IMTAP : Impact of the Suicide Attempt on the Nearly Entourage in Term of Traumatic Stress and Medico-economic Impact (IMTAP)

October 24, 2011 updated by: University Hospital, Lille

Impact of the Suicide Attempt on the Close Entourage: Traumatic Stress and Medico-economic Concerns, in Medium and Long Term

With 11.000 deaths and 150.000 attempts each year in France, the suicide represents an important public health problem. For each death by suicide, one can count 6 "direct" bereaved people and 20 people in more indirect connection with this mourning (Terra 2001). In term of impact, there is thus 300.000 people (annually) touched by the deaths by suicide and 3.750.000 people (annually) touched by the "suicide attempt" of a close relative. It seems indeed important to have Public Health data on this cascade repercussion of the suicide attempt.

A suicide attempt propagates a suffering cascade on the various circles of the family and close entourage, which can be measured in term of traumatic stress and medico-economic impact.

Objective = To measure the medico-economic impact on the entourage, in the 3 months following the suicide attempt and at 1 year.

Study Overview

Status

Completed

Detailed Description

Secondary objectives = To measure the impact of the suicide attempt in traumatic term of stress on the close relatives of committing suicide confronted with the suicidal scene To compare the evolution of consumption of care of the close relatives and of committing suicide To measure the evolution of the general health condition of the close relatives and of committing suicide

The study participants (committing suicide it and the relatives) will be recontacted by telephone, after 3 months and to 1 year.

Consumption of care (number of consultations, drugs consumption) of the population of the close relatives of committing suicide will be compared with the data of the Research Institute and Documentation in Economy of Health (IRDES) on the French population (sample of 20.000 people, representative of 95% of the French households).

Study Type

Observational

Enrollment (Actual)

372

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

      • Angers, France
        • University Hospital, Angers
      • Brest, France
        • University Hospital, Brest
      • Caen, France
        • University Hospital, Caen
      • Clermont-Ferrand, France
        • University Hospital, Clermont-Ferrand
      • Lille, France
        • University Hospital, Lille
      • Limoges, France
        • University Hospital, Limoges
      • Lyon, France
        • Le Vinatier Hospital
      • Nancy, France
        • University Hospital, Nancy
      • Nice, France
        • University Hospital, Nice
      • Paris, France
        • Tenon Hospital, Paris
      • Quimper, France
        • General Hospital, Quimper
      • Tourcoing, France
        • EPSM Lille Metropole

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

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

500 families; 500 committing suicide and approximately 900 close relatives.

Description

Inclusion Criteria for Suicide attempter :

  • Men or women
  • Older than 18 years
  • Survivor with an suicide attempt going back to less than 15 days

Inclusion Criteria for close relations of committing suicide :

  • Men or women
  • age more than 18 years
  • Members of the entourage of committing suicide
  • Living under the same roof as committing suicide it

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
Suicide attempter and its entourage

Suicide attempter and its close relatives (who are living under the same roof)

Comparison of the population of the close relations of committing suicide with the data of the Research Institute and Documentation in Economy of Health (IRDES) on the French population (sample of 20.000 people, representative of 95% of the French households).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Consumption of care in the close relatives of a suicide attempter
Time Frame: one year
Consumption of care in the close relatives of a suicide attempter, at the various stages of evaluation, compared with a matched sample in general population (data IRDES). One will be able to thus evaluate not only if the consumption of the close relatives is higher than the average, but still if this difference increases or on the contrary decreases during time.
one year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological level of distress
Time Frame: one year
Psychological level of distress in the close relatives
one year
Links between consumption of care and psychological level of distress
Time Frame: one year
Links between consumption of care and psychological level of distress
one year
Prevalence of the post-traumatic stress disorder
Time Frame: one year

Post-traumatic stress disorder at 3 months and one year, as evaluated by the PTSD Check List Symptoms among members of the entourage having been exposed to the scene of the suicide attempt.

Comparison of prevalence of the post-traumatic disorder of stress compared to the index of lethality of the suicide attempt index.

one year
Evolution of consumption of care
Time Frame: one year
Evolution of consumption of care at committing suicide compared to the remainder of the household and the general population
one year

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Guillaume VAIVA, University Hospital, Lille

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

March 1, 2006

Primary Completion (Actual)

September 1, 2010

Study Completion (Actual)

September 1, 2010

Study Registration Dates

First Submitted

October 1, 2010

First Submitted That Met QC Criteria

October 1, 2010

First Posted (Estimate)

October 4, 2010

Study Record Updates

Last Update Posted (Estimate)

October 25, 2011

Last Update Submitted That Met QC Criteria

October 24, 2011

Last Verified

July 1, 2011

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • DGS 2006/0116
  • PHRC 2005/1917 (Other Identifier: DHOS)
  • 2006/0603 (Other Identifier: Sponsor)

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.

Clinical Trials on Suicide, Attempted

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