The primary objective of this study is to compare an integrated, multidisciplinar patient-centered CRP (Cardiac Rehabilitation Program) (intervention group) especially focused on covering the needs for the female and fragile population to the usual care conventional CRP (control group)
Patient aged ≥ 18 years
Patients discharged within the last 30 days after an admission for ACS or in the discharge planning process for an admission for ACS.
The patient is able to fully communicate with the research team and comply with all study procedures.
The patient voluntarily signs and dates the informed consent form approved by the ethics committee
Age <18 years
Participation in another clinical trial
Moderate or severe cognitive impairment in the absence of a competent caregiver
Absence of social support
Institut d'Investigació Biomèdica de Bellvitge
Lead sponsor
Hospital Universitari de Bellvitge
Collaborator
Fundació La Marató de TV3
Collaborator