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Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population

Developmental prosopagnosia (DP) is a neurodevelopmental condition, characterized by lifelong face recognition deficits. Leading research groups diagnose the condition using complementary computer-based tasks and self-report measures. In an attempt to standardize the reporting of self-report evidenc...

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Autores principales: Gray, Katie L. H., Bird, Geoffrey, Cook, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383837/
https://www.ncbi.nlm.nih.gov/pubmed/28405380
http://dx.doi.org/10.1098/rsos.160923
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author Gray, Katie L. H.
Bird, Geoffrey
Cook, Richard
author_facet Gray, Katie L. H.
Bird, Geoffrey
Cook, Richard
author_sort Gray, Katie L. H.
collection PubMed
description Developmental prosopagnosia (DP) is a neurodevelopmental condition, characterized by lifelong face recognition deficits. Leading research groups diagnose the condition using complementary computer-based tasks and self-report measures. In an attempt to standardize the reporting of self-report evidence, we recently developed the 20-item prosopagnosia index (PI20), a short questionnaire measure of prosopagnosic traits suitable for screening adult samples for DP. Strong correlations between scores on the PI20 and performance on the Cambridge Face Memory Test (CFMT) appeared to confirm that individuals possess sufficient insight into their face recognition ability to complete a self-report measure of prosopagnosic traits. However, the extent to which people have insight into their face recognition abilities remains contentious. A lingering concern is that feedback from formal testing, received prior to administration of the PI20, may have augmented the self-insight of some respondents in the original validation study. To determine whether the significant correlation with the CFMT was an artefact of previously delivered feedback, we sought to replicate the validation study in individuals with no history of formal testing. We report highly significant correlations in two independent samples drawn from the general population, confirming: (i) that a significant relationship exists between PI20 scores and performance on the CFMT, and (ii) that this is not dependent on the inclusion of individuals who have previously received feedback. These findings support the view that people have sufficient insight into their face recognition abilities to complete a self-report measure of prosopagnosic traits.
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spelling pubmed-53838372017-04-12 Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population Gray, Katie L. H. Bird, Geoffrey Cook, Richard R Soc Open Sci Psychology and Cognitive Neuroscience Developmental prosopagnosia (DP) is a neurodevelopmental condition, characterized by lifelong face recognition deficits. Leading research groups diagnose the condition using complementary computer-based tasks and self-report measures. In an attempt to standardize the reporting of self-report evidence, we recently developed the 20-item prosopagnosia index (PI20), a short questionnaire measure of prosopagnosic traits suitable for screening adult samples for DP. Strong correlations between scores on the PI20 and performance on the Cambridge Face Memory Test (CFMT) appeared to confirm that individuals possess sufficient insight into their face recognition ability to complete a self-report measure of prosopagnosic traits. However, the extent to which people have insight into their face recognition abilities remains contentious. A lingering concern is that feedback from formal testing, received prior to administration of the PI20, may have augmented the self-insight of some respondents in the original validation study. To determine whether the significant correlation with the CFMT was an artefact of previously delivered feedback, we sought to replicate the validation study in individuals with no history of formal testing. We report highly significant correlations in two independent samples drawn from the general population, confirming: (i) that a significant relationship exists between PI20 scores and performance on the CFMT, and (ii) that this is not dependent on the inclusion of individuals who have previously received feedback. These findings support the view that people have sufficient insight into their face recognition abilities to complete a self-report measure of prosopagnosic traits. The Royal Society Publishing 2017-03-01 /pmc/articles/PMC5383837/ /pubmed/28405380 http://dx.doi.org/10.1098/rsos.160923 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Psychology and Cognitive Neuroscience
Gray, Katie L. H.
Bird, Geoffrey
Cook, Richard
Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title_full Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title_fullStr Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title_full_unstemmed Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title_short Robust associations between the 20-item prosopagnosia index and the Cambridge Face Memory Test in the general population
title_sort robust associations between the 20-item prosopagnosia index and the cambridge face memory test in the general population
topic Psychology and Cognitive Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383837/
https://www.ncbi.nlm.nih.gov/pubmed/28405380
http://dx.doi.org/10.1098/rsos.160923
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