Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05913713

HIIT Following Breast Cancer Chemotherapy

High Intensity Interval Training: Optimizing Exercise Therapy to Mitigate Cardiovascular Disease Risk Following Breast Cancer Chemotherapy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
158 (estimated)
Sponsor
University of Florida · Academic / Other
Sex
Female
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORAL12-week Intervention PeriodResearch participants will be randomly assigned to either high-intensity interval training (HIIT), moderate-intensity continuous training (MICT), or the usual care (UC) group for a 12-week intervention period.
BEHAVIORAL12-week Observation PeriodAfter a 12-week intervention period (HIIT, MICT, or UC), research participants will have a 12-week observation period to assess the durability of two types of different exercises.

Timeline

Start date
2024-03-07
Primary completion
2026-05-31
Completion
2026-05-31
First posted
2023-06-22
Last updated
2025-11-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05913713. Inclusion in this directory is not an endorsement.