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

  1. 23/03/20 23/03/20 -
Titolare del copyright

DZNE

Caricato su

23 marzo 2020

DOI

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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)

Administrative Daten
Descrizione

Administrative Daten

Alias
UMLS CUI-1
C1320722
Studien ID
Descrizione

Study ID

Tipo di dati

text

Alias
UMLS CUI [1]
C2826693
Vor‐ oder Begleiterkrankungen
Descrizione

Vor‐ oder Begleiterkrankungen

Alias
UMLS CUI-1
C0262926
UMLS CUI-2
C0009488
Hatte/hat der/die Proband/in Vor‐ oder Begleiterkrankungen?
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
Nummer, Vor‐ oder Begleiterkrankungen
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
Diagnose
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
Start der Erkrankung
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
Ende der Erkrankung
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
Erkrankung andauernd
Descrizione

Ongoing disease

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C0012634
Checkliste Vorerkrankung
Descrizione

Checkliste Vorerkrankung

Alias
UMLS CUI-1
C1707357
UMLS CUI-2
C0262926
Diagnose
Descrizione

Bitte für jede Diagnose das Datum der Erstdiagnose notieren.

Tipo di dati

integer

Alias
UMLS CUI [1]
C0011900
Ist oder war der Proband / die Probandin aufgrund einer der folgenden Erkrankungen in Behandlung?
Descrizione

Medical history, treatment

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0087111
Erstdiagnose
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)

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative Daten
C1320722 (UMLS CUI-1)
Study ID
Item
Studien ID
text
C2826693 (UMLS CUI [1])
Item Group
Vor‐ oder Begleiterkrankungen
C0262926 (UMLS CUI-1)
C0009488 (UMLS CUI-2)
Item
Hatte/hat der/die Proband/in Vor‐ oder Begleiterkrankungen?
integer
C0262926 (UMLS CUI [1])
C0009488 (UMLS CUI [2])
Code List
Hatte/hat der/die Proband/in Vor‐ oder Begleiterkrankungen?
CL Item
Ja (1)
CL Item
Nein (0)
CL Item
Unbekannt (997)
Medical history/ concomitant diseases record
Item
Nummer, Vor‐ oder Begleiterkrankungen
integer
C0262926 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
C0243087 (UMLS CUI [2,1])
C2348184 (UMLS CUI [2,2])
Diagnosis
Item
Diagnose
text
C0011900 (UMLS CUI [1])
Start of disease
Item
Start der Erkrankung
partialDate
C0012634 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
End of disease
Item
Ende der Erkrankung
partialDate
C0012634 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Ongoing disease
Item
Erkrankung andauernd
boolean
C0549178 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
Item Group
Checkliste Vorerkrankung
C1707357 (UMLS CUI-1)
C0262926 (UMLS CUI-2)
Item
Diagnose
integer
C0011900 (UMLS CUI [1])
Code List
Diagnose
CL Item
Hypertonie (1)
CL Item
Hypercholesterinämie (2)
CL Item
Hypertriglyzeridämie (3)
CL Item
Sonst. Hyper‐ / Dyslipidämie (4)
CL Item
Diabetes Mellitus Typ 1 (5)
CL Item
Diabetes Mellitus Typ 2 (6)
CL Item
Diabetische Polyneuropathie (7)
CL Item
Herzinfarkt (8)
CL Item
Transitorische ischämische Attacke (TIA) (9)
CL Item
Koronare Herzkrankheit (KHK) (10)
CL Item
Schlaganfall (Ischämie) (11)
CL Item
Sinus‐ / Hirnvenenthrombose (12)
CL Item
Subarachnoidalblutung (13)
CL Item
Intracerebrale Blutung (14)
CL Item
Subduralhämatom (15)
CL Item
Schädelhirntrauma (16)
CL Item
Andere hirnorganische Vorerkrankungen (17)
CL Item
Periphere arterielle Verschlusskrankheit (18)
CL Item
Vorhofflimmern (19)
CL Item
Bluterkrankheit (20)
CL Item
Parkinson (21)
CL Item
Rheumatismus / Arthritis (22)
CL Item
Allergien / Unverträglichkeiten (23)
Item
Ist oder war der Proband / die Probandin aufgrund einer der folgenden Erkrankungen in Behandlung?
text
C0262926 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Code List
Ist oder war der Proband / die Probandin aufgrund einer der folgenden Erkrankungen in Behandlung?
CL Item
Ja (Ja)
CL Item
Nein (Nein)
CL Item
Unbekannt (Unb.)
CL Item
keine Angabe (k.A.)
Date of initial diagnosis
Item
Erstdiagnose
partialDate
C2316983 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])

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