[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100514284":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":36,"centralContacts":40,"locations":45,"responsibleParty":66,"collaborators":35,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":35,"eligibilityCriteria":75,"healthyVolunteers":71,"sex":76,"minAge":77,"maxAge":35,"enrollmentInfo":78,"targetDuration":35,"studyType":81,"phases":82,"briefSummary":84,"conditions":85,"keywords":89,"overallStatus":48,"whyStopped":35,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":103},{"fullName":5,"class":6},"Massachusetts General Hospital","OTHER",[8,14,18],{"label":9,"type":10,"description":11,"interventionNames":12},"NeuroPathways Open Pilot","EXPERIMENTAL","Enrolled patients will receive an intervention guide with information about navigating life with a brain tumor diagnosis, and will participate in four weekly or biweekly, individual sessions with a clinician (e.g. nurse or behavioral health specialist).\n\nParticipants will be asked to complete surveys at baseline, 8 weeks and 12 weeks, as well as an exit interview after the intervention.",[13],"Behavioral: Information and Support Intervention",{"label":15,"type":10,"description":16,"interventionNames":17},"NeuroPathways Pilot RCT","Enrolled patients will receive an intervention guide with information about navigating life with a brain tumor diagnosis, and will participate in four weekly or biweekly, individual sessions with a clinician (e.g. nurse or behavioral health specialist).\n\nParticipants will be asked to complete surveys at baseline, 8 weeks and 12 weeks.",[13],{"label":19,"type":20,"description":21,"interventionNames":22},"Usual supportive care","ACTIVE_COMPARATOR","Participants will receive usual supportive care, which includes referral to cancer center supportive care services (e.g., social work) upon request from the patient, caregiver, or clinician.\n\nParticipants will be asked to complete surveys at baseline, 8 weeks and 12 weeks.",[23],"Other: Usual supportive care",[25,32],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":30},"BEHAVIORAL","Information and Support Intervention","Information guide and four one-on-one coaching sessions",[9,15],[31],"NeuroPathways",{"type":6,"name":19,"description":33,"armGroupLabels":34,"otherNames":35},"Referral to cancer center supportive care services (e.g., social work) upon request from the patient, caregiver, or clinician",[19],null,[37],{"name":38,"affiliation":5,"role":39},"Deborah A Forst, MD","PRINCIPAL_INVESTIGATOR",[41],{"name":38,"role":42,"phone":43,"phoneExt":35,"email":44},"CONTACT","617-724-4000","dforst@partners.org",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"Massachusetts General Hospital Cancer Center","RECRUITING","Boston","Massachusetts","02114","United States","US",{"type":55,"coordinates":56},"Point",[57,58],-71.05977,42.35843,{"lat":58,"lon":57},[61,64],{"name":62,"role":42,"phone":63,"phoneExt":35,"email":44},"Deborah Forst, MA","617-726-2000",{"name":65,"role":39,"phone":35,"phoneExt":35,"email":35},"Deborah Forst, MD",{"type":39,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":35,"oldOrganization":35},"Deborah A Forst","Principal Investigator","100514284","neuropathways-intervention-for-brain-tumor-patients-100514284",false,"NCT05976490","NeuroPathways Intervention for Brain Tumor Patients","NeuroPathways: An Information and Support Intervention for Patients With Malignant Brain Tumors","Inclusion Criteria:\n\n* Age ≥18\n* Massachusetts General Hospital Cancer Center patient\n* Within 6 weeks of diagnosis with a primary malignant brain tumor\n* Able to speak and read in English\n\nExclusion Criteria:\n\n* Inability to provide informed consent as assessed by the study team (e.g., due to neurological impairment such as severe cognitive impairment\u002Fdementia or moderate-to-severe receptive aphasia)\n* Deemed inappropriate to approach by patient's oncologist or study PI","ALL","18 Years",{"count":79,"type":80},50,"ESTIMATED","INTERVENTIONAL",[83],"NA","This goal of this study is to test an information and support intervention for patients with malignant (or \"high-grade\") brain tumors. This study was developed to help patients cope after a brain tumor diagnosis. The main question this study aims to answer is whether this intervention (which includes access to an information guide and one-on-one coaching sessions) is feasible (i.e., possible to carry out) and acceptable (i.e., considered helpful) to patients. Participants will be asked to take part in the coaching sessions, use the guide as desired, and complete a small group of short surveys at three different points in time; some participants will be asked to share feedback via exit interviews.",[86,87,88],"Malignant Brain Tumor","Glioma","Coping Skills",[90,91,92,93],"glioma","supportive care","psychoeducation","information","2025-12-16",{"date":96,"type":97},"2025-12-17","ACTUAL",{"date":99,"type":97},"2023-11-07",{"date":101,"type":80},"2027-04-10",{"name":5,"class":6},1]