Answer:
cross-sectional study
Explanation:
Dr. Milano compares the performance of a group of 20-year-olds, a group of 45-year-olds, and a group of 70-year-olds on several tests of fluid intelligence and several tests of crystallized intelligence. Dr. Milano's investigation BEST exemplifies a <u>cross-sectional study</u>. A cross-sectional study is a type of observational study that analyzes data from a population, or a representative subset, at a specific point in time, it involves the use of different set of people who differ in the trait of interest. For example, the effect of age on intelligence level will involve the selection of subjects across the cross-section of ages of interest.
Maybe physical, mental, or emotional withdrawals
Answer:
I think I’m gonna need Moreno information
It's not true that there might be a light rain, actually, there might be a heavy rain (but not necessarily). In any case, if a cold front is coming, a sun block is not very useful, an umbrella might be better!
So the correct answer is: Get inside the house and close the windows because a storm is coming! (again, not necessarily, but there is a high chance)
Answer:
The answer to:
Which of the following is the most appropriate action to take for the investigator? Is:
We need to send a copy of the informed consent to the subject's wife. Then, after she speaks with the investigator she can sign the consent and send it back.
The correct answer for:
Which of the following statements in a consent form is an example of an exculpatory language?
Is:
I reject any possible compensation for injuries that might affect me as a result of my participation in this research.
Explanation:
The reasons behind the answers are: In the first question we need to find the quickest way to send the consent. It can be scanned, faxed, etc. But we need to understand that it has to be signed by the wife as she is the one with the authority to provide us the consent as the subject is unable to do so. The reason for the second question is that in the first place the consent has to include a direct statement of liberating the research, the organization behind it, and the person from any responsibility of complication.
