Suicide, AttemptedETICNCT01333215
Study of Cognitive Inhibition Disorders in Depressed Older Suicide Attempters
An observational study of Suicide, Attempted and Cognitive Symptoms, run by University Hospital, Angers at 1 site in France.
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. Read more about this study
- Who is it for?
- Ages 65 years and olderHealthy volunteers can take part
- Conditions the study is for
- Suicide, Attempted, Cognitive Symptoms
- How many people
- 40 participants
- Where
- 1 siteFrance
- Study dates
- Dec 2010to Jul 2011
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- Healthy volunteers accepted
- Older adult
Study population: Patients are recruited during their hospitalisation at Angers University Hospital with respect to the eligibility criteria
Who may be able to join
- 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
Who cannot join
- Neurological history or medical-surgical affection in the past 3 months.
- Dependence or alcohol abuse.
- Use of neuroleptics
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
University Hospital
Angers, 49933
Stephane Richard-Devantoy, Mr., ++33 2 41 35 32 43, stricharddevantoy@chu-angers.fr
About this study
Official title: Etude Des Troubles de l'Inhibition Cognitive Chez le Sujet âgé déprimé Suicidant
The purpose of this study is to compare the cognitive inhibition deficit among depressed older suicide attempters compared to depressed older suicide non-attempters.
Read the detailed description
The main objective consists in examining the association between cognitive inhibition and suicide attempt in depressed older adults (> 65 year old).
- Conditions
- Suicide, Attempted, Cognitive Symptoms
- Keywords
- Suicide, Attempted, Cognitive Symptoms
- Medical subject headings
- Suicide, Attempted, Neurobehavioral Manifestations
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Group 1 | Depressed older suicide non-attempters | |
| Group 2 | Depressed older suicide attempters |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cognitive inhibition deficit
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Apr 2011 (estimated)
- Study startDec 2010
- Primary completionJul 2011 (estimated)
- Study completionJul 2011 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Suicide, AttemptedStudies of the same condition, open and under way.
- More trials run by University Hospital, AngersThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Angers
- Sponsor type
- Other government
- Investigators
- Stephane Richard-Devantoy, Mr., Principal investigator, University Hospital, Angers
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01333215
- Sponsor's protocol ID
- 2010/24
- Acronym
- ETIC
- Status last verified
- Dec 2010
- First submitted
- 7 Apr 2011
- Last updated
- 11 Apr 2011
- Results posted
- No
- Data monitoring committee
- Yes
Publications
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.
PubMed 21733483
Study at a glance
From the registry record, last updated by the sponsor on 11 Apr 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Etude Des Troubles de l'Inhibition Cognitive Chez le Sujet âgé déprimé Suicidant
- ClinicalTrials.gov ID
- NCT01333215
- Acronym / sponsor ID
- ETIC / 2010/24
- Conditions
- Suicide, Attempted, Cognitive Symptoms
- Keywords
- Suicide, Attempted, Cognitive Symptoms
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- University Hospital, AngersOther government
- Study start
- Dec 2010
- Primary completion
- Jul 2011 (estimated)
- Study completion
- Jul 2011 (estimated)
- First posted
- 11 Apr 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to compare the cognitive inhibition deficit among depressed older suicide attempters compared to depressed older suicide non-attempters.
Detailed description
The main objective consists in examining the association between cognitive inhibition and suicide attempt in depressed older adults (> 65 year old).
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group 1 | – | –Depressed older suicide non-attempters |
| Group 2 | – | –Depressed older suicide attempters |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Older adult
- Study population
- Patients are recruited during their hospitalisation at Angers University Hospital with respect to the eligibility criteria
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (3 listed)
- Neurological history or medical-surgical affection in the past 3 months.
- Dependence or alcohol abuse.
- Use of neuroleptics
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Cognitive inhibition deficit
Time frame: baseline
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Apr 2011.
- Derived from this study: PubMed 21733483Richard-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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stephane Richard-Devantoy, Mr. principal investigator
University Hospital, Angers
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Suicide, Attempted and Cognitive Symptoms, run by University Hospital, Angers at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 11 Apr 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Stephane Richard-Devantoy, Mr. (++33 2 41 35 32 43, stricharddevantoy@chu-angers.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cognitive inhibition deficit (time frame: baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01333215, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2011.