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Pedopsychiatric and Multidisciplinary Research Devoted to Children Exposed to the Attack in Nice on July 14, 2016

Pedopsychiatric and Multidisciplinary Research (Public Health, Psychodynamics, Neuroscience and Human and Social Sciences) Devoted to Children Exposed to the Attack in Nice on July 14, 2016

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03356028
Acronym
Program14-7
Enrollment
728
Registered
2017-11-29
Start date
2017-11-21
Completion date
2044-12-31
Last updated
2023-09-29

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

Conditions

Psychiatric Disorder, Trauma, Psychological

Keywords

Trauma, Psychiatric Disorder, mass trauma

Brief summary

On July 14, 2016, in Nice, children and their families were attacked by the organization EI. In Nice, 86 deaths, including 10 children, the youngest at 4, were recorded. A number of children, still difficult to assess exactly but over 100, was bereaved. After a traumatic event, multiple clinical consequences may appear in children. Among these consequences, the most common is Post-Traumatic Stress Disorder (PTSD). The aim of the study is to characterize the psycho-social factors of risk and / or protection interfering in the children's future, following the mass trauma of 14 July 2016 in Nice on a sample of pediatric population exposed in comparison of children controls. Ancillary study, entilted The Physalis Child, prospectively observe the presence or not of non-psychotic acousto-verbal hallucinations (AVH) in the population with PTSD from the Program 14-7. The main objective of this ancillary study will be to identify factors of social and emotional cognition linked to the presence of non-psychotic HAV within the cohort of children exposed to the mass trauma of July 14, 2016 in Nice but also to any type of individual trauma. Ancillary study, entilted trail of the 14 July attack, prospectively observe the risk of traumatic reactivation.

Detailed description

On July 14, 2016, in Nice, children and their families were attacked by the organization EI. This is the second time in our country that children are victims of this organization after the attack on the school Ozar Hotarah in March 2012 in Toulouse where four children were killed touching end. In Nice, 86 deaths, including 10 children, the youngest at 4, were recorded. A number of children, still difficult to assess exactly but over 100, was bereaved. After a traumatic event, multiple clinical consequences may appear in children. Among these consequences, the most common is Post-Traumatic Stress Disorder (PTSD). This pathology includes 4 main symptoms: the reviviscences of the event, avoidance behaviors, alterations of cognition and mood and neurovegetative overactivation. In addition, PTSD contributes to the development of many other mental disorders. It is estimated that 75% of adolescents or children having a comorbid disorder with PTSD. In the literature, the main comorbidities identified in pediatric populations are: anxiety disorders, Attention Deficit Hyperactivity Disorder (ADHD) and depression. There is no recommendation as to the therapeutics to be used in psychotraumatism in pediatric population. Epidemiological studies conducted on the consequences of trauma reveal a high variability in the development of psychopathologies. 6 to 20% of exposed children would develop PTSD after a potentially traumatic situation. Several factors can explain the heterogeneity of the results, including the age, the type of trauma experienced, the violence suffered during this trauma. In Nice, to date, more than 2200 children have consulted: 700 children between July 14 and July 28, 2016, 1100 children were seen between August and December, and about 400 since the creation of the Post Traumatic Pediatric Intersectoral Assessment Center (CE2P), in January 2017. The aim of the study is to characterize the psycho-social factors of risk and / or protection interfering in the children's future, following the mass trauma of 14 July 2016 in Nice on a sample of pediatric population exposed in comparison of children controls. Non-psychotic hallucinations represent a significant symptomatology in child psychiatry (1) and remain clinical question. The results of our previous study the physalis child showed a significant correlation between the persistence of non-psychotic acousto-verbal hallucinations (AVH) and the presence of negative emotions, linked to post traumatic stress disorder (PTSD). It seems important to understand the link between trauma and the presence of non-psychotic AVH in children as the literature shows the risk of progression to psychosis when these AVH persist.The interest of the ancllary study of the physalis child would be to prospectively observe the presence or not of non-psychotic AVH in the population with PTSD from the Program 14-7. The question would then be: Why in two subjects diagnosed with PTSD, one has non-psychotic HAV and the other does not? The main objective of this ancillary study will be to identify factors of social and emotional cognition linked to the presence of non-psychotic HAV within the cohort of children exposed to the mass trauma of July 14, 2016 in Nice but also to any type of individual trauma. The impending opening of the trial of the 14 July attack, the conduct and the media coverage associated with the trial are all factors that could be distressing for the children and families exposed to the attack in Nice. Re-exposure to testimonials and certain images can increase the risk of traumatic reactivation with a return of suppressed fears and the symptoms associated. Some factors have been identified as protective: social and family support, cognitive functioning, the presence of residual symptoms or the quality of sleep. Therefore, an assessment of these factors before and after the opening of the trial would identify children and families with traumatic reactivation, as well as identify protective or risk factors for relapse of traumatic symptoms

