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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00563888
Other study ID # SOSS-B6
Secondary ID SOSS-B6
Status Active, not recruiting
Phase N/A
First received November 23, 2007
Last updated November 23, 2007
Start date January 2007
Est. completion date December 2008

Study information

Verified date November 2007
Source University of Konstanz
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

Effective Treatment of PTSD involves talking about the traumatic event in detail.It is unclear how this process influences the sensory-specific trauma network (fear structure)in the traumatized person. The goal of the project is to test the hypothesis that treatment-facilitated recovery does not change the original fear structure but establishes an inhibitory mechanism that depends on verbal activity. An affective visual steady-state paradigm in magnetencephalography (MEG) using positive, aversive and neutral picture stimuli will be used to examine the spatial and temporal pattern of the processing of emotional stimuli. To examine the effects of treatment this paradigm will be used as outcome measure within a randomized controlled trial of Narrative Exposure Therapy and a waiting-list control condition for severely traumatized torture victims.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30
Est. completion date December 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- experiences of organized violence/torture

- PTSD diagnosis

Exclusion Criteria:

- psychotic disorder

- neurological disease or seizures

- current drug/alcohol abuse

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
NET
Narrative Exposure Therapy for traumatized survivors of organized violence

Locations

Country Name City State
Germany University of Konstanz, Department of Psychology Konstanz

Sponsors (2)

Lead Sponsor Collaborator
University of Konstanz German Research Foundation

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary PTSD diagnosis and severity score according to the Clinicians Administered PTSD Scale (CAPS) 4 & 9 months after completion of treatment
Secondary steady state visual evoked magnetic fields in response to affective stimuli 4 & 9 months after completion of treatment
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