Including People with Parkinson's Disease in Clinical Study Design and Execution: A Call to Action
- PMID: 35404289
- PMCID: PMC9198722
- DOI: 10.3233/JPD-223190
Including People with Parkinson's Disease in Clinical Study Design and Execution: A Call to Action
Abstract
The proactive inclusion of patients in the design and execution of clinical studies has been an emerging focus for decades. Such participatory research helps to design studies better, by addressing relevant research questions and defining outcomes that matter to patients. Yet, much remains to be learned about the best methods and exact impacts of patient engagement in research in general, and more specifically, about the specific challenges that come with Parkinson's disease. Here we present the lived experiences of patient researchers living with Parkinson's disease, as a motivation for the value of their perspectives in research and as a call to action for empirical research on how to successfully include patient researchers.
Keywords: Parkinson’s disease; Patient participation; patient advocacy; patient preference.
Conflict of interest statement
The authors have no conflict of interest to report.
References
-
- Anderson M, McCleary KK (2015) From passengers to co-pilots: Patient roles expand. Sci Transl Med 7, 291fs225. - PubMed
-
- Laurance J, Henderson S, Howitt PJ, Matar M, Al Kuwari H, Edgman-Levitan S, Darzi A (2014) Patient engagement: Four case studies that highlight the potential for improved health outcomes and reduced costs. Health Aff (Millwood) 33, 1627–1634. - PubMed
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