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The study team obtained administrative clearance to access the patients from the Executive Director of the Uganda Cancer Institute. All methods were carried out in accordance with the relevant ethical guidelines and regulations. The research assistants were trained in the study procedures, and they provided adequate information about the study to the participants before recruitment and data collection. All study participants provided written informed consent prior to recruitment into the study. Participants who were unable to read or write were assisted by their attendants as witnesses. Information about the study was provided in the language chosen by the prospective participants. Data collection tools were designed in English and translated into two local languages\u2014Luganda and Acoli\/Luo. Participants were informed that participation in the study was voluntary; therefore, they were free to join the study, decline to participate, and\/or start to participate and withdraw from the study at any time without any negative consequences on their treatment at the UCI. Participants\u2019 privacy and confidentiality of data were observed by conducting the interviews in private rooms without non-participants and de-identifying data before analysis, respectively. Participants received nominal compensation for their time and transport of USD 3.5 after the interviews.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval and consent to participate"}},{"value":"Not applicable.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}}]}}