ID

34264

Description

Effectiveness of the Self Monitoring of Capillary Blood Glucose at Home; ODM derived from: https://clinicaltrials.gov/show/NCT01475422

Link

https://clinicaltrials.gov/show/NCT01475422

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 NCT01475422

Eligibility Diabetes Mellitus NCT01475422

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ages 18 years and older;
Description

ID.1

Data type

boolean

diagnosis of type 1 and 2 diabetes mellitus;
Description

ID.2

Data type

boolean

in follow-up in the self-monitoring of capillary blood glucose at home program;
Description

ID.3

Data type

boolean

have cognitive conditions that enable participation (minimum ability of users to understand issues of data collection instruments, observation of the researcher and/or of the caregivers).
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with gestational dm;
Description

ID.5

Data type

boolean

patients with dm who are not located;
Description

ID.6

Data type

boolean

those who die in the proposed period for the research;
Description

ID.7

Data type

boolean

those who dropout the self-monitoring of capillary blood glucose at home program;
Description

ID.8

Data type

boolean

those who report difficulties to participate of the study due to work and those with amaurosis;
Description

ID.9

Data type

boolean

used conversation maps as an educational tool.
Description

ID.10

Data type

boolean

Similar models

Eligibility Diabetes Mellitus NCT01475422

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
ages 18 years and older;
boolean
ID.2
Item
diagnosis of type 1 and 2 diabetes mellitus;
boolean
ID.3
Item
in follow-up in the self-monitoring of capillary blood glucose at home program;
boolean
ID.4
Item
have cognitive conditions that enable participation (minimum ability of users to understand issues of data collection instruments, observation of the researcher and/or of the caregivers).
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
patients with gestational dm;
boolean
ID.6
Item
patients with dm who are not located;
boolean
ID.7
Item
those who die in the proposed period for the research;
boolean
ID.8
Item
those who dropout the self-monitoring of capillary blood glucose at home program;
boolean
ID.9
Item
those who report difficulties to participate of the study due to work and those with amaurosis;
boolean
ID.10
Item
used conversation maps as an educational tool.
boolean

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