About this trial
The purpose of this study is to assess the feasibility of a 4-week intervention combining exercise and transcranial alternating current stimulation (Ex+tACS) in breast cancer survivors who report experiencing cancer-related cognitive impairment. Feasibility will be assessed by measuring participant retention, adherence, satisfaction with the intervention, and safety. The researchers will also examine pre-to-post intervention changes in attention, executive function, working memory, perceived cognitive function, and physical function before, after, and four weeks post intervention completion in the Ex+tACS group compared to a control group who will receive exercise and a placebo tACS condition (CON).
Eligibility criteria
Qualifiers
Diagnosed non-metastatic breast cancer (stages 0-3)
Completed primary breast cancer treatment (surgery, chemotherapy, radiation) for at least 3 months
Self-reported cognitive impairment after cancer treatment
Disqualifiers
Current participation in aerobic exercise for ≥60 min/wk
Contraindication or impairment that precludes the potential participant from exercise as defined by the American College of Sports Medicine
The presence of serious medical illnesses, metal implants, previous brain trauma, epilepsy or history of seizures, previous surgery to the head or spinal cord, or skin problems at the forehead area where the tACS electrodes will be applied
Uncontrolled cardiovascular disease
Trial design
Treatments tested in this trial
- Exercise + transcranial alternating current stimulation (Ex+tACS)
- Control
Treatment groups
Sponsors and collaborators
Florida Atlantic University
Lead sponsor
Memorial Sloan Kettering Cancer Center
Collaborator
Florida Department of Health
Collaborator