PRECLIP: Predictability of the Clinical Global Impression Scale (CGI) in Post Immediate in Psychotraumatic Impact

Sponsor
Centre Hospitalier Arras (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05358067
Collaborator
F2RSM Psy (Hauts-de-France Regional Federation for Research in Psychiatry and Mental Health) (Other)
241
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40
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1.5

Study Details

Study Description

Brief Summary

The objective of this study is to evaluate correlation between Clinical Global Impression Scale (CGI) score immediately in patients who have experienced psychotrauma and occurrence of posttraumatic stress disorder at distance from traumatic event. This could allow, in future, implementation of a systematic telephone reminder of psychotraumatized patients when they have a high score on the CGI scale, and thus detect onset of a stress disorder as early as possible, post-traumatic and orientation of these patients on specialized care.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    A functional unit of Urgent Medical Aid Service (SAMU), Medical-psychological emergency cell (CUMP) is an emergency medical device and provides immediate and post-immediate medico-psychological care for mentally injured people in psychotraumatic situations. CUMP also ensures immediate post follow-up of these patients, as well as departmental organization of psychotrauma consultation.

    During the course of the treatment, victims are oriented, with a telephone callback which can be decided, allowing a remote reassessment of any psychotraumatic sequelae of the event. This phone reminder is part of routine practice following a CUMP intervention. The objective is then early detection of sequelae allowing rapid orientation on specific care pathways, in particular on the consultation of psychotrauma.

    Post-traumatic stress disorder is a syndromic entity reactive to experience of a traumatogenic event (defined by the brutal, sudden and unexpected confrontation with death, or the loss of physical or psychological integrity), bringing together intrusive symptoms of reliving, behavioral avoidance of stimuli related to the traumatic event, persistent negative alterations in cognitions and mood, and neurovegetative hyperactivity, causing clinically significant distress and impaired the usual functioning of the subject.

    Experiencing a psychotraumatic event in one's life is a frequent experience. Epidemiological data show a lifetime prevalence of around 30%. During and/or in the hours following a psychotraumatic event, people experience psychological, physiological and emotional upheavals called peritraumatic distress. Although most people recover on their own, a portion (8.3%) develop post-traumatic stress disorder.

    However, one of the main characteristics of post-traumatic stress disorder is the presence of avoidance symptoms. Avoidance can take different forms such as non-confrontation with all the evocative clues of the traumatic event such as places, people and situations related to the traumatic event, but also the avoidance of thoughts, memories, conversations related to the traumatic event. This avoidance of thoughts and conversations can be a barrier to entry into trauma-focused psychotherapy. Indeed, talking about the traumatic event goes against this avoidance. A proactive approach at a distance from the event to re-evaluate the symptomatology of the people involved and thus propose an orientation towards specialized care in the field of psychotrauma in order to counter avoidance would seem entirely relevant.

    Indeed, studies show the interest of a telephone follow-up by the Medical-Psychological Unit 15 days before an emergency repatriation of French people during the Lebanon war in 2016. On the one hand, remote telephone reminder of event is experienced positively by the people involved in the event and was able to highlight the presence of post-traumatic stress symptoms in 23% of cases. On the other hand, 56% of people were able to be referred to appropriate medio-psychological care following this telephone interview.

    However, depending on the situation, all of the subjects involved in a psychotraumatic event cannot be reassessed, especially when event involves too many people. On the other hand, a significant proportion of subjects will not present psychotraumatic sequelae. Under these conditions, it seems appropriate to be able to define the proportion of psychotraumatized subjects most at risk of developing post-traumatic stress disorder (PTSD). Data from literature find that a high level of peritraumatic distress is largely associated with severity of post-traumatic stress symptoms .

    Thus, peritraumatic distress reactions would be a good indicator of risk of developing a subsequent post-traumatic stress disorder. Several questionnaires exist to assess this peritraumatic distress. However, in a disaster situation and in view of the large number of victims potentially involved, it may be interesting to use a rapid and global assessment tool.

    To do this, the severity item of the global clinical impression scale would respond to this clinical reality.

    Research hypothesis

    Hypothesis is that the severity item of the global clinical impression scale evaluated immediately after in a subject who has experienced a psychotraumatic event is a predictor of post-traumatic stress symptoms at 1 month and 6 months. Investigators expect a correlation between the scores of the PDI and the severity item of the global clinical impression while controlling the socio-demographic characteristics of the worker as well as his clinical experience. Patients included will have similar profiles and will be confronted with the same type of traumatic event.

    Brief Protocol

    • Inclusion visit : psychiatric assessment, socio-demographic data, questionnaire (CGI and Peritraumatic Distress Inventory scale(PDI))

    • Follow-up visit: M1 and M6 : phone call (Post traumatic stress disorder Checklist Scale questionnaire (PCL 5), Mini International Neuropsychiatric Interview (MINI) : major depressive episod, alcohol consumption disorder, substance-related disorder (non-alcoholic).

