Linnemayr, Sebastian
Huang, Haijing Crystal http://orcid.org/0000-0002-8696-557X
Wagner, Zachary
Onkundi, Faith Kemunto
Mukasa, Barbara
Odiit, Mary
Funding for this research was provided by:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (1R01HD104555-01)
RAND Corporation
Article History
Received: 10 May 2023
Accepted: 10 June 2023
First Online: 9 August 2023
Declarations
:
: We obtained IRB approval from the Mildmay Uganda Research Ethics Committee IRB (# MUREC-2022–102), as well as the Uganda National Council for Science and Technology (# HS2207ES). The study objectives, and risks and benefits will be explained to participants in advance at the time they are consenting to participate in the study. The study coordinators will obtain signed consent and assent forms from all participants prior to the pre-baseline visit. Participation is voluntary, and they are welcome to withdraw at any point during the study.The conduct of the study will conform to the principles and relevant ethical guidelines covering informed consent, confidentiality, and data storage. No separate and/or additional procedures are needed for auditing trial conduct.
: Not applicable. No identifying images or other personal or clinical details of participants are presented here or will be presented in reports of the trial results. Informed consent materials are attached as supplementary materials.
: The authors declare that they have no competing interests.