Psychiatric Future of Young Patients Hospitalized in the Pass'Aje Service Between 2006 and 2010 (After Pass'Aje)

February 1, 2019 updated by: University Hospital, Clermont-Ferrand

The emergence of adult psychic disorders occurs in about three quarters of cases before 25 years. The Pass-Aje service of Clermont-Ferrand University Hospital is a psychiatric unit specializing in the management of disorders of young adults. This unit evaluates the first episodes among the diversity of the clinical presentations of the psychic disorders. Suicidal attempts or ideations account for a large part of the reasons for entering the unit and are found transversely in many disorders. Among the reasons for hospitalization are a wide variety of situations that are not initially associated with an accurate diagnosis such as withdrawal, de-schooling, runaways, behavioral disorders (disorders of social interactions, self and hetero aggression, eating disorders).

Investigator propose to study the psychiatric outcome of hospitalized patients in the Pass-Aje unit and their psychosocial evolution in order to compare them with the data of the general population and to identify the factors influencing their future.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Former young psychiatric patients hospitalized in the Pass'Aje units are contacted by phone several years later to determine their psychiatric outcome.

Study Type

Observational

Enrollment (Anticipated)

660

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Clermont-Ferrand, France, 63003
        • Recruiting
        • CHU Clermont-Ferrand
        • Principal Investigator:
          • Eve COURTY

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

23 years to 36 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Young patients hospitalized in psychiatric service

Description

Inclusion Criteria:

  • all patients hospitalized in the Pass'Aje unit between 2006 and 2010
  • Aged from 16 to 25 years when hospitalized

Exclusion Criteria:

  • Patient refusing or not understanding the purpose of the study.
  • Patients who died.
  • Patient phone number unavailable or non-functional

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Formers young patients
all patients hospitalized between 2006 and 2010 in the Pass'Aje unit
Other: Psychiatric future
Former young psychiatric patients are contacted to determine their psychiatric outcome.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychiatric rehospitalisation
Time Frame: at day 1 during the phone call

the psychiatric outcome comprises 3 parameters :

  • ongoing psychiatric follow-up (yes / no)
  • psychotropic treatment in progress (yes / no)
  • psychiatric hospitalizations after the first hospitalization in Pass'Aje (yes / no)
at day 1 during the phone call

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Determination of social outcomes
Time Frame: at day 1 during the phone call
Educational level of obtained by patients will be compared to data of the general population according to sex, age and parents' social environment
at day 1 during the phone call
Percentage of patients with an occupational activity
Time Frame: at day 1 during the phone call
Percentage of patients with an occupational activity will be compared to data of the general population according to sex, age and parents' social environment
at day 1 during the phone call

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Clermont-Ferrand

Investigators

  • Principal Investigator: Eve COURTY, University Hospital, Clermont-Ferrand

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 14, 2017

Primary Completion (Actual)

September 15, 2017

Study Completion (Anticipated)

May 15, 2019

Study Registration Dates

First Submitted

October 2, 2017

First Submitted That Met QC Criteria

October 12, 2017

First Posted (Actual)

October 13, 2017

Study Record Updates

Last Update Posted (Actual)

February 4, 2019

Last Update Submitted That Met QC Criteria

February 1, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CHU-355

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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