Noémie Treichel, Daniel Dukes, Koviljka Barisnikov, Andrea C. Samson
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引用次数: 0
Abstract
Objectives
Previous studies on the comprehension and appreciation of humour in individuals with Williams syndrome (WS) have only included complex types of humour that required complex cognitive abilities. Additionally, although individuals with WS have been described as having a bias towards positive emotions, no study has investigated their expressive responses to humour.
Methods
The present study examined basic humour processing skills, as well as expressive responses to simple humorous and non-humorous stimuli in individuals with WS (N = 8) compared to mental-age matched typically developing (TD) children (N = 9). Participants were shown short funny and non-funny excerpts of the movies “Ice Age” and “Madagascar” and were asked to rate their level of amusement. Their expressive responses, namely smiles and laughs, were coded and analysed.
Results
Individuals with WS seem to be able to discriminate between humorous and non-humorous conditions and appreciate simple humorous content as much as TD individuals. As such, they are equally able to process simple types of humour as their mental-age matched counterparts. Additionally, and in line with their positivity bias, individuals with WS expressed more frequent and more intense laughter than the control group.
Conclusion
Individuals with WS appreciate simple humour as much as TD individuals, and they seem to display a particularly high expressivity in response to humorous stimuli.
期刊介绍:
Advances in Neurodevelopmental Disorders publishes high-quality research in the broad area of neurodevelopmental disorders across the lifespan. Study participants may include individuals with:Intellectual and developmental disabilitiesGlobal developmental delayCommunication disordersLanguage disordersSpeech sound disordersChildhood-onset fluency disorders (e.g., stuttering)Social (e.g., pragmatic) communication disordersUnspecified communication disordersAutism spectrum disorder (ASD)Attention-deficit/hyperactivity disorder (ADHD), specified and unspecifiedSpecific learning disordersMotor disordersDevelopmental coordination disordersStereotypic movement disorderTic disorders, specified and unspecifiedOther neurodevelopmental disorders, specified and unspecifiedPapers may also include studies of participants with neurodegenerative disorders that lead to a decline in intellectual functioning, including Alzheimer’s disease, amyotrophic lateral sclerosis, Creutzfeldt-Jakob disease, vascular dementia, Lewy body dementia, frontotemporal dementia, corticobasal degeneration, Huntington’s disease, and progressive supranuclear palsy. The journal includes empirical, theoretical and review papers on a large variety of issues, populations, and domains, including but not limited to: diagnosis; incidence and prevalence; and educational, pharmacological, behavioral and cognitive behavioral, mindfulness, and psychosocial interventions across the life span. Animal models of basic research that inform the understanding and treatment of neurodevelopmental disorders are also welcomed. The journal is multidisciplinary and multi-theoretical, and encourages research from multiple specialties in the social sciences using quantitative and mixed-method research methodologies.