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CompletedNCT01213797IMTAPUpdated Oct 25, 2011

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

An observational study in Suicide, Attempted and Relatives, sponsored by University Hospital, Lille. Completed at 12 sites in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-10-25.

Sponsored by University Hospital, Lille · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
372
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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).

02

Conditions studied

  • Suicide, Attempted
  • Relatives

Keywords

  • Suicide
03

In context

Suicide

701 studies on the registry are indexed under Suicide; 183 are open to participants now.

This study's enrollment of 372 is above the median of 159 across 122 observational studies indexed under Suicide.

Browse Suicide studies →

Lead sponsor

University Hospital, Lille is the lead sponsor of 625 studies on the registry; 141 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

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

Eligibility criteria

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
05

Study design

Time perspective
Prospective
Enrollment
372 participants (actual)

Groups and cohorts

  • 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).

06

What researchers measure

Primary outcomes

  1. Consumption of care in the close relatives of a suicide attempter

    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.

    Time frame: one year

Secondary outcomes

  1. Psychological level of distress

    Psychological level of distress in the close relatives

    Time frame: one year

  2. Links between consumption of care and psychological level of distress

    Links between consumption of care and psychological level of distress

    Time frame: one year

  3. Prevalence of the post-traumatic stress disorder

    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.

    Time frame: one year

  4. Evolution of consumption of care

    Evolution of consumption of care at committing suicide compared to the remainder of the household and the general population

    Time frame: one year

07

Study locations

12 sites
  • University Hospital, Angers
    Angers, France
  • University Hospital, Brest
    Brest, France
  • University Hospital, Caen
    Caen, France
  • University Hospital, Clermont-Ferrand
    Clermont-Ferrand, France
  • University Hospital, Lille
    Lille, France
  • University Hospital, Limoges
    Limoges, France
  • Le Vinatier Hospital
    Lyon, France
  • University Hospital, Nancy
    Nancy, France
  • University Hospital, Nice
    Nice, France
  • Tenon Hospital, Paris
    Paris, France
  • General Hospital, Quimper
    Quimper, France
  • EPSM Lille Metropole
    Tourcoing, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 25, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01213797
Lead sponsor
University Hospital, Lille
Responsible party
Sponsor
First posted
Oct 4, 2010
Start date
Mar 2006
Primary completion
Sep 2010
Completion
Sep 2010
Last update
Oct 25, 2011

Study contacts

Guillaume VAIVA
principal investigator · University Hospital, Lille

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2011. You cannot join it, but the record below documents what was studied.

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