ID
40208
Descrizione
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 - medical history/ comorbidities . Prior medical history should be filled in at baseline. If there are newly diagnosed diseases during the study period, add in the course of the study.
collegamento
https://www.dzne.de/en/research/studies/clinical-studies/delcode/
Keywords
versioni (1)
- 23/03/20 23/03/20 -
Titolare del copyright
DZNE
Caricato su
23 marzo 2020
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 4.0
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DELCODE: DZNE – Longitudinal Cognitive Impairment and Dementia Study
Cumulative documentation - medical history/ comorbidities (Kumulative Dokumentation - Vor-/ Begleiterkrankung)
Descrizione
Vor‐ oder Begleiterkrankungen
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0009488
Descrizione
(Falls ja, tragen Sie diese bitte in das folgende Item ein)
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0262926
- UMLS CUI [2]
- C0009488
Descrizione
Medical history/ concomitant diseases record
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C2348184
- UMLS CUI [2,1]
- C0243087
- UMLS CUI [2,2]
- C2348184
Descrizione
Bitte berücksichtigen Sie die folgenden Diagnosen: Arterieller Hypertonus, Diabetes Mellitus, Hypercholesterinämie, Schlaganfall, Epilepsie, Herzinfarkt/KHK, rezidivierende depressive Episode, Krebserkrankungen, Schilddrüsenerkrankungen, Niereninsuffizienz, Lungenentzündungen, bronchiale Infekte, Probleme beim Schlucken, Dysphagie. Zur Unterstützung können Sie das Formular Checkliste Vorerkrankungen zu Hilfe nehmen. In der Datenbank kann nach Eingabe der Diagnose der entsprechende ICD‐10‐Code ausgewählt werden.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0011900
Descrizione
Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.
Tipo di dati
partialDate
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0808070
Descrizione
Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.
Tipo di dati
partialDate
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0806020
Descrizione
Ongoing disease
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0012634
Descrizione
Checkliste Vorerkrankung
Alias
- UMLS CUI-1
- C1707357
- UMLS CUI-2
- C0262926
Descrizione
Bitte für jede Diagnose das Datum der Erstdiagnose notieren.
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0011900
Descrizione
Medical history, treatment
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0087111
Descrizione
Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.
Tipo di dati
partialDate
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0262926
- UMLS CUI [1,3]
- C0087111
Similar models
Cumulative documentation - medical history/ comorbidities (Kumulative Dokumentation - Vor-/ Begleiterkrankung)
C0009488 (UMLS CUI-2)
C0009488 (UMLS CUI [2])
C2348184 (UMLS CUI [1,2])
C0243087 (UMLS CUI [2,1])
C2348184 (UMLS CUI [2,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0262926 (UMLS CUI-2)
C0087111 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])