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Juliet Fockler
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Publications
Juliet Fockler's Publications
Community-engaged efforts to increase retention of Black American online registry participants.
Digital efforts in Spanish for enrolling Latino adults in the Brain Health Registry.
Evaluating the Accuracy of Web-Based and In-Clinic Subjective Cognitive Decline Assessments in Detecting Cognitive Impairment: Multicohort Study.
Self- and Informant-Report Cognitive Decline Discordance and Mild Cognitive Impairment Diagnosis.
Test taking location and practice effects as factors contributing to scores on remotely administered neurocognitive performance tests in a sample of older adults.
Participant completion of longitudinal assessments in an online cognitive aging registry: The role of medical conditions.
The ADNI Administrative Core: Ensuring ADNI's success and informing future AD clinical trials.
The ADNI4 Digital Study: A novel approach to recruitment, screening, and assessment of participants for AD clinical research.
Unsupervised Online Paired Associates Learning Task from the Cambridge Neuropsychological Test Automated Battery (CANTAB®) in the Brain Health Registry.
Associations between Participant Characteristics and Participant Feedback about an Unsupervised Online Cognitive Assessment in a Research Registry.
Brain Health Registry Study Partner Portal: Novel infrastructure for digital, dyadic data collection.
Brain health registry updates: An online longitudinal neuroscience platform.
Evaluation of the Electronic Clinical Dementia Rating for Dementia Screening.
The Community Engaged Digital Alzheimer's Research (CEDAR) Study: A Digital Intervention to Increase Research Participation of Black American Participants in the Brain Health Registry.
Understanding Online Registry Facilitators and Barriers Experienced by Black Brain Health Registry Participants: The Community Engaged Digital Alzheimer's Research (CEDAR) Study.
Association of Major Depressive Disorder with remotely administered measures of cognition and subjective report of cognitive difficulties across the adult age spectrum.
Digital culturally tailored marketing for enrolling Latino participants in a web-based registry: Baseline metrics from the Brain Health Registry.
Remote blood collection from older adults in the Brain Health Registry for plasma biomarker and genetic analysis.
Brain health registry GenePool study: A novel approach to online genetics research.
Data-Driven Participant Recruitment: Findings from the Alzheimer's Disease Neuroimaging Initiative 3.
Effects of sex, race, ethnicity, and education on online aging research participation.
Predicting amyloid status using self-report information from an online research and recruitment registry: The Brain Health Registry.
Online study partner-reported cognitive decline in the Brain Health Registry.
The Brain Health Registry: An internet-based platform for recruitment, assessment, and longitudinal monitoring of participants for neuroscience studies.
