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
Abstract Background Informed 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 tri...
Main Authors: | Masunga K. Iseselo, Edith A. M. Tarimo |
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Format: | Article |
Language: | English |
Published: |
BMC
2024-03-01
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Series: | BMC Medical Ethics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12910-024-01033-z |
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