[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Trustees of Princeton University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":69},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":14,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100624320",false,"NCT07408102","Online Study on the Impact of a Self-Help Tool for Social Anxiety","Inclusion Criteria:\n\n* Age 18 to 65 years\n* Live in the United States\n* Comfortable reading and writing in English\n* Have regular access to the internet and a desktop\u002Flaptop computer\n* Report wanting to feel more comfortable in social situations, to improve social confidence, and\u002For to reduce symptoms of social anxiety as primary reason for joining the study\n* Have a valid photo ID and be willing to complete a video-based identity verification call if requested\n\nExclusion Criteria:\n\n* Lack of attention when completing parts of the study, and\u002For not completing the study tasks as instructed",true,"ALL","18 Years","65 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to understand which individuals benefit most from an internet-based cognitive behavioral intervention for social anxiety. Adults aged 18-65 will complete a self-guided online program designed to reduce anxiety symptoms. The investigators will use a combination of self-reported clinical information and data from computerized decision-making and cognitive tasks to predict changes in symptom scores from the intervention.",[26],"Social Anxiety",[28,29,30,31,26,32,33],"Cognitive Restructuring","Exposure Therapy","Cognitive Behavioral Therapy","Internet-Based Intervention","Predictive Models","Patient-Specific Modeling","NOT_YET_RECRUITING","2026-04-17",{"date":37,"type":38},"2026-04-20","ACTUAL",{"date":40,"type":20},"2026-06",{"date":42,"type":20},"2027-04",{"name":44,"class":45},"Trustees of Princeton University","OTHER",1,{"id":48,"slug":4,"hasResults":10,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":14,"sex":15,"minAge":16,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":46},"100602379","NCT07122739","Neurofeedback to Reduce Spontaneous Recovery of Threat Expectancy","Reducing Spontaneous Recovery Using Functional Connectivity Based Real-time Functional Magnetic Resonance Imaging Neurofeedback Targeting the Memory Control Network","Inclusion Criteria:\n\n* Adults aged 18-50\n* No history of psychiatric disorders or neurological disorders affecting the central nervous system.\n* Are not currently taking psychoactive medication or drugs of abuse.\n* Must be eligible to enter an MRI (i.e., no permanent metal or medical implants)\n* Normal color vision\n* Right-handed\n* Full reading and writing English comprehension\n* Must exhibit spontaneous recovery behavior as determined by an experimenter in a prescreening experimental session\n* Must be able to provide informed consent\n\nExclusion Criteria:\n\n* Pregnancy (female participants)\n* Outside of age range\n* History of psychiatric or neurological disease\n* Currently taking psychoactive medication or drugs of abuse\n* Color blindness\n* Primary left-handedness\n* Less than full reading and writing English comprehension\n* Do not exhibit spontaneous recovery behavior as determined by an experimenter in a prescreening experimental session\n* Refusing to provide informed consent","50 Years",{"count":55,"type":20},40,[23],"This study tests the efficacy of a new behavioral intervention with the goal of reducing spontaneous recovery of threat expectancy in healthy adults. This real-time functional magnetic resonance imaging (fMRI) neurofeedback intervention delivers feedback based on a functional connection between the prefrontal cortex and the hippocampus.",[59],"Healthy","RECRUITING","2026-02-20",{"date":63,"type":38},"2026-02-23",{"date":65,"type":38},"2025-07-17",{"date":67,"type":20},"2028-06",{"name":44,"class":45},""]