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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03519802
Other study ID # 2015_84
Secondary ID 2016-A00881-50
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2016
Est. completion date October 2022

Study information

Verified date September 2020
Source University Hospital, Lille
Contact Vincent JARDON, MD
Email vincent.jardon@chru-lille.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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


Recruitment information / eligibility

Status Recruiting
Enrollment 165
Est. completion date October 2022
Est. primary completion date October 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Normal or corrected vision

- Having understood the information not and having signed the form of consent

- Being hospitalized for suicidal ideas (Score with inclusion at the level of Beck > 3) or after a suicide attempt of less than one week.

Exclusion criteria:

- 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHRU,Hôpital Fontan Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of patients having a score in MoCA test strictly under 26 at inclusion
Secondary Variation in MoCA test scores between before (V1) and after hospitalization (V2) an average at 3 months after inclusion
Secondary Variation in scores to the subtests between between before (V1) and after hospitalization (V2) an average at 3 months after inclusion
Secondary Rate of patients having lower subtests scores than the standards an average at 3 months after inclusion
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