COVID-19 Vaccines Safety Tracking (CoVaST): Protocol of a Multi-Center Prospective Cohort Study for Active Surveillance of COVID-19 Vaccines’ Side Effects
dc.contributor.author | Riad, A. | |
dc.contributor.author | Schünemann, H. | |
dc.contributor.author | Attia, S. | |
dc.contributor.author | Periˇci´c, T.P. | |
dc.contributor.author | Žuljevi´c, M.F. | |
dc.contributor.author | Jürisson, M. | |
dc.contributor.author | Kalda, R. | |
dc.contributor.author | Lang, K. | |
dc.contributor.author | Morankar, S. | |
dc.contributor.author | Yesuf, E.A. | |
dc.contributor.author | Mekhemar, M. | |
dc.contributor.author | Danso-Appiah, A. | |
dc.contributor.author | Sofi-Mahmudi, A. | |
dc.contributor.author | Pérez-Gaxiola, G. | |
dc.contributor.author | Dziedzic, A. | |
dc.contributor.author | Apóstolo, J. | |
dc.contributor.author | Cardoso, D. | |
dc.contributor.author | Marc, J. | |
dc.contributor.author | Moreno-Casbas, M. | |
dc.contributor.author | Wiysonge, C.S. | |
dc.contributor.author | Qaseem, A. | |
dc.contributor.author | Gryschek, A. | |
dc.contributor.author | Tadi´c, I. | |
dc.contributor.author | Hussain, S. | |
dc.contributor.author | Khan, M.A. | |
dc.contributor.author | Klugarova, J. | |
dc.contributor.author | Pokorna, A. | |
dc.contributor.author | Košˇcík, M. | |
dc.contributor.author | Klugar, M. | |
dc.date.accessioned | 2021-11-15T11:12:39Z | |
dc.date.available | 2021-11-15T11:12:39Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Background:Coronavirus disease (COVID-19) vaccine-related side effects have a deter minant role in the public decision regarding vaccination. Therefore, this study has been designed to actively monitor the safety and effectiveness of COVID-19 vaccines globally. Methods: A multi country, three-phase study including a cross-sectional survey to test for the short-term side effects of COVID-19 vaccines among target population groups. In the second phase, we will monitor the booster doses’ side effects, while in the third phase, the long-term safety and effectiveness will be investigated. A validated, self-administered questionnaire will be used to collect data from the target population; Results: The study protocol has been registered at ClinicalTrials.gov, with the identifier NCT04834869. Conclusions: CoVaST is the first independent study aiming to monitor the side effects of COVID-19 vaccines following booster doses, and the long-term safety and effectiveness of said vaccines. | en_US |
dc.identifier.other | https://doi.org/10.3390/ijerph18157859 | |
dc.identifier.uri | http://ugspace.ug.edu.gh/handle/123456789/37104 | |
dc.language.iso | en | en_US |
dc.publisher | International Journal of Environmental Research and Public Health | en_US |
dc.subject | cohort studies | en_US |
dc.subject | cross-sectional studies | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | drug-related side effects and adverse reactions | en_US |
dc.subject | health personnel | en_US |
dc.subject | mass vaccination | en_US |
dc.subject | prevalence | en_US |
dc.title | COVID-19 Vaccines Safety Tracking (CoVaST): Protocol of a Multi-Center Prospective Cohort Study for Active Surveillance of COVID-19 Vaccines’ Side Effects | en_US |
dc.type | Article | en_US |
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