[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570262":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":19,"centralContacts":23,"locations":33,"responsibleParty":47,"collaborators":50,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":18,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":74,"overallStatus":35,"whyStopped":18,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"University of Washington","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"Use of AMPERE EMA prototype","An EMA risk monitoring system using a smartphone EMA app to collect self-reported data from participating patients experiencing suicidal ideation.",[12],"Other: AMPERE EMA app",[14],{"type":6,"name":15,"description":16,"armGroupLabels":17,"otherNames":18},"AMPERE EMA app","AMPERE EMA smartphone app using MyCap",[9],null,[20],{"name":21,"affiliation":5,"role":22},"Ian M Bennett, MD, PhD","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":18,"email":28},"Mindy Vredevoogd, MS","CONTACT","206-465-0099","mindyv@uw.edu",{"name":30,"role":26,"phone":31,"phoneExt":18,"email":32},"Tess Grover, BA","206-830-1950","grovet@uw.edu",[34],{"facility":5,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":18},"RECRUITING","Seattle","Washington","98195","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-122.33207,47.60621,{"lat":45,"lon":44},{"type":22,"investigatorFullName":48,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Ian Bennett","Professor: Psychiatry & Behavioral Sciences",[51],{"name":52,"class":53},"National Institute of Mental Health (NIMH)","NIH","100570262","augmented-momentary-personal-ecological-risk-evaluation-100570262",false,"NCT06704958","Augmented Momentary Personal Ecological Risk Evaluation","AMPERE","Inclusion Criteria:\n\n* Young adults (age 16-30 years)\n* Receiving care at University of Washington Primary Care for suicidal ideation as determined by Electronic Health Record problem list or PHQ-9 suicide risk item \\>0 in previous year and\u002For recent (past year) history of suicide attempt and\u002For active suicidal ideation.\n* Ability to consent to participate\n\nExclusion Criteria:\n\n* Age \\\u003C16 or \\>30,\n* Non-English speaking\n* No smart phone access\n* Any clinical medical\u002Fpsychiatric condition, severity of that condition, or life situation that would compromise safe and voluntary study participation.","ALL","16 Years","30 Years",{"count":65,"type":66},50,"ESTIMATED","INTERVENTIONAL",[69],"NA","The goal of this intervention study is to co-design and test an Ecological Momentary Assessment (EMA) prototype tool with young adults aged 16-30 experiencing suicidality to see if it is an acceptable and usable clinical tool for risk management.\n\nThe main study aims are:\n\n* To co-design a prototype EMA suicide risk monitoring system with patients and health care provider input using Human Centered Design (HCD) methods.\n* To test the developed EMA protype with providers and their young adult patients aged 16-30 experiencing suicidality to determine if the EMA prototype is an acceptable and usable clinical tool.\n\nYoung adult participants receiving care for active suicidal ideation will\n\n* Download and use the EMA prototype for a total of two months.\n* Complete 3 online surveys at 0, 1 and 2 months after enrolled in the study.",[72,73],"Suicidal Ideation","Self Harm",[75,76],"suicidal ideation","self harm","2025-11-20",{"date":79,"type":80},"2025-11-26","ACTUAL",{"date":82,"type":80},"2025-09-25",{"date":84,"type":66},"2026-07-01",{"name":5,"class":6},1]