Patients and Research Subjects
Research subjects are an integral piece of all successful human subjects research and the Medical College of Wisconsin/Froedtert Hospital recognizes the importance of your decision whether or not to participate in a research study. Your participation is voluntary and you may choose not to participate or to discontinue participation at any time. Your decision whether or not to participate will not affect your current or future relations with the Medical College of Wisconsin. We hope this website will answer any questions you may have. Thank you for your interest in our research.
Generally, students, staff and faculty across campus, and members of the surrounding Milwaukee County and greater southeastern Wisconsin community may have an opportunity at one time or another to participate in research currently taking place at the Medical College of Wisconsin/Froedtert Hospital. In addition, our research includes both national and international participants. Frequently, participation requires filling out a survey, responding to service or opinion questionnaires, being interviewed or may be a component in the treatment plan for your disease. Typically, participants respond in person, by phone, email, regular mail or may be a part of the clinic visits you have with your physicians. Some of the research involves kinesthetic, physiological, or psychological experiments. The level of risk involved in a study depends upon its design, methodology, subject matter, and intervention or interaction with human subjects. It is important to consider the level of risk and compare it to any benefits when deciding whether or not to participate in human subjects research.
The Investigator conducting the study should provide you with answers to specific questions about the study. You may contact the Investigator or their research team with questions at any time before, during or after the study. If you would like to obtain information about a research study, or if you have questions, concerns, complaints or wish to discuss problems or your rights as a research subject with someone unaffiliated with the study, please contact the IRB Office at (414) 955-8844. Anonymity, if desired, will be protected to the extent possible. As an alternative method of contact, an email may be sent to email@example.com or a letter sent to Director- Human Research Protections Program, attn: Rsch Subject Advocate Medical College of Wisconsin, 8701 Watertown Plank Road, PO Box 26509, Milwaukee WI 53226-0509
Additional contact information is available on our contacts page.
Informed Consent Process
Informed Consent is a process of collaborative education and decision making that a prospective research participant must go through before freely volunteering to participate in a research study. The Principal Investigator, his/her research staff and the participant need to clearly understand the informed consent process. The Medical College of Wisconsin, with support by the National Institutes of Health, presents interactive web sites on the Informed Consent Process.