Recap: In Stage 1 – You identified your main point of contact: to access your hospital database. So, to reliably quantify the target populations, set the baseline of your current population and be able to measure the impact of the new pathways of care.
Aim & Objective: Define the measure of success. If you are unable to access the clinical data from your institution – you need to determine how to measure the outcomes of your intervention/s.
Method: It’s difficult to show any improvements without a baseline comparison or a reliable source of data & metrics. You can create a dedicated registry e.g. CaReMe Registry.