Assessment of Dissociative Traumatic Disorders

NCT ID: NCT04379648

Last Updated: 2020-05-07

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

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-05

Study Completion Date

2021-09-05

Brief Summary

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More than 70% of ambulatory patients with IDD have attempted suicide (APA, 2015). This disorder, as well as all the disorders on the dissociation spectrum, must therefore be clarified and better diagnosed.

The goal of this research is :

1. to assess the prevalence of dissociative disorders using specific tools in patients suffering from PTSD.
2. to validate the French version of the DDIS interview (Ross, 1997) that the investigators have translated.

Detailed Description

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Conditions

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Posttraumatic Stress Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

All patients with a diagnosis of Post Traumatic Stress Disorder will be seen by a physician psychiatrist or psychologist who will introduce them to the study. They will be given an information letter and a consent form. If patients agree to participate in the study, and after signing the consent form, they will be included and will complete the assessment scales.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Posttraumatic stress disorder

cohort of patients with Posttraumatic stress disorder PTSD

Group Type OTHER

self-assessment and hetero-assessment

Intervention Type OTHER

Self assessment for the passing of the following rating scales CTQ-SF36-ITQ-PCL5-DES Hetero-assessment for the pasing of the following rating scales DDIS FR and medical interview

Interventions

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self-assessment and hetero-assessment

Self assessment for the passing of the following rating scales CTQ-SF36-ITQ-PCL5-DES Hetero-assessment for the pasing of the following rating scales DDIS FR and medical interview

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient diagnosed with PTSD according to DSM 5 criteria
* Over 18 years of age
* Informed consent signed

Exclusion Criteria

* Neurological disorders
* Serious and/or unstable somatic pathologies
* Patient not affiliated with social security
* Patient hospitalized under restraint in psychiatric care by decision of the state representative or in psychiatric care at the request of a third party
* Patient under guardianship
* Patient participating in parallel in another biomedical research
* Change of antidepressant in the last three months
* Patient not mastering the French language
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Januel

OTHER

Sponsor Role lead

Responsible Party

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Januel

Clinical research unit manager

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Khalid KALALOU, Psychiatrist

Role: PRINCIPAL_INVESTIGATOR

EPS Ville Evrard

Locations

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Youcef BENCHERIF

Neuilly-sur-Marne, Île-de-France Region, France

Site Status RECRUITING

Countries

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France

Central Contacts

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BENCHERIF Youcef, CRA

Role: CONTACT

0143093030

Rusheenthira THAVASEELAN, CRA

Role: CONTACT

0143093030

Facility Contacts

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Youcef BENCHERIF, CRA

Role: primary

0143093030

Other Identifiers

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10477M-TEDI

Identifier Type: -

Identifier Source: org_study_id

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