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Effects of a physical exercise program on cardiac function of patients with Heart Failure

Effects of a combined physical exercise program on cardiac function and biochemical and cardiovascular genetic markers of patients with heart failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6djxqz
Enrollment
Unknown
Registered
2020-01-15
Start date
2017-02-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Interventions

Intervention Group (IG n=41): will undergo a supervised combined exercise program consisting of continuous walking type aerobic exercise plus strength exercise for 16 weeks, three times a week, for 45
Other

Sponsors

Hospital das Clínicas da Faculdade de Medicina de Botucatu
Lead Sponsor
Faculdade de Medicina de Botucatu (FMB) - Universidade Estadual Paulista "Júlio de Mesquita Filho" (UNESP)
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Will be included participants older than 18 years; both sexes; heart failure with reduced ejection fraction (HFrEF) of various etiologies and optimized drug therapy.

Exclusion criteria

Exclusion criteria: Patients with heart failure grade III and IV and stage D; Hypertrophic cardiomyopathy; Deposit diseases; Mitral and aortic stenosis; Decompensated heart failure in the last three months; Persistent or permanent atrial fibrillation and/or artificial pacemaker rhythm; Chronic obstructive pulmonary disease; Biomechanical limitations that prevent them from participating in the proposed combined physical exercise program.

Design outcomes

Primary

MeasureTime frame
a) Echocardiographic cardiac evaluation: 20% improvement of left ventricular diastolic and systolic function; ;b) Evaluation of circulating miRNAs: assess the profile as biomarkers to monitor the treatment of heart failure; ;c) Evaluation of plasma BNP concentration: 30% reduction after intervention; ;d) Evaluation of plasma nitrite / nitrate concentration: 30% increase after intervention.

Secondary

MeasureTime frame
a) Evaluation of inflammatory cytokines: improvement of inflammatory response in the range of 30 to 50% after the intervention; ;b) Handgrip assessment: increase after intervention;;c) Assessment of functional capacity: improvement at or above 300 meters in the Cooper Walking or Running Test 12 minutes the following week after 16 weeks of intervention;;d) Quality of life assessment: 15% improvement in perception on the quality of life scale after the intervention;;e) Bioimpedance assessment: improvement in the range of 5 to 10% of the total body fat index after the intervention.

Countries

Brazil

Contacts

Public ContactSilméia Zanati Bazan

Faculdade de Medicina de Botucatu - UNESP

sgzanati@fmb.unesp.br+55(14)38801171

Outcome results

None listed

Source: REBEC (via WHO ICTRP)