    Expected results

    Investigators expect this work to confirm the prediction between the initial score on the CGI and the score at M1 and M6 on the PCL5. This result will make it possible to define an initial threshold for the CGI allowing the occurrence of a constituted post-traumatic stress disorder to be predicted, defined by a score greater than or equal to 33 on the PCL5. The objective is to set up a systematic recall protocol for subjects presenting with a state of acute stress for which an initial CGI score will be higher than the determined threshold, in order to be able, depending on the subsequent symptomatology, to offer early management. and focus of post traumatic stress disorder. This reminder protocol will be integrated into routine practices and deployed on the emergency reception service of Hospital.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    241 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Predictability of the Clinical Global Impression Scale (CGI) in Post Immediate in Psychotraumatic Impact
    Anticipated Study Start Date :
    May 1, 2022
    Anticipated Primary Completion Date :
    Apr 30, 2025
    Anticipated Study Completion Date :
    Aug 31, 2025

    Outcome Measures

    Primary Outcome Measures

    1. Psychometric properties of the CGI as a predictor of occurrence of post-traumatic stress disorder [inclusion]

      Clinical Global Impression Scale (CGI) severity item provided with a seven-point scale of severity of patient's clinical condition (1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients.)

    Secondary Outcome Measures

    1. Correlation between CGI score and Peritraumatic Distress Inventory scale score (PDI) [Inclusion]

      Clinical Global Impression Scale (CGI) severity item provided with a seven-point scale of severity of the patient's clinical condition (1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients). PDI consists of 13 likert-style items and total score can range from 0 to 52. Higher total scores represent greater symptom burden. Lower scores represent better outcomes.

    2. Correlation coefficient between CGI score and PCL 5 score at 1 month. [1 month]

      Clinical Global Impression Scale (CGI) severity item provided with a seven-point scale of severity of the patient's clinical condition (1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients). The PCL-5 (Post-traumatic stress disorder Checlist version DSM-5) is a self-assessment comprising 20 items that measures the 20 symptoms of a post-traumatic stress disorder from the DSM-5 (MANUAL. DIAGNOSTIC AND STATISTICS. OF DISORDERS MENTALS. 5th edition.). The objectives of the PCL-5 are numerous, such as monitoring changes in symptoms during and after treatment, screening individuals with an episode of post-traumatic stress, making a provisional diagnosis.

    3. Correlation coefficient between CGI score and PCL 5 score at 6 months. [6 months]

      Clinical Global Impression Scale (CGI) severity item provided with a seven-point scale of severity of the patient's clinical condition (1=normal, not at all ill; 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among the most extremely ill patients). The PCL-5 (Post-traumatic stress disorder Checlist version DSM-5) is a self-assessment comprising 20 items that measures the 20 symptoms of a post-traumatic stress disorder from the DSM-5 (MANUAL. DIAGNOSTIC AND STATISTICS. OF DISORDERS MENTALS. 5th edition.). The objectives of the PCL-5 are numerous, such as monitoring changes in symptoms during and after treatment, screening individuals with an episode of post-traumatic stress, making a provisional diagnosis.

    4. Presence/absence of a major depressive episode at 1 month in connection with traumatic event [1 month]

      Presence/absence of a major depressive episode assessed by the MINI at 1 month. Search for an association between the CGI score and the presence of a major depressive episode. Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    5. Presence/absence of a major depressive episode at 6 months in connection with traumatic event [6 months]

      Presence/absence of a major depressive episode assessed by the MINI at 6 month. Search for an association between the CGI score and the presence of a major depressive episode. Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    6. Presence/absence of a consumption of alcohol at 1 month in connection with traumatic event [1 month]

      Presence/absence of a consumption of alcohol assessed by the MINI at 1 month. Search for an association between the CGI score and the presence of a consumption of alcohol. Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    7. Presence/absence of a consumption of alcohol at 6 months in connection with traumatic event [6 months]

      Presence/absence of a consumption of alcohol assessed by the MINI at 6 month. Search for an association between the CGI score and the presence of a consumption of alcohol. Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    8. Presence/absence of a consumption of substances (except alcohol) at 1 month in connection with traumatic event [1 month]

      Presence/absence of a consumption of substances (except alcohol) assessed by the MINI at 1 month. Search for an association between the CGI score and the presence of a consumption of substances (except alcohol). Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    9. Presence/absence of a consumption of substances (except alcohol) 6 months in connection with traumatic event [6 months]

      Presence/absence of a consumption of substances (except alcohol) assessed by the MINI at 6 month. Search for an association between the CGI score and the presence of a consumption of substances (except alcohol). Mini International Neuropsychiatric Interview (MINI) is a short structured clinical interview which enables researchers to make diagnoses of psychiatric disorders according to DSM-IV or ICD-10 and was designed for epidemiological studies and multicenter clinical trials.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patient who has experienced a traumatic event in the last 48 hours;

    • Patient speaking French;

    Exclusion Criteria:
    • Patient participating in another clinical trial on the treatment of his psychotraumatic experience.

    • Person deprived of liberty (prisoners, defendants);

    • Persons under legal protection (protected adults: under guardianship, curatorship, etc.);

    • Opposition of the patient to participate in the research.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Arras General Hospital Arras France 62000
    2 Douai General Hospital Douai France 59507
    3 Lens General Hospital Lens France 62300
    4 Lille University Hospital Lille France 59000

    Sponsors and Collaborators

    • Centre Hospitalier Arras
    • F2RSM Psy (Hauts-de-France Regional Federation for Research in Psychiatry and Mental Health)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Centre Hospitalier Arras
    ClinicalTrials.gov Identifier:
    NCT05358067
    Other Study ID Numbers:
    • 2021-02
    First Posted:
    May 3, 2022
    Last Update Posted:
    May 3, 2022
    Last Verified:
    Apr 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Centre Hospitalier Arras
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 3, 2022