Actively Recruiting
Exercise in Triple- Negative Breast Cancer
Led by Technical University of Munich · Updated on 2025-05-31
120
Participants Needed
2
Research Sites
195 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, randomized, controlled mono-center study investigating the effects of a combined, supervised aerobic exercise and resistance training in female patients with newly diagnosed, therapy-naive triple-negative breast cancer (TNBC, stage I-III) between 18 and 50 years of age scheduled for anthracycline-based chemotherapy and immunotherapy with checkpoint inhibitors. All patients will receive smart watches for rhythm monitoring. Patients will be randomized (1:1) into a control group, receiving 24 weeks of standard exercise recommendations during neoadjuvant therapy, and an intervention group receiving 24 weeks of home-based, video-supervised exercise training consisting of endurance and resistance training. The primary endpoint is the change of peak oxygen consumption (VO2peak) between baseline and 24 weeks in the groups. Secondary endpoints include changes of physical function (short physical performance battery, SPPB), as well as cardiac biomarkers, quality of life, and changes of strength of the upper and lower body between baseline and 24 weeks. In addition, variables of cardiopulmonary exercise testing (CPET), resting and stress echocardiography, and burden of atrial fibrillation (AF) will be assessed. All changes in variables will be analyzed from baseline until 52 weeks as well. Both groups will receive standard exercise recommendations after 24 weeks and will be followed-up by clinical examination after 52 weeks. Echocardiographic variables (at rest and during exercise), quality of life, CPET, SPPB, strength testing, burden of AF, and cardiac biomarkers will be assessed. Changes between the end of the intervention period 24 weeks after diagnosis and the end of follow-up after 52 weeks will be analyzed. In addition, changes in variables between baseline and 52 weeks will be analyzed. As an exploratory endpoint the incidence of cancer therapy-related cardiac dysfunction (CTRCD) and immune-checkpoint inhibitor- associated myocarditis (ICI-myocarditis) will be assessed after 24 and 52 weeks.
CONDITIONS
Official Title
Exercise in Triple- Negative Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients with newly diagnosed, local triple-negative breast cancer (stage I-III)
- Age between 18 and 65 years
- Scheduled for immunochemotherapy with pembrolizumab and anthracycline-based chemotherapy
You will not qualify if you...
- Unstable cardiac condition (such as suspected progression or unstable coronary artery disease, signs of acute heart failure, or significant arrhythmias)
- Orthopaedic disability preventing exercise
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Preventive Sports Medicine and Sports Cardiology
Munich, Bavaria, Germany, 80992
Actively Recruiting
2
Department of Medicine, Division of Prevention and Sports Medicine TU Munich
Munich, Germany, 80809
Actively Recruiting
Research Team
M
Martin Halle, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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