ID

29165

Description

Telephone Delivered Behavioral Skills Intervention for Blacks With T2DM; ODM derived from: https://clinicaltrials.gov/show/NCT00929838

Link

https://clinicaltrials.gov/show/NCT00929838

Keywords

Versions (1)
  1. 3/3/18 3/3/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 3, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT00929838

English

Eligibility Diabetes Mellitus, Type 2 NCT00929838

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1) age ≥18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
2) clinical diagnosis of t2dm and hba1c ≥9% at the screening visit
Description

Diabetes Mellitus, Non-Insulin-Dependent | Glucohemoglobin measurement

Data type

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2]
C0202054
3) self-identified as black or african american
Description

African American

Data type

boolean

Alias
UMLS CUI [1]
C0085756
4) subject must be taking at least one oral medication for diabetes, hypertension, or hyperlipidemia and must be willing to use the mems cap and bottle for 12 months
Description

Oral medication Quantity Diabetes | Oral medication Quantity Hypertensive disease | Oral medication Quantity Hyperlipidemia | MEMS Cap Use of

Data type

boolean

Alias
UMLS CUI [1,1]
C0175795
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0011847
UMLS CUI [2,1]
C0175795
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0020538
UMLS CUI [3,1]
C0175795
UMLS CUI [3,2]
C1265611
UMLS CUI [3,3]
C0020473
UMLS CUI [4,1]
C2600049
UMLS CUI [4,2]
C1524063
5) subjects must be able to communicate in english
Description

Able to communicate English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C2364293
UMLS CUI [1,2]
C0376245
6) subjects must have access to a telephone (landline or cell phone) for the 12 week intervention period
Description

Access to telephone | Access Cell Phone

Data type

boolean

Alias
UMLS CUI [1]
C1822200
UMLS CUI [2,1]
C0444454
UMLS CUI [2,2]
C1136359
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1) mental confusion on interview suggesting significant dementia
Description

Confusion Patient interview | Dementia Suggestive of

Data type

boolean

Alias
UMLS CUI [1,1]
C0009676
UMLS CUI [1,2]
C0683518
UMLS CUI [2,1]
C0497327
UMLS CUI [2,2]
C0332299
2) participation in other diabetes clinical trials
Description

Study Subject Participation Status | Diabetes

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0011847
3) alcohol or drug abuse/dependency
Description

Substance Use Disorders | Substance Dependence

Data type

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2]
C0038580
4) active psychosis or acute mental disorder
Description

Psychotic Disorders | Mental disorders

Data type

boolean

Alias
UMLS CUI [1]
C0033975
UMLS CUI [2]
C0004936
5) life expectancy <6 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
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Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00929838

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1) age ≥18 years
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus, Non-Insulin-Dependent | Glucohemoglobin measurement
Item
2) clinical diagnosis of t2dm and hba1c ≥9% at the screening visit
boolean
C0011860 (UMLS CUI [1])
C0202054 (UMLS CUI [2])
African American
Item
3) self-identified as black or african american
boolean
C0085756 (UMLS CUI [1])
Oral medication Quantity Diabetes | Oral medication Quantity Hypertensive disease | Oral medication Quantity Hyperlipidemia | MEMS Cap Use of
Item
4) subject must be taking at least one oral medication for diabetes, hypertension, or hyperlipidemia and must be willing to use the mems cap and bottle for 12 months
boolean
C0175795 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0011847 (UMLS CUI [1,3])
C0175795 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0020538 (UMLS CUI [2,3])
C0175795 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0020473 (UMLS CUI [3,3])
C2600049 (UMLS CUI [4,1])
C1524063 (UMLS CUI [4,2])
Able to communicate English Language
Item
5) subjects must be able to communicate in english
boolean
C2364293 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Access to telephone | Access Cell Phone
Item
6) subjects must have access to a telephone (landline or cell phone) for the 12 week intervention period
boolean
C1822200 (UMLS CUI [1])
C0444454 (UMLS CUI [2,1])
C1136359 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Confusion Patient interview | Dementia Suggestive of
Item
1) mental confusion on interview suggesting significant dementia
boolean
C0009676 (UMLS CUI [1,1])
C0683518 (UMLS CUI [1,2])
C0497327 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
Study Subject Participation Status | Diabetes
Item
2) participation in other diabetes clinical trials
boolean
C2348568 (UMLS CUI [1])
C0011847 (UMLS CUI [2])
Substance Use Disorders | Substance Dependence
Item
3) alcohol or drug abuse/dependency
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
Psychotic Disorders | Mental disorders
Item
4) active psychosis or acute mental disorder
boolean
C0033975 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Life Expectancy
Item
5) life expectancy <6 months
boolean
C0023671 (UMLS CUI [1])
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