ID

41508

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 form contains information about the MRI investigation.

Link

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

Keywords

  1. 10/30/20 10/30/20 -
Copyright Holder

DZNE (German Center for Neurodegenerative Diseases)

Uploaded on

October 30, 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

Magnetic resonance imaging investigation (3T‐MRT‐Untersuchung)

Administrative Daten
Description

Administrative Daten

Alias
UMLS CUI-1
C1320722
Studien ID
Description

Study ID

Data type

text

Alias
UMLS CUI [1]
C2826693
Visitendatum
Description

Tag Monat Jahr

Data type

date

Alias
UMLS CUI [1]
C1320303
Visite
Description

Bitte geben Sie an, für welche Visite das vorliegende Dokument ausgefüllt werden soll.

Data type

integer

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0332307
Aufklärung zum MRT
Description

Aufklärung zum MRT

Alias
UMLS CUI-1
C0024485
UMLS CUI-2
C1533716
Datum der Aufklärung
Description

Date of information

Data type

date

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C2985782
Aktueller MRT‐Kontraindikationsbogen vorliegend?
Description

Wenn ja, bitte Datum und Daten unter fortlaufenden Daten aktualisieren. Wenn Händigkeit noch nicht dokumentiert ist, bitte ebenfalls unter fortlaufende Daten eingeben.

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [1,3]
C0684224
UMLS CUI [1,4]
C0150312
Durchführung des 1. MRT
Description

Durchführung des 1. MRT

Alias
UMLS CUI-1
C0205435
UMLS CUI-2
C0024485
UMLS CUI-3
C1518965
MRT‐ Untersuchungsdatum:
Description

MRI-Investigation date

Data type

date

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0011008
Durchgeführt nach MRT‐Protokoll:
Description

Performed according to MRI protocol

Data type

text

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0597198
UMLS CUI [1,3]
C1550543
UMLS CUI [1,4]
C2348563
Lokal archiviert
Description

Locally archived

Data type

boolean

Alias
UMLS CUI [1,1]
C1517927
UMLS CUI [1,2]
C4724030
Durchführung des 2. MRT
Description

Durchführung des 2. MRT

Alias
UMLS CUI-1
C0205436
UMLS CUI-2
C0024485
UMLS CUI-3
C1518965
MRT‐ Untersuchungsdatum:
Description

MRI-Investigation date

Data type

date

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0011008
Durchgeführt nach MRT‐Protokoll:
Description

Performed according to MRI protocol

Data type

text

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0597198
UMLS CUI [1,3]
C1550543
UMLS CUI [1,4]
C2348563
Lokal archiviert
Description

Locally archived

Data type

boolean

Alias
UMLS CUI [1,1]
C1517927
UMLS CUI [1,2]
C4724030

Similar models

Magnetic resonance imaging investigation (3T‐MRT‐Untersuchung)

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])
Date of Visit
Item
Visitendatum
date
C1320303 (UMLS CUI [1])
Item
Visite
integer
C0545082 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Visite
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)
CL Item
Baseline (0)
Item Group
Aufklärung zum MRT
C0024485 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
Date of information
Item
Datum der Aufklärung
date
C0024485 (UMLS CUI [1,1])
C2985782 (UMLS CUI [1,2])
MRI contraindication document present
Item
Aktueller MRT‐Kontraindikationsbogen vorliegend?
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0684224 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,4])
Item Group
Durchführung des 1. MRT
C0205435 (UMLS CUI-1)
C0024485 (UMLS CUI-2)
C1518965 (UMLS CUI-3)
MRI-Investigation date
Item
MRT‐ Untersuchungsdatum:
date
C0024485 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Performed according to MRI protocol
Item
Durchgeführt nach MRT‐Protokoll:
text
C0024485 (UMLS CUI [1,1])
C0597198 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
Locally archived
Item
Lokal archiviert
boolean
C1517927 (UMLS CUI [1,1])
C4724030 (UMLS CUI [1,2])
Item Group
Durchführung des 2. MRT
C0205436 (UMLS CUI-1)
C0024485 (UMLS CUI-2)
C1518965 (UMLS CUI-3)
MRI-Investigation date
Item
MRT‐ Untersuchungsdatum:
date
C0024485 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Performed according to MRI protocol
Item
Durchgeführt nach MRT‐Protokoll:
text
C0024485 (UMLS CUI [1,1])
C0597198 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
Locally archived
Item
Lokal archiviert
boolean
C1517927 (UMLS CUI [1,1])
C4724030 (UMLS CUI [1,2])

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