The Italian Alliance for Cardiovascular Rehabilitation and Prevention (ITACARE-P) Registry: An Observational Study on Cardiac Rehabilitation in Patients With Coronary Disease or Heart Failure
NCT ID: NCT07094737
Last Updated: 2025-07-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1600 participants
OBSERVATIONAL
2025-05-01
2027-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Transcultural Digital Solutions in Phase III Cardiac Rehabilitation
NCT07252856
RECOVER WITH INOCA: A Study of a Cardiac Rehabilitation Program in Patients With Ischemia With Nonobstructive Coronary Artery Disease (INOCA)
NCT06887257
Cardiac Rehabilitation Program in Patients with Cardiovascular Disease
NCT06211361
Autonomic and Metabolic Response to Cardiac Rehabilitation After Acute MI
NCT06298513
Comparison of Cardiac Rehabilitation Benefits Between Coronary and Non-coronary Patients Through a 24 Months Follow-up After Myocardial Infarction: the "INCARD" Study
NCT01683903
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The main goal of the present study is to better understand how cardiac rehabilitation (CR) is being delivered to patients who have experienced heart-related conditions (coronary deseases or heart failure). Cardiac rehabilitation is a structured program that includes exercise, lifestyle education, and psychological support. It is known to help patients recover faster, reduce the risk of future heart problems, lower hospital readmissions, and improve quality of life.
Despite strong recommendations from international guidelines, not all eligible patients are referred to cardiac rehabilitation, and CR programs are not always delivered in a consistent way. This study aims to collect real-world data to:
* Describe how CR programs are implemented in different hospitals,
* Evaluate whether patients are meeting treatment goals (such as improved fitness, lower cholesterol, or better medication use),
* Identify patient groups that may need different types of care,
* Support future improvements in heart care services in Italy and beyond.
The central idea behind the study is that systematically collecting and analyzing data on patients undergoing cardiac rehabilitation can highlight what works best, help standardize care, and improve long-term health outcomes for people with heart disease. By understanding how care is delivered and what results are achieved, the study aims to improve the quality and equity of cardiac rehabilitation services across Italy.
Adults who recently had a heart condition that qualifies them for cardiac rehabilitation will be included.
This is not a treatment trial, and no experimental therapies are given. Instead, the study observes what happens during standard care. Patients will continue to receive their normal rehabilitation program/care. Information will be collected about:
Basic personal and medical data (such as age, blood pressure, cholesterol),
Risk factors (like smoking, diabetes, weight),
Emotional well-being and quality of life,
Functional improvements (like exercise capacity),
Medication use.
Patients will also be contacted by phone at 6 and 12 months after their program to check on their health and whether they have had any additional heart-related problems.
There are no added risks because this study does not involve any changes to a patient's usual care. While there are no direct personal benefits, participants may experience better tracking of their health indicators. More importantly, their participation helps researchers and healthcare providers improve care for future patients.
All personal health data will be kept confidential and protected according to European Union data protection regulations (GDPR). A secure online system (REDCap) will be used to collect and manage the data. The information will be pseudo-anonymized, meaning names and personal identifiers will ben removed, so no one can be identified and only authorized staff will have access to the data and it will only be used for scientific and quality improvement .
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
cardiorehab patients
cardiological rehabilitation patients with heart conditions (heart coronary deseases and/or heart failure).
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Planned hospital readmission within six months after completion of the cardiac rehabilitation program.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istituti Clinici Scientifici Maugeri SpA
OTHER
ASST Crema
UNKNOWN
IRCCS Ospedale San Raffaele
OTHER
AORN Sant'Anna e San Sebastiano - Caserta
UNKNOWN
IRCCS Fondazione Don Gnocchi-Firenze
UNKNOWN
Fondazione Don Gnocchi Parma
UNKNOWN
U.O.S. Riabilitazione Cardiologica Area Sud Azienda USL Toscana
UNKNOWN
S.O.D. Riabilitazione Cardiologica Azienda Ospedaliero Universitaria Careggi Firenze
UNKNOWN
UOSD Cardiologia Riabilitativa Azienda Ospedaliera San Giovanni-Addolorata
UNKNOWN
IRCCS Istituti clinici Maugeri, Istituto di Montescano
UNKNOWN
IRCCS Istituti clinici Maugeri, Istituto di Pavia
UNKNOWN
IRCCS Istituti clinici Maugeri, Istituto di Gattico-Veruno
UNKNOWN
Struttura complessa Riabilitazione Cardiologica
UNKNOWN
Casa di cura villa gemma
UNKNOWN
Cardiologia Riabilitativa Tagliacozzo
UNKNOWN
ASST Brianza
UNKNOWN
Riabilitazione del Cardiopatico
UNKNOWN
UOS Cardiologia Riabilitativa ULSS Serenissima
UNKNOWN
Ospedale Riabilitativo di Alta Specializzazione
UNKNOWN
Istituto clinico Maugeri Lumezzane
UNKNOWN
U.O.C. Cardiologia ASL 3 Genovese
UNKNOWN
Fondazione Don Carlo Gnocchi Onlus
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
IRCCS Dongnocchi
Milan, , Italy
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CardioRehab
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.