Skip to main content
Clinical Trials/NCT03421587
NCT03421587
Completed
Not Applicable

Abnormal Processing of Stressful Social Stimuli After Trauma Exposure, in Particular After Childhood Maltreatment.

University Hospital, Bonn1 site in 1 country100 target enrollmentNovember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post-traumatic Stress Disorder
Sponsor
University Hospital, Bonn
Enrollment
100
Locations
1
Primary Endpoint
Neural substrates of social tactile stimuli processing.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Post-traumatic stress disorder is associated with altered processing of sensory stimuli. The clinical phenotype PTSD has predominantly been described for the visual and auditory sensory modalities. However, PTSD symptoms such as intrusive memories are often evoked by olfactory and tactile cues in the environment. Moreover, little is known about whether aberrant responses to social olfactory and tactile stimuli are also present in a subclinical population.The purpose of this study is to compare trauma-exposed subjects (e.g. childhood maltreatment) with non-exposed controls in the processing of olfactory and tactile stimuli. This sensory characterizations hold potential to identify potential biomarkers for the course of trauma-related disorders and to inform trauma therapies focusing on sensory integration.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
December 2018
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Bonn
Responsible Party
Principal Investigator
Principal Investigator

Rene Hurlemann

Vice Chair of the Department of Psychiatry and Chair of the Medical Psychology Division

University Hospital, Bonn

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent
  • Subjects that have experienced a traumatic event that meets the DSM-5 criteria

Exclusion Criteria

  • Schizophrenia, schizoaffective or other psychotic disorder
  • Neurological disorders
  • Psychotropic medication
  • Subjects suffering from a respiratory tract infection or other respiratory disorder known to affect olfactory functioning at investigator's discretion
  • Subjects with anosmia or other previous primary olfactory dysfunction (olfactory threshold score using the "Sniffin' Sticks" ≤ 5)
  • Dermatitis of the extremities or other skin disorders that affect the skin sensitivity of the extremities

Outcomes

Primary Outcomes

Neural substrates of social tactile stimuli processing.

Time Frame: The neural substrates will be assessed througout fMRI scanning over the course of 20 minutes.

fMRI scanning will be used to measure neural respones to tactile stimuli.

Valence ratings of social tactile stimuli.

Time Frame: Ratings will be assessed throughout fMRI scanning over the course of 20 minutes.

Emotion recognition ratings obtained during a forced-choice emotional face recognition task with stimuli of varying intensities (neutral to fearful).

Time Frame: Ratings will be assessed throughout fMRI scanning over the course of 25 minutes.

Neural substrates of social olfactory stimuli processing.

Time Frame: The neural substrates will be assessed througout fMRI scanning over the course of 25 minutes.

Secondary Outcomes

  • Oxytocin plasma concentrations.(The oxytocin plasma concentrations of all participants will be assessed 15 minutes before fMRI scanning onset..)
  • Olfactory performance in a n-butanol odor staircase threshold test.(The olfactory threshold of all participants will be assessed in a screening session at least 24 hours prior to fMRI scanning.)

Study Sites (1)

Loading locations...

Similar Trials