Sloot, Rosa
Glenshaw, Mary T.
van Niekerk, Margaret
Meehan, Sue-Ann
Funding for this research was provided by:
U.S. President’s Emergency Plan for AIDS Relief (U2GGH000320)
Article History
Received: 8 July 2019
Accepted: 2 April 2020
First Online: 19 April 2020
Ethics approval and consent to participate
: The Health Research Ethics Committee of Stellenbosch University (N08/10/307) approved the study, which was conducted according to the guiding principles within the Declaration of Helsinki. The study was also reviewed in accordance with the Centers for Disease Control and Prevention (CDC) human research protection procedures and was determined to be research, but CDC did not interact with human subjects nor have access to identifiable data or specimens for research purposes. All clients who underwent an HIV rapid test provided written consent on their client record form. No incentives were provided.
: Not applicable.
: The authors declare that they have no competing interests.