Article Text

Download PDFPDF
Advancing child health research in the UK: the Royal College of Paediatrics and Child Health Infants’ Children's and Young People's Research Charter
  1. Lindsey Hunter1,
  2. Emma Sparrow1,
  3. Neena Modi1,2,
  4. Anne Greenough1,3,4
  1. 1Royal College of Paediatrics and Child Health, London, UK
  2. 2Department of Medicine, Section of Neonatal Medicine, Imperial College London, London, UK
  3. 3Division of Asthma, Allergy and Lung Biology, MRC-Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London, UK
  4. 4NIHR Biomedical Centre at Guy's and St Thomas NHS Foundation Trust and King's College London, London, UK
  1. Correspondence to Professor Anne Greenough, Royal College of Paediatrics and Child Health, 5-11 Theobalds Road, London WC1X 8SH, UK; anne.greenough{at}kcl.ac.uk

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

The participation of children, young people and their families is an important component of the child health research process. Children and young people's right to participate in and benefit from research is laid out in the United Nations Convention on the Rights of the Child (UNCRC).1 Researchers and healthcare professionals have a duty to respect, protect and help fulfil those rights. The Ethical Research Involving Children Partnership2 built on the work of the UNCRC and produced the International Charter for Ethical Research Involving Children. It called on researchers to be open, reflective and collaborative in their ethical decision making. In recent years, there has been considerable activity in the UK advancing this agenda. INVOLVE3 was established in 1996 to support active public involvement in the National Health Service, public health and social care research. This is now funded by the National Institute of Health Research (NIHR), as is the Generation R network, a national young people's advisory group with local groups across the UK to support the design and delivery of paediatric research. Organisations, such as the Nuffield Council,4 have determined how healthcare professionals can ethically involve children and young people in research to ensure that healthcare services are safe and effective. This has begun a cultural shift in perceptions about involving children and young people in research design and delivery. It, however, continues to be important that all the perceived barriers to involvement of infants, children and young people in research are removed.2–5

In 2012, the Royal College of Paediatrics and Child health (RCPCH) ‘Turning the Tide’ report5 highlighted the importance of child health research. It emphasised the need for …

View Full Text

Footnotes

  • Contributors LH and ES undertook the literature review and delivered the workshops. AG supported the development work and NM identified the need for a Research Charter. All the authors were involved in the production of the manuscript.

  • Competing interests None declared.

  • Provenance and peer review Commissioned; internally peer reviewed.

  • Data sharing statement These data can be open for sharing if required.