Our approach to research

We are committed to working with individuals and organisations to deliver innovations in research and practice that can save vulnerable babies’ lives, improve their long-term quality of life and raise standards of care.

At Bliss, we welcome research projects which evaluate the impact their projects have on families and babies, and on the culture of a neonatal unit. We believe this is especially important to make sure that babies and families are able to support any new developments in neonatal care and that any new changes are sustainable.

Learn about the different ways we approach supporting and funding research.

Supporting research

Bliss works in collaboration with organisations to support neonatal research in different ways.

We can support a research project by:

  • Reviewing application materials and parent/patient information leaflets
  • Writing a letter of support for the project
  • Supporting parent advisory/patient and public involvement groups
  • Participating in the project’s steering group
  • Being a co-applicant on the project
  • Helping communication around the project through the Bliss website and social media, including dissemination of results

We can also support research by finding people with lived experience to be involved in a project.

Through our network of parents and relatives of babies born premature or sick, and ex-neonatal patients, we can find people willing to:

Please read our Research Support Policy to understand our approach to supporting research. Use our Public Involvement Role Description Template to inform members of the public about involvement opportunities.

Would you like Bliss to support your research?

Send your request form to research@bliss.org.uk
Bliss Support in Research Request Form

If you are only interested in posting on our social media pages, or to the Insight and Involvement Group, please complete our Social Media Request Form.

Funding research

We want to make sure that the projects we fund are achievable, will contribute something new to improve the care and development of babies who are born premature or sick, and are run by a team which is able to carry out the work they have proposed.

In order to achieve this, we have worked with a panel of healthcare professionals, research experts, parents and with someone who was born premature, to identify our key priority areas.

Our research panel help us to make sure that the research projects we award funding to will address the key areas highlighted in our research strategy.

Our research panel

We have worked with an independent panel of parents, someone who was born premature and neonatal health professionals to identify areas and research questions that would benefit most from Bliss’ funding.
Read more

Please note that we are not opening funding rounds for research projects in 2019.

Find out how the National Neonatal Research Database (NNRD) can be used for research, audit or quality improvement by visiting the website or downloading this leaflet.