ID

34404

Descripción

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

Link

https://clinicaltrials.gov/show/NCT01597882

Palabras clave

  1. 17/1/19 17/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

17 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Multiple Conditions NCT01597882

Eligibility Multiple Conditions NCT01597882

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.2

Tipo de datos

boolean

2. preclude consent:
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

3. preclude participation/ collection of data
Descripción

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

receiving end of life care.
Descripción

ID.7

Tipo de datos

boolean

current illness that would preclude data collection.
Descripción

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

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

ID.10

Tipo de datos

boolean

Similar models

Eligibility Multiple Conditions NCT01597882

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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