Maintaining informed consent validity during lengthy research protocols.
نویسندگان
چکیده
Are you participating in a research study? What is the general purpose of the study? Are you required to participate in this research study? Is the treatment you are getting now the same as it was before you started the study? [Follow-up: How it is different?] Are you allowed to withdraw from the study? If you decide to withdraw, will you be able to receive treatment? Are there any possible risks or discomforts in the study? [Follow-up: Can you tell me about them?] Maintaining Informed Consent Validity during Lengthy Research Protocols
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ورودعنوان ژورنال:
- IRB
دوره 29 6 شماره
صفحات -
تاریخ انتشار 2007