Discuss how you would approach informed consent and IRB Approval if you were to implement your action research study. Explain how you would ensure that participants enter the research of their free will and with an understanding of the study and any potential dangers.
Freedom from Harm:
Explain how the literature you reviewed and your plan for implementation leads you to believe what you are doing is an appropriate intervention and not exposing your participants to risk.
Anonymity and Confidentiality:
Explain your planned measures to use anonymity and confidentiality to avoid privacy invasion and potential harm.
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