Consider the ethics of the following research scenario:
A researcher wants to understand the relationship between horror movies and memory in teenagers. The researchers had teens ages 14 through 17 view various types of horror movies over the course of six hours (roughly 3 movies). Prior to viewing, the teens were given visual and auditory memory tasks. After viewing, they were readministered tests of visual and auditory memory. The researchers found that after six hours of viewing horror films, visual memory declined but auditory memory remained the same.
Imagine you are a member of the IRB reviewing this study before it is conducted. What issues might it have with the research?
What are the risks to the participants in the study?
Can you think of any other way that this study could be designed to reduce the risks to the participants?
1. Potential Psychological Harm:
2. Informed Consent and Comprehension:
3. Debriefing and Support:
4. Alternative Research Design:
5. Data Collection and Confidentiality:
Conclusion:
While understanding the relationship between horror movies and memory is an interesting research question, the potential risks to the participants in this study are significant. By addressing the concerns outlined above and implementing alternative research designs that minimize risks, the IRB can ensure ethical and responsible research practices that protect the well-being of adolescent participants.
Remember, ethical research prioritizes participant safety and informed consent. Balancing scientific curiosity with protecting human subjects is paramount in any research, especially when involving potentially vulnerable populations like teenagers.