Evaluation of Cognitive Function in a Suicidal Crisis
CocaCS
2 other identifiers
observational
140
1 country
1
Brief Summary
The aftermath of suicide is devastating, being the cause of 800 000 deaths every year worldwide. In France, suicide still causes about 10 000 deaths per year and the number of suicide attempts (SA) is estimated between 170 000 and 200 000 per year (InVS). It is often thought that a suicidal crisis is only related to depression, as it actually is a far more complex phenomenon. A suicidal crisis can occur on various grounds like psychiatric disorders but also contextual events or somatic diseases and it has been hypothesized that suicidal ideas or inclinations could have a common and independent cognitive origin
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 20, 2016
CompletedFirst Submitted
Initial submission to the registry
April 26, 2018
CompletedFirst Posted
Study publicly available on registry
May 9, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 25, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 25, 2024
CompletedDecember 23, 2025
September 1, 2020
7.5 years
April 26, 2018
December 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Rate of patients having a score in MoCA test strictly under 26
at inclusion
Secondary Outcomes (3)
Variation in MoCA test scores between before (V1) and after hospitalization (V2)
an average at 3 months after inclusion
Variation in scores to the subtests between between before (V1) and after hospitalization (V2)
an average at 3 months after inclusion
Rate of patients having lower subtests scores than the standards
an average at 3 months after inclusion
Eligibility Criteria
patients hospitalized for less than a week and presenting with a suicidal crisis
You may qualify if:
- Normal or corrected vision
- Having understood the information not and having signed the form of consent
You may not qualify if:
- Pregnant woman and/or nursing
- Diagnosed irrational pathology
- Known proven intellectual deficiency
- Patient whose physical or mental status does not allow to pass the tests of the study
- Being under supervision or trusteeship or private of freedom or in emergency
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHRU,Hôpital Fontan
Lille, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Vincent JARDON, MD
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 26, 2018
First Posted
May 9, 2018
Study Start
September 20, 2016
Primary Completion
March 25, 2024
Study Completion
March 25, 2024
Last Updated
December 23, 2025
Record last verified: 2020-09
Data Sharing
- IPD Sharing
- Will not share