The ATTD conference is, by its nature, very technology-centric. This is absolutely not a negative; in fact, it was one of the reasons that I had always wanted to attend because I am such a DTech junkie.
However, as it turns out, it wasn’t the promise of hearing about, or seeing, the latest devices that had me most excited as I perused the program, setting out my schedule for my busy days in Paris.
No, it was this session on the afternoon of the Thursday that really piqued my interest:
I knew we were off to a good start when session co-chair and first speaker, Dr Lori Laffel, flashed this slide up, announcing ‘Diabetes is Stressful’.
Sometimes, there is an assumption that diabetes technology automatically reduces stress. To a degree – and for some – that may be true. For me, the thought of wearing CGM all the time reduces the stress of not being aware of hypos. But it also adds stress with the never-ending, pervasive data data-feed.
There was also this dichotomy that so many of us face:
Acknowledgement of the terminology we use was a welcome addition to this talk. I think that at times our expectations are not being particularly well managed with the way technology is named.
Expectations were covered again when Dr Kath Barnard took the stage.
I love that Kath discussed the responsibilities of health psychology researchers when it comes to improving the outcomes of tech. She mentioned the importance of developing and using device-specific measures to assess psychosocial impacts on both people with diabetes as well as their carers. Most important was the point of ensuring robust and consistent psychological assessments in clinical trials to better understand participant experiences. This often seems to be a missing component when it comes to researching technology.
This is a recurring theme from Kath: that the juggernaut of diabetes technology advances needs to stop being only about button pushing and changes to clinical outcomes if their full potential is to be realised.
It’s important to note Kath is not anti-tech – in fact she frequently acknowledged the ground-breaking nature and significant potential of diabetes technologies. But her dedication to individualising technology use for each person with diabetes is her over-riding message.
Overall, the take-home from this whole session was this comment from Kath, which became a mantra for me for the remainder of the meeting:
Next up, Dr Andrea Scraramuzza from Italy explored the human factor in technology in paediatric diabetes, however his talk was relevant to adults too. Human Factor brings together information from psychology, education, engineering and design to focus on the individual and their interaction with products, technology and their environments with the aim of better understanding the connection between human and technology.
I really loved this presentation because it brought home the idea that it doesn’t matter how whiz-bang the tech is, if the education is not right, if human limitations are not considered and if people with diabetes are not willing to learn – or clinicians are not willing to teach – the potential of that tech will never be reached.
The session closed with the always brilliant Professor Stephanie Amiel who spoke about hypoglycaemia – specifically, where to go when the technology hasn’t worked. I thought this was a really sensible way to round out the session because it reminded us all that technology is never a silver bullet that will fix all situations. Sometimes, we need to revert to other ideas (possibly alongside the technology) to search for solutions.
I was really grateful for this session at the conference. All too often psychology is ignored when we talk and think tech. The focus is on advances – and the speed of these advances – all of which are, of course, super important.
But it is undeniable that alongside currently available and still-in-development technology is the fact that there is a very personal aspect to it all. Whether it be considerations of actually attaching the tech to our bodies (unfortunately this wasn’t really discussed) or tech fatigue and burnout, or simply not wanting to use the tech, this is the side of diabetes and technology that needs to be researched and understood because how we feel about using the tech absolutely impacts on the results we get from it.
Well done to Professor Tadej Battelino and the ATTD organising committee for including this session in the ATTD program. It really was most useful and hopefully the HCPs and researchers in the room walked out thinking a little differently. I know that there were a lot of advocates in the room who really appreciated the session – because we always are thinking about this side of diabetes!
I do, however, have a challenge for the organising committee. As excellent as this session was, it could have been even better if they had dedicated some of it to hearing from people with diabetes talk about this issues being discussed by the clinicians and researchers. That would have really brought home the message. Perhaps next year…?
Disclosures
My flights and accommodation costs to attend the Roche Blogger #DiabetesMeetUp were covered by Roche Diabetes Care (Global). They also provided me with press registration to attend ATTD. My agreement to attend their blogger day did not include any commitment from me, or expectation from them, to write about the day or their products, however I have shared my thoughts on the event here. Plus, you can read my live tweets from the event via my Twitter stream.
3 comments
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February 28, 2017 at 5:59 pm
Andrew Bassett-Smith
Great read Renza, and a critical comment is the right tech for the right person at the right time
It will be interesting once the 4000 kid CGMS trial thingy goes ahead. How many will be jumping on board thinking it is a godsend when it is simply a tool that you need to understand how to use properly to get the right outcome
I see many with say high alarms at like 15-20 etc. I have mine set at 8.9 (on my Animas Vibe – the receiver has the high alarm turned off). I want to take action before my BSL even thinks about hitting double digits rather than fighting it when its already there
Maybe thats one of the various reasons for my HbA1c of 4.7-5.1 for over 2 years now
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March 1, 2017 at 11:57 am
Rick Phillips
I believe we have to acknowledge that diabetes is one of many chronic conditions which offer psychological burdens to those who have them. I think we will make better progress in this area, by reaching out than by closing ranks and suggesting that diabetes is an overly terrible condition.
I know so many others who look at me and say yes you have a 24/7/365 day condition, guess what we have 6 months live. Do we want to compare?
My life with 3 major chronic diseases helps inform me that no one has it worse or better we have different, and as such we should not give ourselves permission to feel worse, rather we should give ourselves permission to find commonality. There is much more common than not.
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March 3, 2017 at 5:58 am
Whitney C
I’ve been on dexcom since a week or so after diagnosis. But I stopped using them a few weeks ago — first because of an insurance hiccup but now because I noticed my blood sugars were great. I loved dexcom so much and I may go back, but I’m starting to think that I may have been overcompensating (both ways) when staring at that little screen! Another way psychology can determine what devices are best for that individual.
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