Phase
Condition
Cardiac Ischemia
Chest Pain
Acute Pain
Treatment
Aerobic exercise (MIT)
Aerobic exercise (Short HIIT)
Aerobic exercise (Long HIIT)
Clinical Study ID
Ages 45-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Men and women aged between 45 and 75 years.
Diagnosed with acute myocardial infarction, unstable or stable angina.
Treated with percutaneous coronary intervention, coronary artery bypass grafting, orconservative treatment.
Event or intervention within 3 to 12 months prior to participation in the study.
Fluency in speaking and reading Spanish.
Residing in Elche or surrounding areas and able to attend evaluations and theexercise programme (not planning to be absent for more than one week during theprogramme).
Functional Class I-II according to the New York Heart Association (NYHA)classification.
No physical limitations for exercise.
Stable optimal medical treatment.
Physically inactive, defined as 1) not meeting the World Health Organizationrecommendations for both aerobic and strength exercise, and 2) not participating ina structured exercise programme at least 3 days per week for more than 3 months.Both conditions must be met for inclusion. Note: Casual walking is not consideredgrounds for exclusion.
Exclusion
Exclusion Criteria:
Use of walking assistive devices.
Treatment with chemotherapy for any type of cancer in the past 2 years.
Hospitalisation in an intensive care unit in the past 6 months for reasons otherthan the ischaemic event.
Acute myocardial infarction group IV Killip-Kimball.
Obesity grade III (≥40.0 kg/m²).
Medical contraindication for inclusion in an exercise programme.
Diabetes with uncontrolled blood glucose levels.
Poorly controlled hypertension: resting blood pressure > 180/110 mmHg.
Chest pain with exertion or ST-segment changes suggestive of residual ischemiaduring ergometry. Residual ischemia.
Severely reduced functional capacity on initial ergometry (<5 metabolicequivalent of task).
Left ventricular ejection fraction less than 50%.
Severe stenosis of the left main coronary artery (>50% significant disease).
Severe aortic stenosis, left ventricular outflow tract obstruction (e.g.,obstructive hypertrophic cardiomyopathy) or aortic dissection.
Severe valvulopathy.
Acute pulmonary embolism or deep vein thrombosis.
Severe pulmonary hypertension.
Acute heart failure.
Acute endocarditis, myocarditis, or pericarditis.
Acute or chronic renal insufficiency (estimated glomerular filtration rate <30ml/min).
Pulmonary fibrosis or interstitial disease (severe respiratory insufficiency orconfirmed chronic obstructive pulmonary disease).
Uncontrolled cardiac arrhythmias/hemodynamically unstable.
Permanent or persistent/paroxysmal atrial fibrillation with episodes in the past 6months.
High-grade cardiac block.
Presence of implantable devices: cardiac resynchronization therapy pacemaker,implantable cardioverter defibrillators, or pacemaker.
Presence of ischaemic symptoms during the incremental exercise test performed beforethe intervention.
Severe autonomic or peripheral neuropathy.
Use of nitrates in pharmacological treatment.
Any planned surgical or medical intervention during the study period.
Plans to participate in or current participation in other studies that may interferewith this study.
Current pregnancy or intention to become pregnant during the study period.
Study Design
Connect with a study center
Centro de Investigación del deporte
Elche, Alicante 03202
SpainActive - Recruiting
Instituto de Investigación Sanitaria y Biomédica de Alicante
Alicante, 03010
SpainActive - Recruiting
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