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Note on licensure: The MS in Forensic Psychology is not a licensure program and does not prepare an individual to become a licensed psychology professional. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
It is said to be the most common cause of neurological disability in young adults in the Western world ; however, as life expectancy is only minimally affected , the impact of disability can be felt across a relatively long lifespan.Clinical symptoms characteristically first present in people in their mid-20s to 30s; however, a wide spectrum exists, and as the general population ages, the prevalence of MS in older adults rises .Despite the average age of those living with MS in western countries having reached an all-time high (mid-50s) , relatively little is known about the clinical characteristics of “older” adults with MS or their use of and response to treatment.The study was approved by the University of British Columbia’s Clinical Research Ethics Board, which includes informed patient consent.Patients had to be registered with a BCMS clinic between August 1980 and December 2004 and diagnosed with definite MS (based on Poser or Mc Donald criteria) [13, 22]. Please note that the materials you are required to submit may vary depending on the academic program to which you apply. Walden’s MS in Forensic Psychology allows you to choose the General Program or from a variety of specializations that focus on a specific population or subject.
The programs of study for the General Program and specializations each consist of 10 courses.
The Kaplan-Meier survival curves and the log-rank test were used to compare time from MS onset to confirmed and sustained EDSS 6.
The independent effect of potential risk factors on time to reach EDSS 6 was examined using a multivariable Cox regression model, with sex, onset symptoms, and onset age category (AOMS versus LOMS), with relapsing-onset and primary-progressive MS patients examined separately. Firstly, patients with an unknown time to EDSS 6 (because EDSS 6 had already been reached at the first clinic visit) were included by imputing the midway time between MS onset and the first clinic assessment.
Secondly, data were censored once a DMD was initiated.
For aim 2, similar bivariate statistics were used when comparing the baseline characteristics of the IFNβ-treated versus contemporary and historical untreated cohorts, along with the Mann-Whitney-Wilcoxon test for ordinal variables.
Patient characteristics (clinical and demographic) are shown in Table 1. Paul Gustafson is supported by the Natural Sciences and Engineering Research Council of Canada.