Rowing Following Breast Cancer Chemotherapy
About this study
There are more than 3.8 million breast cancer survivors in the United States and cancer survivors have a higher risk of cardiovascular disease (CVD) due to chemotherapy than adults without cancer. Cardiovascular rehabilitation can be an effective strategy to decrease the incidence of CVD and its risk factors in this population. The proposed study may help to examine the effect of a novel exercise intervention on cardiovascular rehabilitation in breast cancer survivors.
- Condition
- Breast Cancer Survivors
- Tested
- Exercise training
- Sponsor
- University of Florida
Who can join
- Age
- 40 to 80 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
Inclusion 11
- Minimum age: 40 years
- Maximum age: 80 years
- Eligible sex: Female
- Study condition: Breast Cancer Survivors
- 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 6
- 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
Where
1 site, 1 recruiting
Integrative Cardiovasculal Physiology Laboratory, University of Florida
Gainesville, Florida, United States
Contact
-
Demetra Christou, PhD
352-294-1746 ddchristou@ufl.edu
Potential match only. Final eligibility is determined by the study team.