Wales Electronic Cohort for Children

NCT ID: NCT01136681

Last Updated: 2014-12-10

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 900000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2009-04-30
• Study Completion Date: 2013-03-31

Brief Summary

The investigators are developing a research platform capable of improving children's health through the generation of knowledge from analysis of routinely collected data from within and outside the health service.

The investigators are using the data that are routinely collected in Wales to answer specific questions about child health and well-being, with the aim of informing policy and practice in Wales, whilst also being internationally relevant.

Routinely collected datasets are publicly funded, and have already been incorporated into the Secure Anonymised Information Linkage databank. The investigators are combining these datasets on children from health and social care to establish an anonymised Wales wide Electronic Cohort for Children (WECC). WECC will serve as the platform for future work in translating information into child population health policy.

There are 35,000 births in Wales per year, and data are available for the previous ten years. Thus, WECC will be sufficiently powered to answer important social, economic and health policy questions. WECC will also act as a demonstration project which would inform the development of e-cohorts to support translational research across the life course and disease spectrum.

Detailed Description

Lack of access to the enormous amount of information collected on children's health status and treatment has been a major contributor to both gaps in the translational pathway to improving child health at individual and population levels. The creation of the Wales Electronic Child Cohort is designed to remove this block and support both explanatory and interventional studies. This proposal is considered to be the best way to address this issue as it is built upon previous strategic investments by WORD and thus should achieve its goals in a very cost effective manner.

This type of E-Cohort with 35,000 additional children every year can answer questions where exposures, outcomes and potential confounders are routinely collected or available through individual or ecological linkages. This is a retrospective and prospective cohort, however, both cohort and nested case-control studies can be supported. Developments in geographical information systems (GIS), network analysis and the creation of a system for anonymising households means that is possible to anonymously link environmentally derived data to health data. The huge numbers of individuals involved in WECC means that the study has enormous power to answer important social, economic and health policy questions.

Examples of research questions which can be answered are:

1. What factors determine the future health service need for individuals that are vulnerable at birth, and inform the development of interventions to reduce health inequalities for these groups?

2. What is the influence of the social and physical environment on childhood obesity?

3. What is the impact of health conditions in childhood on educational outcomes for children?

4. Are birth anomalies more common in households in which any member received antibiotics during early pregnancy (marker for infectious cause)?

5. What is the relationship between maternal depression, family composition and childhood injury risk?

6. Can perinatal environmental and biological parameters be used to predict common illness such as asthma in later childhood and adults?

7. To what extent can E-Cohorts replicate findings from traditional cohorts (e.g. Millennium Cohort Study) and replace the need for some non-routine data collection?

In this first instance we will focus on answering the first two questions.

Conditions

Macrosomia; Low Birth Weight; Premature Birth; Childhood Obesity; Poverty

Keywords

Anonymised Electronic Cohort; Record Linkage; Routine Data; Environment; Childhood Obesity; Low birth weight; Premature birth

Study Design

• Observational Model Type: COHORT

Eligibility Criteria

Inclusion Criteria

• Present in routine data and recorded as born or resident in Wales (1998-2008)

Exclusion Criteria

• Not recorded in routine data as being born of resident in Wales (1998-2008)

• Maximum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cardiff University

OTHER

Sponsor Role: collaborator

Swansea University

OTHER

Sponsor Role: lead

Responsible Party

Dr Sarah E. Rodgers

Professor Ronan Lyons

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ronan A Lyons

Role: PRINCIPAL_INVESTIGATOR

Swansea University

Locations

Health Information Research Unit

Swansea, Swansea, United Kingdom

Department of Primary Care and Public Health

Cardiff, , United Kingdom

Countries

United Kingdom

Other Identifiers

TPR08-006

Identifier Type: -

Identifier Source: org_study_id