PRO-RED is a prospective, longitudinal, and multicenter observational study. Enrolled patients will be followed for 6 months in at least monthly intervals in terms of their received red blood cell transfusions and routine myelodysplastic neoplasms (MDS)-associated clinical parameters. In addition, the participating subjects will be provided with a digital/mobile application covering a smartphone app or paper-based questionnaires to answer a set of quality of life (QoL) questions once a week. During routine visits in the clinical trials center performed by the treating physician (at least every month), patients will answer standardized questionnaires for the assessment of MDS-related QoL. Also, included patients will take a photo of fingernails/eyelids with their smartphone camera with the aim to further analyze these pictures in a way to potentially deduct correlated hemoglobin (Hb)-values. As a long term aim beyond the PRO-RED study, the data will serve as a training cohort for the development of an algorithm for image-based calculation of individual Hb levels.
Study Type
OBSERVATIONAL
Enrollment
60
Universitätsklinik Innsbruck
Innsbruck, Austria
Charité Universitätsmedizin Berlin
Berlin, Germany
Klinikum Chemnitz gGmbH
Chemnitz, Germany
Gemeinschaftspraxis Hämatologie-Onkologie
Dresden, Germany
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden, Germany
Universitätsklinikum Düsseldorf
Düsseldorf, Germany
Universitätsklinikum Jena
Jena, Germany
University Hospital Leipzig
Leipzig, Germany
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Mainz, Germany
Universitätsmedizin Mannheim
Mannheim, Germany
...and 1 more locations
health-related quality of life
health-related quality of life assessed by patient reported questionnaires based on EORTC QLQ-C30
Time frame: 6 months
health-related quality of life
health-related quality of life assessed by patient reported questionnaires based on QUALMS
Time frame: 6 months
Course of hemoglobin levels
Hemoglobin level measurements at point of care
Time frame: 6 months
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