Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Florida
With
National Institute on Aging (NIA)
Age
18–85
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
female patients based on biological sex
18 to 85 years of age
diagnosis of primary, invasive, non-metastatic, stages I-III breast cancer
completed chemotherapy for breast cancer (anthracycline, alkylating agent and/or taxane) more than 6 months but less than 18 months prior to study enrollment. Adjuvant endocrine therapy for breast cancer (e.g., ovarian suppression, SERMs, SERDs, AIs), CDK4/6 inhibitors, PARP inhibitors, HER2 targeted agents, immunotherapy, and bisphosphonates are allowed within 6 months of study enrollment and during study participation
absence of contraindications to exercise or to participate in study
study clinician approval
scheduled to receive surgery or radiation therapy during the intervention period
any relevant cardiovascular diseases (stroke, heart failure, myocardial ischemia during maximal graded exercise test, myocardial infarction, angina pectoris, coronary artery bypass surgery or angioplasty or coronary stent)
lymphedema stage ≥2 prior to study enrollment
are pregnant
current participation in other experimental interventions that may confound interpretation of study findings (e.g., dietary intervention for weight loss)
Clareo Health | HIIT Following Breast Cancer Chemotherapy