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Muzafer Sherif studied group dynamics and the role of conflict and cooperation with a group of campers. The counselors were all members of the research team, unbeknownst to the campers. If this experiment were to be repeated, in order to follow the ethical guidelines dictated by the American Psychological Association (APA), before the study commenced, each parent or guardian would need to need to know the nature of the research and express a willingness for their children to participate. This is known as

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Answer:

Informed consent.

Step-by-step explanation:

Informed consent simply means a decision taken by or for an individual after being informed about the proposed research or procedures, risks, benefits, and details about a research or procedures.

There need to be or have a legal informed consent if you have described to your patient or participants the research or procedure you are going to do in detail.

The features of the informed consent process.

1. The act of learning the key informations about a clinical trial before deciding whether or not to participate.

2. It helps individuals to agree or disagree in participating, health care providers involved in the trial explain the details of the study and others.

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