Randomized controlled clinical study to evaluate a web application (App) to manage and optimize medicatio
- Conditions
- T78K71K74I12.0I13N18N14I10E78I25
- Registration Number
- DRKS00027175
- Lead Sponsor
- Charité Campus Virchow-Klinikum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 128
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
- 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
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. The number of PIMs can be reduced significantly using the web application.<br>2. The individual overall score (calculated through drug interactions and individual factors (such as age, sex)) can be improved significantly.
- Secondary Outcome Measures
Name Time Method PROMS<br>1. Reduced side effects due to improved therapy<br>2. Improved quality of life (validated questionnaires)