Description
Inclusion Criteria:
- * diagnosis of primary invasive non-metastatic breast cancer, stages I-III
- * female based on biological sex
- * 40 to 80 years of age
- * completed breast cancer treatment 6 to 24 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 prior to study enrollment and during study participation
- * absence of contraindications to exercise or study participation
- * study clinician approval
Exclusion Criteria:
- * do not meet inclusion criteria
- * receiving or scheduled to receive treatment for breast cancer (i.e., chemotherapy, surgery, or radiation) during study participation is not allowed. Adjuvant endocrine therapy, CDK4/6 inhibitors, PARP inhibitors, HER2 targeted agents, immunotherapy and bisphosphonates are allowed during study participation
- * lymphedema stage ≥ 2 prior to study enrolment
- * 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)
- * current participation in other experimental interventions that may confound interpretation of study findings (e.g., dietary intervention for weight loss)
- * consistent participation in ≥150 min/week of moderate-intensity rowing exercise training in previous 6 months
Ages Eligible for Study:
40 Years to 80 Years (ADULT, OLDER_ADULT)
Sexes Eligible for Study: FEMALE
Accepts Healthy Volunteers:
No