ID

29159

Beschreibung

Effect of Type 2 Diabetes Genetic Risk Information on Health Behaviors and Outcomes; ODM derived from: https://clinicaltrials.gov/show/NCT00849563

Link

https://clinicaltrials.gov/show/NCT00849563

Stichworte

  1. 02.03.18 02.03.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

2. März 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00849563

Eligibility Diabetes Mellitus, Type 2 NCT00849563

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
are male or female outpatients
Beschreibung

Outpatients

Datentyp

boolean

Alias
UMLS CUI [1]
C0029921
no self-reported history of diabetes
Beschreibung

Diabetes Self-Report Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0011847
UMLS CUI [1,2]
C2700446
UMLS CUI [1,3]
C0332197
no self-reported history of prior genetic testing for diabetes
Beschreibung

Genetic test Diabetes | Self-Report Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679560
UMLS CUI [1,2]
C0011847
UMLS CUI [2,1]
C2700446
UMLS CUI [2,2]
C0332197
not pregnant (self report)
Beschreibung

Pregnancy Absent Self-Report

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C2700446
are ≥18 and <81 years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
scheduled to receive serum glucose test in participating clinic
Beschreibung

Serum Glucose measurement Scheduled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0202041
UMLS CUI [1,2]
C0205539
fasting at time of blood draw (no food or drink - except water - previous 8 hours: self report)
Beschreibung

Fasting Blood draw

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0015663
UMLS CUI [1,2]
C0005834
able and willing to give legally effective consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
able and willing to participate in patient questionnaires
Beschreibung

Participation Patient Questionnaire

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0030705
UMLS CUI [1,3]
C0034394
ambulatory
Beschreibung

Ambulatory

Datentyp

boolean

Alias
UMLS CUI [1]
C0439841
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
previously or currently taking medications for lowering glucose (i.e., exenatide, pramlintide, metformin, rosiglitazone, pioglitazone, or future diabetes drugs) based on self-report and/or prescreening
Beschreibung

Hypoglycemic Agents | exenatide | Pramlintide | Metformin | rosiglitazone | pioglitazone

Datentyp

boolean

Alias
UMLS CUI [1]
C0020616
UMLS CUI [2]
C0167117
UMLS CUI [3]
C0537551
UMLS CUI [4]
C0025598
UMLS CUI [5]
C0289313
UMLS CUI [6]
C0071097
self-report of current or prior diabetes diagnosis
Beschreibung

Diabetes Self-Report

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0011847
UMLS CUI [1,2]
C2700446
self-reported prior history of genetic testing for diabetes
Beschreibung

Genetic test Diabetes Self-Report

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679560
UMLS CUI [1,2]
C0011847
UMLS CUI [1,3]
C2700446
baseline serum glucose test result >125
Beschreibung

Glucose measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0202041

Ähnliche Modelle

Eligibility Diabetes Mellitus, Type 2 NCT00849563

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients
Item
are male or female outpatients
boolean
C0029921 (UMLS CUI [1])
Diabetes Self-Report Absent
Item
no self-reported history of diabetes
boolean
C0011847 (UMLS CUI [1,1])
C2700446 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Genetic test Diabetes | Self-Report Absent
Item
no self-reported history of prior genetic testing for diabetes
boolean
C0679560 (UMLS CUI [1,1])
C0011847 (UMLS CUI [1,2])
C2700446 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Pregnancy Absent Self-Report
Item
not pregnant (self report)
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C2700446 (UMLS CUI [1,3])
Age
Item
are ≥18 and <81 years of age
boolean
C0001779 (UMLS CUI [1])
Serum Glucose measurement Scheduled
Item
scheduled to receive serum glucose test in participating clinic
boolean
C0202041 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Fasting Blood draw
Item
fasting at time of blood draw (no food or drink - except water - previous 8 hours: self report)
boolean
C0015663 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
Informed Consent
Item
able and willing to give legally effective consent
boolean
C0021430 (UMLS CUI [1])
Participation Patient Questionnaire
Item
able and willing to participate in patient questionnaires
boolean
C0679823 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0034394 (UMLS CUI [1,3])
Ambulatory
Item
ambulatory
boolean
C0439841 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypoglycemic Agents | exenatide | Pramlintide | Metformin | rosiglitazone | pioglitazone
Item
previously or currently taking medications for lowering glucose (i.e., exenatide, pramlintide, metformin, rosiglitazone, pioglitazone, or future diabetes drugs) based on self-report and/or prescreening
boolean
C0020616 (UMLS CUI [1])
C0167117 (UMLS CUI [2])
C0537551 (UMLS CUI [3])
C0025598 (UMLS CUI [4])
C0289313 (UMLS CUI [5])
C0071097 (UMLS CUI [6])
Diabetes Self-Report
Item
self-report of current or prior diabetes diagnosis
boolean
C0011847 (UMLS CUI [1,1])
C2700446 (UMLS CUI [1,2])
Genetic test Diabetes Self-Report
Item
self-reported prior history of genetic testing for diabetes
boolean
C0679560 (UMLS CUI [1,1])
C0011847 (UMLS CUI [1,2])
C2700446 (UMLS CUI [1,3])
Glucose measurement, serum
Item
baseline serum glucose test result >125
boolean
C0202041 (UMLS CUI [1])

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