ID

38796

Description

Call-2-Health: Preventing Type II Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01827826

Link

https://clinicaltrials.gov/show/NCT01827826

Keywords

  1. 11/4/19 11/4/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 4, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Diabetes Mellitus, Type 2 NCT01827826

Eligibility Diabetes Mellitus, Type 2 NCT01827826

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
age 40-74
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
receives primary care at group health central, rainier, or poulsbo clinics in the greater seattle area
Description

Primary Health Care Medical center

Data type

boolean

Alias
UMLS CUI [1,1]
C0033137
UMLS CUI [1,2]
C0565990
can walk for more than 10 minutes
Description

Able to walk Number of minutes

Data type

boolean

Alias
UMLS CUI [1,1]
C2712089
UMLS CUI [1,2]
C1562039
fasting plasma glucose (fpg) 105-125 mg/dl or glycolated hemoglobin (hba1c) 5.7-6.4
Description

Plasma fasting glucose measurement | Hemoglobin A1c measurement

Data type

boolean

Alias
UMLS CUI [1]
C0583513
UMLS CUI [2]
C0474680
body mass index (bmi) 25 kg/m2 or greater
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 or 2 diabetes
Description

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Data type

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
fpg > 125 mg/dl or < 105mg/dl at screening blood draw
Description

Plasma fasting glucose measurement Blood draw

Data type

boolean

Alias
UMLS CUI [1,1]
C0583513
UMLS CUI [1,2]
C0005834
hba1c > 6.4 or < 5.7 at screening blood draw
Description

Hemoglobin A1c measurement Blood draw

Data type

boolean

Alias
UMLS CUI [1,1]
C0474680
UMLS CUI [1,2]
C0005834
systolic blood pressure > 210 mmhg at the baseline clinic visit
Description

Systolic Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
exercise ≥ 30 minutes/day, at least five days a week
Description

Exercise Minutes per day Days per week

Data type

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C0556973
UMLS CUI [1,3]
C0677547
current participation in another structured weight loss treatment program or another intervention study
Description

Study Subject Participation Status | Weight Reduction Programs | Interventional Study

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C3179079
UMLS CUI [3]
C3274035
severe concurrent disease
Description

Comorbidity Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
unavailable for the 24-week study period
Description

Patient unavailable Clinical Trial Period

Data type

boolean

Alias
UMLS CUI [1,1]
C1301818
UMLS CUI [1,2]
C2347804
unable to read or speak english
Description

Lacking Able to read English Language | Lacking Able to speak English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C0564215
UMLS CUI [2,3]
C0376245
pregnant or planning to become pregnant.
Description

Pregnancy | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
mentally or legally incapacitated such that informed consent cannot be obtained.
Description

Mental handicap | Legal capacity Lacking | Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1]
C1306341
UMLS CUI [2,1]
C0683673
UMLS CUI [2,2]
C0332268
UMLS CUI [3,1]
C0021430
UMLS CUI [3,2]
C1299582

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT01827826

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Age
Item
age 40-74
boolean
C0001779 (UMLS CUI [1])
Primary Health Care Medical center
Item
receives primary care at group health central, rainier, or poulsbo clinics in the greater seattle area
boolean
C0033137 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
Able to walk Number of minutes
Item
can walk for more than 10 minutes
boolean
C2712089 (UMLS CUI [1,1])
C1562039 (UMLS CUI [1,2])
Plasma fasting glucose measurement | Hemoglobin A1c measurement
Item
fasting plasma glucose (fpg) 105-125 mg/dl or glycolated hemoglobin (hba1c) 5.7-6.4
boolean
C0583513 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
Body mass index
Item
body mass index (bmi) 25 kg/m2 or greater
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
type 1 or 2 diabetes
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Plasma fasting glucose measurement Blood draw
Item
fpg > 125 mg/dl or < 105mg/dl at screening blood draw
boolean
C0583513 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
Hemoglobin A1c measurement Blood draw
Item
hba1c > 6.4 or < 5.7 at screening blood draw
boolean
C0474680 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
Systolic Pressure
Item
systolic blood pressure > 210 mmhg at the baseline clinic visit
boolean
C0871470 (UMLS CUI [1])
Exercise Minutes per day Days per week
Item
exercise ≥ 30 minutes/day, at least five days a week
boolean
C0015259 (UMLS CUI [1,1])
C0556973 (UMLS CUI [1,2])
C0677547 (UMLS CUI [1,3])
Study Subject Participation Status | Weight Reduction Programs | Interventional Study
Item
current participation in another structured weight loss treatment program or another intervention study
boolean
C2348568 (UMLS CUI [1])
C3179079 (UMLS CUI [2])
C3274035 (UMLS CUI [3])
Comorbidity Severe
Item
severe concurrent disease
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Patient unavailable Clinical Trial Period
Item
unavailable for the 24-week study period
boolean
C1301818 (UMLS CUI [1,1])
C2347804 (UMLS CUI [1,2])
Lacking Able to read English Language | Lacking Able to speak English Language
Item
unable to read or speak english
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
Pregnancy | Pregnancy, Planned
Item
pregnant or planning to become pregnant.
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Mental handicap | Legal capacity Lacking | Informed Consent Unable
Item
mentally or legally incapacitated such that informed consent cannot be obtained.
boolean
C1306341 (UMLS CUI [1])
C0683673 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial