[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07635940":3,"trial-entities:NCT07635940":148,"trial-summary:NCT07635940":152},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":20,"study_type":35,"primary_purpose":36,"phases":37,"enrollment_info":39,"interventions":42,"primary_outcomes":59,"secondary_outcomes":67,"sex":72,"minimum_age":73,"maximum_age":74,"healthy_volunteers":75,"eligibility_criteria":76,"std_ages":104,"locations":106,"central_contacts":124,"overall_officials":126,"references":127,"see_also_links":144},"NCT07635940","24-2634","Effects of Transcranial Magnetic Stimulation on Social Cognition, Cognitive Processing, and Functional Brain Architecture","Effects of Transcranial Magnetic Stimulation on Social Cognition, Cognitive Processing, and Functional Brain Architecture in Psychopathy","NOT_YET_RECRUITING","2030-08","2026-05","2026-06-11","2026-06","University of Colorado, Denver","OTHER",true,"This clinical trial will examine whether transcranial magnetic stimulation (TMS), a noninvasive form of brain stimulation, can influence social cognition, cognitive processing, and brain function in adults with elevated psychopathic traits. The study will also evaluate the safety and feasibility of delivering TMS in this population.\n\nParticipants will be randomly assigned to receive either active TMS or sham (placebo-like) TMS. The study will compare outcomes between participants receiving active versus sham TMS and will evaluate changes from before to after TMS exposure.\n\nParticipants will:\n\n* Complete a baseline magnetic resonance imaging (MRI) brain scan.\n* Receive three single-session TMS interventions.\n* Complete a post-intervention MRI brain scan.\n* Complete assessments of social cognition.\n* Complete assessments of cognitive processing.\n\nThe primary objectives are to determine whether TMS can influence social cognition, cognitive processing, and functional brain organization and connectivity in adults with elevated psychopathic traits.","Psychopathic traits are associated with impairments in social cognition, cognitive processing, and alterations in functional brain network organization. Neuroimaging studies have implicated abnormalities in brain regions involved in cognitive control and social information processing, including the right dorsolateral prefrontal cortex (dlPFC) and right temporoparietal junction (TPJ). Transcranial magnetic stimulation (TMS) is a noninvasive neuromodulation technique capable of altering neural activity within targeted brain networks and provides an experimental method for examining the causal contribution of these regions to cognitive and social functioning.\n\nThis randomized, sham-controlled clinical trial will evaluate whether theta burst stimulation targeting the right dlPFC or right TPJ influences social cognition, cognitive processing, and functional brain network organization in adults with elevated psychopathic traits. Participants will be randomly assigned to receive inhibitory continuous theta burst stimulation (cTBS) targeting the right dlPFC, excitatory intermittent theta burst stimulation (iTBS) targeting the right TPJ, or sham stimulation. Stimulation targets will be individualized using participant-specific neuroimaging data.\n\nParticipants will complete baseline and post-intervention assessments that include functional magnetic resonance imaging (fMRI), measures of social cognition, and measures of cognitive processing. Functional neuroimaging will be used to evaluate changes in brain network organization and connectivity associated with stimulation. Behavioral assessments will evaluate social cognitive processes, including emotion processing and perspective taking, as well as cognitive processes related to attention and cognitive control.\n\nAnalyses will compare active stimulation conditions with sham stimulation on measures of social cognition and cognitive processing. Neuroimaging analyses will evaluate both within-subject changes from pre- to post-stimulation and between-group differences in functional brain network organization and connectivity.