Breast Cancer Clinical Trial
Health care has an increasingly demand for mobile applications (App), but studies are rare,
which explore the added value and benefits for patient and physician. Patients in different
disease groups or physicians from different specialties are likely to have different
demands. Research should focus on selected groups to better understand their individual
demands. Our study intends to identify the added value of mobile symptom tracking in a
selected subgroup of patients. We designed an App for breast cancer patients, who receive
ambulant chemotherapy in a breast center. The patients track regularly their well-being and
adverse events (AE) with the smartphone- or web-app and share it with the physician in the
medical consultation. The data entry was designed to meet patient needs based on previous
usability testing.
The reporting of AE and well-being are standardized according to the definitions by CTCAE
4.0 and ECOG-Index to ensure the reliability of patient self-reporting.
The primary outcomes are the number of reported AE, the influence on their subjective
well-being and the acceptance of context specific information. We will include 150
participants in this study. The calculated power is 91% respectively 80% for a 10 %
improvement of well-being and a 2.2 increase of detected AEs.
The results will be compared to patients without App and to patients with App but without
shared information.
- Trial with medical device
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Supportive Care
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