 6, is held under SN 5217.<br> <br> Further information about the full NCDS series can be found on the <a href="http://www.cls.ioe.ac.uk/" title="Centre for Longitudinal Studies">Centre for Longitudinal Studies</a> website.<br> <br> <i>How to access genetic and/or bio-medical sample data from a range of longitudinal surveys:</i><br> A useful overview of the governance routes for applying for genetic and bio-medical sample data, which are not available through the UK Data Service, can be found at <a href="http://www.metadac.ac.uk/data-access-through-metadac/" title="Governance of data and sample access">Governance of data and sample access</a> on the METADAC (Managing Ethico-social, Technical and Administrative issues in Data Access) website.<br> <br> <br> The NCDS biomedical survey was funded under the MRC 'Health of the Public' initiative, and was carried out in collaboration with the Institute of Child Health, St George's Hospital Medical School, and NatCen. The survey was designed to obtain objective measures of ill-health and biomedical risk factors in order to address a wide range of specific hypotheses relating to anthropometry: cardiovascular, respiratory and allergic diseases; visual and hearing impairment; and mental ill-health.<br> <br>