Active Involvement in the Design and Delivery of Clinical Trials

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Young Persons Advisory Group In 2006 the NIHR MCRN, with support from the National Children’s Bureau set up a young persons’ advisory group. Click here to find more information about the group and how it’s expanded to form a National Young Persons’ Advisory Group.
Public Engagement Activities Find out how the NIHR MCRN are engaging and empowering young people in schools and communities about where medicines come
Consumer Involvement Steering Group The Consumer Involvement Steering Group was established in March 2007 to provide support to the consumer involvement team. It also acts as an expert forum to discuss implementation of the strategy and promote the research interests and priorities of children, young people, parents and carers within MCRN more generally.
Parent Involvement in CSGs MCRN CSGs have a remit to oversee the development of a National portfolio of high quality studies in specific areas of research. Parents play a crucial role in this development via their membership on MCRN CSGs.
Patient & Public Involvement in LRNs Each MCRN Local Research Network (LRN) have a remit to involve children and families in their activities.
Parent Involvement in Study Assessment Committee Find out how parents are involved in the MCRN Study Assessment Committee and influencing study design.

Do you want to get actively involved in the design and delivery of research into medicines for children?

The MCRN encourage children and families to work with researcher professionals and clinicians (e.g. doctors, nurses) and get actively involved in the different stages of research and associated activities.

Active involvement in clinical research is very different from being a participant in a study.
It means:

  • research done with members of the public, not to, about or for them
  • getting involved in the research process or activity itself
  • making sure that clinical research is relevant, useful and to the benefit of the public.

There are a range of activities that children and family members may be able to get involved in, with opportunity to choose what interests them.
Examples Include:

  • Helping to identify research that is important and relevant
  • Helping to choose important topics for research
  • Helping to develop patient information leaflets
  • Helping to support a research project or advisory group as a member
  • Helping to develop accessible information and research news
  • Helping to support and promote good research

Getting actively involved can lead to:

  • More relevant research questions being asked resulting in more useful research
  • More sensitive approaches to people who take part in studies as ‘participants’
  • Helping to keep the research on track
  • Greater opportunities to share research news with patients and the public.

Children and families may benefit from being actively involved:

  • By having a say in research
  • Through sharing their experience
  • By getting research started that is important to them
  • By learning more about research activities
  • Through meeting new people – researchers, members of the public and other people from different networks
  • By gaining confidence and new skills
  • By having the chance to make a contribution.

Children and families may get paid for their involvement depending on what they are doing. Sometimes getting involved is unpaid. This information will always be made clear at the beginning of involvement. Any expenses you incur will always be reimbursed.


Click on the links on the right, to find out about activities currently on-going in the MCRN. If you have a particular query or would like further information of these activities please contact This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Address: MCRN Coordinating Centre, Department of Women's and Children's Health, Institute of Translational Medicine (Child Health), University of Liverpool, Alder Hey Children's NHS Foundation Trust, Eaton Road, Liverpool L12 2AP, UK
Email: info@mcrn.org.uk     Tel: +44 (0)151 252 5067     Fax: +44 (0)151 282 4719

Copyright © Medicines for Childrens Research Network 2011