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Clinical Trial Summary

A controlled before-after study is performed in order to gain insights into the effectiveness of the CMyLife platform in terms of medication compliance, guideline adherence, quality of life, information provision and patient empowerment. Participants who agreed to use the CMyLife platform for at least 6 months, were enrolled in the treatment group and participants who did not agree to use the platform were enrolled in the control group. After signing informed consent, participants received a baseline questionnaire by mail. Upon completion of the baseline questionnaire, participants used (intervention group) or did not use (control group) the CMyLife platform for at least 6 months, after which they were asked to complete the post-intervention questionnaire.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04595955
Study type Interventional
Source Radboud University
Contact
Status Completed
Phase N/A
Start date July 1, 2019
Completion date August 31, 2020

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