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A researcher submits a protocol for a study that poses significant psychological risks to participants but offers no potential benefits. If the researcher's informed consent procedures are exceptionally thorough and explicitly detail all possible harms, the Institutional Review Board (IRB) should approve the study because participants' right to informed choice has been fully satisfied.

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Updated 2026-06-16

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KPU

Research Methods in Psychology - 4th American Edition @ KPU

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