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Post Traumatic Stress Disorder and Neural Mechanisms Involved in Its Treatment

Post Traumatic Stress Disorder and Neural Mechanisms Involved in Its Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00893568
Enrollment
62
Registered
2009-05-06
Start date
2009-04-30
Completion date
Unknown
Last updated
2014-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Traumatic Stress Disorders

Keywords

Post traumatic stress disorder PTSD

Brief summary

The post traumatic stress disorder PTSD arises when the physiological response to stress does not come to its term. This study aims to explore the cognitive, psycho physiological and cerebral mechanisms involved in PTSD, in fear conditioning and face matching tasks, before and after treatment.PTSD patients will be recruited by Pr Jean-Claude Samuelian in his service at the Conception Hospital and by Pr Jean-Michel Azorin in his service at the Sainte Marguerite Hospital (Marseille) and will undergo either CBT or EMDR within those same services. The tasks they will be asked to perform will study the psycho physiological, cognitive and central mechanisms involved in PTSD and its treatment. All in all, 17 healthy controls will be recruited as well as 17 PTSD patients for each of the two treatment group.In terms of perspectives, this study would help isolate neural systems functionally involved in PTSD and its treatment. A better knowledge of those mechanisms would set room for the optimization of the current PTSD treatment.

Interventions

OTHERresonance magnetic imaging (fMRI),

a cerebral study will be performed at the neuroanatomic and functional levels by resonance magnetic imaging (fMRI) realized in three times (before, one week and six months after treatment)

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* French speakers * Not hospitalized grown-up patients suffering from a post-traumatic stress disorder ( PTSD) connected to one event. * Subjects Controls: grown-up, mated with the patients in age (18 - 50 years; 4 years maximum of difference of age between a patient and his control), in sex and educational level (schooling of the 3rd level, at the level Bac+8; 3 years maximum of difference of educational level between a patient and his control)

Exclusion criteria

* Pregnancy * Feeding * Nobody under guardianship and grown-up persons being the object of a legal protective measure or not able to express their assent * Alcoholic or addicted to drugs (including medicines) * Other neurological disorders or psychiatric that post-traumatic stress disorder (for patients) * Claustrophobia and contraindications in the IRMf * Subjects controls, no known psychiatric or neurological pathology, as well as no psychiatric history. * Persons private of freedom by a court or administrative order, persons hospitalized without assent * Unability to read French

Design outcomes

Primary

MeasureTime frame
To verify the hypothesis of a levying of inhibition of the CPFm on the tonsil, in the PTSD3 years

Secondary

MeasureTime frame
Studies of the peripheral, cognitive and central mechanisms, before, then 1 week and 6 months after treatment by CBT or EMDR3 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026