- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03355781
Childhood Trauma in Schizophrenia: Exploration of Links Between Gene Expression, Cerebral Morphology and Symptomatology (SCHIZO'TRAUMA)
Childhood Trauma in Schizophrenia: Exploration of Links Between Gene Expression, Cerebral Morphology and Symptomatology. SCHIZO' TRAUMA
Childhood trauma is known as a vulnerability factor in schizophrenia. In healthy volunteers, these adversities are linked to a decrease of grey matter of the brain, similar to those observed in schizophrenia.
In a previous study based on Voxel-Based Morphometry (VBM), including 21 schizophrenic patients and 30 healthy volunteers, the investigators shown a negative correlation between emotional neglect (important dimension in childhood trauma) and grey matter decrease. This strong correlation was significantly higher in schizophrenic patients than in healthy volunteers, suggesting a higher genetic predisposition to environmental factors in schizophrenic people.
Currently, interaction between genetic predisposition and environmental stress factors is the major model for understanding in schizophrenia. In order to analyze both effects on human body, particularly on brain, several studies currently focus on the product of genetic expression, the ribonucleic acid (ARN).
The purpose of this study is to provide an explanatory model of links between childhood trauma, candidate gene for schizophrenia expression, cerebral morphology and schizophrenic symptomatology. Using conceptual framework of stress vulnerability, structural equation modeling (SEM) will allow testing causal link between these different variables.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
-
Saint-Étienne, France, 42055
- CHU de Saint Étienne
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria of patients :
- For women with reproductively active age period: suitable contraceptive method and negative pregnancy test
- Schizophrenia diagnosis (according to DSM 5)
- Regular follow-up care at hospital
- No change in antipsychotic medication (medication AND dosage) within at least six weeks
- Patient into remission : constant dosage, out-patient and meeting Andreassen criteria
- Who have given their informed consent before participating in the study.
- Physical examination without significant clinical physical anomaly
- No serious somatic pathology
- Affiliates or entitled to a social security scheme
Exclusion Criteria of patients :
- For women with reproductively active age period: no suitable contraceptive method (oral, hormonal, intramuscular, intrauterine device, or surgical)
- Pregnancy or breastfeeding
- Not meeting schizophrenic criteria according to DSM 5 or presenting resistant schizophrenic criteria according Kane criteria
- Presenting a serious somatic disorder or neurological (particularly Parkinson disease, epilepsy, tardive dyskinesia)
- Cardiovascular, hepatic or serious renal diseases
- Contraindication to MRI examination, particularly ocular or intracranial metallic foreign object,pacemaker, artificial heart valve, surgical clip
- Claustrophobia, significant tatoo in the high part of the body, IUD incompatible with MRI 3Tesla
- Alcohol or drug addiction, within the last year
- Recruited in other clinical trial or exclusion period from previous trial.
- Susceptibility to self-harm behaviour according to investigator
Inclusion Criteria of Related volunteers :
- Age, gender and socio-educational level similar to recruited patients
- Who have given their informed consent before participating in the study.
- First degree relative of schizophrenic patient diagnosed according DSM IV criteria
- No schizophrenia diagnosis according DSM IV criteria
- No psychiatric history and free of psychotropic drugs/treatment
- Physical examination without significant clinical anomaly
- Affiliates or entitled to a social security scheme
Exclusion Criteria of Related volunteers :
- For women with reproductively active age period: no suitable contraceptive method (oral, hormonal, intramuscular, intrauterine device, or surgical)
- Pregnancy or breastfeeding
- Presenting somatic, neurological or psychiatric disorder
- Alcohol or drug addiction, within the last year
- Recruited in other clinical trial or exclusion period from previous trial.
- Contraindication to MRI examination, particularly ocular or intracranial metallic foreign object, pacemaker, artificial heart valve, surgical clip
- Claustrophobia, significant tatoo in the high part of the body, IUD incompatible with MRI 3Tesla
Inclusion Criteria of Healthy volunteers :
- Age, gender and socio-educational level similar to recruited patients
- Who have given their informed consent before participating in the study.
