ID

16074

Descrizione

NINDS Common Data Elements, Multiple Sclerosis Relapse Used from the National Institute of Neurological Disorders and Stroke Common Data Elements (https://www.commondataelements.ninds.nih.gov/) References: Grinnon ST, Miller K, Marler JR, Lu Y, Stout A, Odenkirchen J, Kunitz S. National Institute of Neurological Disorders and Stroke Common Data Element Project - approach and methods. Clin Trials. 2012;9(3):322-9.

collegamento

https://www.commondataelements.ninds.nih.gov/

Keywords

  1. 28/06/16 28/06/16 -
Caricato su

28 giugno 2016

DOI

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Licenza

Creative Commons BY-NC 3.0

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NINDS CDERelapse Multiple Sclerosis

  1. StudyEvent: ODM
    1. Relapse
Relapse
Descrizione

Relapse

Alias
UMLS CUI-1
C0035020
Study ID
Descrizione

Study ID

Tipo di dati

integer

Alias
UMLS CUI [1]
C2826693
Study site name
Descrizione

Study site name

Tipo di dati

text

Alias
UMLS CUI [1]
C2825164
Subject ID
Descrizione

Subject ID

Tipo di dati

integer

Alias
UMLS CUI [1]
C2348585
1. Is the participant/subject having new neurologic symptom(s) or an acute worsening of preexisting neurologic symptoms?
Descrizione

neurologic symptom

Tipo di dati

text

Alias
UMLS CUI [1]
C0235031
a. If Yes, Date of onset:
Descrizione

Date of onset

Tipo di dati

date

Alias
UMLS CUI [1]
C0574845
i. Did the symptoms last more than 24 hours?
Descrizione

neurologic symptom

Tipo di dati

text

Alias
UMLS CUI [1]
C0235031
2. Did the participant/subject have a fever due to intercurrent illness?
Descrizione

fever

Tipo di dati

text

Alias
UMLS CUI [1]
C0015967
3. Prior to the onset of this event, were the participant’s/subject’s MS symptom(s) stable or improving over the last 30 days?
Descrizione

MS symptom

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0026769
UMLS CUI [1,2]
C1457887
a. If Yes, was onset within the last 24 hours?
Descrizione

symptom onset

Tipo di dati

text

Alias
UMLS CUI [1]
C0277793
b. If No, was the onset within the last 7 days?
Descrizione

symptom onset

Tipo di dati

text

Alias
UMLS CUI [1]
C0277793
4. Are the symptom(s) associated with new neurologic findings?
Descrizione

neurologic findings

Tipo di dati

text

Alias
UMLS CUI [1]
C0422837
Pyramidal system
Descrizione

Pyramidal system

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0228060
Sensory system
Descrizione

Sensory system

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0682648
Cerebellar
Descrizione

Cerebellar

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0007765
Bowel and/or Bladder
Descrizione

Bladder and bowel

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2707247
Brainstem
Descrizione

Brainstem

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0006121
Mental
Descrizione

Mental

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0004936
Visual
Descrizione

Visual

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0042789
5. Are the participant’s/subject’s symptom(s) ongoing?
Descrizione

ongoing symptoms

Tipo di dati

text

Alias
UMLS CUI [1]
C2826680
a. If No, End Date:
Descrizione

End Date

Tipo di dati

date

Alias
UMLS CUI [1]
C0806020
6. Please describe event, symptom(s) and treatment that occured with the participant/subject:
Descrizione

symptom; treatment

Tipo di dati

text

Alias
UMLS CUI [1]
C1457887
UMLS CUI [2]
C0039798
7. If applicable, is this a protocol defined qualifying relapse according to the definition set in the study protocol?
Descrizione

study protocol; relapse

Tipo di dati

text

Alias
UMLS CUI [1]
C2348563
UMLS CUI [2]
C0035020
a. If No, please indicate why the event is not a qualifying relapse as defined in the protocol:
Descrizione

