Orientation
Keeping day, date and time visible.
Evidence & learning
We do not race to prove that Frank's Board works. We create the conditions in which other people can tell us whether it works.
Frank's Board is evidence-informed, not clinically proven. Relevant research, accessibility practice, lived experience and product feedback can shape design. They do not automatically demonstrate an outcome caused by the product.
We distinguish between what is known, what is not yet known, what is being learned and what may be evaluated in future.
These domains guide questions and design choices. They are not claims of proven benefit.
Keeping day, date and time visible.
Making upcoming events easier to see.
Making short family or carer messages visible.
Reducing unnecessary interaction and visual competition.
Supporting people without turning the display into a control mechanism.
The product exists, families are using it, and its observable functions can be described accurately.
We do not yet have product-specific evidence for clinical, cognitive or wellbeing outcomes.
We can learn about usability, practical barriers, setup, acceptability and what people value.
Future work may explore feasibility, qualitative experience and suitable outcomes, without pre-deciding the answer.
The person looking at the Board should not be asked to navigate unnecessary menus, controls or competing information. When a feature conflicts with that clarity, simplicity should win.
Understand whether people can set up, manage and view the Board as intended.
Explore delivery, support, access barriers and sustained use.
Listen carefully to users, families, carers and partners.
Only then identify whether particular outcomes are meaningful and measurable.
Progress only if earlier learning supports it and appropriate governance is in place.
These stages describe a future pathway. They are not all currently underway.
Frank's Board began in lived family experience. As the programme develops, feedback should continue to influence decisions without being misrepresented as clinical evidence. Experiences may be quoted publicly only where appropriate consent exists.