NCT06887257Completed
RECOVER WITH INOCA: A Study of a Cardiac Rehabilitation Program in Patients With Ischemia With Nonobstructive Coronary Artery Disease (INOCA)
RECOVER WITH INOCA: A Randomized, Prospective Study of a Cardiac Rehabilitation Program in Patients With Ischemia With Nonobstructive Coronary Artery Disease (INOCA)
Source: ClinicalTrials.gov · Last updated 24 Mar 2025
Brief summary (registry, in English)
The goal of this clinical trial is to learn if a cardiac rehabilitation program (CRP) improves functional capacity in adults with INOCA (ischemia with non obstructive coronary arteries). The main questions it aims to answer are: * Does CRP improves maximal functional capacity (measured by VO2peak) in INOCA patients? * Does CRP improve as well quality of life, adherence to Mediterranean diet, emotional state, functional independence angina episodes and sleep quality? Researchers will compare CRP (treatment group) to standard recommendations (control group) to see if CRP works better for INOCA patients Participants will: Take part of CRP or standard recommendations for 3 months Visit the clinic in the beginning and in the end of the study for checkups and tests
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 24 (actual)
- First submitted
- 14 Mar 2025
- Start date
- 1 Sept 2024
- Primary completion date
- 15 Dec 2024
- Lead sponsor
- Hospital Clinic of Barcelona
- Diseases
- Coronary artery disease
- NCT number
- NCT06887257
What you commit to
- Study type: Interventional
- Participants enrolled: 24
- From 1 Sept 2024 to the primary completion date, 15 Dec 2024
- 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
- Alarm signs in the stress test (ventricular arrhythmias, hypotensive response, ST segment changes, or symptoms of ischemia)
Lab values
- Left ventricular ejection fraction (LVEF) \<40%, or presence of pacemakers/defibrillators
Who the study is looking for
- All men or women \>18 years old with cath lab diagnosis of INOCA of 2 possible endotypes: vasoespasm or microvascular disease.
- All participants must have a mobile device/tablet/computer with internet access to connect to exercise and educational sessions
- Participants should be stable in terms of angina episodes, defined as the absence of hospitalizations or decompensations in the number of angina episodes, as well as no changes in antianginal medications for 3 months prior to inclusion.
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 |
|---|---|---|---|
| Villarroel 170 Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.