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Recruiting NCT05913713

NCT05913713 HIIT Following Breast Cancer Chemotherapy

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Clinical Trial Summary
NCT ID NCT05913713
Status Recruiting
Phase
Sponsor University of Florida
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 158 participants
Start Date 2024-03-07
Primary Completion 2026-05-31

Trial Parameters

Condition Breast Cancer
Sponsor University of Florida
Study Type INTERVENTIONAL
Phase N/A
Enrollment 158
Sex FEMALE
Min Age 18 Years
Max Age 85 Years
Start Date 2024-03-07
Completion 2026-05-31
Interventions
12-week Intervention Period12-week Observation Period

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Brief Summary

Chemotherapy is an effective breast cancer treatment, which helped to increase the 5-year survival rate to approximately 95%. However, breast 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 and durability of a novel high-intensity interval training compared to moderate-intensity continuous training on cardiovascular rehabilitation in breast cancer survivors.

Eligibility Criteria

Inclusion Criteria: * 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 Exclusion Criteria: * do not meet inclusion criteria * 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 by

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