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Cognitive Inhibition, Psychosocial Interactions and Suicide Attempt in Elderly

Cognitive Inhibition Impairment and Suicide Attempt in Elderly: Eye Tracking Characterization and Impact of Psychosocial Interactions

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02858427
Acronym
OBSUIVAL
Enrollment
36
Registered
2016-08-08
Start date
2017-02-06
Completion date
2020-02-06
Last updated
2017-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide

Keywords

cognitive inhibition, elderly, suicide attempt, depression

Brief summary

The study aims to determine the correlation between the cognitive inhibition impairment and the history of suicide attempt in elderly depressed patients.

Detailed description

2 groups of patients will be studied: in the first group, depressed patients with a history of suicide attempt will be included whereas in the second group, depressed patients without a history of suicide attempt will be included. For each group, the cognitive inhibition will be assessed trough an eye tracker task (antisaccade). Both groups will also be compared on their neuropsychological characteristics and the quality of social interactions of participants.

Interventions

BEHAVIORALeye tracking

several oculomotor parameters will be recorded using vide-oculography techniques (eye tracking) trough different tasks: saccade, antisaccade, and picture scanning. Saccade task: the patient is looking at a screen and is asked to fix his gaze as quickly and accurately as possible on the red dot appearing on the periphery of the screen. Prosaccade task: the patient is looking at a screen and is asked to fix his gaze as quickly and accurately as possible on the opposite side relative to the red dot appearing on the periphery of the screen. Picture Scanning: participant is instructed to freely watch pictures with different emotional valence.

BEHAVIORALneuropsychological assessement

the neuropsychological assessment aims to identify any impairment of executive functioning through several tasks: Mini mental state examination (mmse), isaac set test (STI) trail making test (TMT A and B), Grober test, Stroop test, verbal fluency, Go No Go task, memory impairment screen (MIS), picture naming test (DO30), copying figure test, digit span and categorical matching test.

this evaluation aims to characterize the mental status of the patient. Different scales will be used: Montgomery and ASberg depression rating scale (MADRS), Columbia-suicide severity rating scale (C-SSRS), Beck depression inventory (BDI), Barratt impulsiveness scale (BIS-10), Buss and Durkee Hostility Inventory (BDHI), Balloon, analogue risk task (BART), Iowa gambling task (IGT), and Childhood trauma questionnaire (CTQ).

this interview aims to characterize social interactions of the patients, their duration, their evolution and the perception of each participant on this subject.

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* major depressive disorder according to Diagnostic ans Statistical Manual (DSM) V * group 1: with a history of suicide attempt * group 2: without a history of suicide attempt

Exclusion criteria

* other psychiatric disease * guardianship

Design outcomes

Primary

MeasureTime frame
antisaccade error rate1 month max. after inclusion

Secondary

MeasureTime frameDescription
saccade accuracy1 month max. after inclusiondistance between the eye position at the end of the first saccade, and the ideal position to engage the target in central vision
saccadic intrusion1 month max. after inclusiongaze deviation into a saccade greater than 3° during visual fixation
maximal speed of the gaze1 month max. after inclusionmaximum speed of visual tracking without triggering any saccade
saccade reaction time1 month max. after inclusion
fixation duration on pictures1 month max. after inclusion
social interaction quality score6 month max. after inclusion

Other

MeasureTime frame
neuropsychological test score1 month max. after inclusion

Countries

France

Contacts

Primary Contactjulie monnin, PhD
jmonnin@chu-besancon.fr0033381218543
Backup Contactkristina mouyabi
kmouyabi@chu-besancon.fr0033381218356

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026