RESILIENCE helps you survive cancer with a strong heart

More than 300 participants by now in the RESILIENCE clinical trial

In March, the RESILIENCE project passed the halfway point of its recruitment process, with more than 300 people participating in this clinical trial, which aims to reduce the incidence of heart failure in cancer survivors.

Patients are distributed among the 22 hospitals in the six countries participating in this multinational project funded by the European Commission, with Spain leading the recruitment process, followed by Germany, Portugal, Denmark, France, and the Netherlands.

Since February, the spectrum of patients eligible to participate in the RESILIENCE trial has been expanded to include not only people with lymphoma but also those with breast cancer receiving anthracycline treatment who meet the criteria assessed by their oncologists.

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Are you a patient participating in RESILIENCE? Here you will find useful information about the details of your participation, activities specifically designed for you. You will also be able to contact RESILIENCE researchers.

In accordance with the provisions of Regulation (EU) 2016/679 on the protection of personal data of natural persons (GDPR), the personal information you have provided will be incorporated into the data processing systems of the Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.) for the purpose of attending your registration application in the restricted area for patients participating in the RESILIENCE study. The legal basis for processing your personal data for this purpose is your explicit consent. Your personal data will not be disclosed to any recipients other than those to whom you authorise or when required by law to do so. You may exercise your rights of access, right to rectification, to object, to erasure, to restriction of processing, data portability and not to be subject to automated individual decision-making. To exercise these rights, as well as to obtain additional information about the processing of your personal data, you can consult the following link Terms and Conditions