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Define an 'informed consent script' and recall the specific details and components that researchers must include when verbally presenting this script to participants, as well as the correct timing of its delivery relative to the written consent form.
Question: Define an 'informed consent script' and recall the specific details and components that researchers must include when verbally presenting this script to participants, as well as the correct timing of its delivery relative to the written consent form.
Sample answer: An informed consent script is a prepared set of talking points used by researchers to orally describe a study to participants using clear, everyday language. This verbal explanation must occur before presenting the written consent form. The script must clearly detail the study procedures, potential risks and benefits, and the participant's absolute right to withdraw at any time.
Key points:
- An informed consent script is a prepared set of talking points used to orally describe a study in clear, everyday language.
- The verbal explanation must occur before presenting the written consent form.
- The script must clearly detail the study procedures.
- The script must detail potential risks and benefits.
- The script must state the participant's absolute right to withdraw at any time.
Rubric: To earn full credit, the response must: 1) Define the script as a prepared set of talking points used to orally describe the study in clear, everyday language. 2) Specify that the verbal explanation must occur before presenting the written consent form. 3) List the three mandatory components: study procedures, potential risks and benefits, and the participant's absolute right to withdraw at any time.
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Research Methods in Psychology - 4th American Edition @ KPU
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