\n\nThe primary objectives are to determine whether theta burst stimulation can influence social cognition, cognitive processing, and functional brain network organization in adults with elevated psychopathic traits and to evaluate the safety and feasibility of delivering TMS in this population. Findings from this study may help clarify the neural mechanisms underlying psychopathic traits and inform future development of targeted neuromodulation interventions.",[19],"Psychopathy",[19,21,22,23,24,25,26,27,28,29,30,31,32,33,34],"Transcranial Magnetic Stimulation","Theta Burst Stimulation","Neuromodulation","Social Cognition","Emotion Recognition","Theory of Mind","Social Decision Making","Cognitive Processing","Cognitive Control","Executive Function","Functional Connectivity","Resting-State fMRI","Dorsolateral Prefrontal Cortex","Temporal Parietal Junction","INTERVENTIONAL","TREATMENT",[38],"NA",{"count":40,"type":41},60,"ESTIMATED",[43,49,54],{"type":44,"name":45,"description":46,"armGroupLabels":47},"DEVICE","continuous theta burst stimulation (cTBS)","Continuous theta burst stimulation (cTBS) will be delivered using transcranial magnetic stimulation (TMS) targeting the right dorsolateral prefrontal cortex (dlPFC). cTBS is a patterned form of repetitive TMS designed to modulate neural activity within targeted brain networks involved in cognitive control and social cognition. Stimulation targets will be individualized using participant-specific neuroimaging data.",[48],"active dlPFC sham TPJ",{"type":44,"name":50,"description":51,"armGroupLabels":52},"Intermittent theta burst stimulation (iTBS)","Intermittent theta burst stimulation (iTBS) will be delivered using transcranial magnetic stimulation (TMS) targeting the right temporoparietal junction (TPJ). iTBS is a patterned form of repetitive TMS designed to modulate neural activity within targeted brain networks involved in social cognition and perspective taking. Stimulation targets will be individualized using participant-specific neuroimaging data",[53],"active TPJ sham dlPFC",{"type":44,"name":55,"description":56,"armGroupLabels":57},"Sham","Sham transcranial magnetic stimulation will be delivered using procedures designed to mimic the sensory experience of active stimulation without producing the intended neuromodulatory effects. Stimulation targets and study procedures will mirror those used in the active intervention arms.",[58],"sham",[60,64],{"measure":61,"description":62,"timeFrame":63},"Social Cognition Task Battery Performance","Performance on a social cognition task battery assessing facial emotion recognition (Emotion Recognition Task), perspective taking (Visual Perspective Taking Task), theory of mind (Movie Assessment of Social Cognition Task), and social decision-making (Altruistic\u002FAntisocial game). Accuracy and reaction time will be analyzed using mixed-effects models to compare active stimulation versus sham stimulation across tasks. Higher accuracy values indicate better performance, whereas lower reaction times indicate better performance.","within 10 minutes after the intervention.",{"measure":65,"description":66,"timeFrame":63},"Serial and Parallel Cognitive Processing Task Performance","Performance on the Miller serial\u002Fparallel cognitive processing task. Trial-level accuracy and\u002For reaction time will be analyzed using mixed-effects models to compare active stimulation versus sham stimulation across serial and parallel processing conditions.",[68],{"measure":69,"description":70,"timeFrame":71},"Change in Resting-State Functional Connectivity","Resting-state functional magnetic resonance imaging will be used to evaluate changes in functional connectivity within stimulation-relevant brain networks from baseline to post-intervention. Analyses will examine frontoparietal network connectivity for right dorsolateral prefrontal cortex stimulation and default mode network connectivity for right temporoparietal junction stimulation, including within-subject change and between-group comparisons of active versus sham stimulation.","From the date of baseline fMRI until the first TMS session, assessed 2 times (baseline and post-TMS) up to 2 months after the baseline session. Post-TMS fMRI scan will be conducted within 30 minutes after the intervention.","ALL","18 Years","60 Years",false,{"inclusion":77,"exclusion":87,"raw_text":103},[78,79,80,81,82,83,84,85,86],"18-60 years.","Elevated psychopathy as defined by the self-report psychopathy scale.","IQ \\>= 80.","No prior diagnosis or current risk of Autism as defined by the autism spectrum quotient.","Negative urine drug screen.","At least 7 Days of abstinence from substance use (excluding nicotine)","Able to provide informed consent.","No change in psychiatric medication regimen, or medication-free, for 4 weeks before study.","Adequate English proficiency to complete study procedures and assessments.",[88,89,90,91,92,93,94,95,96,97,98,99,100,101,102],"Current or lifetime DSM-5 psychotic disorder, schizophrenia, schizoaffective disorder, bipolar disorder, or autism spectrum disorder.","IQ \\\u003C 80.","Clinically significant neurological disorder or medical illness that would make study participation unsafe, including a history of