ID

40207

Description

DELCODE is conducted by DZNE, the German Center for Neurodegenerative Diseases within the Helmholtz Association. The following information was taken from https://www.dzne.de/en/research/studies/clinical-studies/delcode/. Background and aims: One of the important aims of research into Alzheimer's is to find ways of detecting the disease early – if at all possible, as soon as the first minor symptoms appear, or even before any symptoms at all have appeared. Such detection capabilities are the necessary basis for development of therapies that can be applied at such early stages in the disease. Recent research indicates that such therapies could be more effective than therapies initiated during the disease's later stages. Over a period of several years, the DELCODE study is studying persons in early stages of the disease, along with various risk groups. The research is aimed at the development of procedures for characterizing early stages of the disease, at improving prediction of the course of the disease and at identifying new markers for early diagnosis of Alzheimer's-related dementia. Overview: DELCODE is set up to run for an initial period of three years, and to include a total of 1,000 study participants, who will be examined on a yearly basis. The group of participants will include persons with no complaints (healthy control subjects), patients with slight memory impairment or mild dementia and first-degree relatives of patients with diagnosed Alzheimer's disease. The minimum age for participants is 60. Course of the study: The examinations in the framework of the study will include a comprehensive interview carried out by a study investigator, a detailed neuropsychological examination (testing of memory functions and other areas of cognitive performance), a blood test and a cranial MRI scan. Optionally, subject to the study participant's consent in each case, a lumbar puncture (collection of cerebrospinal fluid) will be carried out." For more information (e.g. principle investigator and study coordination), please visit the above link or https://www.dzne.de. This document contains the cumulative documentation - medication. Prior medication should be filled in at baseline. Medication that are performed during the study period should be added in the course of the study.

Link

https://www.dzne.de/en/research/studies/clinical-studies/delcode/

Keywords

  1. 3/23/20 3/23/20 -
Copyright Holder

DZNE

Uploaded on

March 23, 2020

DOI

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License

Creative Commons BY-NC 4.0

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DELCODE: DZNE – Longitudinal Cognitive Impairment and Dementia Study

Cumulative documentation - Medication (Kumulative Dokumentation - Medikation)

Administrative Daten
Description

Administrative Daten

Alias
UMLS CUI-1
C1320722
Studien ID
Description

Study ID

Data type

text

Alias
UMLS CUI [1]
C2826693
Medikation
Description

Medikation

Alias
UMLS CUI-1
C0013227
Nimmt der/die Proband/in derzeit Arzneimittel ein
Description

(Falls ja, tragen Sie diese bitte in das folgende Item ein).

Data type

integer

Alias
UMLS CUI [1]
C0013227
Nummerierung, Medikation
Description

Medication, record

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C2348184
Arzneimittel / Wirkstoff
Description

Drug

Data type

text

Alias
UMLS CUI [1]
C0013227
Dosis
Description

Bei Kombipräparaten bitte die jeweiligen Einzeldosen aufführen

Data type

float

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0013227
Einheit
Description

Unit dose

Data type

text

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0013227
Einnahme
Description

(wenn nicht täglich): w= wöchentlich, m= monatlich.

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C2982514
Applikationsform
Description

Type of application

Data type

integer

Alias
UMLS CUI [1,1]
C0185125
UMLS CUI [1,2]
C0332307
Applikationsweg
Description

Route of application

Data type

integer

Alias
UMLS CUI [1]
C0013153
Retardform
Description

Modified release dosage form

Data type

boolean

Alias
UMLS CUI [1]
C1709058
Indikation
Description

Indication of medication

Data type

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
Start
Description

Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.

Data type

partialDate

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
End
Description

Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.

Data type

partialDate

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Medikation andauernd
Description

Ongoing medication

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0549178

Similar models

Cumulative documentation - Medication (Kumulative Dokumentation - Medikation)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Daten
C1320722 (UMLS CUI-1)
Study ID
Item
Studien ID
text
C2826693 (UMLS CUI [1])
Item Group
Medikation
C0013227 (UMLS CUI-1)
Item
Nimmt der/die Proband/in derzeit Arzneimittel ein
integer
C0013227 (UMLS CUI [1])
Code List
Nimmt der/die Proband/in derzeit Arzneimittel ein
CL Item
Ja (1)
CL Item
Nein (0)
CL Item
Unbekannt (997)
Medication, record
Item
Nummerierung, Medikation
integer
C0013227 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Drug
Item
Arzneimittel / Wirkstoff
text
C0013227 (UMLS CUI [1])
Dosis
Item
Dosis
float
C0178602 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Unit dose
Item
Einheit
text
C0869039 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Item
Einnahme
integer
C0013227 (UMLS CUI [1,1])
C2982514 (UMLS CUI [1,2])
Code List
Einnahme
CL Item
w (1)
CL Item
m (2)
Item
Applikationsform
integer
C0185125 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Applikationsform
CL Item
Tablette (1)
CL Item
Creme (2)
CL Item
Spray (3)
CL Item
Spritze (4)
CL Item
Zäpfchen (5)
CL Item
Tropfen (6)
CL Item
Infusion (7)
CL Item
andere (8)
Item
Applikationsweg
integer
C0013153 (UMLS CUI [1])
Code List
Applikationsweg
CL Item
p.o. (1)
CL Item
i.v. (2)
CL Item
i.m. (3)
CL Item
s.c. (4)
CL Item
rektal (5)
CL Item
lokal (6)
CL Item
p.inh. (7)
CL Item
transdermal (8)
CL Item
anderer (9)
Modified release dosage form
Item
Retardform
boolean
C1709058 (UMLS CUI [1])
Indication of medication
Item
Indikation
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start of medication
Item
Start
partialDate
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
End of medication
Item
End
partialDate
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Ongoing medication
Item
Medikation andauernd
boolean
C0013227 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])

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