Reflecting on our science festival journey – and what’s next
15 October 2024 | Author: Anna Woolman, Public Engagement and Communications Manager
Over the past year, HDR UK have brought health data research to science festivals and events across the UK. Anna Woolman, Public Engagement Manager, reflects on our journey so far and what’s next.
I joined Health Data Research UK (HDR UK) as Public Engagement and Communications Manager back in May. This makes it almost 6 months since I was tasked with continuing the team’s efforts of exploring how science festivals could help us to engage different audiences with health data research across the UK’s four nations.
Hitting the ground running was something I’d been expecting – in fact in my interview I’d been tasked with coming up with an event plan for Orkney International Science Festival in September. Having been out of the science festival scene for the last 2 years (I’d worked on the British Science Festival before that), I was excited to get stuck back into the highs (and, yes, even the lows) of in-person public engagement events.
By the time I joined, the team had already attended Humber Science Festival and Northern Ireland Science Festival. My role was to keep momentum going and develop relevant content for the upcoming festival in Orkney and identify an appropriate festival in Wales for us to attend – which ended up being Broadlands Fun Day, a lovely community festival based in Bridgend.
Making health data accessible (and sparkle)
Thanks to my predecessor, Rachel Edwards (who is now involved in some great public engagement work over at Research Data Scotland), our Public Advisory Board and HDR UK Voices contributors, table-top activities had already been developed to make health data research more accessible for family audiences.
The beauty of these activities is that they can really be adapted to any kind of data science engagement and research and are cheap and easy to run. We will eventually make these activities readily available for anyone to adapt and use, but in the meantime, get in touch if you’d like to find out more about them:
Speed lego data sorting: Participants have to race against the clock to sort lego pieces that represent different data points. This activity aims to show how data is de-identified, sorted, and analysed in a 3-step game, by highlighting, on a small scale, what researchers do with millions of individual data points on a daily basis.
Hook-a-data-duck: Participants are invited to hook 5 ducks to identify the data they will use for their research. If they hook a duck with ‘duplicate’ data, they win a prize. They’re then asked to think about what experiment they would do with the data they’re given. This activity helps to start conversations about how researchers decide which data they are going to use for research in the real-world.
What does health data look like?: Audiences cut, stick or draw what they think health data looks like. People’s drawings are collected and displayed throughout the event. While simple, this served as a good opportunity to spark conversations around the issues of trust and health data – plus who doesn’t love the opportunity to get creative!
In addition to the activities, we made sparkly stickers to giveaway with “My voice matters” on them which, while simple, was a joyful way to celebrate the role the public can play shaping health data science. In Bridgend, we also translated these into Welsh, as well as our banners, which was appreciated by the local audience.
Trying different approaches
In Orkney and Bridgend, we trialed a few new things: An ‘in-conversation’ style event, aimed at an adult audience, at Orkney Theatre with former HDR UK Chief Scientist, Professor Cathie Sudlow and public contributor Chris Monk, and introducing some new audience evaluation questions to understand more about who we were reaching through our activities.
New evaluation additions included using the British Science Association’s audience model to understand more about people’s levels of engagement with science generally, asking questions about awareness and trust of health data research and some demographic questions.
To my delight, “Fun” was the word that was most used by audiences to describe our table-top activities which goes to show that while health data topics can be serious, they don’t always need to be dry.
A team effort
At all festivals we’ve attended, HDR UK colleagues, public contributors, local researchers and regional HDR UK hubs (like HDR UK Scotland and Wales) have supported the activities. As with any public engagement programme, this pilot has been a true team effort and I am so grateful to everyone – past and present – for the role they had to play, including the festival organisers themselves.
On the horizon
HDR UK started the pilot science festival journey back in 2023 to cover a science festival in all four UK nations to reach new audiences, develop activities that made health data research accessible and involve public contributors and regional researchers in the process. I can safely say that this has been achieved! While I didn’t start this journey, I am glad I was able to be there to see it through.
With this chapter drawing to a close, the PPIE team will use the learnings from this programme as we embark on our soon to be published 2024-2028 PPIE strategy. I feel lucky to have been able to contribute to the development of this strategy in my short time here and am excited about the possibilities there are to make health data research accessible, equitable, trustworthy and, dare I say, fun?
If you’re interested in finding out more about our public engagement plans, I’m always up for a chat – just reach out at anna.woolman@hdruk.ac.uk. You can also contact the wider PPIE team at involvement@hdruk.ac.uk.
Finally, do check out the Public Engagement in Data Research Initiative (PEDRI), a network HDR UK coordinate for anyone interested in any aspect of public engagement with data. There’s a new website (and branding) coming soon.