[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644084":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":36,"centralContacts":40,"locations":48,"responsibleParty":66,"collaborators":24,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":24,"eligibilityCriteria":75,"healthyVolunteers":71,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":24,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":90,"overallStatus":51,"whyStopped":24,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"Tel Aviv University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Active ABM Training","ACTIVE_COMPARATOR","Mechanized Dot-Probe Attention Bias Modification (ABM) training attention away from threat faces. Participants identify the direction of an arrowehead presented at the location of neutral faces.",[13],"Behavioral: Dot-Probe Attention Bias Modification (ABM)",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo Training","PLACEBO_COMPARATOR","Mechanized Intervention: Placebo Training, presenting a single, centered, non-face oval shape in each trial. Participants identify the direction of an arrowehead centrally presented.",[19],"Behavioral: Placebo Training",{"label":21,"type":22,"description":23,"interventionNames":24},"Wait-List Control","NO_INTERVENTION","No Intervention \u002F Wait-List, assessments at the same intervals as the active and placebo conditions without intervention in between.",null,[26,33],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"BEHAVIORAL","Dot-Probe Attention Bias Modification (ABM)","Participants complete a computerized dot-probe attention training task designed to train attention away from threat-related stimuli. During each trial, angry and neutral facial expressions are presented simultaneously, followed by a probe that consistently appears in the location of the neutral face. Participants complete eight training sessions over four weeks.",[9],[32],"ABM",{"type":27,"name":15,"description":34,"armGroupLabels":35,"otherNames":24},"Participants complete a computerized task matched to the active training condition in duration, structure, and task demands, but without exposure to emotional stimuli or attentional training contingencies. The task is designed to control for nonspecific factors such as expectancy and engagement. Participants complete eight sessions over four weeks.",[15],[37],{"name":38,"affiliation":5,"role":39},"Yair Bar-Haim, PhD","PRINCIPAL_INVESTIGATOR",[41,45],{"name":38,"role":42,"phone":43,"phoneExt":24,"email":44},"CONTACT","97236405465","yair1@tauex.tau.ac.il",{"name":46,"role":42,"phone":43,"phoneExt":24,"email":47},"Lital Kohn, MA","litalkohn@tauex.tau.ac.il",[49],{"facility":50,"status":51,"city":52,"state":24,"zip":24,"country":53,"countryCode":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Tel Aviv university","RECRUITING","Tel Aviv","Israel","IL",{"type":56,"coordinates":57},"Point",[58,59],34.78057,32.08088,{"lat":59,"lon":58},[62],{"name":63,"role":42,"phone":64,"phoneExt":24,"email":65},"Yuval Regev, masters","+97245-333-4472","yuvalregev4@mail.tau.ac.il",{"type":39,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Yair Bar-Haim","Professor","100644084","efficacy-of-attention-bias-modification-vs-placebo-for-social-anxiety-disorder-100644084",false,"NCT07666776","Efficacy of Attention Bias Modification vs. Placebo for Social Anxiety Disorder","Placebo Effects in Dot-Probe Attention Bias Modification (ABM) Among Adults With Social Anxiety Disorder.","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* Primary diagnosis of generalized Social Anxiety Disorder based on clinical evaluation, the MINI International Neuropsychiatric Interview (MINI), and a Liebowitz Social Anxiety Scale (LSAS) score greater than 50\n* Normal or corrected-to-normal vision without color blindness\n* Sufficient Hebrew proficiency to complete clinical interviews, self-report questionnaires, and computerized cognitive tasks\n\nExclusion Criteria:\n\n* Previous participation in attention bias modification training using a dot-probe task\n* Previous participation in eye-tracking-based attention training\n* Current diagnosis of Post-Traumatic Stress Disorder\n* Current or past diagnosis of psychotic disorder or bipolar disorder\n* Neurological disorder (e.g., epilepsy or traumatic brain injury)\n* Severe suicidal ideation\n* Current substance or alcohol use disorder\n* Concurrent pharmacological or psychosocial treatment, unless medication has been stable for at least 45 days\n* Pregnancy\n* Uncorrected visual impairment or use of multifocal glasses","ALL","18 Years","65 Years",{"count":80,"type":81},90,"ESTIMATED","INTERVENTIONAL",[84],"NA","This study examines whether a computerized attention-training intervention called attention bias modification (ABM) can reduce symptoms of social anxiety disorder (SAD) in adults, and whether symptom improvement is specifically related to changes in attentional processing or to nonspecific factors such as expectancy and placebo effects.",[87,88,89],"Social Anxiety Disorder (SAD)","Attention Bias Modification Treatment (ABMT)","Placebo Effect",[91],"Social Anxiety; Placebo; Treatment; Attention Bias","2026-06-18",{"date":94,"type":95},"2026-06-24","ACTUAL",{"date":97,"type":95},"2026-06-15",{"date":99,"type":81},"2027-06-30",{"name":5,"class":6},1]