Mekonnen, Y
Wolde, E
Bekele, A
Mehari, Z
Abebe, S
Hagos, T
Tadesse, Y
Taye, T
Asire, G
Nigatu, T
Kumar, S
Girma, S
Salasibew, M
Funding for this research was provided by:
Children’s Investment Fund Foundation (2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463, 2001-04463)
Article History
Received: 7 May 2023
Accepted: 9 August 2023
First Online: 29 August 2023
Declarations
:
: The study obtained informed verbal consent from study participants and this was approved by the ethical board of the Amhara Public Health Institute (APHI). Written consent was not required for this study. The ethical approval number was APHI/D.G-01/3/1026.All methods of this study were carried out in accordance with the Helsinki Declaration on the ethical principles for medical research involving human subjects [CitationRef removed].All experimental protocols of the study were approved by the Amhara Public Health Institute (APHI) ethical board.The study did not involve gathering sensitive information from the pregnant women, and there was no invasive procedure or test of drugs or procedures used in the ENAT intervention. The ENAT intervention simply improved availability and access of point of care testing and infection prevention which are within the Ethiopia national ANC guideline. The services given to the pregnant women were in accordance with the Ethiopia National ANC guideline [CitationRef removed].Basic socio-demographic information was obtained at enrolment into the study. Following enrollment services provided to the pregnant women during their routine ANC visits were extracted from the routine ANC and delivery registration books. No name was used to link the pregnant women with the services they obtained and their pregnancy outcomes. Information were linked through unique identifiers.Study midwives/nurses were specifically instructed on the importance of obtaining informed consent and respecting the voluntary participation of respondents, their privacy, and the confidentiality of the data collected. There was no remuneration to pregnant women who participated in this study. All the information and data were accumulated, organized, stored, analyzed, and retrieved, guaranteeing confidentiality.
: Not applicable.
: MS, AB, ZM, TT are employees of CIFF. Their participation in this research did not in any manner undermine the professional impartiality and integrity of the results presented in this manuscript. The remaining authors have no conflicts of interest to declare.