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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University Hospital, Lille
ClinicalTrials.gov Identifier:
NCT01213797
First received: October 1, 2010
Last updated: October 24, 2011
Last verified: July 2011
  Purpose

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.


Condition
Suicide, Attempted
Relatives

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Impact of the Suicide Attempt on the Close Entourage: Traumatic Stress and Medico-economic Concerns, in Medium and Long Term

Resource links provided by NLM:


Further study details as provided by University Hospital, Lille:

Primary Outcome Measures:
  • Consumption of care in the close relatives of a suicide attempter [ Time Frame: one year ] [ Designated as safety issue: No ]
    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.


Secondary Outcome Measures:
  • Psychological level of distress [ Time Frame: one year ] [ Designated as safety issue: No ]
    Psychological level of distress in the close relatives

  • Links between consumption of care and psychological level of distress [ Time Frame: one year ] [ Designated as safety issue: No ]
    Links between consumption of care and psychological level of distress

  • Prevalence of the post-traumatic stress disorder [ Time Frame: one year ] [ Designated as safety issue: No ]

    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.


  • Evolution of consumption of care [ Time Frame: one year ] [ Designated as safety issue: No ]
    Evolution of consumption of care at committing suicide compared to the remainder of the household and the general population


Enrollment: 372
Study Start Date: March 2006
Study Completion Date: September 2010
Primary Completion Date: September 2010 (Final data collection date for primary outcome measure)
Groups/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).


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).

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

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

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01213797

Locations
France
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
Sponsors and Collaborators
University Hospital, Lille
Investigators
Principal Investigator: Guillaume VAIVA University Hospital, Lille
  More Information

No publications provided

Responsible Party: University Hospital, Lille
ClinicalTrials.gov Identifier: NCT01213797     History of Changes
Other Study ID Numbers: DGS 2006/0116, PHRC 2005/1917, 2006/0603
Study First Received: October 1, 2010
Last Updated: October 24, 2011
Health Authority: France: Direction Générale de la Santé

Keywords provided by University Hospital, Lille:
Suicide

Additional relevant MeSH terms:
Suicide
Suicide, Attempted
Self-Injurious Behavior
Behavioral Symptoms

ClinicalTrials.gov processed this record on July 31, 2014