relapse

Tipo di dati

text

Alias
UMLS CUI [1]
C0277556

Similar models

Relapse

  1. StudyEvent: ODM
    1. Relapse
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Relapse
C0035020 (UMLS CUI-1)
Study ID
Item
Study ID
integer
C2826693 (UMLS CUI [1])
Study site name
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
integer
C2348585 (UMLS CUI [1])
Item
1. Is the participant/subject having new neurologic symptom(s) or an acute worsening of preexisting neurologic symptoms?
text
C0235031 (UMLS CUI [1])
Code List
1. Is the participant/subject having new neurologic symptom(s) or an acute worsening of preexisting neurologic symptoms?
CL Item
yes (1)
CL Item
no (stop) (2)
CL Item
unknown (3)
Date of onset
Item
a. If Yes, Date of onset:
date
C0574845 (UMLS CUI [1])
Item
i. Did the symptoms last more than 24 hours?
text
C0235031 (UMLS CUI [1])
Code List
i. Did the symptoms last more than 24 hours?
CL Item
yes (1)
CL Item
no (Skip to Q8) (2)
CL Item
unknown (3)
Item
2. Did the participant/subject have a fever due to intercurrent illness?
text
C0015967 (UMLS CUI [1])
Code List
2. Did the participant/subject have a fever due to intercurrent illness?
CL Item
Yes (Skip to Q8)  (1)
CL Item
No (2)
Item
3. Prior to the onset of this event, were the participant’s/subject’s MS symptom(s) stable or improving over the last 30 days?
text
C0026769 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
Code List
3. Prior to the onset of this event, were the participant’s/subject’s MS symptom(s) stable or improving over the last 30 days?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item
a. If Yes, was onset within the last 24 hours?
text
C0277793 (UMLS CUI [1])
Code List
a. If Yes, was onset within the last 24 hours?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item
b. If No, was the onset within the last 7 days?
text
C0277793 (UMLS CUI [1])
Code List
b. If No, was the onset within the last 7 days?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
Item
4. Are the symptom(s) associated with new neurologic findings?
text
C0422837 (UMLS CUI [1])
Code List
4. Are the symptom(s) associated with new neurologic findings?
CL Item
yes [If Yes, in which system(s) was/is the deficit present? (Choose all that apply)] (1)
CL Item
no  (2)
CL Item
unknown (3)
Pyramidal system
Item
Pyramidal system
boolean
C0228060 (UMLS CUI [1])
Sensory system
Item
Sensory system
boolean
C0682648 (UMLS CUI [1])
Cerebellar
Item
Cerebellar
boolean
C0007765 (UMLS CUI [1])
Bladder and bowel
Item
Bowel and/or Bladder
boolean
C2707247 (UMLS CUI [1])
Brainstem
Item
Brainstem
boolean
C0006121 (UMLS CUI [1])
Mental
Item
Mental
boolean
C0004936 (UMLS CUI [1])
Visual
Item
Visual
boolean
C0042789 (UMLS CUI [1])
Item
5. Are the participant’s/subject’s symptom(s) ongoing?
text
C2826680 (UMLS CUI [1])
Code List
5. Are the participant’s/subject’s symptom(s) ongoing?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
End Date
Item
a. If No, End Date:
date
C0806020 (UMLS CUI [1])
symptom; treatment
Item
6. Please describe event, symptom(s) and treatment that occured with the participant/subject:
text
C1457887 (UMLS CUI [1])
C0039798 (UMLS CUI [2])
Item
7. If applicable, is this a protocol defined qualifying relapse according to the definition set in the study protocol?
text
C2348563 (UMLS CUI [1])
C0035020 (UMLS CUI [2])
Code List
7. If applicable, is this a protocol defined qualifying relapse according to the definition set in the study protocol?
CL Item
yes (1)
CL Item
no (2)
CL Item
unknown (3)
relapse
Item
a. If No, please indicate why the event is not a qualifying relapse as defined in the protocol:
text
C0277556 (UMLS CUI [1])

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