

What exactly were you doing? In my case, it was counted as research, not clinical experience. You should probably get some additional clinical experience just to be safe unless you were doing procedures or otherwise spending time working with physicians.I have 1 year to volunteer and get as much medically related Extracurricular activities as I can. Because I only recently decided on going Pre-Med.
Does Clinical Research Count As Clinical Experience?
What do you mean that it was classified as research? You mean the adcoms disagreed with your classification or AMCAS changed it for you?What exactly were you doing? In my case, it was counted as research, not clinical experience. You should probably get some additional clinical experience just to be safe unless you were doing procedures or otherwise spending time working with physicians.
What do you mean that it was classified as research? You mean the adcoms disagreed with your classification or AMCAS changed it for you?
I have a clinical research job for my gap year that I REALLY want to be considered clinical exp.
Oh phew okay! Thanks.
How would it be classified under research then? If you just sit in a cubicle in a hospital and data mine most of the time? Hopefully my boss got my drift when I said I want patient contact.
Is the research subject a patient?... is research "patient care" or is it research? Clinical research can look a lot like medical care or it can be nothing like medical care and you throw in the "therapeutic misconception" (research subjects confuse their role as a subject in a research study with getting treatment as a patient) and you have a very confusing picture.
Regarding the therapeutic misconception, if patients are studied but get no treatment out of the study, then would that still be considered clinical exp? Or are you just trying to describe the ambiguity with the definition in general?
Therapeutic misconception refers to the phenomenon by which patients who are invited to enroll in clinical trials that test new and unproven therapies (most often against a placebo) believe that they will be helped by the study drug and disregard the probability that they will be assigned to placebo. They do not see what they are doing as participation in an experiment but rather an offer of a new treatment for their condition. They often believe the the new drug will be of benefit to them (although the only way to do an ethically designed study is to be at a point where you have equipoise, that is to say you don't know (haven't proven) that the new drug is better than the existing therapy for this disorder).
So, if you are involved in this type of project, what do adcoms think?