[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100633540":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":10,"locations":18,"responsibleParty":49,"collaborators":51,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":57,"sex":62,"minAge":63,"maxAge":10,"enrollmentInfo":64,"targetDuration":67,"studyType":68,"phases":10,"briefSummary":69,"conditions":70,"keywords":72,"overallStatus":21,"whyStopped":10,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Salma Health, Inc.","OTHER",[8,12,15],{"label":9,"type":10,"description":11,"interventionNames":10},"Esketamine",null,"Patients receiving esketamine for the treatment of depressed mood.",{"label":13,"type":10,"description":14,"interventionNames":10},"Conventional rTMS","Patients receiving conventional rTMS for the treatment of depressed mood.",{"label":16,"type":10,"description":17,"interventionNames":10},"SAINT","Patients receiving SAINT for the treatment of depressed mood.",[19,39],{"facility":20,"status":21,"city":22,"state":23,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":33},"Salma Health","RECRUITING","La Jolla","California","92037","United States","US",{"type":28,"coordinates":29},"Point",[30,31],-117.2742,32.84727,{"lat":31,"lon":30},[34],{"name":35,"role":36,"phone":37,"phoneExt":10,"email":38},"Clinical Research Coordinator","CONTACT","858-294-0161","research@salmahealth.com",{"facility":20,"status":21,"city":40,"state":23,"zip":41,"country":25,"countryCode":26,"cosmosGeoPoint":42,"geoPoint":46,"contacts":47},"Laguna Hills","92653",{"type":28,"coordinates":43},[44,45],-117.71283,33.61252,{"lat":45,"lon":44},[48],{"name":35,"role":36,"phone":37,"phoneExt":10,"email":38},{"type":50,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[52],{"name":53,"class":54},"Center for Neurohealth, Inc","UNKNOWN","100633540","atlas-1-advanced-trial-for-longitudinal-assessment-in-salma-1-100633540",false,"NCT07528014","ATLAS-1: Advanced Trial for Longitudinal Assessment in Salma 1","ATLAS-1","Inclusion Criteria:\n\n* Adults (≥18 years) of any gender identity presenting for care with a depressed mood.\n* Prescribed treatment with esketamine, conventional TMS, or SAINT as part of standard clinical care.\n* Able to provide informed consent and comply with all study requirements.\n\nExclusion Criteria:\n\n* Any condition deemed by the investigator to preclude safe participation in study assessments.","ALL","18 Years",{"count":65,"type":66},5000,"ESTIMATED","12 Months","OBSERVATIONAL","This study will evaluate the feasibility and clinical utility of developing predictive models of treatment response for patients with depressed mood using multimodal clinical data collected in real-world clinical settings. The study will examine outcomes among patients treated with interventions including esketamine, conventional transcranial magnetic stimulation (TMS), or Stanford Accelerated Intelligent Neuromodulation Therapy (SAINT). Retrospective clinical and research data from existing databases may also be incorporated, when available and authorized, to support model development and validation. The goal is to assess whether integrated clinical datasets can be used to support the development of predictive tools that may inform personalized treatment selection in depression.",[71],"Depressed Mood",[73,74,75,16,76,77,78,79],"Depression","transcranial magnetic stimulation (TMS)","accelerated TMS","Spravato","esketamine","Treatment-resistant depression (TRD)","Major depressive disorder (MDD)","2026-04-07",{"date":82,"type":83},"2026-04-14","ACTUAL",{"date":85,"type":83},"2026-03-25",{"date":87,"type":66},"2037-03",{"name":5,"class":6},2]