Low- versus high-volume high-intensity interval training for people with chronic heart failure
Official title: Effectiveness of Low -Versus High -Volume High -Intensity Interval Training in Patients With Chronic Heart Failure
Run by Cairo University · NCT07325942 · Data updated 2026-11-12
This trial will try two different amounts of high-intensity interval exercise to see which better improves fitness and quality of life in adults with chronic heart failure and reduced ejection fraction.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 45 (estimated) |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Cairo, Giza Governorate) |
| Status | Recruiting |
| Started | December 10, 2025 |
| Main results expected | June 6, 2026 |
| Study ends | June 6, 2026 |
| Registry record updated | January 8, 2026 |
| Trial ID | NCT07325942 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (over 18) with stable chronic heart failure and reduced ejection fraction (EF <40) who can provide informed consent are ideal candidates.
✕Probably not a fit
Patients with acute or unstable cardiac conditions, decompensated heart failure, recent myocardial infarction, other AHA-listed contraindications to exercise testing/training, or physical disabilities preventing safe exercise are unlikely to benefit and are excluded.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults with stable chronic heart failure and reduced ejection fraction (EF <40) will be enrolled and placed into one of three groups: low-volume HIIT, high-volume HIIT, or standard medical treatment. Participants in the exercise groups will follow supervised high-intensity interval training programs with different total training volumes while continuing usual medical care. Functional capacity and quality of life will be measured before and after the intervention to compare effects across groups. Safety monitoring will follow contemporary exercise contraindication guidance to exclude patients at high risk for adverse events.
Why it matters
Potential benefit: If successful, the comparison could identify a more time-efficient exercise approach that improves exercise capacity and quality of life for patients with reduced‑EF heart failure.
How similar studies have gone: Previous trials of high-intensity interval training in heart failure have shown improvements in exercise capacity and quality of life compared with usual care or moderate training, though direct comparisons of low- versus high-volume HIIT are relatively limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
Cairo University
Cairo, Giza Governorate, Egypt Recruiting
Study contacts
- Study coordinator: Aya I Elshenawy
- Email: dr.aya_ebrahime@yahoo.com
- Phone: +01098811085
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.