ID

34281

Descripción

DREAM Project Community Health Worker Intervention; ODM derived from: https://clinicaltrials.gov/show/NCT02041598

Link

https://clinicaltrials.gov/show/NCT02041598

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT02041598

Eligibility Diabetes Mellitus, Type 2 NCT02041598

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
confirmed clinical diagnosis of t2dm with a hemoglobin a1c (hba1c) of ≥ 6.5%; and
Descripción

ID.1

Tipo de datos

boolean

male or female between the ages of 21-85 years old; and
Descripción

ID.2

Tipo de datos

boolean

willingness to be randomized to either treatment or control groups.
Descripción

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
is or was on renal dialysis;
Descripción

ID.4

Tipo de datos

boolean

experiencing an acute or terminal illness or serious mental illness;
Descripción

ID.5

Tipo de datos

boolean

had a history of recent coronary event within the last 3 months of recruitment;
Descripción

ID.6

Tipo de datos

boolean

is pregnant at the time of recruitment;
Descripción

ID.7

Tipo de datos

boolean

experienced other severe medical conditions that might preclude participation;
Descripción

ID.8

Tipo de datos

boolean

has poor short-term prognosis (expected death in <2 years); or
Descripción

ID.9

Tipo de datos

boolean

is participating in another research study.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT02041598

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
confirmed clinical diagnosis of t2dm with a hemoglobin a1c (hba1c) of ≥ 6.5%; and
boolean
ID.2
Item
male or female between the ages of 21-85 years old; and
boolean
ID.3
Item
willingness to be randomized to either treatment or control groups.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
is or was on renal dialysis;
boolean
ID.5
Item
experiencing an acute or terminal illness or serious mental illness;
boolean
ID.6
Item
had a history of recent coronary event within the last 3 months of recruitment;
boolean
ID.7
Item
is pregnant at the time of recruitment;
boolean
ID.8
Item
experienced other severe medical conditions that might preclude participation;
boolean
ID.9
Item
has poor short-term prognosis (expected death in <2 years); or
boolean
ID.10
Item
is participating in another research study.
boolean

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