Study of the Links Between Suicidal Intentionality and Acute Alcoholism (ISA)

August 30, 2017 updated by: University Hospital, Toulouse

There is a strong link between the alcohol consumption and the suicidal risk. Indeed there is an increase of the risk of suicide in case of chronic or acute alcohol consumption. However why the alcohol consumption increase the suicidal risk is unknown.

The hypothesis of this study is that the alcohol consumption induced disinhibition and facilitates the suicide attempt without premeditation

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

People hospitalized after a suicide attempt will answer to two questionnaires about the suicide intentionality and the acute alcohol consumption.

There is 2 arms:

people doing suicide attempt and with positive level of alcohol (up to 0.1g.L) people doing suicide attempt and with negative level of alcohol

110 patients will be included in this study so 55 in each arm.

Study Type

Observational

Enrollment (Actual)

110

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
      • Toulouse, France, 31000
        • University Hospital of Toulouse

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

Sampling Method

Non-Probability Sample

Study Population

people hospitalized in the emergency department after a suicide attempt by voluntary drug intoxication

Description

Inclusion Criteria:

  • patient hospitalized in emergency department for a suicide attempt by voluntary drug intoxication
  • speaking and understanding french

Exclusion Criteria:

  • Patient who has used other psychoactive substances (attested by toxicological analyzes and / or interrogation)
  • Known neurodegenerative pathology

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
positive alcoholism
positive acute alcoholism had questionnaire about suicidal intentionality
Other: questionnaire
after the inclusion patient will answer to a questionnaire about the suicidal intentionality and a second about the alcool consumption
negative alcoholism
negative acute alcoholism had questionnaire about suicidal intentionality
Other: questionnaire
after the inclusion patient will answer to a questionnaire about the suicidal intentionality and a second about the alcool consumption

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
compare the score of suicidal intentionality in patient presenting a positive or a negative alcohol level and doing suicide attempt
Time Frame: 15 minutes
patient will complete the PIERCE questionnaire about the suicidal intentionality
15 minutes

Collaborators and Investigators

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

Sponsor

University Hospital, Toulouse

Investigators

  • Principal Investigator: Juliette SALLES, MD, University Hospital of Toulouse

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)

May 29, 2017

Primary Completion (Actual)

July 31, 2017

Study Completion (Actual)

July 31, 2017

Study Registration Dates

First Submitted

July 24, 2017

First Submitted That Met QC Criteria

July 24, 2017

First Posted (Actual)

July 26, 2017

Study Record Updates

Last Update Posted (Actual)

August 31, 2017

Last Update Submitted That Met QC Criteria

August 30, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RC31/17-0074
  • 2017-A00641-52 (Other Identifier: ID-RCB)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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