ID

40212

Descrição

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 - procedures. Prior procedures should be filled in at baseline. Procedures that are performed during the study period should be added in the course of the study.

Link

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

Palavras-chave

  1. 23/03/2020 23/03/2020 -
Titular dos direitos

DZNE

Transferido a

23 de março de 2020

DOI

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Licença

Creative Commons BY-NC 4.0

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DELCODE: DZNE – Longitudinal Cognitive Impairment and Dementia Study

Cumulative documentation - Procedures (Kumulative Dokumentation - Prozeduren)

Administrative Daten
Descrição

Administrative Daten

Alias
UMLS CUI-1
C1320722
Studien ID
Descrição

Study ID

Tipo de dados

text

Alias
UMLS CUI [1]
C2826693
Prozeduren
Descrição

Prozeduren

Alias
UMLS CUI-1
C0087111
Hatte der Proband / die Probandin in der Vergangenheit eine oder mehrere Behandlungen erhalten?
Descrição

(Falls ja, tragen Sie diese bitte in das folgende Item ein)

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1444637
Nummerierung der Prozeduren
Descrição

Procedures, record

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2348184
Prozedur
Descrição

Bitte berücksichtigen Sie: Herzschrittmacherimplantationen, Gewebetransplantationen, Bluttransfusionen, Geburten und Gelenkersatz‐Operationen.

Tipo de dados

text

Alias
UMLS CUI [1]
C0087111
Indikation
Descrição

(optional)

Tipo de dados

text

Alias
UMLS CUI [1]
C3146298
Datum
Descrição

Tag Monat Jahr. Tages‐ und Monatsangabe ist optional. Jahresangabe muss dokumentiert werden.

Tipo de dados

partialDate

Alias
UMLS CUI [1]
C2584899

Similar models

Cumulative documentation - Procedures (Kumulative Dokumentation - Prozeduren)

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Administrative Daten
C1320722 (UMLS CUI-1)
Study ID
Item
Studien ID
text
C2826693 (UMLS CUI [1])
Item Group
Prozeduren
C0087111 (UMLS CUI-1)
Item
Hatte der Proband / die Probandin in der Vergangenheit eine oder mehrere Behandlungen erhalten?
integer
C0087111 (UMLS CUI [1,1])
C1444637 (UMLS CUI [1,2])
Code List
Hatte der Proband / die Probandin in der Vergangenheit eine oder mehrere Behandlungen erhalten?
CL Item
Ja (1)
CL Item
Nein (0)
CL Item
Unbekannt (997)
Procedures, record
Item
Nummerierung der Prozeduren
integer
C0087111 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Procedure
Item
Prozedur
text
C0087111 (UMLS CUI [1])
Indication
Item
Indikation
text
C3146298 (UMLS CUI [1])
Date of procedure
Item
Datum
partialDate
C2584899 (UMLS CUI [1])

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