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Effectiveness of Low -Versus High -Volume High -Intensity Interval Training in Patients With Chronic Heart Failure

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Chronic Heart Failure

Treatments

Drug: Standard medical treatment
Other: High volume high intensity interval training
Other: low-volume high intensity interval training

Study type

Interventional

Funder types

Other

Identifiers

NCT07325942
P.T.REC/012/005825

Details and patient eligibility

About

this study aims to investigate the effect of low vs high volume- high intensity interval training on functional capacity and quality of life in chronic heart failure patients

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Chronic stable heart failure patient with reduced ejection fraction (EF <40)
  2. Age Above 18 years old
  3. Both males and females
  4. The ability to provide informed consent

Exclusion criteria

  1. Based on the Scientific Statement from the American Heart Association: contraindications for exercise Testing and Training. (Fletcher et al., 2013)

    1. Acute myocardial infarction (MI), within 2 days
    2. Ongoing unstable angina
    3. Uncontrolled cardiac tachy or brady arrhythmia with hemodynamic compromise
    4. Active endocarditis
    5. Symptomatic severe aortic stenosis
    6. Decompensated heart failure
    7. Acute pulmonary embolism, pulmonary infarction, or deep vein thrombosis
    8. Acute myocarditis or pericarditis
    9. Acute aortic dissection
    10. Physical disability that precludes safe and adequate testing or training
    11. Known obstructive left main coronary artery stenosis
    12. Hypertrophic obstructive cardiomyopathy with severe resting gradient
    13. Recent stroke or transient ischemic attack
    14. Mental impairment with limited ability to cooperate
    15. Resting hypertension with systolic or diastolic blood pressures >200/110 mmHg
    16. Uncorrected medical conditions, such as significant anemia, important electrolyte imbalance, and hyperthyroidism
  2. Acute decompensated heart failure NYHA class IV

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Low volume high intensity interval training
Experimental group
Description:
This group will receive the usual care (standard medical treatment) in addition to LV-HIIT on a treadmill for 8 weeks, 2 sessions per week.
Treatment:
Other: low-volume high intensity interval training
Drug: Standard medical treatment
high volume high intensity interval training
Experimental group
Description:
In this group, the patients will receive the usual care (standard treatment) in addition to HV-HIIT on a treadmill for 8 weeks, 2 sessions per week
Treatment:
Other: High volume high intensity interval training
Drug: Standard medical treatment
control group
Other group
Description:
It includes 15 patients who will receive standard medical treatment only
Treatment:
Drug: Standard medical treatment

Trial contacts and locations

1

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Central trial contact

Aya I Elshenawy

Data sourced from clinicaltrials.gov

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