Mobile-Health Delivery of Lifestyle Interventions for Women With Breast Cancer Multicenter Pilot Trial
Sponsor: M.D. Anderson Cancer Center
Trial Details
| Condition | Breast Carcinoma |
| Intervention | Behavioral Intervention; Best Practice; FitBit; Nutrition Education; Physical Activity; Questionnaire Administration |
| Phase | NA |
| Status | Active |
| Participants | 30 |
| Est. Completion | 15 June 2026 |
| Last Updated | 12 June 2026 |
Primary Outcome
Assess the feasibility of delivering a mobile, standardized, comprehensive lifestyle program in women with BCa.
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Women with stage I-III BCa scheduled to undergo radiation therapy (RT) or within the first 12 months of having completed primary treatment (they do not need to have undergone RT) * Underwent chemotherapy and surgery * Able to read, write, and speak English * BMI of 25 or higher * 18 years of age or older * Oriented to person, place, and time * Participants must meet at least two of the following criteria related to their lifestyle at the time of diagnosis: * Consume less than 3 servings of fruit and vegetable/day * Engage in less than 75 minutes of moderate/vigorous intensity activity per week, defined as anything that causes small increases in breathing or heart rate for a sustained amount of time (e.g., brisk walking, bicycling) * Engage in a mind-body practice less than 4 times a month * Access to internet connection * Access to a tablet, laptop or computer * Able to come to University of Texas (UT) MD Anderson or Wake Forest for blood collection * Able to perform light physical activity. if any medical issues exist or arise that may limit performing physical activity, a medical release will be required Exclusion Criteria: * Have not completed chemotherapy; have a recurrent BCa diagnosis; another primary cancer diagnosis within past 5 years (not including non-melanoma skin cancers) * Any major thought disorder (e.g., schizophrenia, dementia) * Any major communication barriers that would preclude being able to complete the intervention (e.g., visually or hearing impaired) * Poorly or uncontrolled diabetes in the opinion of the physician(s) * Extreme mobility issues (e.g., unable to get in and out of a chair unassisted)
Trial Sites
Countries
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