Institutional Trust in Times of Corona

During the corona pandemic, governments of all countries appealed strongly to the trust of their populations by implementing drastic social and economic measures to prevent the spread of the virus. This study seeks to understand mechanisms that influence the level of institutional trust at the time of the corona pandemic. We are specifically interested in how three explanatory factors (socioeconomic status, experienced economic insecurity and dissatisfaction with the implemented corona policies) can, in mutual association, explain differences in institutional trust. This study is based on data from a large-scale panel survey on the social impact of COVID-19, carried out by Kieskompas research agency (N=22,696). Using a serial mediation analysis, we show that SES has both a direct and indirect effect on the level of institutional trust. People with higher SES experience less economic insecurity and have less dissatisfaction with the corona policies and, partly as a result of this, stronger institutional trust. It is also true that economic insecurity increases dissatisfaction with the corona policies and, partly as a result of this, weakens the level of trust. ### Competing Interest Statement The authors have declared no competing interest. ### Funding Statement This study was sponsored by The Netherlands Organisation for Health Research and Development (Dutch acronym ZonMw) project De maatschappelijke impact van COVID-19 (The social impact of COVID-19), project number: 10430032010034. The study was also sponsored by the Dutch municipalities of Rotterdam and The Hague ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: This research is approved by the Research Ethics Review Committee of the Faculty of Social Sciences, Free University (VU-FSW), Amsterdam, The Netherlands. I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable. Yes The data underlying the results presented in the study are available from the corresponding author.