Answer:
informed consent is a process through
Ca
A
which a person is provided with all the relevant information about a research study, medical procedure, or treatment and then they voluntarily agree to participate or undergo the procedure. Informed consent is an essential ethical principle in research and healthcare, as it ensures that people are fully informed about the potential risks and benefits of a study or procedure, and they can make an autonomous decision about whether or not to participate
in the context of a research study, the
information that should be provided to
potential participants includes
•The purpose and goals of the research
study The potential risks and benefits of participating in the study
The procedures that will be followed
during the study The duration of the study and the time
comment required from participants
• Any costs or compensation associated with participation
The right to withdraw from the study at
any time
The confidentiality of the data collected and how it will be used The contact information of the
researchers in case of any questions or coocens
Providing this information to potential participants helps them to make an informed decision about whether or not to participate in the study. It also helps to ensure that people are not coerced or misled into participating in a study, and that their rights and welfare are protected throughout the study