ID

34601

Description

The I-KAN Study: Internet Insulin Education for Kansans; ODM derived from: https://clinicaltrials.gov/show/NCT01408628

Link

https://clinicaltrials.gov/show/NCT01408628

Keywords

Versions (3)
  1. 1/19/19 1/19/19 -
  2. 4/17/20 4/17/20 -
  3. 4/18/20 4/18/20 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 19, 2019

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Type 2 Diabetes NCT01408628

English

Eligibility Type 2 Diabetes NCT01408628

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
t2dm, meets provider criteria for insulin initiation; starting or having started insulin treatment no longer than six months prior to enrollment or has not yet committed to starting insulin but has agreed to participate in the education
Description

ID.1

Data type

boolean

broadband internet and experience with logging into a password-protected site (e.g., ecommerce or social networking);
Description

ID.2

Data type

boolean

ability to purchase or otherwise acquire glargine/detemir insulin and testing supplies.
Description

ID.3

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
use of oral glucocorticoids or second generation anti-psychotics;
Description

ID.4

Data type

boolean

previous use of self-administered insulin more than six months prior to enrollment;
Description

ID.5

Data type

boolean

gestational diabetes or other endocrine conditions causing hyperglycemia; treatment for a malignant condition other than basal cell carcinoma in situ within prior two years;
Description

ID.6

Data type

boolean

renal insufficiency (ast/alt >2 or concurrent liver disease except nash);
Description

ID.7

Data type

boolean

pregnant or planning to become pregnant within 6 months;
Description

ID.8

Data type

boolean

hba1c < 7.0% or ongoing weight loss or persistent fasting hyperglycemia > 250 mg/dl.
Description

ID.9

Data type

boolean

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Similar models

Eligibility Type 2 Diabetes NCT01408628

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
t2dm, meets provider criteria for insulin initiation; starting or having started insulin treatment no longer than six months prior to enrollment or has not yet committed to starting insulin but has agreed to participate in the education
boolean
ID.2
Item
broadband internet and experience with logging into a password-protected site (e.g., ecommerce or social networking);
boolean
ID.3
Item
ability to purchase or otherwise acquire glargine/detemir insulin and testing supplies.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
use of oral glucocorticoids or second generation anti-psychotics;
boolean
ID.5
Item
previous use of self-administered insulin more than six months prior to enrollment;
boolean
ID.6
Item
gestational diabetes or other endocrine conditions causing hyperglycemia; treatment for a malignant condition other than basal cell carcinoma in situ within prior two years;
boolean
ID.7
Item
renal insufficiency (ast/alt >2 or concurrent liver disease except nash);
boolean
ID.8
Item
pregnant or planning to become pregnant within 6 months;
boolean
ID.9
Item
hba1c < 7.0% or ongoing weight loss or persistent fasting hyperglycemia > 250 mg/dl.
boolean
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