What is informed consent? Why was it developed? How does it protect research subjects?

Question

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The Answer is Informed consent is a process in which a person is given all the necessary information about a medical procedure, clinical trial, or research study before deciding whether or not to participate. This includes details about the purpose of the study, potential risks and benefits, and the right to withdraw from the study at any time.

Informed consent was developed to ensure that individuals are fully aware of what they are agreeing to when participating in research or medical procedures. It is based on the ethical principle of respect for persons, which emphasizes the importance of allowing individuals to make autonomous decisions about their own health and well-being.

Informed consent protects research subjects by ensuring that they have all the information they need to make an informed decision about participating in a study. This helps to prevent coercion or manipulation and allows individuals to weigh the potential risks and benefits before agreeing to participate. It also helps to protect their rights and welfare throughout the duration of the study, as they have the right to withdraw at any time if they feel uncomfortable or if new information arises that may affect their decision. Overall, informed consent is a crucial component of ethical research and medical practice, as it prioritizes the well-being and autonomy of the individual.

What Is informed Consent? Why Was It Developed? How Does