NCT00641498

Brief Summary

Very few studies have proved the effectiveness of treatment for suicide attempt patients. Our objective is to evaluate the addition of the resources of an suicide prevention centre to standard psychiatric treatment in the Emergency Department. Consecutive suicide attempt patients in 2 Emergency departments (multicenter study) were included after standard psychiatric treatment and referral. After Written informed consent, psychological assessment (depression, suicide intention) was carried out After randomisation, control patients were given an information card describing the Suicide Prevention Center (SPC); experimental patients had a first meeting with a psychologist of the SPC. To verify the hypothesis of a decrease in suicidal behaviors in the experimental group, an evaluation of these behaviors was carried out every month during a two year follow-up.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
607

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2007

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2007

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

March 17, 2008

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 24, 2008

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2009

Completed
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2011

Completed
Last Updated

March 30, 2015

Status Verified

March 1, 2015

Enrollment Period

2.8 years

First QC Date

March 17, 2008

Last Update Submit

March 27, 2015

Conditions

Keywords

suicideparasuicidepreventionindividual supportive psychotherapy

Outcome Measures

Primary Outcomes (1)

  • Suicide behavior defined by self poisoning or other suicidal attempts in the emergency departments of the region. Death by suicide will be identified by the examination of information obtained from the national death statistics office (INSERM).

    2 years

Secondary Outcomes (1)

  • Level of depression, suicide ideation, level of despair, level of alexithymia

    2 years

Study Arms (2)

Control

NO INTERVENTION

Usual therapy

Active group

EXPERIMENTAL

Individual supportive psychotherapy initiated in the Emergency department

Behavioral: Psychotherapy

Interventions

PsychotherapyBEHAVIORAL

Individual supportive

Active group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • parasuicide by self-poisoning
  • Glasgow score=15
  • Standard psychiatric treatment

You may not qualify if:

  • No speaking french
  • committed inpatient

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Service d'Accueil des Urgences

Brive-la-Gaillarde, 19100, France

Location

Laboratoire de Stress Post-Traumatique

Toulouse, 31059, France

Location

Related Publications (2)

  • Cailhol L, Marcoux M, Mathur A, Yrondi A, Birmes P. Predictors of prospective suicide attempts in a group at risk of personality disorder following self-poisoning. Front Psychiatry. 2023 Jun 9;14:1084730. doi: 10.3389/fpsyt.2023.1084730. eCollection 2023.

  • Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2.

MeSH Terms

Conditions

Suicide, AttemptedSuicide

Interventions

Psychotherapy

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Behavioral Disciplines and Activities

Study Officials

  • Philippe BIRMES, PhD

    University Hospital, Toulouse

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 17, 2008

First Posted

March 24, 2008

Study Start

March 1, 2007

Primary Completion

December 1, 2009

Study Completion

October 1, 2011

Last Updated

March 30, 2015

Record last verified: 2015-03

Locations