- No schizophrenia diagnosis according DSM IV criteria
- No personal or family history of psychiatric disorders
- Free of psychotropic drugs/treatment
- Physical examination without significant clinical anomaly
- Affiliates or entitled to a social security scheme
Exclusion Criteria of Healthy volunteers :
Beside the absence of schizophrenia diagnosis, healthy volunteers should meet the same exclusion criteria as patients
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Schizophrenic patients
Patients will have clinical psychiatric evaluation, brain imaging and blood sample
|
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)
|
|
Related volunteers (first degree relative of patient)
Related volunteers will have clinical psychiatric evaluation, brain imaging and blood sample
|
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)
|
|
Healthy volunteers
Healthy volunteers will have clinical psychiatric evaluation, brain imaging and blood sample
|
brain imaging : structural anatomy, emotional congruence, anatomic connectivity, functional connectivity
27,5 ml of blood sample : genetic analysis and biobank
Global Assessment Scale(GAS),Mini International Neuropsychiatric Interview(MINI),Positive and Negative Symptoms Scale(PANSS),Family Interview for Genetic Studies(FIGS),Calgary Depression Scale for Schizophrenia(CDSS),extrapyramidal side effects evaluation or Simpson-Angus scale evaluation(ESRS),Apathy Evaluation Scale(AES-C),State-Trait Anxiety Inventory(STAI),Beck Depression Inventory(BDI-13),Eysenck Personality Questionnaire-Revised(EPQ-R),Assessment of Schizotypal Personality(SPQ),Emotion Regulation Questionnaire(ERQ),Emotional Reactivity Scale(ERS),Toronto Alexithymia Scale(TAS-20),social anhedonia scale(SAS),Childhood Trauma Questionnaire(CTQ),Clinical-administered Post Traumatic Stress Disorder Scale(CAPS),Wechsler Adult Intelligence Scale(WAIS-III),Trail Making Test(TMT),Pen and paper visuospatial working memory(DOT-test),impulsivity test(GoStop),Stroop test,National Adult Reading Test(NART),Wechsler Adult Intelligence Scale(WAIS-III),Facial Emotion Recognition task(FER)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Childhood Trauma Questionnaire (CTQ) for childhood trauma.
Time Frame: 5 days
|
development of an etiopathogenic model characteristic of schizophrenia Childhood Trauma Questionnaire : to assess five types of childhood trauma :
Each item being rated in 5 answer choice from 1 to 5 (never, rarely, sometimes, often or very often) |
5 days
|
|
Quantitative measurement of RNAs
Time Frame: 5 days
|
development of an etiopathogenic model characteristic of schizophrenia
|
5 days
|
|
Voxel-based morphometry (VBM) for total gray matter
Time Frame: 5 days
|
development of an etiopathogenic model characteristic of schizophrenia
|
5 days
|
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Voxel-based morphometry (VBM) for regional gray matter density.
Time Frame: 5 days
|
development of an etiopathogenic model characteristic of schizophrenia
|
5 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Connectivity in the cortico-limbic circuit
Time Frame: 5 days
|
5 days
|
|
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Volumetry of the brain
Time Frame: 5 days
|
5 days
|
|
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Correlation of BOLD activity in the cortico-limbic circuit in patients with patients with symptomatic variables
Time Frame: 5 days
|
symptomatic variables : PANSS scale
|
5 days
|
|
Correlation of BOLD activity in the cortico-limbic circuit with emotional variables
Time Frame: 5 days
|
emotional variables : ERS scale, ERQ scale, TAS-20 scale, SAS scale, AES-C scale
|
5 days
|
|
Correlation of BOLD activity in the cortico-limbic circuit with personality characteristics
Time Frame: 5 days
|
personality characteristics : EPQ-R scale, SPQ scale
|
5 days
|
|
Correlation of BOLD activity in the cortico-limbic circuit with history of trauma in childhood
Time Frame: 5 days
|
history of trauma in childhood : CTQ scale
|
5 days
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1608039
- 2017-A00408-45 (Other Identifier: ANSM)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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