ID

40207

Beschrijving

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/

Trefwoorden

  1. 23-03-20 23-03-20 -
Houder van rechten

DZNE

Geüploaded op

23 maart 2020

DOI

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Licentie

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
Beschrijving

Administrative Daten

Alias
UMLS CUI-1
C1320722
Studien ID
Beschrijving

Study ID

Datatype

text

Alias
UMLS CUI [1]
C2826693
Medikation
Beschrijving

Medikation

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

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

Datatype

integer

Alias
UMLS CUI [1]
C0013227
Nummerierung, Medikation
Beschrijving

Medication, record

Datatype

integer

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

Drug

Datatype

text

Alias
UMLS CUI [1]
C0013227
Dosis
Beschrijving

Bei Kombipräparaten bitte die jeweiligen Einzeldosen aufführen

Datatype

float

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

Unit dose

Datatype

text

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

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

Datatype

integer

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

Type of application

Datatype

integer

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

Route of application

Datatype

integer

Alias
UMLS CUI [1]
C0013153
Retardform
Beschrijving

Modified release dosage form

Datatype

boolean

Alias
UMLS CUI [1]
C1709058
Indikation
Beschrijving

Indication of medication

Datatype

text

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

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

Datatype

partialDate

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

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

Datatype

partialDate

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

Ongoing medication

Datatype

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)
Datatype
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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