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80 results for “Clinical High Risk for Psychosis”
FIGURE 39 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 39. Mesoceration reticulatum, dorsal and lateral habitus of holotype.
FIGURE 16 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 16. Parasthetops pampinus, dorsal and lateral habitus of holotype.
FIGURE 36 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 36. Mesoceration disjunctum, dorsal and lateral habitus of holotype.
FIGURE 37 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 37. Mesoceration repandum, dorsal and lateral habitus of holotype.
FIGURE 17 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 17. Parasthetops lemniscus, dorsal and lateral habitus of holotype.
FIGURE 15 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 15. Parasthetops semiplanus, dorsal and lateral habitus of holotype.
FIGURE 9 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 9. Parasthetops unicornus, dorsal and lateral habitus of holotype.
FIGURE 10 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 10. Parasthetops buunicornus, dorsal and lateral habitus of holotype.
FIGURE 8 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 8. Parasthetops propitius, dorsal and lateral habitus of holotype.
FIGURE 7 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 7. Parasthetops sebastiani, dorsal and lateral habitus of holotype.
FIGURE 2 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 2. Pterosthetops hawequas, dorsal and lateral habitus of holotype.
FIGURE 1 in Facial affect recognition in individuals at clinical high risk for psychosis
FIGURE 1. Prosthetops gladiator, dorsal and lateral habitus of holotype.
Developing Clinical Tools to Communicate Genetic Risk for Individuals Who Are Clinical High Risk for Psychosis
ClinicalTrials.gov study NCT04325568. IPD Sharing: NO. Countries: 1. Publications: 0.
A Treatment Engagement Protocol for Psychiatrically Hospitalized Adolescents at Clinical High Risk for Psychosis
ClinicalTrials.gov study NCT04314635. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Mentalization Based Treatment (MBT) in Help Seeking Youths With a Clinical High-Risk Condition for Psychosis (CHR-P)
ClinicalTrials.gov study NCT07093671. IPD Sharing: NO. Countries: 1. Publications: 0.
Targeted Cognitive Training in Clinical High Risk (CHR) for Psychosis
ClinicalTrials.gov study NCT02404194. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Study Exploring Changes in a Variety of Biomarkers Following Dosing With MT1988 in Participants at Clinical High Risk for Psychosis
ClinicalTrials.gov study NCT07226895. IPD Sharing: YES. Countries: 1. Publications: 0.
Effects of Cognitive Remediation on Cognition in Young People at Clinical High Risk of Psychosis
ClinicalTrials.gov study NCT01619319. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Perceived family functioning profile in adolescents at clinical high risk for psychosis: rigidity as a possible preventive target
<p><strong>Introduction</strong></p> <p>This database includes the raw data linked with the paper “Perceived family functioning profile in adolescents at Clinical High-Risk for Psychosis: rigidity as a possible preventive target”, currently under submission.</p> <p>In this paper, we reported sociodemographic characteristics, family history of any DSM-5 psychiatric disorder, personal history of any DSM-5 psychiatric disorder, psychopathological assessment, and level of functioning. We aimed at investigating the role of family functioning for APS adolescents compared to adolescents suffering from early onset psychosis and with other psychiatric disorders.</p> <p><strong>Methods</strong></p> <p>Participants were then divided into three groups: 1) adolescents with established Early Onset Psychosis (EOP), 2) adolescents meeting DSM-5 Attenuated psychotic Syndrome (APS) criteria and the attenuated psychotic symptoms subgroup of the Clinical High Risk for Psychosis (CHR-P), 3) adolescents with other DSM-5 psychiatric disorders who did not meet APS/EOP criteria.</p> <p><strong>Results</strong></p> <p>Our results suggest that family functioning has a central role and could represent a worthwhile target of intervention for adolescents at CHR-P, leading the way to new preventive approaches.</p>
Neurocognition and functioning in adolescents at clinical high risk for psychosis
<p><strong>Introduction. </strong>This database includes the raw data linked with the paper “Neurocognitive Functioning of Adolescents at Clinical High Risk for Psychosis”<strong>. </strong>In this paper, we reported sociodemographic characteristics, family history of any DSM-5 psychiatric disorder, personal history of any DSM-5 psychiatric disorder, psychopathological assessment, and level of functioning. We aimed to identify differences in overall and neurocognitive functioning in three groups of adolescent patients divided according to the semi-structured interview Comprehensive Assessment of At-Risk Mental States (CAARMS) criteria.</p> <p><strong>Methods </strong>Participants were divided into three groups: 1) adolescents with established Early Onset Psychosis (EOP), 2) adolescents meeting DSM-5 Attenuated psychotic Syndrome (APS) criteria and the attenuated psychotic symptoms subgroup of the Clinical High Risk for Psychosis (CHR-P), 3) adolescents with other DSM-5 psychiatric disorders who did not meet APS/EOP criteria.</p> <p><strong>Results . </strong>We found that non-CHR-P exhibited better functioning and performances than psychosis group in processing speed, forward and backward verbal digit span, visual attention, categorial fluency, executive functions, processing speed, and planning and attention. No differences emerged between non-CHR-P and CHR-P. CHR-P and psychosis groups differed in processing speed, in TMT-A, in BVN forward verbal digit span, visual attention, categorial fluency and in ROCF drawing from memory task.</p>
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