ID

23080

Beschrijving

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

Link

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

Trefwoorden

Versies (1)
  1. 22-06-17 22-06-17 -
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22 juni 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Anxiety Disorders DRKS00008743 NCT02605668 DRKS00008743

Engels

Eligibility Anxiety Disorders NCT02605668 DRKS00008743

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Age

Datatype

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
Beschrijving

Anxiety disorders

Datatype

boolean

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

Hamilton Anxiety Rating Scale Questionnaire

Datatype

boolean

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

Clinical Global Impression Questionnaire

Datatype

boolean

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

Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
Informed Consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Beschrijving

Control Group

Datatype

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.)
Beschrijving

Study protocol

Datatype

boolean

Alias
UMLS CUI [1]
C2348563
Current suicidal tendency
Beschrijving

Suicidal tendency

Datatype

boolean

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

Bipolar Disorder

Datatype

boolean

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

Psychotic Disorder

Datatype

boolean

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

Borderline Personality Disorder

Datatype

boolean

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

Treatment of mental disorder

Datatype

boolean

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

Substance Use Disorders

Datatype

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)
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
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Similar models

Eligibility Anxiety Disorders NCT02605668 DRKS00008743

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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