CompletedNot Applicable

RECOVER WITH INOCA: A Study of a Cardiac Rehabilitation Program in Patients With Ischemia With Nonobstructive Coronary Artery Disease (INOCA)

Spain24 participantsStarted 2024-09-01

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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. Exclusion Criteria: * Alarm signs in the stress test (ventricular arrhythmias, hypotensive response, ST segment changes, or symptoms of ischemia) * Left ventricular ejection fraction (LVEF) \<40%, or presence of pacemakers/defibrillators

What they're measuring

Maximal functional capacity

Timeframe: 3 months

Trial details

NCT IDNCT06887257

SponsorHospital Clinic of Barcelona

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-12-15