NCT07038265Recruiting
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)
Source: ClinicalTrials.gov · Last updated 26 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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)
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 202 (estimated)
- First submitted
- 4 Apr 2025
- Start date
- 26 May 2025
- Primary completion date
- 30 Nov 2027
- Lead sponsor
- Institut d'Investigació Biomèdica de Bellvitge
- Diseases
- Coronary artery disease
- NCT number
- NCT07038265
What you commit to
- Study type: Interventional
- Planned participants: 202
- From 26 May 2025 to the primary completion date, 30 Nov 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Moderate or severe cognitive impairment in the absence of a competent caregiver
- Severe psychiatric illness
- Planned cardiac surgery including transplant or circulatory support implant
- Carrier of heart transplant.
Age
- Age \<18 years
Other
- Participation in another clinical trial
- Absence of social support
- Institutionalized patient
- Life expectancy \<1 year
- Candidates for end-of-life care
- Death before hospital discharge in patients included in the hospital discharge planning phase
- 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
Who the study is looking for
- 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 in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital Universitari de Bellvitge Coordinator of this site? Confirm its status | L'Hospitalet de Llobregat | Spain | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.