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ABSTRACT: Background
The informed consent process in clinical trials has been extensively studied to inform the development processes which protect research participants and encourage their autonomy. However, ensuring a meaningful informed consent process is still of great concern in many research settings due to its complexity in practice and interwined socio-cultural factors.Objectives
This study explored the practices and meaning of the informed consent process in two clinial trials conducted by Oxford University Clinical Research Unit in collaboration with the Hospital for Tropical Diseases in Ho Chi Minh City, Vietnam.Methods
We used multiple data collection methods including direct observervations, in-depth interviews with study physicians and trial participants, review
SUBMITTER: Nguyen YHT
PROVIDER: S-EPMC9843952 | biostudies-literature | 2023 Jan
REPOSITORIES: biostudies-literature