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Clinical Trials/DRKS00011405
DRKS00011405
Completed
Not Applicable

eural and behavioral markers for the motivational negative symptoms of schizophrenia – a longitudinal approach - SyMoNe

Charité - Universitätsmedizin BerlinKlinik für Psychiatrie und Psychotherapie0 sites175 target enrollmentApril 5, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
F20
Sponsor
Charité - Universitätsmedizin BerlinKlinik für Psychiatrie und Psychotherapie
Enrollment
175
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 5, 2017
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Charité - Universitätsmedizin BerlinKlinik für Psychiatrie und Psychotherapie

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in this study, all participants must meet all of the following criteria:
  • 18\-60 years old
  • Written informed consent
  • In patients the diagnostic criteria are:
  • DSM\-5 diagnosis of schizophrenia on the basis of the Structured Clinical Interview for DSM\-5 (SCID\-I)
  • Clinical stability as judged by the treating psychiatrist and indicated by no change in medication in the two weeks prior to the initial assessment

Exclusion Criteria

  • Any potential subject who meets any of the following criteria will be excluded from participation in this study:
  • Any previous neurosurgery or neurological disorder, including epilepsy
  • History of head injury resulting in unconsciousness lasting at least 1 hour
  • Pregnancy or lactation
  • Any contraindications for MRI such as ferromagnetic/non\-MRI\-compatible items or medical devices on or in the body (for example pacemaker, brain stimulator, clips, metal implants)
  • sensorineural hearing loss of 30dB or more or history of tinnitus
  • Incompetency to fully comprehend the purpose of the study or to make a rational decision whether or not to participate
  • In patients additional exclusion criteria are:
  • Benzodiazepine use of more than 1mg lorazepam equivalents per day
  • Comorbid axis\-I disorder

Outcomes

Primary Outcomes

Not specified

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