Limit the continuous request of information coming from patients and caregivers who are looking for some help in the management of the home-therapy?
Design different communication channels to ensure the wellbeing of people involved into care paths (patients, relatives, nurses, doctors...)?
Give patients an estimated waiting time before medical examinations?
Train and accompany patients and caregivers in the management and control of the characteristic side effects of the therapies?
Avoid the patient/caregiver gets lost in the hospitals/clinical structures?
Make clearer and effective/efficient the communication of informed consent?