Rattanaprom, Panida
Ratinthorn, Ameporn
Sindhu, Siriorn
Viwatwongkasem, Chukiat
Article History
Received: 23 August 2022
Accepted: 30 July 2023
First Online: 15 August 2023
Declarations
:
: Ethical approval for the study was obtained from the Siriraj Institutional Review Board of the Faculty of Medicine, Mahidol University (No. Si 705/2018); the Human Research Ethics Committee, Faculty of Medicine, Prince of Songkla University (REC. 61–317-19–6); and the Research Ethics Committee, Faculty of Medicine, Chiang Mai University (ID: 5649). The ethics committee complies fully with international guidelines for human research protection, such as the Declaration of Helsinki, the Belmont Report, CIOMS Guidelines and the International Conference on Harmonization in Good Clinical Practice (ICH-GCP). The research proposal, participant information sheet, informed consent form, case record form and questionnaire were approved. Before data collection, human research protection certificates were presented to each hospital director of the research setting for permission. All agreed to permit data collection before the data collection began. All the enrolled head nurses of the intrapartum unit were accurately informed about the research purpose, and the researcher randomly selected the samples based on the inclusion criteria.The data collection progress must be reported at least once a year except where required more frequent by the Research Ethics Committee. Prior Research Ethics Committee approval is required before implementing any changes in the consent documents or protocol unless those changes are needed urgently for the safety of subjects. In addition, any event or new information that may affect the benefit/risk ratio of the study must be reported to the research ethic committee promptly.The informed consent was performed in a voluntary approached before data collection from the participant. Each participant was adequately informed of the aims, methods, possible conflicts of interest, institutional affiliations of the researcher, the anticipated benefits and potential risks of the study and the discomfort it may entail, post-study provisions and any other relevant aspects of the study. In addition, the participant was informed about the right to withdraw consent to participate at any time without reprisal.
: Not applicable.
: The authors declare no competing interests.