Actively Recruiting
Effects of Upper Extremity Low Volume HIIT in Heart Failure
Led by Tarsus University · Updated on 2025-01-03
30
Participants Needed
2
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study was planned to investigate the effects of upper extremity low-volume high-intensity interval training (LV-HIIT) on physical and cognitive function in patients with heart failure with preserved ejection fraction(HFpEF).The research was planned as a randomized controlled trial. Patients with clinically stable HFpEF at cardiology clinic will be included in the study. These cases will be randomly divided into two groups: intervention group and control grup. After 8 weeks intervention physical functions before and after treatment; functional exercise capacity, arm exercise capacities , peripheral muscle strength , fatigue cognitive functions; anxiety and depression and fear of movement will be evaluated.
CONDITIONS
Official Title
Effects of Upper Extremity Low Volume HIIT in Heart Failure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical condition stable for 64 weeks.
- New York Heart Association functional classification I-II to III
- Over 18 years old
You will not qualify if you...
- History of CABG surgery
- Unstable angina pectoris
- Severe arrhythmia
- Acute pericarditis, endocarditis, myocarditis
- Severe left ventricular failure (EF <40%)
- Acute pulmonary embolism
- History of syncope
- Dissecting aneurysm
- Thrombophlebitis
- Orthopedic disorders that may interfere with exercise
- Uncontrolled hypertension, severe pulmonary arterial hypertension
- Moderate-severe valve disease
- Decompensated Congestive Heart Failure
- Electrolyte abnormalities
- Hypertrophic Cardiomyopathy
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Tarsus University, TARSUS, Mersin
Mersin, Mersin, Turkey (Türkiye)
Actively Recruiting
2
Nurel Ertürk, TARSUS, Mersin
Yenişehir, Mersin, Turkey (Türkiye)
Actively Recruiting
Research Team
N
Nurel ERTÜRK
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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