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Effects of Treatment of PTSD on Reduced Recall for Fear Extinction

Primary Purpose

Post-traumatic Stress Disorder

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
rTMS: repetitive transcranial magnetic stimulation
SHAM rTMS: repetitive transcranial magnetic stimulation is off
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-traumatic Stress Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • French mother tongue
  • major
  • patient out of hospital
  • patient with health insurance

Exclusion Criteria:

  • patient with dysthymia
  • alcohol dependence, drug dependence
  • acute or chronic psychosis

Sites / Locations

  • Chu de Nice

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

No Intervention

No Intervention

No Intervention

No Intervention

Sham Comparator

Experimental

Arm Label

1

2

3

4.3

4.2

4.1

Arm Description

Safe voluntary.

patient with psychotrauma but without PSTD and without any psychiatric trouble at the time of inclusion

patient with psychotrauma and PTSD (post-traumatic stress disorder) and in full remission at the time of inclusion

patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion

patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion

patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion

Outcomes

Primary Outcome Measures

prefrontal hyperactivation
recall test of extinction (at D21)

Secondary Outcome Measures

neuropsychological tests
two other tests will indirectly assess prefrontal hyperactivation (emotional Stroop and attentional bias)

Full Information

First Posted
October 25, 2010
Last Updated
September 29, 2015
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT01228253
Brief Title
Effects of Treatment of PTSD on Reduced Recall for Fear Extinction
Official Title
Effects of Treatment of Post-traumatic Stress Disorder on Reduced Recall for Fear Extinction
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This preliminary study will examine the differential effects of rTMS on the recall of extinction of conditioned fear in patients suffering from PTSD (post-traumatic stress disorder ) compared with subjects without PTSD but with high risk of relapse.
Detailed Description
It is estimated that nearly 70% of individuals will experiment at least once in their life a traumatic event (eg war, natural disaster, accident or assault). The psychotrauma, whose symptoms (including revivalism, hypersensitivity to the environment, anxiety, avoidance behavior), may be sustainable and thus constitute a posttraumatic stress disorder (PTSD). One characteristic of PTSD can be studied in the laboratory is the lack of recall of extinction of conditioned fear, caused largely by a lack of induction of hyperactivation in the prefrontal cortex. Knowing that this hyperactivation may occur in some cases of remission of symptoms of PTSD, it is possible that the deficit in recall of extinction is lifted in such cases. This idea is also supported by animal models showing that the induction of natural or artificial prefrontal hyperactivation facilitates the recall of extinction. However, no study has yet addressed so far the effects of different treatments (conventional: pharmacotherapy and psychotherapy, or rTMS: repetitive transcranial magnetic stimulation) for PTSD, supposed to induce prefrontal hyperactivation and avoid the recall deficit of extinction of conditioned fear. The persistence of this deficit beyond the remission of PTSD symptoms could represent a situation with a high risk of relapse. Objective. Our main objective is to examine performance in recall of extinction of conditioned fear on the one hand, in patients in remission of PTSD after conventional treatment and, secondly, in patients who received rTMS at 10 Hz Population: THIS PRELIMINARY STUDY will include 9 patients with PTSD, 3 individuals in remission from PTSD, 3 psychotraumatized subjects without secondary PTSD and 3 individuals without a history of psychotrauma. These groups will be matched for age, sex and sociocultural level. Method: All studies will be conducted at the Nice University Hospital. The pre-inclusion visit (D-7), including different clinical evaluations (MINI-DSM-IV, CAPS, PDI, Hamilton Depression Scale and Covi Anxiety), will be held at the Emergency Psychiatric Unit (Hospital Saint-Roch). The study will take place at the Psychiatry University Department and at the Neurology Exploration Department (Hospital Pasteur), where the subjects will have other clinical assessments (at D0, D17-D19, D21), the conditioning test and extinction (day 0) and recall test of extinction (at D21). The fear conditioning (measured by increases in heart rate and skin conductance) corresponds to presentations coupled with an image and tactile stimulation (the intensity of which will be chosen by the subject), while sessions of extinction and extinction recall that correspond to presentations of the image alone (without tactile stimulation). In addition to these sessions, one third of PTSD patients will be treated with rTMS at 10 Hz (D3 to D7 and D10-D14, 1 session / day), another third with placebo treatment and one third without treatment. Eventually (D21), two other tests will indirectly assess prefrontal hyperactivation (emotional Stroop and attentional bias) and self-questionnaires will be performed in all subjects immediately after the recall of extinction. The persistent failure to recall extinction in some individuals in remission from PTSD would sign the maintenance of prefrontal dysfunction, and therefore a high risk of relapse. The induction of hyperactivation using prefrontal rTMS at 10 Hz would not only reduce symptoms of PTSD, but also reduce the risk of recurrence of these symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-traumatic Stress Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
No Intervention
Arm Description
Safe voluntary.
Arm Title
2
Arm Type
No Intervention
Arm Description
patient with psychotrauma but without PSTD and without any psychiatric trouble at the time of inclusion
Arm Title
3
Arm Type
No Intervention
Arm Description
patient with psychotrauma and PTSD (post-traumatic stress disorder) and in full remission at the time of inclusion
Arm Title
4.3
Arm Type
No Intervention
Arm Description
patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion
Arm Title
4.2
Arm Type
Sham Comparator
Arm Description
patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion
Arm Title
4.1
Arm Type
Experimental
Arm Description
patient with psychotrauma and with activ PTSD (post-traumatic stress disorder)at the time of inclusion
Intervention Type
Device
Intervention Name(s)
rTMS: repetitive transcranial magnetic stimulation
Intervention Description
patients will be treated with rTMS at 10 Hz (D3 to D7 and D10-D14, 1 session / day)
Intervention Type
Device
Intervention Name(s)
SHAM rTMS: repetitive transcranial magnetic stimulation is off
Other Intervention Name(s)
SHAM rTMS: repetitive transcranial magnetic stimulation
Intervention Description
patients will be treated with rTMS at 10 Hz (D3 to D7 and D10-D14, 1 session / day with the stimulator on off
Primary Outcome Measure Information:
Title
prefrontal hyperactivation
Description
recall test of extinction (at D21)
Time Frame
Day 21
Secondary Outcome Measure Information:
Title
neuropsychological tests
Description
two other tests will indirectly assess prefrontal hyperactivation (emotional Stroop and attentional bias)
Time Frame
Day 21

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: French mother tongue major patient out of hospital patient with health insurance Exclusion Criteria: patient with dysthymia alcohol dependence, drug dependence acute or chronic psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel BENOIT, PhD
Organizational Affiliation
psychiatry department, Nice University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chu de Nice
City
Nice
ZIP/Postal Code
06000
Country
France

12. IPD Sharing Statement

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Effects of Treatment of PTSD on Reduced Recall for Fear Extinction

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