Evaluation of the Effects of Sauna Therapy on Congestion and Loop Diuretic Use in Patients With Heart Failure With Reduced or Moderately Reduced Ejection Fraction
Sauna: A 15-minute sauna session at 60 degrees Celsius, five times a week for three weeks during hospitalization for cardiac rehabilitation. The sauna sessions will be followed by 30 minutes of recovery in a seated position. In addition to the sauna, patients will benefit from cardiac rehabilitation care for 3 weeks.
Study summary
This study aims to evaluate the effect of sauna therapy on congestion levels during cardiac rehabilitation in patients with heart failure who have an impaired or moderately impaired ejection fraction, compared to standard cardiac rehabilitation care. To investigate this, patients with reduced cardiac function who are hospitalized as part of a cardiac rehabilitation program will be included. These patients will be randomly assigned to two groups: standard cardiac rehabilitation program (control group) and sauna group (intervention group). The study will also assess whether this approach could allow for a reduction in the dose of diuretics, which are commonly used to remove excess fluid, thereby helping to avoid certain side effects. The expected benefits include a reduction in symptoms such as shortness of breath and swelling, improvements in quality of life and physical fitness, and enhanced blood vessel function.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥ 18 years.
* Heart failure with ejection fraction \<50% confirmed by an echocardiogram within the past year.
* NYHA class II-III.
* Loop diuretic dose ≥ 40 mg/day of furosemide (or equivalent) for at least 30 days.
* NT-proBNP \> 400 pg/ml or BNP \> 100 pg/ml.
* Systolic blood pressure ≥ 100 mmHg.
* Estimated glomerular filtration rate (eGFR) ≥ 20 ml/min/1.73 m².
* Patient scheduled for a hospital-based cardiac rehabilitation program for a minimum of 3 weeks.
* Person who has undergone a preliminary clinical examination suitable for clinical research.
* Person affiliated with a social security system or a beneficiary of such a system.
* Person who has received complete information about the organization of the clinical research and has signed informed consent.
Exclusion Criteria:
* Person presenting a contraindication to sauna therapy (for example, intolerance to heat).
* Serum sodium \< 130 mmol/L.
* Serum potassium \> 5.5 mmol/L.
* Active infection, liver disease, or peripheral vascular disease.
* Acute coronary syndrome or recent stroke (\<90 days).
* Participation in another interventional clinical trial.
* Person subject to Articles L. 1121-5, L. 1121-7, and L. 1121-8 of the Public Health Code (applicable in France) :- pregnant, giving birth, or breastfeeding woman , minor (non-emancipated), person adult subject to a legal protection measure (guardianship, curatorship, judicial protection) , adult unable to express consent, persons deprived of liberty by judicial or administrative decision, persons receiving psychiatric care under Articles L. 3212-1 and L. 3213-1…
Primary outcome measure(s)
Median change in NT-proBNP levels. — Between randomization and the end of the third week.
Trial sites (1)
Facility
City
Region
Status
Centre Hospitalier Régional Universitaire de Nancy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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