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This study investigates the use of digital and standardized documentation by patients of frequently occurring adverse events in oncological therapies.
Full description
This research study is structured as a Phase I and II clinical trial. In phase I, the feasibility of using a smartphone application to document adverse events that have occurred during oncological therapies by the patient will be investigated. In phase II we will investigate whether the use of the smartphone app allows an improvement of patient care by reducing occurred adverse events.
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Exclusion criteria
Participants who meet any of the following criteria will be excluded:
66 participants in 1 patient group
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Central trial contact
Thomas Seufferlein, Prof. Dr.
Data sourced from clinicaltrials.gov
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