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

Terminated

• Conditions: Behavior Disorders

• Registration Number: NCT03485898
• Lead Sponsor: Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

Brief 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.

Study Timeline

• Study First Submitted: 2018-02-22
• Study First Submitted QC: 2018-03-26
• Study First Posted: 2018-04-03
• Study Start: 2018-04-12
• Primary Completion: 2019-07-31
• Study Completion: 2019-07-31
• Status Verified: 2019-09
• Last Update Submitted: 2019-09-13
• Last Update Posted: 2019-09-16

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 58

Inclusion Criteria

• Inpatient at the UCC of Toulon

Exclusion Criteria

• Patient already included in the study ( a patient cannot be included twice during the study)
• Non-affiliated to a social security regimen
• Objection of the patient, the trusted person, the legal representative, the relative or the member of the family (depending on the overall condition of the patient)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mortality rate at 12 month after patient's discharge from UCC	12 months	Number of dead patient at 12 month on the total number of patient included

Secondary Outcome Measures

Name	Time	Method
Analysis of the treatment's mode of delivery	12 months	Descriptive analysis
Assess the primary mortality risk factors regarding all the collected data.	12 months	correlation analysis of collected data and survival data will lead to prediction of survival model with the most relevant survival variable
Create a predictive score for 6 and 12 month mortality	6 and 12 months	all the survival variable will have a score according to the survival prediction model - this endpoint is adressed in order to create a predictive scale/score.
Mortality rate at 3 and 6 month after patient's discharge from UCC	3 and 6 months	Number of dead patient at 3 and 6 month on the total number of patient included
Analysis of the number of treatment taken during the study	12 months	Descriptive analysis
Analysis of the different classes of treatment taken during the study	12 months	Descriptive analysis of the rate of different classes of treatment taken by patient during the study
Mortality rate during the hospitalization in the UCC	12 months	Number of all dead patient on the total number of patient included
Analysis of hospitalisation rate	12 months	Descriptive analysis

Trial Locations

Locations (1)

Centre Hospitalier Intercommunal de Toulon La-Seyne-sur-Mer; 🇫🇷 Toulon, France