ID

34404

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01597882

Nyckelord

  1. 2019-01-17 2019-01-17 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

17 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Multiple Conditions NCT01597882

Eligibility Multiple Conditions NCT01597882

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.2

Datatyp

boolean

2. preclude consent:
Beskrivning

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

3. preclude participation/ collection of data
Beskrivning

ID.5

Datatyp

boolean

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

ID.6

Datatyp

boolean

receiving end of life care.
Beskrivning

ID.7

Datatyp

boolean

current illness that would preclude data collection.
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

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

ID.10

Datatyp

boolean

Similar models

Eligibility Multiple Conditions NCT01597882

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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