Interventions

BEHAVIORALChild and adolescent psychiatry and Epidemiology

psychosocial risk assessment questionnaire, structured diagnostic interview, pedopsychiatric questionnaire

OTHERsalivary biological collection

Saliva sampling will be done using a specific kit

BEHAVIORALqualitative analysis of the discourse

two semi-structured interviews, the first with the teenager alone, the second with the lone parents

BEHAVIORALParenthood

Parenting Sense of Competence (PSOC) questionnaires completed online.Two visits will be realized: a first in the month preceding the start of the trial and a second in the month following the end of the trial

BEHAVIORALCognitive alterations

Episodic memory will be assessed using Grober and Buschke. The evaluation of the cognitive alterations will include two stages: a first in the month preceding the start of the trial and a second in the month following the end of the trial. For child and parents

BEHAVIORALImpact on schooling

collect of several data about the number of absences of the child, the number of exclusions and hours of detention of the child, as well as the school reports of the child

BEHAVIORALSleep disorders and associated somatizations

Evaluation of sleep disorders and associated somatizations by connected watche and sleep questionnaire

Sponsors

Fondation Lenval
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Interventional research involving the category 2 human person at minimal risk and constraint, excluding health product, multicentre

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Children and / or young adults who have consulted at the pediatric consultation center of the CHU Lenval or who are listed in the ORSAN organization of the health system response in exceptional health situations file or who have made an appointment following the call by press; * Children and / or young adults under 18 at the time of the Nice attack of 14/07/2016. * Affiliated to a social security scheme; * Having a good command of the French language (French); * Children whose parents have accepted participation in the study (collection of informed consents). Non inclusion: * Children and / or young adults with average intellectual disability (Intelligence Quotient IQ less than 50); * Person deprived of liberty by judicial or administrative decision; * Person subject to an exclusion period for another search.

Exclusion criteria

* a simple request from the child / adolescent and / or young adults or their parents (interruption of participation or withdrawal of consent); * failure to comply with the instructions defined and exposed at the time of inclusion.

Design outcomes

Primary

MeasureTime frameDescription
psychosocial risk assessment questionnaire after 2 yearDifference between baseline and after 2 yearCompletion of the psychosocial risk assessment questionnaire

