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NCT01333215 Clinical Trial

Study of Cognitive Inhibition Disorders in Depressed Older Suicide Attempters

Suicide, Attempted Clinical Trial

— ETIC  

Official title:
Etude Des Troubles de l'Inhibition Cognitive Chez le Sujet âgé déprimé Suicidant

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01333215
Other study ID # 2010/24
Secondary ID
Status Recruiting
Phase N/A
First received April 7, 2011
Last updated April 8, 2011
Start date December 2010
Est. completion date July 2011

Study information
Verified date December 2010
Source University Hospital, Angers
Contact Stephane Richard-Devantoy, Mr.
Phone ++33 2 41 35 32 43
Email stricharddevantoy@chu-angers.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare the cognitive inhibition deficit among depressed older suicide attempters compared to depressed older suicide non-attempters.

Description:

The main objective consists in examining the association between cognitive inhibition and suicide attempt in depressed older adults (> 65 year old).

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Age > 65 years old

- Score of Mini-Mental State Examination (MMSE) > 23

- Score of Hamilton Depression Scale >27

- For Group 1 (depressed older suicide non-attempters): No history of suicide attempt

- For Group 2 (depressed older suicide attempters) : History of suicide attempt

Exclusion Criteria:

- Neurological history or medical-surgical affection in the past 3 months.

- Dependence or alcohol abuse.

- Use of neuroleptics

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
France University Hospital Angers

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cognitive inhibition deficit baseline No
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