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Clinical Trials/DRKS00009687
DRKS00009687
Completed
未知

Providing Tools for Effective Care and Treatment of Anxiety Disorders (AD): Outcomes, Mediators and Moderators of Enhanced Extinction Learning (MRI subproject P4: Neural response and Fear Circuitry Activity Related to Extinction Learning and Outcome) - PROTECT-AD subproject P4

Technische Universität Dresden, Institut für Klinische Psychologie und Psychotherapie0 sites445 target enrollmentNovember 18, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
F40.1
Sponsor
Technische Universität Dresden, Institut für Klinische Psychologie und Psychotherapie
Enrollment
445
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 18, 2015
End Date
July 24, 2019
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Technische Universität Dresden, Institut für Klinische Psychologie und Psychotherapie

Eligibility Criteria

Inclusion Criteria

  • on or more of the following DSM\-V Anxiety Disorders: Panic disorder, Agoraphobia, Social
  • Anxiety Disorder, Specific Phobia
  • HAMA – Score \= 18
  • CGI – Score \= 3
  • Can attend Therapie regularly (with or without suppot)
  • Informed Consent
  • Healthy control group: • No DSM\-5 Diagnosis • Informed Consent

Exclusion Criteria

  • Every reason the protocol may not be upheld (e.g. planned hospitalization within study time frame, planning to move away, etc.)
  • Current Suicidal tendency
  • DSM\-V Bipolar Disorder
  • DSM\-V Psychotic Disorder
  • DSM\-V Borderline PD
  • Current treatment of other Mental Disorder (Drugs, Psychotherapy)
  • Current Alcohol, Benzodiazepine or other Substance Use Disorders
  • Severe medical illness/condition (every serious physical illness, including cardiovascular, kidney, endocrinological and neurological conditions, Hepatitis or other clinical findings that suggest a severe illness and may affect participation in the study)
  • Pregnancy
  • MRI exclusion criteria (e.g., metal in body)

Outcomes

Primary Outcomes

Not specified

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