ID

34264

Beschrijving

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

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus NCT01475422

Eligibility Diabetes Mellitus NCT01475422

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
ages 18 years and older;
Beschrijving

ID.1

Datatype

boolean

diagnosis of type 1 and 2 diabetes mellitus;
Beschrijving

ID.2

Datatype

boolean

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

ID.3

Datatype

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).
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with gestational dm;
Beschrijving

ID.5

Datatype

boolean

patients with dm who are not located;
Beschrijving

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

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

ID.8

Datatype

boolean

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

ID.9

Datatype

boolean

used conversation maps as an educational tool.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Diabetes Mellitus NCT01475422

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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