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...

Full description

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