seizures or significant cardiovascular disease.","Clinically significant abnormality identified on baseline MRI.","Contraindication to MRI or inability to undergo MRI scanning.","Current pregnancy or breastfeeding.","History of head injury resulting in loss of consciousness greater than 15 minutes.","Diagnosis of dementia.","Current prescription for benzodiazepines or anticonvulsants.","Metal implants or non-removable metal objects above the waist.","Lifetime history of prior clinical treatment with transcranial magnetic stimulation (TMS).","Serious risk of suicide or homicide.","Unable or unwilling to comply with study procedures.","History of intractable migraine.","Claustrophobia or inability to tolerate enclosed spaces required for MRI procedures.","Inclusion Criteria:\n\n* 18-60 years.\n* Elevated psychopathy as defined by the self-report psychopathy scale.\n* IQ \\>= 80.\n* No prior diagnosis or current risk of Autism as defined by the autism spectrum quotient.\n* Negative urine drug screen.\n* At least 7 Days of abstinence from substance use (excluding nicotine)\n* Able to provide informed consent.\n* No change in psychiatric medication regimen, or medication-free, for 4 weeks before study.\n* Adequate English proficiency to complete study procedures and assessments.\n\nExclusion Criteria:\n\n* Current or lifetime DSM-5 psychotic disorder, schizophrenia, schizoaffective disorder, bipolar disorder, or autism spectrum disorder.\n* IQ \\\u003C 80.\n* Clinically significant neurological disorder or medical illness that would make study participation unsafe, including a history of seizures or significant cardiovascular disease.\n* Clinically significant abnormality identified on baseline MRI.\n* Contraindication to MRI or inability to undergo MRI scanning.\n* Current pregnancy or breastfeeding.\n* History of head injury resulting in loss of consciousness greater than 15 minutes.\n* Diagnosis of dementia.\n* Current prescription for benzodiazepines or anticonvulsants.\n* Metal implants or non-removable metal objects above the waist.\n* Lifetime history of prior clinical treatment with transcranial magnetic stimulation (TMS).\n* Serious risk of suicide or homicide.\n* Unable or unwilling to comply with study procedures.\n* History of intractable migraine.\n* Claustrophobia or inability to tolerate enclosed spaces required for MRI procedures.",[105],"ADULT",[107],{"facility":108,"city":109,"state":110,"zip":111,"country":112,"contacts":113,"geoPoint":121},"University of Colorado Anschutz Medical Campus","Aurora","Colorado","80045","United States",[114,119],{"name":115,"role":116,"phone":117,"email":118},"Drew E Winters, PhD.","CONTACT","303-724-1000","ascend@ucdenver.edu",{"name":115,"role":120},"PRINCIPAL_INVESTIGATOR",{"lat":122,"lon":123},39.72943,-104.83192,[125],{"name":115,"role":116,"phone":117,"email":118},[],[128,132,135,138,141],{"pmid":129,"type":130,"citation":131},"33821459","BACKGROUND","Tillem S, Weinstein H, Baskin-Sommers A. Psychopathy is associated with an exaggerated attention bottleneck: EEG and behavioral evidence from a dual-task paradigm. Cogn Affect Behav Neurosci. 2021 Aug;21(4):881-893. doi: 10.3758\u002Fs13415-021-00891-z. Epub 2021 Apr 5.",{"pmid":133,"type":130,"citation":134},"24592204","Jeurissen D, Sack AT, Roebroeck A, Russ BE, Pascual-Leone A. TMS affects moral judgment, showing the role of DLPFC and TPJ in cognitive and emotional processing. Front Neurosci. 2014 Feb 13;8:18. doi: 10.3389\u002Ffnins.2014.00018. eCollection 2014.",{"pmid":136,"type":130,"citation":137},"12948738","Saxe R, Kanwisher N. People thinking about thinking people. The role of the temporo-parietal junction in \"theory of mind\". Neuroimage. 2003 Aug;19(4):1835-42. doi: 10.1016\u002Fs1053-8119(03)00230-1.",{"pmid":139,"type":130,"citation":140},"29531085","Drayton LA, Santos LR, Baskin-Sommers A. Psychopaths fail to automatically take the perspective of others. Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):3302-3307. doi: 10.1073\u002Fpnas.1721903115. Epub 2018 Mar 12.",{"pmid":142,"type":130,"citation":143},"37172923","Song Z, Jones A, Corcoran R, Daly N, Abu-Akel A, Gillespie SM. Psychopathic traits and theory of mind task performance: A systematic review and meta-analysis. Neurosci Biobehav Rev. 2023 Aug;151:105231. doi: 10.1016\u002Fj.neubiorev.2023.105231. Epub 2023 May 10.",[145],{"label":146,"url":147},"NIH reporter","https:\u002F\u002Freporter.nih.gov\u002Fsearch\u002F381eapZMS02WeEDulNIPZQ\u002Fproject-details\u002F11102801",{"nct_id":4,"conditions":149,"biomarkers":151},[150],"Antisocial Personality Disorder",[],{"nct_id":4,"found":75,"summary":153,"prompt_version":153},null]