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Clinical Trial Summary

Each investigator will have to collect data for 50 hospitalized patients in the Internal Medicine wards. If the center is randomized to Intentional Rounding, the staff of nurses and OSS will have to implement the new care strategy.


Clinical Trial Description

The centers participating in the study are randomized to the Intentional Roundig group and the Control group, in a 1: 1 ratio. In the randomized centers for experimental intervention, a training intervention lasting about 4 hours was conducted by a nurse expert in Intentional Rounding. At the end of the study, training is also scheduled for the Control Centers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04257422
Study type Interventional
Source Fadoi Foundation, Italy
Contact
Status Terminated
Phase N/A
Start date October 21, 2019
Completion date March 29, 2020

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