Welcome to our survey entitled "Urinary Symptoms and Parkinson’s Disease."
We would like ALL individuals with PD to participate, including individuals with and without urinary symptoms.
In our previous research assessing non-motor symptoms of PD, urinary symptoms were reported to have the greatest impact on day-to-day activities for many individuals with PD. Research has indicated that the frequency of urinary symptoms in patients with PD has been found to be up to 85%; symptoms may include increased frequency and urgency, needing to go to the bathroom at night (while sleeping), incomplete emptying, weak urinary stream, and urine leakage (i.e., incontinence). Although there are some improvements in the management of such symptoms, continued research focusing on understanding the experience of urinary symptoms through the eyes and voice of the person with PD is very important.
The information you provide will benefit individuals with PD and care partners as well as treatment providers so that they can better help you. We encourage your participation, but want to emphasize that your participation is completely voluntary and that all information that you provide will be kept strictly confidential.
The data collection for this report will conclude on December 1, 2019.
Please use the PREV and NEXT buttons at the bottom of each page to move through the survey. Using your browser's navigation buttons will take you out of the survey.