[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT06880640":3,"trial-entities:NCT06880640":101,"trial-summary:NCT06880640":106},{"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":15,"conditions":17,"keywords":20,"study_type":21,"primary_purpose":22,"phases":23,"enrollment_info":25,"interventions":28,"primary_outcomes":37,"secondary_outcomes":42,"sex":46,"minimum_age":47,"maximum_age":48,"healthy_volunteers":49,"eligibility_criteria":50,"std_ages":70,"locations":72,"central_contacts":88,"overall_officials":91,"references":95,"see_also_links":100},"NCT06880640","24-3120","Affect-based Impulsivity in Borderline Personality Disorder","Affect-based Impulsivity in Borderline Personality Disorder: Developing a Neurocomputational Phenotype","RECRUITING","2026-08","2025-09","2026-06-26","2025-09-21","University of North Carolina, Chapel Hill","OTHER",null,"The purpose of this research study is to investigate how personality traits and neuroendocrine systems relate to decision-making patterns in individuals 18-45 years old. The main question it aims to answer is how neuroendocrine activity impacts decision-making.\n\nParticipants will complete online behavioral tasks, a stress induction procedure, self-report surveys, and a cognitive assessment. During the session, psychophysiological measures will be collected, including electrocardiogram (ECG) and cardiac impedance (ICG) to monitor heart rate and blood flow, as well as electrodermal activity (EDA), blood drop samples, and saliva collection to assess nervous system activity.",[18,19],"Borderline Personality Disorder (BPD)","Healthy Controls Group - Age and Sex-matched",[],"INTERVENTIONAL","BASIC_SCIENCE",[24],"NA",{"count":26,"type":27},106,"ESTIMATED",[29],{"type":30,"name":31,"description":32,"armGroupLabels":33,"otherNames":35},"BEHAVIORAL","Stress Induction","Participants will complete the Trier Social Stress Test to induce stress, which includes a public speaking simulation and mental arithmetic.",[34],"Stress",[36],"Trier Social Stress Test (TSST)",[38],{"measure":39,"description":40,"timeFrame":41},"Goal-directed decision-making in the Social Decision Tree Task (SDTT)","Measured by choice behavior in SDTT, which is based on the decision tree framework. After each action, participants receive feedback about the effect of that action and the extent to which it added to or took away from their points. If participants make a given choice, the subsequent actions that they can choose are different than if they were to initially make a different choice.\n\nAn action in SDTT is goal-directed if the possible net gain an individual can earn before the end of the current epoch (a \"day\" in the SDTT) is equal to or higher than the amount they could gain by choosing the alternative action. The investigators will subset trials so that 1 is coded as choosing the immediately valuable action at the expense of the optimal and 0 is coded as choosing the optimal at the expense of the immediately valuable action. This outcome variable is binary.","Collected for 40 minutes ~2 hours into one-time study visit",[43],{"measure":44,"description":45,"timeFrame":41},"Bias toward social actions in the Social Decision Tree Task (SDTT)","Measured by choice behavior in SDTT, which is based on the decision tree framework. An action in SDTT is defined as social if it is paired with a visual cue with a face on it and non-social if not. This outcome variable is binary.","ALL","18 Years","45 Years",true,{"inclusion":51,"exclusion":63,"raw_text":69},[52,53,54,55,56,57,58,59,60,61,62],"Score of 38 or higher on Personality Assessment Inventory-Borderline Scale (PAI-BOR)","Participants in the BPD group will be primarily recruited from the two","Score of 12 or lower on PAI-BOR","Score below 50th percentile on World Health Organization Disability Assessment Schedule (WHODAS)","Absence of any current or lifetime psychiatric disorder, including personality disorders as determined by diagnostic interviews (SIDP and SCID), if the participant had participated in the lab's other studies (IRB Nos. 20-1735 and 21-0602).","Ages 18-45","Provision of signed and dated informed consent form","Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study","Willingness to participate in all components of the study","Participants must be able to speak, understand and read English.","Participants must have at least 20\u002F40 visual acuity (correct or uncorrected).",[64,65,66,67,68],"Use of as needed antihypertensive agents within 12 hours prior to lab visit","Inability to refrain from using as needed psychotropic medications for 12 hours prior to lab visit","History of psychotic disorder, Bipolar I disorder, autism spectrum disorder, reactive attachment disorder, pervasive developmental disorder, motor disorder, head injury, mental retardation, neurological disorder, or current substance dependence","Family history of Bipolar I disorder in a first degree relative.","Participants are also excluded for any of the following: cardiac pacemaker, aneurysm clip, cochlear implants, pregnancy, shrapnel, history of metal fragments in eyes, neurostimulators, weight