ID

34404

Beschrijving

Improving Monitoring of Patients Receiving Case Management; ODM derived from: https://clinicaltrials.gov/show/NCT01597882

Link

https://clinicaltrials.gov/show/NCT01597882

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Conditions NCT01597882

Eligibility Multiple Conditions NCT01597882

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients aged 65 years or over receiving health case management in the community.
Beschrijving

ID.1

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. enrolled in any other research study
Beschrijving

ID.2

Datatype

boolean

2. preclude consent:
Beschrijving

ID.3

Datatype

boolean

significant cognitive impairment resulting in lack of capacity to consent. b. unable to communicate without significant aids e.g. non-english speaking.
Beschrijving

ID.4

Datatype

boolean

3. preclude participation/ collection of data
Beschrijving

ID.5

Datatype

boolean

significant emotional distress or psychotic illness active within the last 6 months.
Beschrijving

ID.6

Datatype

boolean

receiving end of life care.
Beschrijving

ID.7

Datatype

boolean

current illness that would preclude data collection.
Beschrijving

ID.8

Datatype

boolean

upper limb pathology that would limit participation e.g. bone fracture within the previous 6 months.
Beschrijving

ID.9

Datatype

boolean

identified as high risk patients with regards to lone working safety by their case manager.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Multiple Conditions NCT01597882

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients aged 65 years or over receiving health case management in the community.
boolean
Item Group
C0680251 (UMLS CUI)
ID.2
Item
1. enrolled in any other research study
boolean
ID.3
Item
2. preclude consent:
boolean
ID.4
Item
significant cognitive impairment resulting in lack of capacity to consent. b. unable to communicate without significant aids e.g. non-english speaking.
boolean
ID.5
Item
3. preclude participation/ collection of data
boolean
ID.6
Item
significant emotional distress or psychotic illness active within the last 6 months.
boolean
ID.7
Item
receiving end of life care.
boolean
ID.8
Item
current illness that would preclude data collection.
boolean
ID.9
Item
upper limb pathology that would limit participation e.g. bone fracture within the previous 6 months.
boolean
ID.10
Item
identified as high risk patients with regards to lone working safety by their case manager.
boolean

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