Secondary

MeasureTime frameDescription
psychosocial risk assessment questionnaire after 10 yearDifference between baseline and after 10 yearCompletion of the psychosocial risk assessment questionnaire
psychosocial risk assessment questionnaire after 15 yearDifference between baseline and after 15 yearCompletion of the psychosocial risk assessment questionnaire
psychosocial risk assessment questionnaire after 20 yearDifference between baseline and after 20 yearCompletion of the psychosocial risk assessment questionnaire
psychosocial risk assessment questionnaire after 25 yearDifference between baseline and after 25 yearCompletion of the psychosocial risk assessment questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 2 yearDifference between baseline and after 2 yearCompletion of the MINI questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 5 yearDifference between baseline and after 5 yearCompletion of the MINI questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 10 yearDifference between baseline and after 10 yearCompletion of the MINI questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 15 yearDifference between baseline and after 15 yearCompletion of the MINI questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 20 yearDifference between baseline and after 20 yearCompletion of the MINI questionnaire
Structured diagnostic interview MINI (Mini International Neuropsychiatric Interview) after 25 yearDifference between baseline and after 25 yearCompletion of the MINI questionnaire
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 2 yearDifference between baseline and after 2 yearCompletion of the CGI-S
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 5 yearDifference between baseline and after 5 yearCompletion of the CGI-S
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 10 yearDifference between baseline and after 10 yearCompletion of the CGI-S
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 15 yearDifference between baseline and after 15 yearCompletion of the CGI-S
psychosocial risk assessment questionnaire after 5 yearDifference between baseline and after 5 yearCompletion of the psychosocial risk assessment questionnaire
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 25 yearDifference between baseline and after 25 yearCompletion of the CGI-S
General operation CGA-S (Children's Global Assessment Scale) after 2 yearDifference between baseline and after 2 yearCompletion of the CGA-S
General operation CGA-S (Children's Global Assessment Scale) after 5 yearDifference between baseline and after 5 yearCompletion of the CGA-S
General operation CGA-S (Children's Global Assessment Scale) after 10 yearDifference between baseline and after 10 yearCompletion of the CGA-S
General operation CGA-S (Children's Global Assessment Scale) after 15 yearDifference between baseline and after 15 yearCompletion of the CGA-S
General operation CGA-S (Children's Global Assessment Scale) after 20 yearDifference between baseline and after 20 yearCompletion of the CGA-S
General operation CGA-S (Children's Global Assessment Scale) after 25 yearDifference between baseline and after 25 yearCompletion of the CGA-S
identify factors of social cognition linked to the presence of non-psychotic acousto-verbal hallucinations (AVH)at baselinecompletion of the NEPSY II for a complete neuropsychological assessment
identify factors of emotional cognition linked to the presence of non-psychotic AVHat baselinecompletion of the EED IV , French version of the Differential Emotions Scale IV (DES-IV
identify the factors of persistence of AVHafter 6 months, 1 year and 2 year from baselinecomplete neuropsychological assessment
impact of trial of the attack July 14th on Parenthoodbaseline and month9Parenthood assessment will be offered to parents of children included in the arm impacted by attack The Parenting Sense of Competence (PSOC) questionnaire is a widely used scale to assess and measure parenting abilities perceived by parents with two subscales: competence/knowledge and appreciation/comfort. The PSOC is a scale with a score ranging from 17 to 102. The higher the score, the more the parent feels a sense of high parenting competence. To demonstrate a minimum difference of 20 points on this questionnaire before and after the trial, with a standard deviation of 20, the number of participants required is 44 Two visits will be realized: a first in the month preceding the start of the trial (baseline) and a second in the month following the end of the trial.
impact of trial of the attack July 14th on Cognitive alterationsbaseline and month 6Evaluation of cognitive alterations, in particular memory disorders and executive functions, will be aimed at children aged 0 to 6 at the time of the July 14, 2016 attack Episodic memory will be assessed using Grober and Buschke (Grober and Buschke, 1988). This test includes 16 items to memorize belonging to 16 different semantic categories. The duration of this test is approximately 20 minutes. This test starts with a control phase of the semantic encoding of words with an immediate cued recall, 3 free and cued recall phases with a 20-second interferential task, a recognition phase and finally a free and deferred cued recall phase to test learning. Previous studies using this test show a mean difference of 2 points between the control groups and the experimental groups. The evaluation of the cognitive alterations will include two stages: a first in the month preceding the start of the trial (baseline) and a second in the month following the end of the trial
impact of trial of the attack July 14th on schooling2 years from baselineEvaluation of the impact of schooling will focus on middle and high school students, using Pronote software and included in the arm impacted by attack . In order to test the impact of the trial on children's education, several data will be requested from parents. Using the Pronote software, they will be able to communicate to us the number of absences of the child, the number of exclusions and hours of detention of the child, as well as the school reports of the child to obtain the effective grades of children and adolescents. This data will be collected for the 2021-2022 school year (3 terms of the previous school year) and for the 2022-2023 school year (3 terms of the current year).
impact of trial of the attack July 14th on Sleep disorders and associated somatizationsbaseline and month 6Evaluation of sleep disorders and associated somatizations will be offered to adolescents in the 14-7 cohort, are children aged 7 to 12 at the time of the attack. The screening scale for sleep disorders in children aged 4 to 16 years by Bruni et al. 1996 . This questionnaire includes an overall sleep quality score, but also sub-indices evaluating insomnia, parasomnia, respiratory problems, non-restorative sleep and excessive daytime sleepiness. The threshold score is 39 and an average score around 25 for the control population. This questionnaire will be carried out during the month preceding the opening of the trial (baseline), then every month, until the end of the trial. From baseline to the end of trial, participants will receive a connected watches to continuously record sleep quality and daytime activity. A questionnaire on Post Traumatic Stress Disorder (PTSD) symptoms will also be completed by the participants at baseline and at the end of trial.
Overall assessment of the individual CGI-S (Clinical Global Impression - Severity) after 20 yearDifference between baseline and after 20 yearCompletion of the CGI-S

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026