[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100483368":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":32,"centralContacts":36,"locations":46,"responsibleParty":62,"collaborators":40,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":40,"eligibilityCriteria":70,"healthyVolunteers":71,"sex":72,"minAge":73,"maxAge":40,"enrollmentInfo":74,"targetDuration":40,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":49,"whyStopped":40,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Memorial Sloan Kettering Cancer Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Older Adult Cancer Survivors (OACS) - Behavioral Activation (BA)","EXPERIMENTAL","Older adult cancer survivors (OACS) will receive a Behavioral Activation intervention",[13],"Behavioral: Behavioral Activation",{"label":15,"type":10,"description":16,"interventionNames":17},"Older Adult Cancer Survivors (OACS) - Supportive Psychotherapy (SP)","Older adult cancer survivors (OACS) will receive a Supportive Psychotherapy intervention",[18],"Behavioral: Supportive Psychotherapy",[20,27],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Behavioral Activation","Sessions for both arms (BP \\& SP) will be administered remotely via video-conference and\u002For telephone (per patient preference) at the following timeline:\n\n* Full participants (not training cases): Ten sessions (30-50 minutes each) will be delivered approximately weekly over a 10-week period (+10 weeks).\n* Training case participants: Ten sessions (30-50 minutes each) will be delivered over an approximately 5-week period (+10 weeks).",[9],[26],"BA",{"type":21,"name":28,"description":23,"armGroupLabels":29,"otherNames":30},"Supportive Psychotherapy",[15],[31],"SP",[33],{"name":34,"affiliation":5,"role":35},"Rebecca Saracino, PhD","PRINCIPAL_INVESTIGATOR",[37,42],{"name":34,"role":38,"phone":39,"phoneExt":40,"email":41},"CONTACT","646-888-0263",null,"jamesr@mskcc.org",{"name":43,"role":38,"phone":44,"phoneExt":40,"email":45},"Christian Nelson, PhD","646-888-0030","nelsonc@MSKCC.ORG",[47],{"facility":48,"status":49,"city":50,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"Memorial Sloan Kettering Cancer Center (All Protocol Activities)","RECRUITING","New York","10065","United States","US",{"type":55,"coordinates":56},"Point",[57,58],-74.00597,40.71427,{"lat":58,"lon":57},[61],{"name":34,"role":38,"phone":39,"phoneExt":40,"email":40},{"type":63,"investigatorFullName":40,"investigatorTitle":40,"investigatorAffiliation":40,"oldNameTitle":40,"oldOrganization":40},"SPONSOR","100483368","phase-2-a-study-of-brief-behavioral-activation-for-the-treatment-of-depression-in-older-adult-cancer-survivors-100483368",false,"NCT05574127","A Study of Brief Behavioral Activation for the Treatment of Depression in Older Adult Cancer Survivors","Brief Behavioral Activation for the Treatment of Depression in Older Adult Cancer Survivors","Inclusion Criteria:\n\n* As per self-report or medical record, ≥65 years old\n* As per self-report or medical record, has a history of cancer\n* As per medical record and\u002For clinician confirmation:\n\n  * a patient in MSK Survivorship Clinics AND\u002FOR\n  * no evidence of disease (NED) AND\u002FOR\n  * 6 months or more post-treatment (patients on maintenance hormonal therapies are eligible)\n* Fluent in English, as per self-reported fluency of \"well\" or \"very well\"\\*\n* As per self-report, able to communicate over video-conference and\u002For phone for sessions\n* Elevated score on the PHQ-9: ≥5 (N\u002FA for Training Case participants)\n* Received a Blessed Orientation-Memory-Concentration Scale (BOMC) score of ≤ 11 (N\u002FA for Training Case participants)\n\nExclusion Criteria:\n\n* As per PI determination, requires a higher level of care for current passive or active suicidal ideation than current protocol is able to provide. If a participant receives a score of \\> 0 on item 9 of the PHQ-9, they will be referred to study PI for further evaluation. They will be excluded from participation in this study if the PI determines they would be appropriate for a higher level of care than BA may be able to provide.\n* As per self-report or as documented in the medical record, current untreated (e.g., no medication, no therapy) major psychotic disorder (schizotypal personality disorder, schizophreniform disorder, schizoaffective disorder). Patients diagnosed with a major psychiatric disorder will be reviewed by the study PI to determine eligibility prior to consent.\n* As per self-report or medical record, currently taking antidepressant medication for \\\u003C 3 month\n* As per medical record, patient has impaired decision-making capacity",true,"ALL","65 Years",{"count":75,"type":76},90,"ESTIMATED","INTERVENTIONAL",[79],"PHASE2","The purpose of this study is to find out if a psychotherapy method called behavioral activation (BA) can be successfully delivered by telephone or videoconference (remotely) and can effectively treat depression in Older Adult Cancer Survivors (OACS)",[82],"Survivorship",[84,85,86,5],"Older Adult Cancer Survivors","history of cancer","22-248","2026-06-18",{"date":89,"type":90},"2026-06-22","ACTUAL",{"date":92,"type":90},"2022-10-06",{"date":94,"type":76},"2027-06-01",{"name":5,"class":6},1]