ID

29159

Descripción

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

Palabras clave

Versiones (1)
  1. 2/3/18 2/3/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

2 de marzo de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT00849563

Inglés

Eligibility Diabetes Mellitus, Type 2 NCT00849563

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
are male or female outpatients
Descripción

Outpatients

Tipo de datos

boolean

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

Diabetes Self-Report Absent

Tipo de datos

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
Descripción

Genetic test Diabetes | Self-Report Absent

Tipo de datos

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)
Descripción

Pregnancy Absent Self-Report

Tipo de datos

boolean

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

Age

Tipo de datos

boolean

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

Serum Glucose measurement Scheduled

Tipo de datos

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)
Descripción

Fasting Blood draw

Tipo de datos

boolean

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

Informed Consent

Tipo de datos

boolean

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

Participation Patient Questionnaire

Tipo de datos

boolean

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

Ambulatory

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0439841
Exclusion Criteria
Descripción

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
Descripción

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

Tipo de datos

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
Descripción

Diabetes Self-Report

Tipo de datos

boolean

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

Genetic test Diabetes Self-Report

Tipo de datos

boolean

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

Glucose measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202041
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Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00849563

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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