Mental health trajectories and protective factors in individuals affected by natural disasters

Overview
Related items

This study systematically synthesizes evidence on mental health trajectories after natural disasters using the ResiMETA database to identify common patterns of mental distress and well-being, their prevalence, determinants, and the predictive role of psychosocial resilience factors.

SEEK ID: https://ldh.lir-mainz.imise.uni-leipzig.de/studies/6

Investigation: ResiMETA Meta-Analyses

Projects: ResiMETA

Study position:

Extended Metadata (Nfdi4Health MDS 3.3)

Expand All Collapse All

Resource classification(*)

Type of the resource : Substudy

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

Title/name : Mental health trajectories and protective factors in individuals affected by natural disasters
Language of the title/name : English

Acronym(s) of the Study

Acronym : n/a
Language of the acronym : English

Description(s) of the Study

Description : This study systematically synthesizes evidence on mental health trajectories after natural disasters using the ResiMETA database to identify common patterns of mental distress and well-being, their prevalence, determinants, and the predictive role of psychosocial resilience factors.
Language of the description : English

Keyword(s) describing the Study

Keyword(*) : systematic review

Keyword(*) : meta-analysis

Contributor(s) of the Study

Is it a personal or organisational contribution?(*) : Personal
Details about the contributing organisation(s)/institution(s)/group(s)
Contributor type(*) : Creator/Author
Funding identifier(s) : Not specified
Name of the organisation/institution/group(*) : Not specified
Details about the contributing person(s)
Contributor type(*) : Not specified
Given name(*) : Lea M.
Family name(s)(*) : Schaubruch
Digital identifier(s)
Identifier(*) : Not specified
Scheme(*) : Not specified
Email address : Not specified
Phone number : Not specified
Organisation(s) associated with the contributor
Name(*) : Leibniz Institute for Resilience Research (LIR)
Address : Wallstr. 7, 55122 Mainz, Germany
Web page : https://lir-mainz.de
Digital identifier(s)
Identifier(*) : 00q5t0010
Scheme(*) : ROR

Alternative identifiers

Type of the registry(*) : Not specified
Identifier(*) : Not specified

Characteristics of the Study

Is it an interventional or non-interventional Study? : Non-interventional
Specification of the type of the Study
Interventional Study type : []
Non-interventional Study type : []
Primary health condition(s) or disease(s) considered in the Study
Primary health condition or disease name(*) : Not specified
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 Study
Status of the ethics committee approval : Not specified
Overall Study status : Not specified
Participants enrolled by invitation? : Not specified
Start date : Not specified
End date : Not specified
Mono- or multicentric? : Not specified
Number of centers : Not specified
One or more data providers? : Not specified
Number of data providers : Not specified
Primary subject(*) : Person
Eligibility criteria for Study participants
Eligibility criteria: Minimum age
Minimum eligible age(*) : Not specified
Unit of age(*) : Not specified
Eligibility criteria: Maximum age
Maximum eligible age(*) : Not specified
Unit of age(*) : Not specified
Eligible gender : []
Inclusion criteria : Not specified
Exclusion criteria : Not specified
Population of the Study(*)
Coverage : International
Country(ies) : []
Region(s) and/or city(ies) : Not specified
Interventions of the Study
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 Study
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 Study
Name of the outcome measure(*) : Not specified
Description of the outcome measure : Not specified
Type of the outcome measure : Not specified
Time point(s) of assessment : Not specified
Additional information about the Study : Not specified
Additional assessments/measurements in the Study : []
Data sharing strategy of the Study(*)
Is it planned to share the data?(*) : Not specified
Supporting documents available in addition to the data : []
When and for how long will the data be available? : Not specified
Criteria for data access : Not specified
Additional information about data sharing : Not specified
DataSHIELD/Opal infrastructure available? : Not specified
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 Study
Temporal design : []
Target follow-up duration of the Study
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 Study
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