RecruitingNot ApplicableNCT07038265

Patient-centered Personalized Cardiac Rehabilitation in Post Acute Coronary Syndrome (BREAK-trial)

Patient-centered Cardiac rehaBilitation pRogramE in Post Acute Coronary Syndrome:Identification of Key Barriers and Evaluation of Personalized Intervention (BREAK-trial)

Sponsor

Institut d'Investigació Biomèdica de Bellvitge

Enrollment

202 participants

Start Date

May 26, 2025

Study Type

INTERVENTIONAL

Conditions

Women Frailty Cardiac Rehabilitation Women's Health acute coronary syndromes (ACS)

Summary

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)

Eligibility

Min Age: 18 Years

Inclusion Criteria4

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

Exclusion Criteria13

Age <18 years
Participation in another clinical trial
Moderate or severe cognitive impairment in the absence of a competent caregiver
Absence of social support
Institutionalized patient
Life expectancy <1 year
Candidates for end-of-life care
Severe psychiatric illness
Planned cardiac surgery including transplant or circulatory support implant
Death before hospital discharge in patients included in the hospital discharge planning phase
Carrier of heart transplant.
Patient unable or refusing to give written informed consent to participate
Patients who, in the opinion of the investigator, are unsuitable candidates for the study