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Study of Patients Hospitalized in Specialized Cognitive-behavioral Unit (UCC) — UCC  

Behavior Disorders Clinical Trial

Official title:
Patient Outcomes After an Hospitalization in the Specialized Cognitive-behavioral Unit (UCC) of Toulon

Clinical Trial Summary

The purpose of the study is to assess the mortality of patient discharged from the specialized cognitive-behavioral unit (UCC) of Toulon.

Clinical Trial Description

The purpose of specialized cognitive-behavioral unit is to take care of patients demented, valid and with disruptive behavior disorders. The hypothesis is that analyzing the healthcare of these discharged patients might provide a view of the benefices of these units.

The study will be explained to the eligible subjects if they are able to understand it, or to their trusted person, primary caregiver or legal representative.

Medical information will be collected during and after the hospitalization in the specialized cognitive-behavioral unit. The investigator will call the medical staff and the primary caregiver at 3, 6, and 12 months after the patient's discharge, in order to collect study data. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03485898
Study type Observational
Source Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Contact
Status Terminated
Phase
Start date April 12, 2018
Completion date July 31, 2019
View Details
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