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Dynamic Digital Biomarkers of Motor and Cognitive Function in Parkinson's Disease
Published on: July 24, 2019
Differences in Parkinson's Disease Populations: Teaching Hospitals Versus Other Settings and Implications for
Priti Gros1,2,3,4, Connie Marras1,2,3,4, Xuesong Wang4
1Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, University Health Network Toronto, Toronto, Ontario, Canada.
Insights
Parkinson disease (PD) patients seen at teaching hospitals for disease-modifying therapy (DMT) trials are younger and socioeconomically advantaged. These findings suggest PD clinical trials may not represent the general PD population, highlighting health equity concerns.
Area of Science:
- Neurology
- Clinical Trials
- Health Equity
Background:
- Parkinson disease (PD) disease-modifying therapy (DMT) trials typically recruit participants from teaching hospitals.
- It remains unclear if these trial participants accurately represent the broader PD population.
Purpose of the Study:
- To compare individuals with PD seen by neurologists in teaching hospitals (early disease stage, proxy for DMT trial eligibility) with those seen in other settings.
- To identify demographic and clinical differences between these groups.
Main Methods:
- Retrospective cohort study utilizing population-based data from Ontario, Canada (1995-2017).
- Identified individuals with PD and ≥1 visit to a teaching hospital neurologist within 3 years as a proxy for DMT trial eligibility.
- Compared demographic factors (age, sex, income, rurality, marginalization) and comorbidities.
- Assessed time to key clinical milestones (drug escalation, surgery/infusion, home care, dementia, long-term care, death).
Main Results:
- Out of 19,948 individuals with PD, 22.0% were seen by a teaching hospital neurologist.
- Individuals seen at teaching hospitals were younger, from more socioeconomically advantaged areas, and had fewer comorbidities.
- They experienced more drug escalation, surgical/infusion therapies, and home care.
- Conversely, they had less dementia, long-term care admission, and lower mortality rates compared to those seen in other settings.
Conclusions:
- Individuals with PD seen early by teaching hospital neurologists differ significantly from the general PD population.
- Disease-modifying therapy (DMT) trials in PD may potentially exclude individuals with faster disease progression and those from marginalized communities.
- These disparities underscore significant health equity issues within PD research and care, impacting the generalizability of trial findings.
Background:
Parkinson disease (PD) disease-modifying therapy (DMT) trials generally recruit individuals from teaching hospitals. Whether these participants represent the broader PD population is unclear.
Objective:
The objective was to compare individuals with PD seen by neurologists in teaching hospitals early in their disease-a proxy for DMT trial-eligible cohorts-with individuals seen in other settings.
Methods:
This retrospective cohort study using population-based data from Ontario (Canada) included individuals with PD from 1995 to 2017. Individuals with ≥1 PD visit with a teaching hospital neurologist within 3 years served as a proxy for DMT trial-eligible participants. Comparators were individuals with PD seen in other settings. We compared age, sex, income, rurality, marginalization, and comorbidities. We measured time to milestones, including drug escalation, surgical/infusion therapies, home care, dementia, long-term care admission, and death.
Results:
We identified 19,948 individuals with PD, of whom 4386 (22.0%) were seen by a teaching hospital neurologist and 15,562 (78.0%) in other settings. Compared to other settings, individuals with teaching hospital neurology visits were younger, belonged to socioeconomically advantaged neighborhoods, and had fewer comorbidities. They had more drug escalation (unadjusted hazard ratio = 1.30; 95% confidence interval [CI] = (1.21, 1.38), surgical or infusion therapies (2.35 [2.09, 2.64]), and home care (1.06 [1.02, 1.10]). They had less dementia (0.813 [0.77, 0.86]), long-term care admission (0.62 [0.58, 0.67]), and death (0.68 [0.64, 0.72]).
Conclusions:
Individuals with PD seen early by teaching hospital neurologists exhibited differences from the PD population. DMT trials in PD may exclude individuals with faster PD progression and from marginalized groups, impacting generalizability. Our study highlights health equity issues. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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