What an amazing year 2024 has been

As we come to the end of another year and look to the future in 2025, we just wanted to take a moment to reflect on the amazing things that the award-winning Rapid Eczema Trials project has achieved over the last year. You have all played a part in that – thank you! Our first …

Just one thing…

Last month (15-22 September) was National Eczema Week. This annual campaign aims to raise awareness about eczema – so of course the Rapid Eczema Trials team wanted to do our bit to mark the week and support such an important cause! We put our heads together and came up with the idea of making a …

Exploring community beliefs around clinical research

A wedding planner wouldn’t plan a wedding without input from the couple who are to be married… So why would anyone do health research without input from the populations that they’re hoping to help? Just like nearly weds will prefer certain arrangements over others, so will people find certain interventions more acceptable. And there’s no …

Talking eczema flare-ups

When studying something, we need to use words that everyone understands. That way, our findings make sense and can help people. Even common words like a “flare-up” in eczema can mean different things to different people. Everyone in the eczema world talks about “flare-ups” as a term for worsening of the eczema. But that is …

When the answers from health research are not what you want to hear

When the answers from health research are not what you want to hear, how do you make sense of them? Negative reactions, disagreement with the findings or disengaging with the research team will not make the results of a clinical trial change or disappear. But I have experienced all those responses when sharing results, which …

Getting out and about with Rapid Eczema Trials

The ‘traditional route’ for publicising research is to publish the results in scientific and medical journals and talk about what’s been done at scientific conferences. This means a lot of research is only accessible to a limited audience of other researchers and healthcare professionals. But patients and the public are users of research too and …

Being a Rapid Eczema Trials Community Champion

In Rapid Eczema Trials, Community Champions are people with experience of eczema, insight, local knowledge and networks who have been prepared to gather and share information in specific communities or localities. With their unique knowledge, Community Champions can act as a bridge between academic research and practical community-based solutions by giving people in their locality …

Addressing the Eczema PSP priorities with citizen science

In 2011, the Centre of Evidence Based Dermatology (CEBD) at the University of Nottingham worked with the James Lind Alliance to run an Eczema Priority Setting Partnership (PSP) exercise. The aim was to identify and prioritise uncertainties around how best to treat and manage eczema. Over 500 individuals took part. The exercise identified 14 priority …

Understanding the evidence behind eczema treatments

Would you like to know more about the research evidence that supports treatment decisions for people with eczema? If so, this evidence summary from the National Institute for Health and Care Research (NIHR) is a ‘must read’ for you. This article summarises the amazing research that has taken place over the last decade. It has …

Boosting study recruitment by engaging with Be Part of Research

We were all so excited when the Eczema Bathing Study opened to recruitment on 29 January. It’s the first study to come out of the Rapid Eczema Trials research programme and is trying to find out whether it’s better to have a shower (or bath) daily or just once or twice a week when you have …