Phase
Condition
Arrhythmia
Vascular Diseases
Williams Syndrome
Treatment
Intermittent hypoxic-hyperoxic training
Intermittent hypoxic-hyperoxic training/control
Clinical Study ID
Ages 40-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Written informed consent to participate in the study;
Age 40 and over;
Male and female;
One or more cardiovascular pathologies in the anamnesis:
a reliably confirmed diagnosis of hypertension, stage I-III (the diagnosis wasmade in accordance with the National Clinical Guidelines - 2019);
stable angina pectoris I-III functional class, confirmed by complaints,anamnesis and physical examination and with the help of diagnostic tests (bicycle ergometry or daily electrocardiography monitoring);
confirmed diagnosis of arrhythmias and conduction disorders based onelectrocardiography data and 24-hour Holter monitoring (prematuredepolarization, supraventricular tachycardia, atrial fibrillation, sick sinussyndrome, atrioventricular block I-II, bundle branch blocks);
chronic heart failure stage I-IIB, I-III functional class (New York HeartAssociation Functional Classification), confirmed by the presence of clinicalsigns and at least one of two criteria: myocardial dysfunction of leftventricle or / and an increase in the level of the N-terminal fragment of brainnatriuretic peptide over 125 pg / ml;
the presence of signs of systolic or diastolic dysfunction of the leftventricle according to echocardiography.
- COVID-19 infection confirmed by laboratory tests (polymerase chain reaction testing,enzyme-linked immunosorbent assay (positive result at least 1 time) with a CT degreeof 3 or higher.
Non-inclusion criteria:
Acute infectious diseases, tuberculosis;
Chronic somatic diseases in the acute stage;
Congenital anomalies of the heart and large vessels;
Valvular heart defects (congenital and acquired);
Severe atherosclerosis of the lower extremities'vessels (chronic ischemia of thelower extremities,stage 3-4);
Acute decompensated heart failure (II-IV class according to Killip classification);
Chronic heart failure IV functional class (New York Heart Association FunctionalClassification classification);
Secondary arterial hypertension;
Acute coronary syndrome within 4 weeks before the start of the study;
Life-threatening rhythm and conduction disturbances;
Bronchial asthma with the development of respiratory failure II-III degree;
Acute cerebrovascular accident within the last 4 months;
Chronic kidney disease (glomerular filtration rate<30 ml / min / 1.73 m2 via CKD-EPI (chronic kidney disease epidemiology collaboration) formula);
Pregnancy;
Mental illness (severe dementia, schizophrenia, severe depression, manic-depressivepsychosis);
Oncology, diagnosed within a year or receiving a course of radiation / chemotherapyfor cancer at the present time;
Severe cognitive impairment (MOS) and clinically significant anxiety and / ordepression (HADS) interfering with observation;
Individual intolerance to oxygen deficiency.
Exclusion
Exclusion Criteria:
Refusal to further participation in the study;
Acute psychotic reactions arising in the process of the study;
Exacerbation of chronic diseases, requiring a change in patient management tacticsand preventing his or her further participation in the study.
Study Design
Study Description
Connect with a study center
University Clinical Hospital No. 4 of I.M. Sechenov First Moscow State Medical University (Institute for personalized cardiology, Center "Digital biodesign and personalized healthcare").
Moscow, 119435
Russian FederationSite Not Available

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