ID

34314

Beschrijving

Improving Heart Failure Outcomes Rural; ODM derived from: https://clinicaltrials.gov/show/NCT02395588

Link

https://clinicaltrials.gov/show/NCT02395588

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 Heart Failure NCT02395588

Eligibility Heart Failure NCT02395588

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
admitted to hospital with a diagnosis of heart failure
Beschrijving

ID.1

Datatype

boolean

age > 20
Beschrijving

ID.2

Datatype

boolean

cognitively intact
Beschrijving

ID.3

Datatype

boolean

english speaking
Beschrijving

ID.4

Datatype

boolean

plan for discharge to home, assisted living or intermediate care
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with planned discharge to sub-acute or nursing home facilities
Beschrijving

ID.6

Datatype

boolean

patients enrolled in another research study to test interventions to improve heart failure knowledge, self-management or reduce readmission to the hospital within 30 days post discharge
Beschrijving

ID.7

Datatype

boolean

patients that are cognitively impaired
Beschrijving

ID.8

Datatype

boolean

patients that are transferred to another unit in the hospital, and will be discharged from that unit
Beschrijving

ID.9

Datatype

boolean

patients who undergo or have a planned surgical intervention during their hospital stay
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Heart Failure NCT02395588

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
admitted to hospital with a diagnosis of heart failure
boolean
ID.2
Item
age > 20
boolean
ID.3
Item
cognitively intact
boolean
ID.4
Item
english speaking
boolean
ID.5
Item
plan for discharge to home, assisted living or intermediate care
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients with planned discharge to sub-acute or nursing home facilities
boolean
ID.7
Item
patients enrolled in another research study to test interventions to improve heart failure knowledge, self-management or reduce readmission to the hospital within 30 days post discharge
boolean
ID.8
Item
patients that are cognitively impaired
boolean
ID.9
Item
patients that are transferred to another unit in the hospital, and will be discharged from that unit
boolean
ID.10
Item
patients who undergo or have a planned surgical intervention during their hospital stay
boolean

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