(formerly known as Oregon MS Registry)The Providence Multiple Sclerosis Center, in partnership with the Oregon Chapter of the National Multiple Sclerosis Society, is trying to identify every person with multiple sclerosis (MS) in the Pacific Northwest. If successful, this registry project will provide a better measure of the number of people with MS, and where they live, in this region of the country. The information could be used to better understand MS and to improve care for people with the condition. If you agree to take part in this project, please fill out the online registration form. Once we receive your completed form as your consent to participate, we will send you surveys to learn about you, your disease, and the medicines or services you use to manage your disease. Participation is voluntary, and you will not receive payment for participating. Whether you take part in the registry will have no effect on your relationship with your doctor. The information that you and other persons with MS provide will be used only for research purposes: for example, to compare the rate of MS between different states, or to compare the health care available to MS patients living in rural versus urban areas. Your personal identity will not be shown as part of any reports or made available to insurance or other companies. We will make every effort to protect your privacy. Instead of using your name, we will assign a number to represent your information. All information about you will be kept in secure, locked cabinets and password-protected computer files. We may send you additional surveys from time to time, but your privacy will always be protected. Only the MS Registry researchers will have access to the information you provide for the registry. You are not required to answer all survey questions. Also, you may choose to stop your participation at any time. If you decide to stop taking part in the MS Registry, please notify us by using the Pacific Northwest MS Registry contact information at the bottom of this page. Information that you have already provided will still be used in the registry, but no more information about you will be collected. If you have any questions about the registry, please call Dr. Stanley Cohan’s office at 503-216-1060. If you have any questions about the use of your information for research purposes, please call the Providence Health & Services Institutional Review Board at 503-215-6512, or the HIPAA privacy officer at 503-574-9123. Our sincere thanks for your willingness to participate in this very important project. Yours truly, 
Stanley Cohan, M.D., Ph.D.
Director, Pacific Northwest Multiple Sclerosis Registry Project
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