THREE FACTORS CHARACTERISTIC OF EXPERIMENTAL SETTINGS WERE HYPOTHESIZED TO INFLATE ARTIFACTUALLY THE RELIABILITY OF OBSERVATIONAL RECORDINGS: (a) knowledge by observers of when and by whom their reliability is being assessed, (b) the absence of the experimenter or a monitor to prevent cheating, and (c) computation of reliability within- (versus between-) observer group. Three groups of four observers used a standard nine-category observational code for disruptive behavior in recording from videotapes of a classroom for 22 days. Analyses revealed considerable increases in average occurrence reliability as a function of the main effects of each of the experimental factors. The specific increases in reliability associated with each of the 12 combinations of the experimental factors are presented for each category of behavior. The possible role of observer-training procedures and behavioral definitions as determiners of nonartifactual reliability is discussed.
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http://dx.doi.org/10.1901/jaba.1977.10-317 | DOI Listing |
Background: Clinical trial sponsors rely on research sites to identify and enroll appropriate study participants and to correctly and reliably assess symptom severity and function over the course of the trial. Low-recruiting sites represent a large financial and operational burden and may negatively impact trial success either by selecting inappropriate participants and/or high prevalence of data quality issues. We previously reported that >60% of sites in schizophrenia clinical trials recruited ≤5 participants.
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Alzheimers Dement
December 2024
Center for Health + Technology, University of Rochester Medical Center, Rochester, NY, USA.
Background: To bolster clinical trial infrastructure, there is a need to develop novel, valid, and reliable patient-reported outcome (PRO) measures capable of tracking clinically-relevant changes in Alzheimer's disease (AD), Mild Cognitive Impairment (MCI) and dementia over time. This research describes the development and validation of the Alzheimer's Disease-Health Index (AD-HI) as a tool to measure how patients feel and function in response to therapeutic intervention.
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Alzheimers Dement
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Background: Paper-and-pencil neuropsychological tests have traditionally been considered the "gold standard" for clinical testing in AD/ADRD, but they have significant limitations: They are time-consuming, costly to administer, vulnerable to examiner bias and error, and unavailable to some patients due to location, transportation challenges, and cost. Manual tests also fail to comprehensively analyze many aspects of test performance. Computerized neuropsychological test batteries have been developed to address these shortcomings.
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