ID

34281

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT02041598

Keywords

  1. 16/01/19 16/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

16 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT02041598

Eligibility Diabetes Mellitus, Type 2 NCT02041598

Inclusion Criteria
Descrizione

Inclusion Criteria

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

ID.1

Tipo di dati

boolean

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

ID.2

Tipo di dati

boolean

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

ID.3

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

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

ID.4

Tipo di dati

boolean

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

ID.5

Tipo di dati

boolean

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

ID.6

Tipo di dati

boolean

is pregnant at the time of recruitment;
Descrizione

ID.7

Tipo di dati

boolean

experienced other severe medical conditions that might preclude participation;
Descrizione

ID.8

Tipo di dati

boolean

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

ID.9

Tipo di dati

boolean

is participating in another research study.
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT02041598

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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