ID

23179

Descripción

Responsible Party: Universitätsklinikum Hamburg-Eppendorf ClinicalTrials.gov Identifier: NCT01879111 History of Changes Other Study ID Numbers: 01-GX-1004 DRKS00003277 ( Registry Identifier: German Clinical Trials Register ) Study First Received: June 12, 2013 Last Updated: December 15, 2014 Increasing the Efficiency of Depression-screening Using Patient-targeted Feedback (DEPSCREEN-INFO); ODM derived from: https://clinicaltrials.gov/show/NCT01879111

Link

https://clinicaltrials.gov/show/NCT01879111

Palabras clave

Versiones (1)
  1. 26/6/17 26/6/17 -
Subido en

26 de junio de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Depressive Episode DRKS00003277 NCT01879111 DRKS00003277

Inglés

Eligibility Depressive Episode NCT01879111 DRKS00003277

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
Gender: both, male and female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
Minimum age: 18 years Maximum age: no maximum age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Attendance in a cardiac clinic;
Descripción

Hospitalization

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019993
Clinical diagnosis of coronary heart disease or hypertension;
Descripción

Coronary heart disease or hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2]
C0020538
Sufficient language skills;
Descripción

Language Ability

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1145677
Informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
Life threatening health status;
Descripción

Health Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018759
Severe somatic or/and psychological disorder that needs urgent treatment;
Descripción

Comorbidity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
Acute suicidal tendency;
Descripción

Suicidal tendency

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0235196
Severe cognitive or/and visual difficulties;
Descripción

Cognitive or/and visual difficulties

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2]
C3665347
not being able to fill out questionnaires
Descripción

Questionnaire

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0034394
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Similar models

Eligibility Depressive Episode NCT01879111 DRKS00003277

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
Gender: both, male and female
boolean
C0079399 (UMLS CUI [1])
Age
Item
Minimum age: 18 years Maximum age: no maximum age
boolean
C0001779 (UMLS CUI [1])
Hospitalization
Item
Attendance in a cardiac clinic;
boolean
C0019993 (UMLS CUI [1])
Coronary heart disease or hypertension
Item
Clinical diagnosis of coronary heart disease or hypertension;
boolean
C0010068 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
Language Ability
Item
Sufficient language skills;
boolean
C1145677 (UMLS CUI [1])
Informed Consent
Item
Informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Health Status
Item
Life threatening health status;
boolean
C0018759 (UMLS CUI [1])
Comorbidity
Item
Severe somatic or/and psychological disorder that needs urgent treatment;
boolean
C0009488 (UMLS CUI [1])
Suicidal tendency
Item
Acute suicidal tendency;
boolean
C0235196 (UMLS CUI [1])
Cognitive or/and visual difficulties
Item
Severe cognitive or/and visual difficulties;
boolean
C0338656 (UMLS CUI [1])
C3665347 (UMLS CUI [2])
Questionnaire
Item
not being able to fill out questionnaires
boolean
C0034394 (UMLS CUI [1])
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