Informações:
Falhas:
ID
29159
Descrição
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
Palavras-chave
Versões (1)
- 02/03/2018 02/03/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
2 de março de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT00849563
Eligibility Diabetes Mellitus, Type 2 NCT00849563
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus, Type 2 NCT00849563
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
C0030705 (UMLS CUI [1,2])
C0034394 (UMLS CUI [1,3])
Ambulatory
Item
ambulatory
boolean
C0439841 (UMLS CUI [1])
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])
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])
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])
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])