NCT01333215

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2010

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

December 1, 2010

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 7, 2011

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 11, 2011

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2011

Completed
Last Updated

April 11, 2011

Status Verified

December 1, 2010

Enrollment Period

7 months

First QC Date

April 7, 2011

Last Update Submit

April 8, 2011

Conditions

Suicide, AttemptedCognitive Symptoms

Keywords

Suicide, AttemptedCognitive Symptoms

Outcome Measures

Primary Outcomes (1)

  • Cognitive inhibition deficit

    baseline

Study Arms (2)

Group 1

Depressed older suicide non-attempters

Group 2

Depressed older suicide attempters

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodProbability Sample
Study Population

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

You may qualify if:

  • 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

You may not qualify if:

  • Neurological history or medical-surgical affection in the past 3 months.
  • Dependence or alcohol abuse.
  • Use of neuroleptics

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital

Angers, 49933, France

RECRUITING

Related Publications (1)

  • Richard-Devantoy S, Annweiler C, Le Gall D, Garre JB, Olie JP, Beauchet O. Cognitive inhibition in suicidal depressed elderly: a case-control pilot study. J Clin Psychiatry. 2011 Jun;72(6):871-2. doi: 10.4088/JCP.10l06797. No abstract available.

    PMID: 21733483DERIVED

MeSH Terms

Conditions

Suicide, AttemptedNeurobehavioral Manifestations

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehaviorNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Stephane Richard-Devantoy, Mr.

    Angers University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Stephane Richard-Devantoy, Mr.

CONTACT

++33 2 41 35 32 43stricharddevantoy@chu-angers.fr

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

April 7, 2011

First Posted

April 11, 2011

Study Start

December 1, 2010

Primary Completion

July 1, 2011

Study Completion

July 1, 2011

Last Updated

April 11, 2011

Record last verified: 2010-12

Locations

FR(1)