Study of Cognitive Inhibition Disorders in Depressed Older Suicide Attempters (ETIC)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2010 by University Hospital, Angers.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University Hospital, Angers
ClinicalTrials.gov Identifier:
NCT01333215
First received: April 7, 2011
Last updated: April 8, 2011
Last verified: December 2010
  Purpose

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


Condition
Suicide, Attempted
Cognitive Symptoms

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Etude Des Troubles de l'Inhibition Cognitive Chez le Sujet âgé déprimé Suicidant

Resource links provided by NLM:


Further study details as provided by University Hospital, Angers:

Primary Outcome Measures:
  • Cognitive inhibition deficit [ Time Frame: baseline ] [ Designated as safety issue: No ]

Estimated Enrollment: 40
Study Start Date: December 2010
Estimated Study Completion Date: July 2011
Estimated Primary Completion Date: July 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts
Group 1
Depressed older suicide non-attempters
Group 2
Depressed older suicide attempters

Detailed Description:

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

  Eligibility

Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Patients are recruited during their hospitalisation at Angers University Hospital with respect to the eligibility criteria

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01333215

Contacts
Contact: Stephane Richard-Devantoy, Mr. ++33 2 41 35 32 43 stricharddevantoy@chu-angers.fr

Locations
France
University Hospital Recruiting
Angers, France, 49933
Contact: Stephane Richard-Devantoy, Mr.    ++33 2 41 35 32 43    stricharddevantoy@chu-angers.fr   
Sponsors and Collaborators
University Hospital, Angers
Investigators
Principal Investigator: Stephane Richard-Devantoy, Mr. Angers University Hospital
  More Information

No publications provided by University Hospital, Angers

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Stéphane Richard-Devantoy, Angers University hospital
ClinicalTrials.gov Identifier: NCT01333215     History of Changes
Other Study ID Numbers: 2010/24
Study First Received: April 7, 2011
Last Updated: April 8, 2011
Health Authority: France: Ministry of Health

Keywords provided by University Hospital, Angers:
Suicide, Attempted
Cognitive Symptoms

Additional relevant MeSH terms:
Suicide
Suicide, Attempted
Neurobehavioral Manifestations
Self-Injurious Behavior
Behavioral Symptoms
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms

ClinicalTrials.gov processed this record on August 28, 2014