Assessing the Effect of an Aerobic Exercise Program on Vascular Function in Women With Non-Metastatic Breast Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorLoyola University

About this trial

The goal of this clinical trial is to assess the feasibility of an 8-week aerobic exercise program and its effect on arterial function in breast cancer survivors.

The main questions it aims to answer are:

* Is an 8-week aerobic exercise program feasible in breast cancer survivors after the completion of chemotherapy? * Is this 8-week aerobic exercise program beneficial for vascular function in breast cancer survivors?

Participants will:

* Begin an 8-week aerobic exercise program, three days per week, after the completion of chemotherapy. * Visit our facility three times before the exercise program, 1 month after, and after the completion of the program. * Complete questionnaires, physical functional tests, and body composition and vascular measurements at every visit.

Eligibility criteria

Qualifiers

Women (18+ years) with a stage I-III breast cancer diagnosis who have completed chemotherapies.

Completed the final chemotherapy cycle within the past 4 weeks.

Sedentary by self-reporting inactivity (<90 min of moderate or vigorous exercise per week)

Body mass index ≤40 kg/m²

Disqualifiers

Current pregnant and lactating patients. Must have completed lactation prior to study start.

Metastatic disease.

Diagnosed cardiovascular disease prior to the initiation of chemotherapy, as evidenced by cardiomyopathy (reduced regional or global left ventricular contractility), diastolic dysfunction grade 2 or above, symptomatic coronary artery disease, ejection fraction below 50%.

History of prior chemotherapy received for other cancer diagnosis.

Trial design

Treatments tested in this trial

  • Aerobic Exercise

Treatment groups

40 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators