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    <titlStmt>
      <titl>«The assessment of EMDR* to treat post-traumatic-stress-disorder » Involvement of corticotropic and sympathetic axes.</titl>
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      <titl>
                «The assessment of EMDR* to treat post-traumatic-stress-disorder » Involvement of corticotropic and sympathetic axes.            </titl>
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                    EVEREST                </altTitl>
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                FRESH-PEF8571-en            </IDNo>
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                    8571                </IDNo>
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                    FRESH-PEF8571                </IDNo>
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                    Isabelle CHAUDIEU                                                                                                                            </AuthEnty>
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      <othId affiliation="ABC of psychotraumas, Biological" type="collaboration">
                                    </othId>
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      <producer role="sponsor">
                                            INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)                    
                                    </producer>
      <producer role="sponsor">
                                            CENTRE HOSPITALIER UNIVERSITAIRE DE MONTPELLIER (CHU)                    
                                    </producer>
      <producer role="sponsor">
                    
                                    </producer>
      <prodPlac>
                Epidemiology France Portal (PEF)            </prodPlac>
      <fundAg>
                                            MINISTERE DU TRAVAIL, DE LA SANTE, DES SOLIDARITES ET DES FAMILLES                    
                                    </fundAg>
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      <distrbtr abbr="null">
                    null</distrbtr>
      <contact affiliation="INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)" email="isabelle.chaudieu@inserm.fr">
                    Isabelle;CHAUDIEU
                                            <ExtLink title="ROR" URI="https://ror.org/02vjkv261" role="organisation id"/>
                                            <ExtLink title="SIREN" URI="180036048" role="organisation id"/>
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      <depDate date="2026-06-16"/>
      <distDate date="2026-06-16"/>
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    <biblCit format="">
            </biblCit>
    <holdings URI="null"/>
    <notes> </notes>
  </citation>
  <stdyInfo>
    <studyBudget/>
    <subject>
      <keyword vocab="" vocabURI="">
                    Prospective study</keyword>
      <keyword vocab="" vocabURI="">
                    psychiatry</keyword>
      <keyword vocab="" vocabURI="">
                    naturalistic study</keyword>
      <keyword vocab="" vocabURI="">
                    EMDR psychotherapy assessment</keyword>
      <keyword vocab="" vocabURI="">
                    biological markers</keyword>
      <keyword vocab="" vocabURI="">
                    corticotropic and sympathetic axes</keyword>
      <keyword vocab="" vocabURI="">
                    salivary cortisol</keyword>
      <keyword vocab="" vocabURI="">
                    metabolic marker</keyword>
      <keyword vocab="" vocabURI="">
                    heart rate</keyword>
      <keyword vocab="" vocabURI="">
                    cutaneous conductance</keyword>
      <keyword vocab="" vocabURI="">
                    randomized study</keyword>
      <keyword vocab="" vocabURI="">
                    multicenter study</keyword>
      <keyword vocab="" vocabURI="">
                    psychiatric comorbidities.</keyword>
      <keyword vocab="" vocabURI="">
                    Post traumatic stress disorder</keyword>
      <keyword vocab="" vocabURI="">
                    PTSD</keyword>
      <keyword vocab="" vocabURI="">
                    clinical research</keyword>
      <keyword vocab="" vocabURI="">
                    allostatic load</keyword>
      <topcClas vocab="health theme">
                        Endocrinology                                                        <ExtLink title="ESV" URI="http://data.europa.eu/8mn/euroscivoc/d1dd1bac-5313-4ab3-837f-4acd3ec521a7"/>
                                                            <ExtLink title="MeSH" URI="http://id.nlm.nih.gov/mesh/D004704"/>
                                                </topcClas>
      <topcClas vocab="health theme">
                        Psychiatry                                                        <ExtLink title="ESV" URI="http://data.europa.eu/8mn/euroscivoc/3de50dee-da1c-4791-a386-56bca24a5fed"/>
                                                            <ExtLink title="MeSH" URI="http://id.nlm.nih.gov/mesh/D011570"/>
                                                </topcClas>
    </subject>
    <abstract contentType="purpose">The main objective is to compare the effectiveness of EMDR psychotherapy and a supportive psychotherapy in chronic post-traumatic stress disorder patients, through a pragmatic-trial based on a daily practice of a psychiatry sector. Secondary objectives are 1)To study the link between diurnal salivary cortisol secretion and post traumatic symptoms 11)Over all the participants in the survey both at the inclusion and the 3 months visits 12)Over all the EMDR group participants, one year after the beginning of the cares. 2)To study the link between salivary cortisol levels during the EMDR sessions and post traumatic symptoms at 3 months (group 1) 3)To study the link between neurovegetative excitation regulation during the EMDR sessions and post traumatic symptoms at 3 months (group 1) 4)To assess the EMDR psychotherapy effect on a midterm, one year after the first EMDR session.</abstract>
    <abstract contentType="abstract">null</abstract>
    <sumDscr>
      <collDate event="start" date="2010-01-01"/>
      <collDate event="end" date="2014-01-01"/>
      <nation abbr="fr">
                    France
                                            <concept vocab="ISO" vocabURI="fr"/>
                                    </nation>
      <geogCover>Occitanie</geogCover>
      <geogUnit/>
      <anlyUnit>
                Individuals            </anlyUnit>
      <universe level="type" clusion="I">Patients population                    </universe>
      <universe level="sex" clusion="I">Male                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D008297"/>
                                                    </universe>
      <universe level="sex" clusion="I">Female                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D005260"/>
                                                    </universe>
      <universe level="age" clusion="I">Young Adult (19 to 24 years)                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D055815"/>
                                                    </universe>
      <universe level="age" clusion="I">Adult (25 to 44 years)                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D000328"/>
                                                    </universe>
      <universe level="age" clusion="I">Middle Aged (45 to 64 years)                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D008875"/>
                                                    </universe>
      <universe level="age" clusion="I">Aged (65 to 79 years)                                                            <concept vocab="MeSH" vocabURI="http://id.nlm.nih.gov/mesh/D000368"/>
                                                    </universe>
      <universe clusion="I">Women and men aged 18-75 years  - Chronical PTSD patients (for more than 3 months,  diagnosed by the CAPS scale/DSM IV criteria - Patients who are not following a psychotherapy focused on PTSD - Patients that never have followedr a CBT (Cognitive behavioral therapy) or a EMDR psychotherapy focused on the traumatic memory - Patients without psychotropic treatment or who have a stabilized treatment for at least 3 months.                    </universe>
      <dataKind>Clinical data</dataKind>
      <dataKind>Participant-reported health data</dataKind>
      <dataKind>Biological data</dataKind>
    </sumDscr>
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      <standardsCompliance>
        <standard>
          <standardName>DSM IV</standardName>
        </standard>
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    <developmentActivity type="primary evaluation">
      <description>Health event/morbidity
Health care consumption and services
Others</description>
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    <dataColl>
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          <unitType>Through organizations (health services or institutions</unitType>
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        <frameUnit>
          <unitType>schools</unitType>
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        <frameUnit>
          <unitType>businesses</unitType>
        </frameUnit>
        <frameUnit>
          <unitType>etc.)</unitType>
        </frameUnit>
      </sampleFrame>
      <targetSampleSize>
        <sampleSizeFormula>&lt; 500 individuals                        </sampleSizeFormula>
      </targetSampleSize>
      <collMode>Self-administered questionnaire                                                            <concept vocab="CESSDA" vocabURI="SelfAdministeredQuestionnaire"/>
                                                    </collMode>
    </dataColl>
    <notes>Observational Study</notes>
    <notes subject="research type">
                        Observational Study                    </notes>
    <anlyInfo>
      <respRate>- 80</respRate>
    </anlyInfo>
    <stdyClas>Unknown</stdyClas>
  </method>
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    <setAvail>
      <avlStatus>
                            Restricted access                                                    </avlStatus>
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      <conditions>Contact the principal investigator</conditions>
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