Hello all!
I’m a health psychologist and PhD candidate. I’m working on identifying what people living with diabetes think about using digital monitoring as part of their usual care. Specifically, which aspects they would find very intrusive in their personal life, and which aspects they would find reassuring.
If you have 10 minutes to spare, please participate in our international survey (by Mayo Clinic, USA and Paris-Descartes University, France): Patient perceptions on the intrusiveness of remote digital monitoring for diabetes
All adults living with diabetes (type 1 or 2) can participate, so please help us by sharing the study on social media, or with friends and family who may be interested.
This post has been approved by forum staff, and the study has an ethics approval (IRB00003888). It was developed in collaboration with french people living with diabetes. When the project is finished, you’ll be able to access a summary of our findings on our study website (I’d be happy to post it here too).
Thank you for your help!
