pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Female breast cancer survivors; aged 30 to 70 years; diagnosis of stage I to III breast cancer; completion of primary cancer treatment, including surgery, chemotherapy and/or radiotherapy, at least three months before enrollment; no evidence of active disease at enrollment; medical clearance from the treating oncologist; medical clearance from the treating cardiologist
Exclusion criteria
Exclusion criteria: Breast cancer recurrence before enrollment; medical contraindication to physical exercise; absence of medical clearance from the treating oncologist or cardiologist; inability to understand or perform the study procedures; clinical conditions that preclude safe participation in the assessments or interventions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in cognition in breast cancer survivors is expected following different physical exercise approaches, determined by changes in Stroop Color and Word Test accuracy and response time, N-back task sensitivity index and response time, as well as task-evoked pupillary response measured by pupillometry, assessed before and after the interventions according to the design of each sub-study;Improvement in pain in breast cancer survivors is expected following different physical exercise approaches, determined by changes in pressure pain threshold and conditioned pain modulation, assessed before and after the interventions according to the design of each sub-study;Improvement in functional status in breast cancer survivors is expected following different physical exercise approaches, determined by changes in completion time in the standard, cognitive, and motor Timed Up and Go tests and dual-task cost, assessed before and after the interventions according to the design of each sub-study;Improvement in cardiovascular health in breast cancer survivors is expected following different physical exercise approaches, determined by changes in pulse wave velocity, augmentation index, blood pressure, heart rate, and heart rate variability, assessed before and after the interventions according to the design of each sub-study | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcome | — |
Countries
BR
Contacts
Universidade Federal de Sergipe