of 250 lbs. or more, or claustrophobia.","Inclusion Criteria:\n\nBorderline Personality Disorder (BPD) group:\n\n* Score of 38 or higher on Personality Assessment Inventory-Borderline Scale (PAI-BOR)\n* Participants in the BPD group will be primarily recruited from the two\n\nDEPENd lab studies that maintain large samples of BPD participants. To ensure maximal similarity between BPD participants recruited from other DEPENd lab studies and BPD participants recruited through other recruitment sources, the investigators will use the same criteria for the BPD group in the current study as the criteria used in the other DEPENd lab studies. BPD participants in the two DEPENd lab studies from which the investigators will be recruiting must meet the following criteria:\n\n1. 3+ BPD symptoms, one of which must be affective instability, per clinical interview\n2. Participants must score at least 80 on the Reynolds Intellectual Screening Test (RIST).\n\nHealth Control (HC) Group:\n\n* Score of 12 or lower on PAI-BOR\n* Score below 50th percentile on World Health Organization Disability Assessment Schedule (WHODAS)\n* Absence of any current or lifetime psychiatric disorder, including personality disorders as determined by diagnostic interviews (SIDP and SCID), if the participant had participated in the lab's other studies (IRB Nos. 20-1735 and 21-0602).\n\nCombined Inclusion Criteria:\n\n* Ages 18-45\n* Provision of signed and dated informed consent form\n* Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study\n* Willingness to participate in all components of the study\n* Participants must be able to speak, understand and read English.\n* Participants must have at least 20\u002F40 visual acuity (correct or uncorrected).\n\nExclusion Criteria:\n\n* Use of as needed antihypertensive agents within 12 hours prior to lab visit\n* Inability to refrain from using as needed psychotropic medications for 12 hours prior to lab visit\n* History of psychotic disorder, Bipolar I disorder, autism spectrum disorder, reactive attachment disorder, pervasive developmental disorder, motor disorder, head injury, mental retardation, neurological disorder, or current substance dependence\n* Family history of Bipolar I disorder in a first degree relative.\n* Participants are also excluded for any of the following: cardiac pacemaker, aneurysm clip, cochlear implants, pregnancy, shrapnel, history of metal fragments in eyes, neurostimulators, weight of 250 lbs. or more, or claustrophobia.",[71],"ADULT",[73],{"facility":74,"status":8,"city":75,"state":76,"zip":77,"country":78,"contacts":79,"geoPoint":85},"University of North Carolina at Chapel Hill","Chapel Hill","North Carolina","27514","United States",[80],{"name":81,"role":82,"phone":83,"email":84},"Keely A Muscatell, PhD","CONTACT","919-843-9113","kmuscatell@unc.edu",{"lat":86,"lon":87},35.9132,-79.05584,[89],{"name":81,"role":82,"phone":90,"email":84},"+1 (919) 843-9113",[92],{"name":93,"affiliation":13,"role":94},"Keely Muscatell, PhD","PRINCIPAL_INVESTIGATOR",[96],{"pmid":97,"type":98,"citation":99},"22412360","BACKGROUND","Huys QJ, Eshel N, O'Nions E, Sheridan L, Dayan P, Roiser JP. Bonsai trees in your head: how the pavlovian system sculpts goal-directed choices by pruning decision trees. PLoS Comput Biol. 2012;8(3):e1002410. doi: 10.1371\u002Fjournal.pcbi.1002410. Epub 2012 Mar 8.",[],{"nct_id":4,"conditions":102,"biomarkers":105},[103,104],"Borderline Personality Disorder","Healthy",[],{"nct_id":4,"found":49,"summary":107,"prompt_version":117},{"design":108,"status":109,"heading":110,"summary":111,"follow_up":112,"word_count":113,"commitments":114,"compensation":115,"drugs_mentioned":116},"This interventional study plans to enroll 106 participants, including those with Borderline Personality Disorder and healthy individuals matched by age and sex. It is not specified if the study is randomized or blinded.","completed","Affect-based Impulsivity in Borderline Personality Disorder Study","This study aims to understand how personality traits and body responses (neuroendocrine systems) affect decision-making in people aged 18-45. Specifically, it's looking at how stress impacts decision-making in individuals with Borderline Personality Disorder (BPD) and healthy individuals. You could be eligible if you are 18-45 years old and have a score of 38 or higher on the Personality Assessment Inventory-Borderline Scale (PAI-BOR) for the BPD group. The study will measure your goal-directed decision-making using a task called the Social Decision Tree Task (SDTT) during a one-time visit. The study is currently recruiting 106 participants.","Your goal-directed decision-making will be measured for 40 minutes, approximately 2 hours into your one-time study visit. No further follow-up is specified.",94,"You would complete online behavioral tasks, a stress induction procedure called the Trier Social Stress Test, self-report surveys, and a cognitive assessment during a single study visit. During this visit, measurements like heart rate (ECG, ICG), skin activity (EDA), blood, and saliva will be collected.","Not stated in the trial record.",[],"v2"]