T78 K71 K74 I12.0 I13 N18 N14 I10 E78 I25 E11 I50 E14 Y57.9
Conditions
Interventions
Group 1: App-User group: Medication plan is scanned.
Analysis of PIMs und QoL at beginning and end of the study.
Group 2: Control group: Medication plan is scanned.
Analysis of PIMs und QoL at beginni
Sponsors
Charité Campus Virchow-Klinikum
Eligibility
Sex/Gender
All
Age
18 Years to 95 Years
Inclusion criteria
Inclusion criteria: - Capability to understand the nature of the study (linguistically, physically, mentally) and to participate - written informed consent - age between 18-95 - prerequisite for national standardized medication plan - smartphone/tablet with internet and willingness to use app
Exclusion criteria
Exclusion criteria: - age under 18 - age over 95 - participation in similar study - no smartphone/tablet with internet - no willingness to use app - operating system older IOS12.0 or Android7.0
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The number of PIMs can be reduced significantly using the web application. 2. The individual overall score (calculated through drug interactions and individual factors (such as age, sex)) can be improved significantly. | — |
Secondary
| Measure | Time frame |
|---|---|
| PROMS 1. Reduced side effects due to improved therapy 2. Improved quality of life (validated questionnaires) | — |
Countries
Germany
Contacts
Public ContactSaskia Preissner
Charité
Outcome results
None listed