Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Washington University School of Medicine
With
National Institute of Mental Health (NIMH)
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Eligibility Criteria Patients:
A physician-confirmed diagnosis of breast cancer (stage I-III)
Female over the age of 18
Scheduled to receive curative-intent breast surgery and chemotherapy (neoadjuvant or adjuvant)
Able to understand and willing to sign an Institutional Review Board (IRB)-approved informed consent document. Given documented mental and cognitive health declines after both neoadjuvant and adjuvant treatment regimens, the investigators are including both patient populations in this exploratory study. Patients of all baseline anxiety, depression, cognitive function, and physical activity levels are eligible to participate.
Eligibility Criteria Stakeholders:
Healthcare personnel with a staked interest in patient care during chemotherapy, including but not limited to surgical oncologists, medical oncologists, physical and occupational therapists, nurses, patient navigators, dietitians, and exercise physiologists
Able to understand and willing to sign an IRB-approved informed consent document
Clareo Health | Mental and Cognitive Health and Physical Activity in the Perioperative Breast Cancer Setting