About this trial
Social interaction is supported by several brain regions, which are involved in encoding socio-perceptual information, attributing affective and mental states to other conspecifics, and ultimately enabling the orchestration of an appropriate response. In this view, cognitive control mechanisms are necessary to select relevant information, allocate resources, and generate inferences. There is a close link between the mechanisms underlying social cognition and social conceptual knowledge, relating, for example, to abstract concepts such as "friendship". For example, children with autism spectrum disorder (ASD) show impairments in social interactions, and also in the ability to use all those abstract concepts that relate to internal states of the individual as well as to interactions between people.
Behavioral studies have shown how experience can impact the characterization of abstract concepts, influencing their personal, introspective, and contextual characteristics. Neuroimaging studies have also reported that, through mechanisms of brain plasticity, experience modulates neural networks shared with non-experts (e.g., by increasing brain volume and/or functional activity), but can also lead to the recruitment of additional brain resources, thus enriching the knowledge gained by experts. To date, the role of different types and levels of expertise in influencing the neural representation of specific categories of abstract concepts, and in particular social concepts, has not yet been fully elucidated.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Participant is willing and able to give informed consent for participation in the study
Male or female, aged between 25 and 50 years
Right-handed dominance
Normal vision or hypo-vision corrected with contact lenses
Disqualifiers
Clinical and/or anamnestic evidence of neurological, psychiatric, or systemic disorders
Drug addiction and/or abuse of neuroactive drugs;
Contraindications and incompatibilities with MRI, and specifically presence of para-magnetic or ferro-magnetic metal body prostheses; presence of permanent biomedical implants (e.g., pacemakers, neuro-stimulators); pregnancy status; claustrophobia. Pregnancy status will be self-reported by the participants.
Trial design
Factorial
Treatments tested in this trial
Behavioral and MR scanning
Other interventionAfter enrollment, participants will be screened on the basis of the inclusion and exclusion criteria. Subsequently, during the single study, participants will be administered a series of questionnaires (Edinburgh Handedness Inventory - Short Form; Evaluation of social related abilities, competences, and traits: Autism Quotient Test, DASS-21, SIAS, DERS, Ekman test; SET; I-TIPI, and conceptual ratings on semantic dimensions (moral, social, political). Then, an MR acquisition without contrast will be performed. Specifically, we will acquire structural, resting state and functional (BOLD) sequences, in the latter case during the administration of a semantic categorization task. The task is aimed to ascertain participants' responses time and accuracy in processing abstract concepts. Participants will be required to indicate the category of each of the visually presented words by means of button press. The study visit will last 3 hours in total.
Treatment groups
Trial outcomes
Primary outcomes
Correlation between participants' accuracy rate and BOLD signal
Evaluate whether and how social expertise modulate the neural representation of different types of abstract concepts, and in particular social concepts.
Secondary outcomes
Correlation between participants' accuracy rate and scores in Autism Quotient Test, DASS-21, SIAS, DERS, Ekman test, SET and I-TIPI
Evaluate whether and how individual affective and social characteristics modulate the characterization and the neural representation of different types of abstract concepts, and in particular social concepts.
Sponsors and contacts
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