Complex Post-traumatic Stress Disorder: What Symptomatological Specificities

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-02-17

Study Completion Date

2023-02-28

Brief Summary

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A better understanding of the Complex Post-Traumatic Stress Disorder would allow a management as close as possible to the specificities of this one, but also a better training of professionals and adapted therapeutic indications.

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Detailed Description

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Post-Traumatic Stress Disorder manifests itself in a multitude of symptoms and self-regulation difficulties in various domains (somatization and biological balance, attention and consciousness, regulation of affects and impulses, interpersonal relationships and relational capacities, perception of the aggressor and of the aggression, self-perception and identity, sense and belief system) as well as profound changes in personality and various comorbidities .In addition, dissociation, the origin and the resulting disorders also have some similarities to Complex Post-Traumatic Stress Disorder. Indeed, dissociation is thought to have a traumatic origin and the symptomatology (eg hyperesthesia, dissociative amnesia, anesthesia) is included in Complex Post-Traumatic Stress Disorder. We can then ask ourselves the following questions: is Complex Post-Traumatic Stress Disorder a dissociative disorder in its own right causing difficulties with self-regulation? What is the share of dissociation in Complex Post-Traumatic Stress Disorder?

Conditions

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Psychiatric Health

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Clinical population

having experienced repeated and prolonged traumatic exposure

clinical population

Intervention Type OTHER

or the general population, students of the University of Lille will be offered the opportunity to participate in a study through posters in the corridors of the faculties and announcements in the lecture halls.

General population

Student volunteers from the University of Lille

clinical population

Intervention Type OTHER

or the general population, students of the University of Lille will be offered the opportunity to participate in a study through posters in the corridors of the faculties and announcements in the lecture halls.

Interventions

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clinical population

or the general population, students of the University of Lille will be offered the opportunity to participate in a study through posters in the corridors of the faculties and announcements in the lecture halls.

Intervention Type OTHER

Other Intervention Names

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general poupulation

Eligibility Criteria

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Inclusion Criteria

For clinical population;

* Age between 18 and 65 years old;
* Having experienced repeated and prolonged traumatic exposure;
* Able to understand and answer self-questionnaires;
* Having expressed their free and informed consent
* Affiliated with a social security scheme

For general population:

* Student volunteers from the University of Lille;
* Aged between 18 and 65 years old;
* Able to understand and answer self-questionnaires;
* Having expressed their free and informed consent.

Exclusion Criteria

For clinical population;

* People with difficulties in answering the self-questionnaires (e.g. incomprehension of items, emotional difficulties);
* Persons under tutorship or curatorship;
* Persons deprived of their liberty.

For general population:

* People with difficulties in answering the self-questionnaires (e.g. incomprehension of items, emotional difficulties);
* Persons under tutorship or curatorship;
* Persons deprived of their liberty;
* Persons having a link of subordination with the investigative team.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes