The Lifestyle and Parkinson’s Disease Longitudinal Study (LPLS) is a multi-year project at Concordia University Irvine assessing how a wide range of personal lifestyle choices—from diet to exercise—impact the progression of Parkinson’s Disease (PD) among people with Parkinson’s living near Orange County. We serve more than 100 participants every summer who volunteer to let us measure their disease state, physical fitness, psychological and cognitive health, and lifestyle habits. Their data contributes to what is one of the most comprehensive databases of lifestyle and PD progression in people diagnosed with the disease and allows our researchers and partners to investigate a wide range of questions relating to:
Non-pharmaceutical symptom management The effects of exercise, medication, and diet on quality of life for people with PD Exciting new technology for assessing PD at home and in the clinic And much more!
All our participants receive personalized health reports that present and explain their data. Participants may share these reports with their physicians, and each measurement includes interpretation and citations.
Every summer, ~20 undergraduate research assistants conduct data collection, gaining valuable skills with clinical human subjects research and learning about movement disorders.
The LPLS is approved by the Institutional Review Board (IRB) at Concordia University Irvine (#6070).
Questions? Email us at [email protected]. If you’re diagnosed with PD and want to participate, click the link below to sign up for this summer.
Sign Up
Who is eligible to participate?
We welcome anyone with a physician’s diagnosis of Parkinson’s Disease to participate in the study. Participants must be able to physically attend data collection at 1530 Concordia W, Irvine, CA 92612 for ~3 hours, once a summer for at least one summer, and to complete basic physical movements like standing, sitting and walking. Participants are under no obligation to return for subsequent years, but it is highly encouraged
Who to expect as a participant? (Measures & Movements)
Data collection happens once a summer and lasts for ~3 hours. The measurements involve interviews, surveys, and simple movements of daily life such as walking, sitting and standing. To learn more about the measurements, visit the What to Expect as a Participant? tab
Health Report
Our health reports are meant to give participants a comprehensive look at their data that they can share with their movement disorder specialist or general practitioner. Visit the Health Report tab to learn more.
Contact Us!
Email us at [email protected]