ID

40206

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 Clinical assessment dementia form. It has to be filled in at follow-up visits of the study.

Link

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

Keywords

  1. 3/16/20 3/16/20 -
  2. 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

Clinical assessment dementia (Klinische Einschätzung Demenz)

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
Visit type
Description

Bitte geben Sie an, für welchen Visit das vorliegende Dokument ausgefüllt werden soll.

Data type

integer

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0332307
Übergang zur Demenz nach klinischer Einschätzung
Description

Übergang zur Demenz nach klinischer Einschätzung

Alias
UMLS CUI-1
C4534461
UMLS CUI-2
C0497327
Hatte der Proband bereits in der letzten Visite eine Demenz?
Description

Falls "Nein", bitte das folgende Item ausfüllen.

Data type

integer

Alias
UMLS CUI [1,1]
C0497327
UMLS CUI [1,2]
C1517741
UMLS CUI [1,3]
C0545082
Hat nach Ihrer klinischen Einschätzung seit der letzten Visite ein Übergang zur Demenz stattgefunden?
Description

Falls "Ja", bitte die folgenden Items ausfüllen. (Bitte berücksichtigen Sie bei Ihrer Einschätzung auch die Ergebnisse von MMSE, CDR und FAQ)

Data type

boolean

Alias
UMLS CUI [1,1]
C2700061
UMLS CUI [1,2]
C0497327
UMLS CUI [1,3]
C1711239
UMLS CUI [1,4]
C1517741
UMLS CUI [1,5]
C0545082
Wenn ja, wählen Sie bitte die Art der Demenz aus und vervollständigen die zugehörigen Diagnosekriterien in den entsprechenden Dokumenten:
Description

Falls "Frontotemporale Demenz", bitte im folgendem Item spezifizieren.

Data type

integer

Alias
UMLS CUI [1,1]
C0497327
UMLS CUI [1,2]
C0332307
FTD Typ
Description

Frontotemporal dementia, type

Data type

integer

Alias
UMLS CUI [1,1]
C0338451
UMLS CUI [1,2]
C0332307

Similar models

Clinical assessment dementia (Klinische Einschätzung Demenz)

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
Visit type
integer
C0545082 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Visit type
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)
Item Group
Übergang zur Demenz nach klinischer Einschätzung
C4534461 (UMLS CUI-1)
C0497327 (UMLS CUI-2)
Item
Hatte der Proband bereits in der letzten Visite eine Demenz?
integer
C0497327 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
Code List
Hatte der Proband bereits in der letzten Visite eine Demenz?
CL Item
Ja (1)
CL Item
Nein (0)
Shift to Dementia since last visit
Item
Hat nach Ihrer klinischen Einschätzung seit der letzten Visite ein Übergang zur Demenz stattgefunden?
boolean
C2700061 (UMLS CUI [1,1])
C0497327 (UMLS CUI [1,2])
C1711239 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
C0545082 (UMLS CUI [1,5])
Item
Wenn ja, wählen Sie bitte die Art der Demenz aus und vervollständigen die zugehörigen Diagnosekriterien in den entsprechenden Dokumenten:
integer
C0497327 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Wenn ja, wählen Sie bitte die Art der Demenz aus und vervollständigen die zugehörigen Diagnosekriterien in den entsprechenden Dokumenten:
CL Item
Wahrscheinliche Demenz bei Alzheimer-Krankheit (AD) (4)
CL Item
Mögliche Demenz bei Alzheimer-Krankheit (AD) (5)
CL Item
Gemischte Demenz (7)
CL Item
Vaskuläre Demenz (VD) (8)
CL Item
Frontotemporale Demenz (FTD) (99)
CL Item
Diffuse Lewykörperchen Erkrankung (DLB) (19)
Item
FTD Typ
integer
C0338451 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
CL Item
Verhaltensvariante der Frontotemporalen Demenz (bvFTD) (9)
CL Item
Primäre progressive Aphasie (PPA) (10)
CL Item
Progressive nicht-flüssige Aphasie (PNFA) (11)
CL Item
Logopenische progressiver Aphasie (LPA) (12)
CL Item
Semantische Demenz (SemD) (13)
CL Item
bvFTD + ALS (14)
CL Item
PPA + ALS (15)
CL Item
ALS cognitively impaired (ALSci) (33)
CL Item
ALS behavioural impaired (ALSbi) (34)
CL Item
ALS + Apraxia of speech (37)
CL Item
ALSni mit genetischem Risiko für FTD (38)

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