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CQXA

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Factorial designs include

Question 2

Because single-subject experimental designs tend to be used in clinical settings, the researcher has an additional ethical obligation to
 
  A) obtain the permission of a legal guardian.
  B) provide a more detailed informed consent form.
  C) provide a less detailed informed consent form.
  D) take into account the client's or patient's developmental, physical, or psychological condition in treatment planning.



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krakiolit

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Reply #1 on: Aug 4, 2018
Answer to Question 1



Answer to Question 2

Answer: D




CQXA

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Reply 2 on: Aug 4, 2018
:D TYSM


upturnedfurball

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Reply 3 on: Yesterday
Wow, this really help

 

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