Bodini, Luca
Bonetto, Chiara
Cheli, Simone
Del Piccolo, Lidia
Rimondini, Michela
Rossi, Alberto
Carta, Angela
Porru, Stefano
Amaddeo, Francesco
Lasalvia, Antonio http://orcid.org/0000-0001-9963-6081
Article History
Received: 2 April 2022
Accepted: 17 August 2022
First Online: 2 September 2022
Declarations
:
: The study protocol will be conducted to ensure adherence to the principles of Good Clinical Practice and procedures and to comply with Italian laws, as described in the following documents and agreed upon by the study investigators:1. ICH Harmonized Tripartite Guidelines for Good Clinical Practice 19962. D. L. vo n.211 del 24 giugno 20034. D. L. vo n.200 6 novembre 20075. D.M. 21 dicembre 20076. Legge n.189 8 novembre 20127. SPIRIT “Standard Protocol Items: Recommendations for Intervention trials” [CitationRef removed].The trial will be conducted according to the principles of the Declaration of Helsinki and in accordance with the Medical Research Involving Human Subjects Act (WMO).Eligible participants will be told that they can withdraw from participating in the study when they change their mind in the time between having contact with the researcher, filling in the questionnaire and participating in the study as well as during the study.Important protocol modifications will be communicated to the intervention participants by email.Data entry by study participants using the online process will be protected by the following measures:UnorderedList removedThe promoter is committed to keeping a hard copy of the informed consent for at least 7 years in compliance with DL 200/2007. All computers in which the data will be stored, once downloaded by the person responsible for data management, will be protected by keywords. The local in which the computers are kept will be locked and protected by alarm systems if unattended. Responsible for the custody is the principal investigator (Prof. Antonio Lasalvia).The study was approved on March 31, 2022, by the Ethics Committee of the Provinces of Verona and Rovigo (approval No. 3717CESC). All participants will be asked to provide a written informed consent to participate in the study. Prof. Antonio Lasalvia is responsible for obtaining informed consent. The trial was registered on ClinicalTrials.gov, Identifier: NCT05308537; April 1, 2022.
: Not applicable.
: The authors declare that they have no competing interests.