DynaCORE-C

Overview
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DynaCORE-C is an international cross-sectional online resilience study, carried out during the time of the first lockdown.

Programme: Dynamic Modelling of Resilience (DynaMORE)

SEEK ID: https://ldh.lir-mainz.imise.uni-leipzig.de/projects/14

Public web page: https://dynamore-project.eu/our-studies/dynacore-study/

NFDI4Health PALs: No PALs for this Project

Project start date: 22nd Mar 2020

Project end date: 20th Apr 2020

Extended Metadata (Nfdi4Health MDS 3.3)

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Id of the project(*) : nfdi4health-29988

Resource classification(*)

Type of the resource : Study

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

Title/name : Dynamic Modelling of Resilience - Cross-sectional Survey Study on Psychological Resilience to the Mental Health Consequences of the Corona Crisis
Language of the title/name : English

Acronym(s) of the Project

Acronym : DynaCORE-C
Language of the acronym : English

Description(s) of the Project

Description : DynaCORE-C was conducted by the European research consortium DynaMORE (Dynamic MOdelling of REsilience). In order to gain mechanistic insights about the relationship between described psycho-social resilience factors and resilience specifically in the COVID-19 crisis, the study assessed resilience factors, exposure to Corona crisis-specific and general stressors, as well as internalizing symptoms in a cross-sectional online survey conducted in 24 languages during the most intense phase of the first lockdown in Europe. Data was collected from N=15790 participants.
Language of the description : English

Keyword(s) describing the Project

Keyword(*) : Resilience

Keyword(*) : Cross-sectional

Keyword(*) : General Population

Keyword(*) : International

Keyword(*) : COVID-19

Language(s) of the project : English

Web page of the project : https://dynamore-project.eu/our-studies/dynacore-study/

Contributor(s) of the Project

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) : Not specified
Name of the organisation/institution/group(*) : Not specified
Details about the contributing person(s)
Contributor type(*) : Principal investigator
Given name(*) : Raffael
Family name(s)(*) : Kalisch
Digital identifier(s)
Identifier(*) : 0000-0002-9503-7601
Scheme(*) : ORCID
Email address : Not specified
Phone number : Not specified
Organisation(s) associated with the contributor
Name(*) : Leibniz Institute of Resilience Research
Address : Wallstr. 7, 55122 Mainz
Web page : https://lir-mainz.de/home
Digital identifier(s)
Identifier(*) : 00q5t0010
Scheme(*) : ROR

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) : Not specified
Name of the organisation/institution/group(*) : Not specified
Details about the contributing person(s)
Contributor type(*) : Principal investigator
Given name(*) : Oliver
Family name(s)(*) : Tüscher
Digital identifier(s)
Identifier(*) : 0000-0002-4023-5301
Scheme(*) : ORCID
Email address : Not specified
Phone number : Not specified
Organisation(s) associated with the contributor
Name(*) : Leibniz Institute for Resilience Research
Address : Wallstr. 7, 55122 Mainz
Web page : https://lir-mainz.de/home
Digital identifier(s)
Identifier(*) : 00q5t0010
Scheme(*) : ROR
Identifier(*) : Not specified
Scheme(*) : Not specified
Name(*) : Not specified
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(*) : Not specified
Identifier(*) : Not specified

Characteristics of the Project

Is it an interventional or non-interventional Project? : Non-interventional
Specification of the type of the Project
Interventional Project type : []
Non-interventional Project type : Cross-sectional
Primary health condition(s) or disease(s) considered in the Project
Primary health condition or disease name(*) : Stress resilience
Terminology/classification(*) : Free text
Code of the health condition or disease : not applicable
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 : Request for approval submitted, approval granted
Overall Project status : Completed: Recruitment, data collection, and data quality management completed normally
Participants enrolled by invitation? : No
Start date : 22 March 2020
End date : 20 April 2020
Mono- or multicentric? : Multicentric
Number of centers : 5
One or more data providers? : Not specified
Number of data providers : Not specified
Primary subject(*) : Person
Eligibility criteria for Project participants
Eligibility criteria: Minimum age
Minimum eligible age(*) : 18
Unit of age(*) : Years
Eligibility criteria: Maximum age
Maximum eligible age(*) : Not specified
Unit of age(*) : Not specified
Eligible gender : Male, Female, Diverse
Inclusion criteria : Informed consent is provided
Exclusion criteria : Not specified
Population of the Project(*)
Coverage : International
Country(ies) : []
Region(s) and/or city(ies) : Not specified
Interventions of the Project
Name of the intervention(*) : Not specified
Type of the intervention : Not specified
Additional information about the intervention : Not specified
Name(s) of the arm(s) associated with the given intervention : Not specified
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(*) : Stressor reactivity
Description of the outcome measure : See preregistration: https://osf.io/3cj8f
Type of the outcome measure : Primary
Time point(s) of assessment : Not specified
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 : []
When and for how long will the data be available? : Not specified
Criteria for data access : Data can be freely accessed via OSF: https://osf.io/rwnjq/files/osfstorage
Additional information about data sharing : Not specified
DataSHIELD/Opal infrastructure available? : Not specified
Link to data request application : https://osf.io/rwnjq/
Web page with additional information about data sharing : https://osf.io/rwnjq/
Record linkage possible? : false
Non-interventional aspects of the Project
Temporal design : Cross-sectional
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 : None retained
Specific types of retained biosamples : Not specified
Interventional aspects of the Project
Numerical phase : Not specified
Masking of intervention(s) assignment
Masking implemented? : Not specified
Who is masked? : []
Additional information about masking : Not specified
Type of allocation of participants to an arm : Not specified
Off-label use of a drug product : Not specified

DynaCORE-C

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