Carta, Mauro Giovanni
Cossu, Giulia
Pintus, Elisa
Zoccheddu, Rosanna
Callia, Omar
Conti, Giuliana
Pintus, Mirra
Gonzalez, Cesar Ivan Aviles
Massidda, Maria Valeria
Mura, Gioia
Sardu, Claudia
Contu, Paolo
Minerba, Luigi
Demontis, Roberto
Pau, Massimiliano
Finco, Gabriele
Cocco, Eleonora
Penna, Maria Petronilla
Orrù, Germano
Kalcev, Goce
Cabras, Federico
Lorrai, Stefano
Loviselli, Andrea
Velluzzi, Fernanda
Monticone, Marco
Cacace, Enrico
Musu, Mario
Rongioletti, Franco
Cauli, Alberto
Ruggiero, Valeria
Scano, Alessandra
Crisafulli, Antonio
Cosentino, Sofia
Atzori, Laura
Massa, Elena
Mela, Quirico
Fortin, Dario
Migliaccio, Gianmario
Nardi, Antonio Egidio
Angermeyer, Matthias
Preti, Antonio http://orcid.org/0000-0001-9003-9838
Funding for this research was provided by:
Fondazione Banco di Sardegna
Article History
Received: 23 May 2020
Accepted: 16 April 2021
First Online: 7 May 2021
Declarations
:
: The Regional Committee for Medical and Health Research Ethics, region of Sardinia, has approved the study with reference number PG/2018/15546 (approved on 25 October 2018). All the protocol modifications are reported to the Regional Committee for Medical and Health Research Ethics for approval and will be detailed in the dissemination of the study. Participants are provided with written and oral information about the study before enrolment. All participants have signed informed consent before enrolment in the study, and the Regional Committee for Medical and Health Research Ethics regulates the use of all data. The consent will be acquired in a quiet room of the enrollment center before the start of any procedure, including the initial assessment. The consent form will be illustrated to each participant with a debriefing about the study. The consent is delivered to a member of the research team. The consent form and other related documents given to participants are available upon request by the authors. There are no current plans for future studies using the data collected in this trial. If the usefulness of the data collected during the trial was to emerge (e.g., stored blood sample to perform some Sars-Cov-2 assessment in the sample, as antigens), the participants will be contacted and their informed consent will be specifically required to the new purpose.
: Not applicable.
: The authors declare that they have no competing interests.