What an amazing year 2024 has been
December 16, 2024
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…
October 31, 2024
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
September 27, 2024
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
August 16, 2024
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
July 19, 2024
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
June 14, 2024
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 …
