Research Participant Rights

Every research participant has the following rights:
  • To be treated with respect, including respect for your decision whether or not you wish to enroll in, continue in, or stop being in a study.
  • To choose to stop being in a study at any time.
  • To be given time to read the consent form and have the study explained to you.
  • To be given time to ask questions, and to be told whom you can contact if you have any more questions.
  • To be given a copy of the consent form after you have signed it.
Questions that you should ask before you agree to participate in a research study:
  • Why is the research being done?
  • What will be done to me as part of the research?
  • How will I benefit from the research?
  • Could the research hurt me?
  • What will the researcher do with my information?
  • Will the research cost me anything?
  • Who pays if I am unexpectedly injured in the study?
  • How long will the study last?
  • What happens if I decide to leave the study early?
Reporting Concerns:

Concerns and complaints are taken very seriously and are treated with the utmost respect and all possible confidentiality.  If you have questions about your participation in a research study, we encourage you to first contact the Principal Investigator (PI) or other study team member listed at the phone number/email on your consent form or information sheet. 

If you remain dissatisfied with the outcome, are unable to receive a response after an appropriate amount of time, or have a concern about your participation that you do not wish to discuss with the PI or study team member, you can contact the Institutional Review Board (IRB).  The IRB is a group of scientists, clinicians and lay persons who review each research study before it starts to ensure that the study is well-designed, does not involve unnecessary risks, and ensures the safety of research participants.

You may report a concern or complaint to the IRB office by calling 701-231-8908 or emailing ndsu.irb@ndsu.edu.

If you contact the IRB office, please try to have your consent form or study information available because you may be asked to provide information about the specific study in question.



Keywords:
participant rights, research subjects, concerns or complaint reporting 
Doc ID:
148433
Owned by:
Kristy S. in NDSU Research and Creative Activity
Created:
2025-02-18
Updated:
2025-02-18
Sites:
NDSU Research and Creative Activity