Search results for " Psicologia clinica"

showing 10 items of 421 documents

A cross-country examination of emotional eating, restrained eating and intuitive eating: Measurement Invariance across eight countries

2020

This study examined the measurement invariance of three scales that assessed emotional eating, restrained eating, and intuitive eating across eight countries (Australia, Belgium, Canada, China, Italy, Japan, Spain and the United States) in order to determine their suitability for cross-country body image research. A total of 6272 young adults took part in this study. Participants completed an online survey including the Emotional Eating subscale of the Three Factor Eating Questionnaire-Revised 21, the Restraint subscale of the Eating Disorder Examination Questionnaire, and the Reliance on Hunger and Satiety Cues subscale of The Intuitive Eating Scale-2. Multi-group confirmatory factor analy…

Male050103 clinical psychologyEmotional eatingHungerEmotionsIntuitive eating050109 social psychologySettore M-PSI/08 - PSICOLOGIA CLINICAEatingBelgiumJapanSurveys and QuestionnairesMultiple indicatorYoung adultGeneral PsychologyApplied PsychologyMeasurement invarianceIntuitive eatingdigestive oral and skin physiology05 social sciencesRestraint eatingEating disorder examination questionnaireEmotional eatingConfirmatory factor analysisItalyFemaleCuesPsychologyClinical psychologyCross-Cultural ComparisonCanadaChinaSocial PsychologyAdolescentPsychometricsSatiationYoung AdultBody ImageHumans0501 psychology and cognitive sciencesMeasurement invarianceCross countryAustraliaFeeding BehaviorUnited StatesSpainCross-countryCross-country Emotional eating Intuitive eating Measurement i nvariance Restraint eating Young adultsFactor Analysis StatisticalYoung adults
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Examining bi-directionality between Fear of Missing Out and problematic smartphone use. A two-wave panel study among adolescents.

2020

Abstract Background In recent years, the Fear of Missing Out (FoMO) construct has been the object of growing attention in digital technology research with previous studies finding support for the relationship between FoMO and problematic smartphone use (PSU) among adolescents and young adults. However, no previous studies clarified the causal link between FoMO and PSU using a longitudinal design. Methods An auto-regressive, cross-lagged panel design was tested by using a longitudinal dataset with two waves of data collection (T0 and T1, one year apart). Participants included two hundred and forty-two adolescents (109 males and 133 females), with a mean age of 14.16 years, who filled out the…

MaleAdolescentTechnology research030508 substance abuseMedicine (miscellaneous)Toxicology03 medical and health sciencesYoung Adult0302 clinical medicineSettore M-PSI/08 - Psicologia ClinicaAutoregressive cross-lagged panelHumans030212 general & internal medicineLongitudinal modelingYoung adultData collectionSmartphone addictionFear of missing outFearSmartphone addictionPsychiatry and Mental healthClinical PsychologyCross-Sectional StudiesScale (social sciences)Fear of Missing OutCausal linkFemaleSmartphone0305 other medical sciencePsychologyConstruct (philosophy)Emotional regulationInternet Addiction DisorderClinical psychologyAddictive behaviors
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The Effects of Attachment, Temperament, and Self-Esteem on Technology Addiction: A Mediation Model among Young Adults

2022

Excessive use of technology has become a worldwide problem due to its high prevalence, fast growth rate, and undesirable consequences. However, little is known about underlying psychological mechanisms that maintain excessive use of technology. We investigated the mediating role of self-esteem, novelty seeking, and persistence on the relationship between attachment dimensions and technology addiction among young adults. Data were collected from 727 young adults (females, N = 478; 66.3 percent), aged 23.44 ± 3.02 years. Participants completed self-report measures of secure and insecure attachment dimensions, personality, and temperament characteristics (i.e., self-esteem, novelty seeking, an…

MaleAttachment; frequency of technology use; personality; technology addiction; temperament;Social PsychologyCommunicationattachment; frequency of technology use; personality; technology addiction; temperamentGeneral MedicinetemperamentPeer GroupSelf ConceptComputer Science ApplicationsHuman-Computer InteractionYoung Adultfrequency of technology usepersonalitytechnology addictionSettore M-PSI/08 - Psicologia ClinicaHumansFemaleSelf ReportApplied Psychologyattachment
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The quality of life in developing age children with celiac disease

2013

The moments that follow the diagnosis of celiac disease and the early stages of the gluten-free diet are extremely difficult and complex for parents and child, because they face an important change punctuated by self-denial and deprivation. The main objective of this research is to assess the impact of celiac disease on quality of life in subjects in developmental age, taking into account the perceptions of parents about the child's illness, with the aim to highlight the effect of disease on the child and the entire family.The study included both parents of 45 children aged between 2 and 10 years, with established celiac disease. To evaluate the effect of celiac disease on the lifestyle of …

MaleCeliac DiseaseCeliac disease Quality of life ChildSettore M-PSI/08 - Psicologia ClinicaChild PreschoolSurveys and QuestionnairesQuality of LifeHumansFemaleChildSettore MED/25 - PsichiatriaSettore MED/39 - Neuropsichiatria Infantile
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Emotional awareness and cognitive performance in borderline intellectual functioning young adolescents

2019

According to DSM-5 and ICD-10, borderline intellectual functioning (BIF) should not be classified properly as a disorder. However, BIF people may present relevant problems of adaptive functioning in several areas of daily activities, and they seem to be more vulnerable to mental diseases. Young adolescence may be considered a particular period for emotional information processing. The "own and others' emotions" awareness can play a crucial role in many daily life situations, such as decision making, interpersonal relationships, and decoding of facial expressions. On this background, a BIF young adolescents group underwent a neuropsychological assessment including emotional and cognitive dom…

MaleElementary cognitive taskEmotional awareneActivities of daily livingAdolescentEmotionsDevelopmental psychology03 medical and health sciencesCognition0302 clinical medicineBorderline intellectual functioningAlexithymiaIntellectual DisabilitySurveys and QuestionnairesSettore M-PSI/08 - Psicologia ClinicamedicineHumansInterpersonal RelationsCognitive skillNeuropsychological assessmentCognitive performanceChildmedicine.diagnostic_testSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicafungiCognitionEmotional awareness borderline intellectual functioning cognitive performance young adolescentsmedicine.disease030227 psychiatryPsychiatry and Mental healthMentalizationYoung adolescentsFemalePsychologyPsychomotor Performance030217 neurology & neurosurgeryBorderline intellectual functioning
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An Initial Study of Alexithymia and Its Relationship With Cognitive Abilities Among Mild Cognitive Impairment, Mild Alzheimer's Disease, and Healthy …

2018

The present study examined the degree to which alexithymia is greater in mild Alzheimer's disease (AD) and mild cognitive impairment (MCI) relative to healthy volunteers (healthy comparison [HC]), and investigated relationships between alexithymia and cognition. Eighty-five participants (MCI = 30, AD = 21, HC = 34) underwent a comprehensive neuropsychological examination and completed the 20-item Toronto Alexithymia Scale (TAS-20). Relative to HC, MCI and AD reported greater alexithymia total scores and higher scores on the TAS factor difficulty in identifying feelings (DIF). The remaining two factors, difficulty in describing feelings (DDF) and externally oriented thinking showed no signif…

MaleEmotionsLuria-Nebraska Neuropsychological BatteryAlexithymia cognition attention executive functions memorybehavioral disciplines and activities03 medical and health sciencesToronto Alexithymia ScaleExecutive Function0302 clinical medicineCognitionAlexithymiaAlzheimer DiseaseMemorySettore M-PSI/08 - Psicologia ClinicamedicineHumansAttentionCognitive DysfunctionAffective SymptomsAgedSettore M-PSI/02 - Psicobiologia E Psicologia Fisiologica030214 geriatricsmedicine.diagnostic_testRecallNeuropsychologyCognitionExecutive functionsmedicine.diseaseHealthy VolunteersPsychiatry and Mental healthFemaleVerbal memoryPsychologyNeurocognitive030217 neurology & neurosurgeryClinical psychologyThe Journal of nervous and mental disease
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A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome.

2019

Benign familial neonatal epilepsy (BFNE) is caused, in about 5% of families, by mutations in the KCNQ3 gene encoding voltage-gated potassium channel subunits. Usually, newborns with BFNE show a normal neurological outcome, but recently, refractory seizures and/or developmental disability have been reported suggesting phenotype variability associated with KCNQ3-related BFNE. Here, we describe a proband from a BFNE family carrying a novel variant in the KCNQ3 gene. Regarding the paucity of data in the literature, we describe the presented case with a view to further establishing: (1) a genotype/phenotype correlation in order to define a BFNE phenotype associated with favourable outcome; (2) a…

MaleGenotypeelectroclinical featureInfantElectroencephalographygenotype-phenotype correlationSettore MED/39 - Neuropsichiatria InfantileEpilepsy Benign NeonatalKCNQ3 Potassium ChannelKCNQSettore MED/38 - Pediatria Generale E SpecialisticaPhenotypevoltage-gated potassium channelsSettore M-PSI/08 - Psicologia ClinicaHumansbenign familial neonatal epilepsyEpileptic SyndromesEpileptic disorders : international epilepsy journal with videotape
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A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability

2015

Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in patients affected with early onset epilepsies with wide phenotypic heterogeneity, ranging from benign familial neonatal seizures (BFNS) to epileptic encephalopathy with cognitive impairment, drug resistance, and characteristic electroencephalography (EEG) and neuroradiologic features. By contrast, only few KCNQ3 mutations have been rarely described, mostly in patients with typical BFNS. We report clinical, genetic, and functional data from a family in which early onset epilepsy and neurocognitive deficits segregated with a novel mutation in KCNQ3 (c.989G>T; p.R330L). Electrophysiological stu…

