ID

23080

Description

Responsible Party: Technische Universität Dresden ClinicalTrials.gov Identifier: NCT02605668 History of Changes Other Study ID Numbers: 01EE1402A DRKS00008743 ( Registry Identifier: German Clinical Trials Register ) Study First Received: August 24, 2015 Last Updated: August 2, 2016 Providing Tools for Effective Care and Treatment of Anxiety Disorders (PROTECT-AD) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT02605668

Lien

https://clinicaltrials.gov/ct2/show/NCT02605668

Mots-clés

Versions (1)
  1. 22/06/2017 22/06/2017 -
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22 juin 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Anxiety Disorders DRKS00008743 NCT02605668 DRKS00008743

Anglais

Eligibility Anxiety Disorders NCT02605668 DRKS00008743

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Ages Eligible for Study: 15 Years to 70 Years (Child, Adult, Senior)
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
one or more of the following DSM-IV/5 anxiety disorders: Panic Disorder, Agoraphobia, Social Anxiety Disorder, Specific Phobia
Description

Anxiety disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0003469
HAMA - Score > 18
Description

Hamilton Anxiety Rating Scale Questionnaire

Type de données

boolean

Alias
UMLS CUI [1]
C3541258
CGI - Score > 3
Description

Clinical Global Impression Questionnaire

Type de données

boolean

Alias
UMLS CUI [1]
C3639708
Can attend therapy regularly (with or without support)
Description

Compliance

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
Informed Consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Description

Control Group

Type de données

boolean

Alias
UMLS CUI [1]
C0009932
Every reason the protocol may not be upheld (e.g. planned hospitalization within study time frame, planning to move away, etc.)
Description

Study protocol

Type de données

boolean

Alias
UMLS CUI [1]
C2348563
Current suicidal tendency
Description

Suicidal tendency

Type de données

boolean

Alias
UMLS CUI [1]
C0235196
DSM-5 Bipolar Disorder
Description

Bipolar Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0005586
DSM-5 Psychotic Disorder
Description

Psychotic Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0033975
DSM-5 Borderline Personality Disorder
Description

Borderline Personality Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0006012
Current treatment of other mental disorder (drugs, psychotherapy)
Description

Treatment of mental disorder

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0087111
Current Alcohol, Benzodiazepine or other Substance Use Disorders
Description

Substance Use Disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0038586
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)
Description

Comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
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Similar models

Eligibility Anxiety Disorders NCT02605668 DRKS00008743

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
Ages Eligible for Study: 15 Years to 70 Years (Child, Adult, Senior)
boolean
C0001779 (UMLS CUI [1])
Anxiety disorders
Item
one or more of the following DSM-IV/5 anxiety disorders: Panic Disorder, Agoraphobia, Social Anxiety Disorder, Specific Phobia
boolean
C0003469 (UMLS CUI [1])
Hamilton Anxiety Rating Scale Questionnaire
Item
HAMA - Score > 18
boolean
C3541258 (UMLS CUI [1])
Clinical Global Impression Questionnaire
Item
CGI - Score > 3
boolean
C3639708 (UMLS CUI [1])
Compliance
Item
Can attend therapy regularly (with or without support)
boolean
C1321605 (UMLS CUI [1])
Informed Consent
Item
Informed Consent
boolean
C0021430 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Study protocol
Item
Every reason the protocol may not be upheld (e.g. planned hospitalization within study time frame, planning to move away, etc.)
boolean
C2348563 (UMLS CUI [1])
Suicidal tendency
Item
Current suicidal tendency
boolean
C0235196 (UMLS CUI [1])
Bipolar Disorder
Item
DSM-5 Bipolar Disorder
boolean
C0005586 (UMLS CUI [1])
Psychotic Disorder
Item
DSM-5 Psychotic Disorder
boolean
C0033975 (UMLS CUI [1])
Borderline Personality Disorder
Item
DSM-5 Borderline Personality Disorder
boolean
C0006012 (UMLS CUI [1])
Treatment of mental disorder
Item
Current treatment of other mental disorder (drugs, psychotherapy)
boolean
C0004936 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Substance Use Disorders
Item
Current Alcohol, Benzodiazepine or other Substance Use Disorders
boolean
C0038586 (UMLS CUI [1])
Comorbidity
Item
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)
boolean
C0009488 (UMLS CUI [1])
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