patients
Ricapps
patients
There are many ways to involve patients and users of the healthcare system in service delivery, and one of them is to listen to their voices when designing and implementing research projects aimed at improving the experiences and outcomes of the care received. This is especially relevant in the management of chronic conditions, as a more empowered patient who is more involved in managing their condition is a patient with a better quality of life.
At RICAPPS we are actively working to set up our advisory group made up of representatives from the most active patient associations active nationwide, which serves as a channel for patients’ voices in order to systematically include their interests in the design and implementation of research projects.
Its members will be announced shortly!
Functions
To collaborate
on the dissemination of the Network’s activities and results at seminars, scientific outreach events, etc.
To act as a connection
to new patient associations to broaden the potential group of members of the public and users who could become involved in the various activities.
To promote
the involvement of patients in the Network’s activities, especially their participation in the design and implementation of research projects.
To review
the various dissemination materials, providing them with clearer language that connects better with the people they are aimed at.
Miembros Comité Asesor