MaleGenotype-phenotype correlationmedicine.medical_specialtyNeurologyBenign familial neonatal seizuresMutantGenotype-phenotype correlationsmedicine.disease_causeMutagenesiKCNQ3 Potassium ChannelEpilepsyKCNQBenign Familial Neonatal Seizures KCNQ cognitive impairment voltage-gated potassium channels epilepsy mutagenesis genotype-phenotype correlationsSeizuresSettore M-PSI/08 - Psicologia ClinicaIntellectual DisabilityIntellectual disabilitymedicineHumansKCNQ2 Potassium ChannelVoltage-gated potassium channelBenign familial neonatal seizuresGenetic Predisposition to DiseaseGenetic TestingChildGenetic testingGeneticsMutationEpilepsymedicine.diagnostic_testGenetic heterogeneitybusiness.industryMedicine (all)Benign familial neonatal seizures; Cognitive impairment; Epilepsy; Genotype-phenotype correlations; KCNQ; Mutagenesis; Voltage-gated potassium channels; Child; Female; Genetic Testing; Humans; Intellectual Disability; KCNQ2 Potassium Channel; KCNQ3 Potassium Channel; Male; Mutation; Pedigree; Seizures; Genetic Predisposition to Disease; Neurology (clinical); Neurology; Medicine (all)Benign familial neonatal seizuremedicine.diseaseSeizureSettore MED/39 - Neuropsichiatria InfantilePedigreeCognitive impairmentNeurologyMutagenesisMutationFemaleNeurology (clinical)businessVoltage-gated potassium channelsHuman
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Behavioral and electrophysiological correlates of cognitive control in ex-obese adults

2017

Impaired cognitive control functions have been documented in obesity. It remains unclear whether these functions normalize after weight reduction. We compared ex-obese individuals, who successfully underwent substantial weight loss after bariatric surgery, to normal-weight participants on measures of resistance to interference, cognitive flexibility and response inhibition, obtained from the completion of two Stroop tasks, a Switching task and a Go/NoGo task, respectively. To elucidate the underlying brain mechanisms, event-related potentials (ERPs) in the latter two tasks were examined. As compared to controls, patients were more susceptible to the predominant but task-irrelevant stimulus …

MaleInhibition (Psychology)Bariatric surgery; ERP; Inhibition; Obesity; Stroop; SwitchingAudiologyDevelopmental psychologyTask (project management)CognitionPostoperative Complications0302 clinical medicineWeight lossPostoperative PeriodEvoked PotentialsInhibitionGeneral Neuroscience05 social sciencesCognitive flexibilityBrainElectroencephalographyCognitionMiddle AgedInhibition PsychologicalNeuropsychology and Physiological PsychologyFemaleStroopEvoked Potentialmedicine.symptomCase-Control StudiePsychologypsychological phenomena and processesERPHumanAdultmedicine.medical_specialtyStimulus (physiology)behavioral disciplines and activities050105 experimental psychologyYoung Adult03 medical and health sciencesSettore M-PSI/08 - Psicologia ClinicaWeight LossReaction TimemedicineHumansCognitive Dysfunction0501 psychology and cognitive sciencesObesityBariatric surgeryNeuroscience (all)Settore M-PSI/02 - Psicobiologia E Psicologia Fisiologicamedicine.diseaseObesityWeight LoElectrophysiologyCase-Control StudiesStroop TestSwitchingPostoperative Complication030217 neurology & neurosurgeryStroop effect
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Recurrent missense variant in the nuclear export signal of FMR1 associated with FXS-like phenotype including intellectual disability, ASD, facial abn…

2021

Fragile X syndrome (FXS; MIM 300624) is an X-linked genetic disorder characterized by physical abnormalities associated with intellectual disability and a wide spectrum of neurological and psychiatric impairments. FXS occurs more frequently in males, 1 in 5000 males and 1 in 8000 females accounting for 1-2% of overall intellectual disability (ID). In more than 99% of patients, FXS results from expansions of a CGG triplet repeat (>200 in male) of the FMR1 gene. In the last years an increasing number, albeit still limited, of FXS subjects carrying FMR1 mutations including deletions, splicing errors, missense, and nonsense variants was reported. Nevertheless, the studies concerning the func…

MaleNuclear Export SignalsSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaAutism Spectrum DisorderMutation MissenseGeneral MedicineFMR1 point mutationSettore MED/39 - Neuropsichiatria InfantileFragile X Mental Retardation ProteinPhenotypeSettore MED/38 - Pediatria Generale E SpecialisticaIntellectual DisabilityAutism spectrum disorders ASDSettore M-PSI/08 - Psicologia ClinicaGeneticsHumansIntellectual disability IDFemaleNuclear export signal NES.Genetics (clinical)Fragile X syndrome
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