ID

34286

Description

Micro-Clinic Obesity and Metabolic Risk Prevention Program; ODM derived from: https://clinicaltrials.gov/show/NCT01651065

Link

https://clinicaltrials.gov/show/NCT01651065

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type II NCT01651065

Eligibility Diabetes Mellitus, Type II NCT01651065

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
must be enrolled in our community health program.
Description

ID.1

Data type

boolean

over the age of 18
Description

ID.2

Data type

boolean

bmi of 30 or higher, or
Description

ID.3

Data type

boolean

bmi of 25 or higher and must be diagnosed with at least one additional risk factor 1) type 2 diabetes, 2) high blood pressure, and/or 3) high cholesterol
Description

ID.4

Data type

boolean

for those who will be participating in the cross-over sub-sample, they must have previously participated in phase 1 as subject of the control group, or
Description

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are not enrolled in the our community health education program (applies to phase 1 only)
Description

ID.6

Data type

boolean

are not able to provide informed consent for themselves
Description

ID.7

Data type

boolean

under the age of 18
Description

ID.8

Data type

boolean

has undergone weight loss surgery
Description

ID.9

Data type

boolean

pregnant women*
Description

ID.10

Data type

boolean

Similar models

Eligibility Diabetes Mellitus, Type II NCT01651065

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
must be enrolled in our community health program.
boolean
ID.2
Item
over the age of 18
boolean
ID.3
Item
bmi of 30 or higher, or
boolean
ID.4
Item
bmi of 25 or higher and must be diagnosed with at least one additional risk factor 1) type 2 diabetes, 2) high blood pressure, and/or 3) high cholesterol
boolean
ID.5
Item
for those who will be participating in the cross-over sub-sample, they must have previously participated in phase 1 as subject of the control group, or
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients who are not enrolled in the our community health education program (applies to phase 1 only)
boolean
ID.7
Item
are not able to provide informed consent for themselves
boolean
ID.8
Item
under the age of 18
boolean
ID.9
Item
has undergone weight loss surgery
boolean
ID.10
Item
pregnant women*
boolean

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