Neurocognition Clinical Trial
Official title:
Translational Research Evaluating Neurocognitive Memory Processes
The purpose of this study is to evaluate the psychometric properties and utility of new,
computerized, neurocognitive measures in humans with depression, and humans with depression
undergoing electroconvulsive therapy (ECT). The benefits of the study outweigh the risk as
there is the possibility of developing better computerized neurocognitive measures, and the
risks are limited to no more than minimal test related fatigue and psychological stress.
Depressed humans, depressed human participants undergoing ECT, and humans diagnosed with
Parkinson's disease (age 18-85) will be invited to participate in this study. After
providing informed consent participants will undergo a clinical psychiatric evaluation to
confirm the inclusion/exclusion criteria. After the clinical psychiatric evaluation,
participants will complete common and new neurocognitive measures. There will be a total of
two testing visits (baseline, 1-month follow-up). The anticipated duration of the
participant's involvement is no more than 2 study visits that can take place over a 4-day
period (i.e., the clinical evaluation can occur on day 1 and the neuropsychological measures
can be administered on day 2 of each study visit) equating to approximately 6-hours (3-hours
each day) per study visit.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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