Participant-reported personal utility of genetic testing for Parkinson’s disease and interest in clinical trial participation

Hannah Oas, Lola Cook, Tae Hwi Schwantes-An, Laurence E. Walsh, Anne Marie Wills, Ignacio F. Mata, Martha A. Nance, James C. Beck, Anna Naito, Karen Marder, Roy N. Alcalay, Jennifer Verbrugge

Résultat de rechercheexamen par les pairs

Résumé

Genetic testing for Parkinson’s disease (PD) is infrequently performed due to perceptions of low utility. We investigated the personal utility in PD GENEration and how results lead to enrollment in additional research studies. Participants (n = 972) underwent genetic testing, results disclosure, genetic counseling, and completed a survey examining the perceived personal utility of their results and interest in participating in additional studies. Most participants found their genetic test results useful, including satisfying curiosity (81%), feeling good about helping the medical community (80%), and having information to share with family (77%). There were no significant differences in responses based on result type. Forty-five percent of participants expressed interest in participating in research studies; whereas 16% of participants confirmed enrollment. Our results suggest that participants find personal utility in genetic testing regardless of results. Although participants may be interested in enrolling in additional research, they may need support and resources.

Langue d'origineEnglish
Numéro d'article202
Journalnpj Parkinson's Disease
Volume10
Numéro de publication1
DOI
Statut de publicationPublished - déc. 2024

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

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