Answer:
Because many patients do not understand what is being asked of them when permission is requested, patients should learn about the HIPPA rules and violations prior to their visits. If they are not informed about HIPPA, it will slow down the process of allowing health researchers to gather the patients records to understand human diseases. A solution is informing them briefly about the HIPPA and asking the patient if researchers could use their info to help gather more data to help understanding human diseases, to determine treatment effectiveness, and to identify health and disease trend.
Step-by-step explanation: