The Choice of a Violent Suicidal Means: a MRI Study With Computational Modeling of Decision-making
SUICIDE_DECIDE
2 other identifiers
observational
40
1 country
1
Brief Summary
The study authors hypothesize a combination of cognitive, brain structural, brain functional and brain connectivity impairments in Suicide Attempters compared to Patient Controls and Healthy Controls, with deficits more marked in suicide attempters using violent suicidal means including:
- 1.Impaired choices at the reversal learning task with responses influenced by immediate outcome. This deficit would be correlated with brain activity in ventromedial Prefrontal Cortex during resting state and with several peripheral markers of the 5HT-system.
- 2.Reduced loss aversion. These deficits would be related to altered dynamics of Blood-Oxygen Level Dependent signal in the dorsal and ventral striatum as well as in ventral Prefrontal Cortex/ orbitofrontal cortex during the loss aversion task. These deficits would also be correlated with several peripheral markers of the 5HT-system.
- 3.Increased pain tolerance facilitating the execution of a violent and possibly painful act. These deficits measured with the algometer would be correlated with several peripheral markers of the 5HT-system.
- 4.Reduced behavioral inhibition in aversive context at the orthogonalized GoNoGo task facilitating the choice of a violent means. These deficits would be associated with altered Blood-Oxygen Level Dependent signal in ventral Prefrontal Cortex/ orbitofrontal cortex and parietal cortex during the resting state and correlated with several peripheral markers of the 5HT-system.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Mar 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 28, 2022
CompletedFirst Posted
Study publicly available on registry
February 8, 2022
CompletedStudy Start
First participant enrolled
March 21, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 8, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 20, 2023
CompletedDecember 10, 2025
December 1, 2025
1.5 years
January 28, 2022
December 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Brain activity between groups
Magnetic Resonance Imaging signal during the resting state and loss aversion task Blood-Oxygen Level Dependent sequences.
Day 0
Secondary Outcomes (4)
Impaired reversal learning between groups
Day 0
Loss aversion between groups
Day 1
Pain tolerance between groups
Day 0
Behavioral inhibition in aversive context between groups
Day 0
Study Arms (4)
Suicide Attempters using Violent Means
A violent suicidal act is any suicidal act conducted with any means except for medication overdose or superficial wrist cutting.
Patient Control
Healthy Controls
Suicide Attempters not using Violent Means
Interventions
The computerized pressure algometer, AlgoMed (Medoc, Ramat Yishai, Israel), will be used for mechanical pain stimulation to assess information about pain threshold and tolerance. A constant rate of pressure is delivered by the examiner, and the pressure is recorded in Kilopascal (kPa). The stimulation will be applied between the medial and distal joints of the phalanges of the dominant hand.
* Two 8s sequences of spin echo field map with phase encoding AP and PA * A 12:00min bold sequence for resting-state * A 15:12min bold sequence for gambling task thickness=2mm, Matrix Size = 105×105, FOV=210×210mm2; * A 6:38min T1w MPR sequence * A 7:40min T1w MPR sequence * A 5:57min T2w SPC sequence * A 8:24min T2w SPC sequence * A 8:32min FLAIR T2w sequence * Two 8:26min Multi-echo GRE sequence * A 8:29min high resolution multi-echo GRE sequence * Two 6:46min multi-echo GRE sequence with and without magnetic transfer contrast * Two 6:03min diffusion weighted images with phase encoding AP and PA
Eligibility Criteria
Four groups of participants will be recruited: 1. 20 individuals with personal history of mood disorder (bipolar disorder or depressive disorders) and at least one suicidal act committed with a violent means within the last 12 months. 2. 20 individuals with personal history of mood disorder (bipolar disorder or depressive disorders) and at least one suicidal act conducted within the last 12 months but no lifetime history of suicidal act with a violent means. 3. 20 individuals with personal history of mood disorder (bipolar disorder or depressive disorders) who never attempted suicide and have no family history of suicidal behavior up to the second biological degree. 4. 20 individuals with no personal history of major mental disorder or suicidal act and no family history of suicidal behavior up to the second biological degree.
You may qualify if:
- Right-handed (as assessed with the Edinburgh Handedness Scale).
- Agreement to participate and sign the informed consent form.
- Is insured or beneficiary of a health insurance plan.
- Speaks French.
- Suicide Attempters using Violent Means group:
- a personal history of mood disorder (bipolar disorder or depressive disorders according to DSM-5 criteria measured with the MINI 7.0);
- at least one suicidal act committed with a violent means within the last 5 years.
- Suicide Attempters using Non-Violent Means group:
- a personal history of mood disorder (bipolar disorder or depressive disorders according to DSM-5 criteria measured with the MINI 7.0);
- at least one suicidal act conducted within the last 5 years;
- no lifetime history of suicidal act with a violent means.
- Patient Control group:
- a personal history of mood disorder (bipolar disorder or depressive disorders according to DSM-5 criteria measured with the MINI 7.0);
- never attempted suicide in their lifetime;
- no family history of suicidal behavior up to the second biological degree.
- +4 more criteria
You may not qualify if:
- Currently under judicial protection, or under adult guardianship.
- Refusal to participate.
- Is pregnant or breast feeding.
- The suicide attempt may have impacted the brain functioning (e.g. following hanging, asphyxia by drowning, head trauma following jumping from height, bullet impact, etc). This criteria will be assessed clinically by the investigator.
- Mental retardation (known or observed during the interview).
- Current psychotic disorder (according to the MINI 7.0).
- Current hypomanic episode (according to the MINI 7.0).
- Current manic, mixed, rapid cycling episodes (according to the MINI 7.0).
- Alcohol or substance disorder within last 3 months (according to the MINI 7.0).
- Past major brain trauma (with loss of consciousness \> 1 minute).
- Contra-indication to MRI (metal in body (including due to suicidal act), claustrophobia, impossibility to lie still on the back during one hour).
- Electroconvulsive therapy within the last three months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU de Nimes
Nîmes, France
Related Publications (1)
Jollant F, Leon C. Suicidal transition rates and their predictors in the adult general population: a repeated survey over 21 years in France. Eur Psychiatry. 2024 Oct 29;67(1):e74. doi: 10.1192/j.eurpsy.2024.1782.
PMID: 39468715RESULT
Biospecimen
Blood and hair samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Fabrice Jollant
CHU Nimes
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 28, 2022
First Posted
February 8, 2022
Study Start
March 21, 2022
Primary Completion
September 8, 2023
Study Completion
September 20, 2023
Last Updated
December 10, 2025
Record last verified: 2025-12