Clinical Trials Directory

Trials / Terminated

TerminatedNCT03485898

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

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

Status
Terminated
Phase
Study type
Observational
Enrollment
58 (actual)
Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Timeline

Start date
2018-04-12
Primary completion
2019-07-31
Completion
2019-07-31
First posted
2018-04-03
Last updated
2019-09-16

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03485898. Inclusion in this directory is not an endorsement.