Descriptive Study of Mental Activity (URGPSYMAY)

April 6, 2017 updated by: University Hospital, Montpellier

Descriptive Study of Mental Activity in the Emergency Department of the Centre Hospitalier de Mayotte

Provide a description of patients admitted in the psychaitric department of the Mayotte Hospital

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This feature and the proximity of Mayotte with developing countries give this department different specificities, both culturally and medically. Indeed, the local population of lifestyle and specific beliefs, combining Islam and animism. Thus, a person with mental suffering is traditionally treated by a wizard who will come into contact with the spirits that inhabit the person, the community that supports the patient remains at home.

Mayotte is far behind compared to the metropolis where the supply of psychiatric care with a fragile population, a care network being created, and few downstream solutions To handle crisis situations, emergency unit and psychiatric liaison, speaking to general emergencies was established in 2010. It is currently the only access to emergency psychiatric care on the island.

The situations covered by this unit are for patients of all ages and all social and geographical origins, reflecting the demographics of the population.

Investigator has only quantitative data (number of patients / year) and has no qualitative analysis tool. No epidemiological research has been done to date in this direction.

The aim of our study was to analyze the impact of various psychiatric disorders represented Mayotte of the emergency hospital to get a statistical picture of its business.

This description will present to the scientific community the specifics of this department

Study Type

Interventional

Enrollment (Actual)

564

Phase

  • Not Applicable

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

    • Mamoudzou
      • Montpellier, Mamoudzou, France
        • CH de MAYOTTE

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Patient in need of psychiatric care in the emergency department

Exclusion Criteria:

  • Patient leaves the emergency department against medical advice or fugue
  • Patient leaves the service without the medical diagnosis is made
  • Patient in exclusion period determined by a previous search
  • Patients for whom it is impossible give clear information
  • Patient who manifested their opposition to participate in research
  • Patient minor whose parental agreement has been reached
  • Patient on safeguarding justice whose guardian will not be contacted

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

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Psychiatry Consultation
Psychiatry Consultation, it is proposed by one of the investigators, patients that clinical data from this psychiatric examination, conducted as part of their usual care, are recorded as part of the research that their is proposed and explained. An information note is then distributed and not collected their opposition
Psychiatry Consultation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Describe the mental activity
Time Frame: 1 day
Describe the mental activity of the emergency hospital of Mayotte (clinical observations obtained during routine psychiatric consultation) That is to say, describe the different psychiatric pathologies of all patients presenting to the emergency department of CH Mayotte.
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Estimated incidence rates of various psychiatric pathologies
Time Frame: 1 day
Estimated incidence rates of various psychiatric pathologies (clinical observations obtained during routine psychiatric consultation)
1 day
Search factors associated with different pathologies
Time Frame: 1 day
Search factors associated with different pathologies (clinical observations obtained during routine psychiatric consultation)
1 day
Creating a database for further research.
Time Frame: 1 day
Creating a database for further research (clinical observations obtained during routine psychiatric consultation)
1 day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Nicolas MOLINARI, University Hospital of Montpellier, Montpellier, France, 34295

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)

November 4, 2014

Primary Completion (Actual)

April 11, 2016

Study Completion (Actual)

April 11, 2016

Study Registration Dates

First Submitted

November 19, 2015

First Submitted That Met QC Criteria

November 23, 2015

First Posted (Estimate)

November 26, 2015

Study Record Updates

Last Update Posted (Actual)

April 7, 2017

Last Update Submitted That Met QC Criteria

April 6, 2017

Last Verified

March 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 9417
  • 2014-A00807-40 (Other Identifier: RCB number)

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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