Actively Recruiting
Patient-centered Personalized Cardiac Rehabilitation in Post Acute Coronary Syndrome (BREAK-trial)
Led by Institut d'Investigació Biomèdica de Bellvitge · Updated on 2025-06-26
202
Participants Needed
1
Research Sites
127 weeks
Total Duration
On this page
Sponsors
I
Institut d'Investigació Biomèdica de Bellvitge
Lead Sponsor
H
Hospital Universitari de Bellvitge
Collaborating Sponsor
AI-Summary
What this Trial Is About
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)
CONDITIONS
Official Title
Patient-centered Personalized Cardiac Rehabilitation in Post Acute Coronary Syndrome (BREAK-trial)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged �3e= 18 years
- Discharged within the last 30 days after admission for acute coronary syndrome or in discharge planning for ACS
- Able to fully communicate with the research team and comply with study procedures
- Voluntarily signed informed consent approved by ethics committee
You will not qualify if you...
- Under 18 years of age
- Currently participating in another clinical trial
- Moderate or severe cognitive impairment without a competent caregiver
- Lack of social support
- Institutionalized patient
- Life expectancy less than 1 year
- Candidate for end-of-life care
- Severe psychiatric illness
- Planned cardiac surgery including transplant or circulatory support implant
- Death before hospital discharge if included in discharge planning phase
- Carrier of heart transplant
- Unable or refusing to give written informed consent
- Considered unsuitable candidates by investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital Universitari de Bellvitge
L'Hospitalet de Llobregat, Barcelona, Spain, 08907
Actively Recruiting
Research Team
C
Cristina Enjuanes Grau, MD, PhD
CONTACT
P
Pablo Morales, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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