Funding for this research was provided by:
National Institute of Mental Health (1R01MH110350-01A1)
Received: 12 November 2018
Accepted: 11 October 2019
First Online: 3 January 2020
Ethics approval and consent to participate
: We obtained IRB approval from the RAND Corporation (HSPC study 2016–0956), Mildmay Uganda Research Ethics Committee (MUREC) (02013–2018), as well as the Uganda National Council for Science and Technology (HS 2394). The study’s objectives, risks, and benefits will be explained to participants before they consent to participate. A signed consent form will be obtained from all participants prior to the pre-baseline visit. Participation is voluntary, and participants may withdraw from the study at any time.The conduct of the study will conform to the principles and relevant ethical guidelines covering informed consent, confidentiality, and data storage. No separate or additional procedures will be used to audit the conduct of the trial.
: Not applicable.
: The authors declare that they have no competing interests.