ID
40213
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 end of study form. It has to be filled in at the end of study or if early withdrawal.
Link
https://www.dzne.de/en/research/studies/clinical-studies/delcode/
Keywords
Versions (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
End of study participation (Studienende)
- StudyEvent: ODM
Description
Ende der Studienteilnahme
Alias
- UMLS CUI-1
- C2348568
- UMLS CUI-2
- C0444930
Description
Tag Monat Jahr
Data type
date
Alias
- UMLS CUI [1]
- C2985720
Description
(bitte geben Sie den primären Grund an) Bei "Erkrankung, die eine weitere Teilnahme verhindert" bitte in der fortlaufenden Dokumentation Begleiterkrankungen ergänzen. Bei "Wunsch des Probanden oder eines Angehörigen": Rücknahme der Einwilligung. Bei Tod bitte die folgende Itemgroup "Mortalität" ausfüllen.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0444930
Description
Other reason for end of participation
Data type
text
Alias
- UMLS CUI [1,1]
- C3840932
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0444930
Description
Mortalität
Alias
- UMLS CUI-1
- C1306577
Description
Tag Monat Jahr
Data type
date
Alias
- UMLS CUI [1]
- C1148348
Description
Place of death
Data type
integer
Alias
- UMLS CUI [1]
- C0421611
Description
In der Datenbank kann nach Eingabe der Todesursache der entsprechende ICD‐10‐Code ausgewählt werden.
Data type
text
Alias
- UMLS CUI [1]
- C0007465
Description
Cause of death ICD-10-Code
Data type
text
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C2598420
Description
Confirmation of cause of death by death certificate
Data type
integer
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C0750484
- UMLS CUI [1,3]
- C0011066
Description
Autopsy
Data type
integer
Alias
- UMLS CUI [1]
- C0004398
Description
Information given by
Data type
integer
Alias
- UMLS CUI [1]
- C0518629
Similar models
End of study participation (Studienende)
- StudyEvent: ODM
C0444930 (UMLS CUI-2)
C2348568 (UMLS CUI [1,2])
C0444930 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C0444930 (UMLS CUI [1,3])
C2598420 (UMLS CUI [1,2])
C0750484 (UMLS CUI [1,2])
C0011066 (UMLS CUI [1,3])