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Aerobic Training and Cardiopulmonary Responses In Heart Failure

A

Ankara City Hospital

Status

Completed

Conditions

Aerobic Capacity
Aerobic Exercise
Cardiopulmonary Exercise Test
Heart Failure

Treatments

Other: Aerobic exercise

Study type

Observational

Funder types

Other

Identifiers

NCT07128784
TABED 2-25-1203

Details and patient eligibility

About

The goal of this observational study is to learn about the short-term effects of aerobic exercise in heart failure patients who were given exercise prescription with cardiopulmonary exercise stres test acocording to aerobic capacity . The main question it aims to answer is:

Does aerobic exercise increase aerobic capacity and quality of life Participants already taking aerobic capacity as part of their regular medical care for Heart failure will asses with cardiopulmonary exercise test and clinical questionaries about quality of life and depression-anxiety level before and after aerobic exercise treatment .

Full description

The goal of this observational study is to learn about the short-term effects of aerobic exercise in heart failure patients who were given exercise prescription with cardiopulmonary exercise stres test acocording to aerobic capacity . The main question it aims to answer is:

Does aerobic exercise increase aerobic capacity and quality of life Participants already taking aerobic capacity as part of their regular medical care for Heart failure will asses with cardiopulmonary exercise test and clinical questionaries about quality of life and depression-anxiety level before and after aerobic exercise treatment .

Enrollment

21 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-75,
  • Diagnosed with compensated HF,
  • BMI 18-30 kg/m²,
  • LVEF < 0.4,
  • NYHA 2-3,
  • Clinical symptoms have been stable for at least 2 weeks, and the dose of angiotensin-converting enzyme inhibitor/angiotensin receptor antagonist/angiotensin receptor inhibitor, beta-blocker, aldosterone inhibitor, and other drugs has been stable for at least 2 weeks.

Exclusion criteria

  • History of a heart implant device within the last 6 weeks or a heart implant device or heart transplant plan within the next 12 months,
  • Acute coronary syndrome within the last 6 weeks, severe valvular heart disease, congenital heart disease, severe hypertrophic obstructive cardiomyopathy, acute myocarditis/pericarditis, intracardiac thrombosis, primary pulmonary hypertension,
  • Uncontrolled hypertension (systolic blood pressure >200 mmHg and/or diastolic blood pressure >110 mmHg),
  • Severe arrhythmias such as ventricular tachycardia, frequent multisource premature ventricular beats, high atrioventricular block, and significant QT interval prolongation during exercise testing,
  • Progressive dyspnea or
  • Loss of exercise endurance at rest within the last 3-5 days under low-intensity exercise load (<2 MET) who have suffered myocardial ischemia,
  • Patients with cognitive impairment.

Trial design

21 participants in 1 patient group

aerobic exercise
Treatment:
Other: Aerobic exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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