Evaluation of a Regional Post-discharge Monitoring System for Suicide Attempters
EVAL-VIGILANS
2 other identifiers
observational
12,989
1 country
28
Brief Summary
VigilanS is an innovative healthcare program. Participants of this program are all patients leaving in the Nord-Pas de Calais region who survived a suicide attempt. General goals of the post hospitalization monitoring system for suicidal attempters are:
- Standardize general healthcare's practices by offering alert networks and innovative response procedures in case of suicidal crisis.
- Coordinate the various health partners' actions around the patient (GP, psychiatrist, psychologist).
- Contribute to reducing mortality and morbidity by suicide (subsequent suicide) in determined territories. The evaluation of VigilanS will be quantitative and qualitative.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2016
Longer than P75 for all trials
28 active sites
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
September 1, 2016
CompletedFirst Submitted
Initial submission to the registry
April 13, 2017
CompletedFirst Posted
Study publicly available on registry
May 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2020
CompletedOctober 27, 2022
April 1, 2021
4.3 years
April 13, 2017
October 24, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
If patients had or not attempted suicide
Yes or no
6 months
Sex
6 months
Age
inclusion
Marital status
inclusion
Means of suicide attempts
6 months
Reason of suicide attempts
6 months
Length of the hospital stay at inclusion
inclusion
Presence of accompanying people
inclusion
MINI (Mini International Neuropsychiatric Interview) lifetime 5.5.0
psychopathological evaluation
6 months
Columbia Suicide Severity Rating Scale C-SSRS
review of suicidal behaviours and thoughts
6 months
Number of emergency calls
6 months
Number of subsequent suicide attempts
6 months
Number of hospitalization after a suicide attempt
6 months
Secondary Outcomes (9)
Number of suicidal attempts in Nord-Pas de Calais region
each year during 3 years
Local mortality by suicide
each year during 3 years
Number of suicidal conducts in Picardie region
1 year
Number of hospital stays after a suicide attempt
each year during 3 years
Care pathway
1 year
- +4 more secondary outcomes
Study Arms (1)
VigilanS Nord-Pas de Calais cohort
All patients leaving in the Nord-Pas de Calais region and entering in the VigilanS program after a suicide attempt
Eligibility Criteria
All patients leaving in the Nord-Pas de Calais region who survived a suicide attempt and entering in the VigilanS program when they discharge from the hospital
You may qualify if:
- leaving in the Nord-Pas de Calais region
- entering in the VigilanS program after a suicide attempt
You may not qualify if:
- refusal to enter in the program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Lillelead
- Regional Agency of Sante Nord Pas-de-Calaiscollaborator
- Région Nord-Pas de Calais, Francecollaborator
Study Sites (28)
General Hospital, Armentieres
Armentières, France
General Hospital, Arras
Arras, France
General Hospital, Bethune
Béthune, France
General Hospital, Boulogne sur Mer
Boulogne-sur-Mer, France
General Hospital, Calais
Calais, France
General Hospital, Cambrai
Cambrai, France
General Hospital, Denain
Denain, France
General Hospital, Douai
Douai, France
General Hospital, Dunkerque
Dunkirk, France
General Hospital, Fourmies
Fourmies, France
General Hospital, Hazebrouck
Hazebrouck, France
Clinic Fleury, Hénin Beaumont
Hénin-Beaumont, France
Polyclinic, Henin-Beaumont
Hénin-Beaumont, France
General Hospital, Lens
Lens, France
Riaumont's Polyclinic, Liévin
Liévin, France
St Vincent's Hospital, Lille
Lille, France
University Hospital, Lille
Lille, France
St Philibert's Hospital, Lomme
Lomme, France
Genral Hospital, Maubeuge
Maubeuge, France
General Hospital, Montreuil sur Mer
Montreuil-sur-Mer, France
General Hospital, Roubaix
Roubaix, France
Lucien Bonnafé Hospital, Roubaix
Roubaix, France
General Hospital, St Omer
Saint-Omer, France
EPSM, St Venant
Saint-Venant, France
General Hospital, Seclin
Seclin, France
EPSM, Tourcoing
Tourcoing, France
General Hospital, Tourcoing
Tourcoing, France
General Hospital, Valenciennes
Valenciennes, France
Related Publications (4)
Demesmaeker A, Creupelandt C, Leroy A, Vaiva G, D'Hondt F. Impact of posttraumatic stress disorder and comorbid psychiatric conditions on suicide reattempts. Eur J Psychotraumatol. 2025 Dec;16(1):2461435. doi: 10.1080/20008066.2025.2461435. Epub 2025 Feb 12.
PMID: 39936356DERIVEDDemesmaeker A, Amad A, Chazard E, Demarty AL, Schlienger H, Lehmann E, Debien C, Jardon V, Bounebache K, Rey G, Vaiva G. Suicide and All-Cause Mortality Within 1 Year After a Suicide Attempt in the VigilanS Cohort. J Clin Psychiatry. 2023 Sep 11;84(6):22m14520. doi: 10.4088/JCP.22m14520.
PMID: 37707316DERIVEDFossi LD, Debien C, Demarty AL, Vaiva G, Messiah A. Suicide reattempt in a population-wide brief contact intervention to prevent suicide attempts: The VigilanS program, France. Eur Psychiatry. 2021 Jul 16;64(1):e57. doi: 10.1192/j.eurpsy.2021.2221.
PMID: 34266505DERIVEDDuhem S, Berrouiguet S, Debien C, Ducrocq F, Demarty AL, Messiah A, Courtet P, Jehel L, Thomas P, Deplanque D, Danel T, Walter M, Notredame CE, Vaiva G. Combining brief contact interventions (BCI) into a decision-making algorithm to reduce suicide reattempt: the VigilanS study protocol. BMJ Open. 2018 Oct 23;8(10):e022762. doi: 10.1136/bmjopen-2018-022762.
PMID: 30355792DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Guillaume Vaiva, MD, PhD
University Hospital, Lille
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 13, 2017
First Posted
May 1, 2017
Study Start
September 1, 2016
Primary Completion
December 31, 2020
Study Completion
December 31, 2020
Last Updated
October 27, 2022
Record last verified: 2021-04
Data Sharing
- IPD Sharing
- Will not share