MDS User Guide I

Overview

Overview
Related items

An example project, showing how the metadata scheme should be filled.

SEEK ID: https://cgnbonn.fdm.digital-medicine.org/projects/20

Public web page: Not specified

Organisms: No Organisms specified

NFDI4Health PIs: No PIs for this Trial Project

Trial Project start date: 3rd Dec 2024

Trial Project end date: 2nd Dec 2124

Extended Metadata (Nfdi4Health MDS 3.3)

Expand All Collapse All

Id of the project(*) : Must be empty while creating the project. The ID will be automatically added when the project is published to the NFDI4Health GCHSH. Afterwards the ID must not be altered, since it is used to update the GCHSH data set.

Resource classification(*)

Type of the resource : Study

Title(s)/name(s) of the Project

Title/name : NFDI MDS 3.3 example for a 'Study'
Language of the title/name : English

Acronym(s) of the Project

Acronym : The acronym or official abbreviation of the project.
Language of the acronym : English

Description(s) of the Project

Description : The description of the project. Due to technical reasons, it is basically a duplication of the description above.
Language of the description : English

Keyword(s) describing the Project

Keyword(*) : Define Keywords for the project

Keyword(*) : One keyword per field

Language(s) of the project : English

Contributor(s) of the Project

Is it a personal or organisational contribution?(*) : Organisational
Details about the contributing organisation(s)/institution(s)/group(s)
Contributor type(*) : Other
Funding identifier(s) : Founding-ID of the organization
Name of the organisation/institution/group(*) : Name of the organization
Details about the contributing person(s)
Contributor type(*) : Not specified
Given name(*) :
Family name(s)(*) :
Digital identifier(s)
Identifier(*) :
Scheme(*) : Not specified
Email address :
Phone number :
Organisation(s) associated with the contributor
Name(*) : This field and the ones below can be filled for both. 'Personal' and 'Organisational' contributors. Fill in the details of the organization.
Address : Not specified
Web page : Not specified
Digital identifier(s)
Identifier(*) : Not specified
Scheme(*) : Not specified

Is it a personal or organisational contribution?(*) : Personal
Details about the contributing organisation(s)/institution(s)/group(s)
Contributor type(*) : Not specified
Funding identifier(s) :
Name of the organisation/institution/group(*) :
Details about the contributing person(s)
Contributor type(*) : Other
Given name(*) : Name of the person
Family name(s)(*) : Name of the person
Digital identifier(s)
Identifier(*) : Identifier of the person
Scheme(*) : Not specified
Email address : of the person
Phone number : of the person
Organisation(s) associated with the contributor
Name(*) : This field and the ones below can be filled for both. 'Personal' and 'Organisational' contributors. Fill in the details of the organization.
Address : Not specified
Web page : Not specified
Digital identifier(s)
Identifier(*) : Not specified
Scheme(*) : Not specified
Identifier(*) : Not specified
Scheme(*) : Not specified

Alternative identifiers

Type of the registry(*) : Other
Identifier(*) : Identifiers from other platforms like ClinicalTrials.gov or the DRKS

Characteristics of the Project

Is it an interventional or non-interventional Project? : Interventional
Specification of the type of the Project
Interventional Project type : Other
Non-interventional Project type : []
Primary health condition(s) or disease(s) considered in the Project
Primary health condition or disease name(*) : Use official terminology
Terminology/classification(*) : Not specified
Code of the health condition or disease : Not specified
Groups of diseases or conditions(*)
Which groups of diseases or conditions were the data collected on? : []
On which diseases or conditions were the data collected? : []
Collects mortality data? : Not specified
Administrative information about the Project
Status of the ethics committee approval : Not specified
Overall Project status : Not specified
Participants enrolled by invitation? : Not specified
Start date : Not specified
End date : Not specified
Mono- or multicentric? : Monocentric
Number of centers : 1
One or more data providers? : One data provider
Number of data providers : 1
Primary subject(*) : Person
Eligibility criteria for Project participants
Eligibility criteria: Minimum age
Minimum eligible age(*) : 6
Unit of age(*) : Minutes
Eligibility criteria: Maximum age
Maximum eligible age(*) : 99
Unit of age(*) : Years
Eligible gender : Male, Female
Inclusion criteria : List multiple criteria as follow: a hyphen before each criterion and a semicolon after each criterion except for the last, e.g.”- criterion1; - criterion 2; - criterion3.”
Exclusion criteria : List multiple criteria as follow: a hyphen before each criterion and a semicolon after each criterion except for the last, e.g.”- criterion1; - criterion 2; - criterion3.”
Population of the Project(*)
Coverage : National
Country(ies) : Germany
Region(s) and/or city(ies) : Bonn
Interventions of the Project
Name of the intervention(*) : Arm 1
Type of the intervention : Other
Additional information about the intervention : Intervention = arm
Name(s) of the arm(s) associated with the given intervention : Not specified
Name of the intervention(*) : Arm 2
Type of the intervention : Other
Additional information about the intervention : This one is linked to Arm 1
Name(s) of the arm(s) associated with the given intervention : Arm 1
Exposures of the Project
Name of the exposure : Not specified
Type of the exposure : Not specified
Additional information about the exposure : Not specified
Name(s) of the group(s) associated with the given exposure : Not specified
Outcome measures in the Project
Name of the outcome measure(*) : Outcome 1
Description of the outcome measure : Outcome measure = end point
Type of the outcome measure : Other
Time point(s) of assessment : After reading
Additional information about the Project : Not specified
Additional assessments/measurements in the Project : []
Data sharing strategy of the Project(*)
Is it planned to share the data?(*) : Yes, there is a plan to make data available
Supporting documents available in addition to the data : Other
When and for how long will the data be available? : Now and forever
Criteria for data access : Open access
Additional information about data sharing : The field "Is it planned to share the data?(*)" must be filled.
DataSHIELD/Opal infrastructure available? : No
Link to data request application : Not specified
Web page with additional information about data sharing : Not specified
Record linkage possible? : Not specified
Non-interventional aspects of the Project
Temporal design : []
Target follow-up duration of the Project
Target follow-up duration(*) : Not specified
Unit of time(*) : Not specified
Number of follow-ups conducted : Not specified
Biosamples retained in a biorepository : []
Specific types of retained biosamples : Not specified
Interventional aspects of the Project
Numerical phase : Other
Masking of intervention(s) assignment
Masking implemented? : false
Who is masked? : []
Additional information about masking : Not specified
Type of allocation of participants to an arm : Randomized
Off-label use of a drug product : Not applicable

MDS User Guide I

Related items