Ethical Response to Adverse Research Outcomes
What is the primary ethical responsibility of a researcher when unanticipated adverse effects are observed in study participants?
A
Promoting continuation without disclosure to maintain integrity of the research design
B
Reporting these effects immediately and considering halting the study if necessary
C
Allowing the study to proceed as planned since participant consent was obtained initially
D
Advising against documenting adverse effects unless they align with the study’s prior defined risks
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