Using Holistic Approaches to Optimize Outcomes for Latina Breast Cancer Survivors
Lay Description
We will assess physical functioning, daily physical activity with wearable activity monitors, biological markers (serum and salivary cortisol), diet, program adherence, as well as psycho-social measures of physical, mental, and spiritual wellbeing. In addition, BCS will be asked to describe their best day possible and their typical day. We will conduct a qualitative analysis from their responses to identify endorsement of themes.
Category
- Cancers and Other Neoplasms
- Breast - Female
- IRB Number
- 20220300HU
- NCT Number
- NCT # not yet entered
Eligibility
- Eligible Ages
- >18
- Eligible Genders
- Female
- Accepts Healthy Volunteers
Inclusion Criteria
1. Adults, age greater than 18 years
2. Have been given a diagnosis of breast cancer in their lifetime:
• Must be post diagnosis
• May be on active treatment or post treatment
3. Have access to a “SMART” device (mobile phone) with internet access to download the BlueJay application to complete questionnaires, respond to app messaging, and watch recorded intervention videos and/or livestream sessions.
4. Be able to speak and understand English or Spanish at the 8th grade level or higher.
5. Able to travel to the UT Health campus at least twice over the 6 months.
6. Oriented to time and place
7. COVID-19 vaccination
Exclusion Criteria
1. They present with any cognitive impairment that limits their ability to understand and provide informed consent, or to comply with the protocol procedures.
2. Are currently enrolled in a competing biobehavioral intervention protocol.
3. Currently in an active yoga program (>weekly classes/practice) for the past 3 months
4. Currently in an active meditation practice, any type > weekly, for the past 3 months
5. Present with any absolute contraindication to exercise testing as detailed by the
American College of Sports Medicine Guidelines on Exercise Testing and
Exercise Prescription. Specifically:
Known significant change in the resting ECG, suggesting significant ischemia.
Recent myocardial infarction (within 2 days).
Unstable angina.
Uncontrolled cardiac arrhythmias causing symptoms or hemodynamic compromise.
Severe symptomatic aortic stenosis.
Uncontrolled symptomatic heart failure.
Acute pulmonary embolus or pulmonary infarction.
Acute myocarditis or pericarditis.
Suspected or known dissecting aneurysm.
Study Design
Arm Groups
Study Contact
Frances Crawford
210-450-5037
crawfordf1@uthscsa.edu
Daniel Hughes
210-562-6506
hughesdc@uthscsa.edu
Myrna Montenegro
210-450-5954
montenegro@uthscsa.edu
Kathleen Rodriguez
210-450-1365
rodriguezk3@uthscsa.edu
Natalie Rodriguez
210-562-6546
rodriguezn6@uthscsa.edu
Benjamin Schleif
210-450-1366
schleifb@uthscsa.edu
Morgan Seekatz
210-450-1133
seekatz@uthscsa.edu
Principal Investigator
Amelie Ramirez