- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02615925
Descriptive Study of Mental Activity (URGPSYMAY)
Descriptive Study of Mental Activity in the Emergency Department of the Centre Hospitalier de Mayotte
Study Overview
Status
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Mamoudzou
-
Montpellier, Mamoudzou, France
- CH de MAYOTTE
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Investigators
- Principal Investigator: Nicolas MOLINARI, University Hospital of Montpellier, Montpellier, France, 34295
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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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