Original Research Article
Are Patients Whose Study Partners Are Spouses More Likely to be Eligible for Alzheimer’s Disease Clinical TrialsGrill J.D.a · Monsell S.b · Karlawish J.c
aMary Easton Center for Alzheimer’s Disease Research, Department of Neurology, UCLA David Geffen School of Medicine, Los Angeles, Calif., bNational Alzheimer’s Coordinating Center, University of Washington, Seattle, Wash., and cPenn Memory Center, Penn Center for Bioethics, Departments of Medicine and Medical Ethics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pa., USA
Joshua D. Grill, PhD
Mary Easton Center for Alzheimer’s Disease Research
UCLA David Geffen School of Medicine
10911 Weyburn Ave, Ste 200
Los Angeles, CA 90095 (USA)
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Background/Aims: Alzheimer’s disease (AD) clinical trials enroll two participants: a patient and a study partner. The primary caregiver most often fills the role of study partner and most trial study partners are spousal caregivers. Methods: AD trial inclusion criteria were applied to baseline data from 5,674 probable AD dementia research participants in the National Alzheimer’s Coordinating Center Uniform Data Set. Eligibility was compared among patients with spousal, adult child, and other types of study partners. Results: Patients with spousal study partners were more frequently eligible than patients with adult child study partners. Compared to patients with spousal study partners, patients with adult child study partners were more frequently ineligible because of age, residence in skilled nursing facility, low scores on the Mini-Mental State Examination, highscores on the Hachinski Ischemia Scale, and failure to fulfill a minimum number of weekly visits with the study partner. Conclusions: In this sample, patients with adult child study partners were less likely to qualify for AD clinical trials than were patients with spousal study partners. This may contribute to the lower representation of patients with adult child caregivers in these studies.
© 2012 S. Karger AG, Basel
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