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  1. Comprehension of informed consent and voluntary participation in registration cohorts for phase IIb HIV vaccine trial in Dar Es Salaam, Tanzania: a qualitative descriptive study.Edith A. M. Tarimo & Masunga K. Iseselo - 2024 - BMC Medical Ethics 25 (1):1-13.
    BackgroundInformed consent as stipulated in regulatory human research guidelines requires volunteers to be well-informed about what will happen to them in a trial. However, researchers may be faced with the challenge of how to ensure that a volunteer agreeing to take part in a clinical trial is truly informed. This study aimed to find out volunteers’ comprehension of informed consent and voluntary participation in Human Immunodeficiency Virus (HIV) clinical trials during the registration cohort.MethodsWe conducted a qualitative study among volunteers who (...)
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  • Examining study participants’ decision-making and ethics-related experiences in a dietary community randomized controlled trial in Malawi.Joseph Mfutso-Bengo, Gabriella Chiutsi-Phiri, Edward Joy, Eric Umar, Kate Millar & Limbanazo Matandika - 2021 - BMC Medical Ethics 22 (1):1-14.
    BackgroundThe participant recruitment process is a key ethical pivot point when conducting robust research. There is a need to continuously review and improve recruitment processes in research trials and to build fair and effective partnerships between researchers and participants as an important core element in ensuring the ethical delivery of high-quality research. When participants make a fair, informed, and voluntary decision to enroll in a study, they agree to fulfill their roles. However, supporting study participants to fulfill study requirements is (...)
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