DESIGN: Controlled clinical trial with single randomization, unmasked, open and multicentric. CENTERS: University Hospital of A Coruña and University Hospital of Ferrol CONDITION TO STUDY: Acute Coronary Syndrome (ACS). INTERVENTION:monitored outhospital not inhospital supervised. MAIN OBJECTIVE: To determine the incidence of major adverse events (total mortality, new ACS, coronary revascularization, all-cause hospitalization) during the one-year period after hospitalization for ACS.
The SPRING study aims to learn whether a remote, nurse-guided secondary prevention program reduces adverse events in patients who suffer an infarction during the subsequent one-year period. The SPRING study focuses not only on adverse events but also on the patients' state of life in terms of diet, physical exercise, emotional state, tobacco use, and adherence to medical treatment. Nursing is a profession in charge of preserving the health of patients, which is why the remote secondary cardiovascular prevention program of this study is coordinated by a nurse.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
484
Offer recommendations of healthy living habits and control of pharmacy administration
University Hospital of Ferrol
Ferrol, A Coruña, Spain
University Hospital of A Coruña
A Coruña, Galicia, Spain
major adverse events
total mortality, new ACS, coronary revascularization, hospitalization for any cause
Time frame: 1 year
cardiovascular mortality
cardiovascular mortality
Time frame: 1 year
cardiovascular hospitalization
cardiovascular hospitalization
Time frame: one year
stroke
stroke
Time frame: 1 year
tobacco
questionnaire
Time frame: 1 year
physical activity
mets
Time frame: 1 year
nutrition
mediterranean diet
Time frame: 1 year
emotion state
questionnaire
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.