[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100399323":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":45,"centralContacts":49,"locations":54,"responsibleParty":73,"collaborators":75,"id":79,"slug":80,"hasResults":81,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":36,"eligibilityCriteria":85,"healthyVolunteers":86,"sex":87,"minAge":88,"maxAge":36,"enrollmentInfo":89,"targetDuration":36,"studyType":92,"phases":93,"briefSummary":95,"conditions":96,"keywords":36,"overallStatus":57,"whyStopped":36,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",[8,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm I (NIRS)","EXPERIMENTAL","Patients receive standard of care verbal and written education materials. Patients also receive a customized video which includes a description of each of their tumor, functional areas of the brain affected, and possible symptoms from the tumor and radiation treatment based on the neuro-imaging features. Patients and their caregivers watch the video together or separately over 1.5-3 minutes before the end of the first week of radiation treatment. Within 2 weeks after watching the NIRS video, patients complete an optional survey over 5-10 minutes.",[13,14,15,16],"Other: Educational Intervention","Other: Questionnaire Administration","Other: Survey Administration","Other: Video",{"label":18,"type":19,"description":20,"interventionNames":21},"Arm II (standard of care)","ACTIVE_COMPARATOR","Patients receive standard of care verbal and written education materials.",[13,14],[23,32,37,41],{"type":6,"name":24,"description":25,"armGroupLabels":26,"otherNames":27},"Educational Intervention","Receive standard of care verbal and written education materials",[9,18],[28,29,30,31],"Education for Intervention","Intervention by Education","Intervention through Education","Intervention, Educational",{"type":6,"name":33,"description":34,"armGroupLabels":35,"otherNames":36},"Questionnaire Administration","Ancillary studies",[9,18],null,{"type":6,"name":38,"description":39,"armGroupLabels":40,"otherNames":36},"Survey Administration","Complete optional survey",[9],{"type":6,"name":42,"description":43,"armGroupLabels":44,"otherNames":36},"Video","Watch NIRS video",[9],[46],{"name":47,"affiliation":5,"role":48},"Caroline Chung","PRINCIPAL_INVESTIGATOR",[50],{"name":47,"role":51,"phone":52,"phoneExt":36,"email":53},"CONTACT","713-745-5422","cchung3@mdanderson.org",[55],{"facility":56,"status":57,"city":58,"state":59,"zip":60,"country":61,"countryCode":62,"cosmosGeoPoint":63,"geoPoint":68,"contacts":69},"M D Anderson Cancer Center","RECRUITING","Houston","Texas","77030","United States","US",{"type":64,"coordinates":65},"Point",[66,67],-95.36327,29.76328,{"lat":67,"lon":66},[70,72],{"name":47,"role":51,"phone":71,"phoneExt":36,"email":36},"713-563-2300",{"name":47,"role":48,"phone":36,"phoneExt":36,"email":36},{"type":74,"investigatorFullName":36,"investigatorTitle":36,"investigatorAffiliation":36,"oldNameTitle":36,"oldOrganization":36},"SPONSOR",[76],{"name":77,"class":78},"National Cancer Institute (NCI)","NIH","100399323","customized-neuro-imaging-referenced-symptom-video-for-the-reduction-of-patient-and-caregiver-anxiety-around-radiation-treatment-for-brain-tumors-100399323",false,"NCT04479696","Customized Neuro-Imaging Referenced Symptom Video for the Reduction of Patient and Caregiver Anxiety Around Radiation Treatment for Brain Tumors","Novel Intervention to Reduce Patient and Caregiver Anxiety Around Radiation Treatment for Brain Tumors With a Customized Neuro-Imaging Referenced Symptom Video","Inclusion Criteria:\n\n* PATIENT ELIGIBILITY CRITERIA: Adult patients with newly diagnosed glioma (World Health Organization \\[WHO\\] grade 2-4) who are planned for a 6-week course of radiotherapy after surgery\n* PATIENT ELIGIBILITY CRITERIA: Able to complete questionnaires in English\n* PATIENT ELIGIBILITY CRITERIA: Has a post-operative diagnostic magnetic resonance imaging (MRI) of the brain with and without contrast acquired within 4 weeks of the start of radiotherapy\n* CAREGIVER ELIGIBILITY CRITERIA: Adult caregiver (\\>= 18 years) who is accompanying an eligible patient consented to the study\n* CAREGIVER ELIGIBILITY CRITERIA: The patient who the caregiver is accompanying is consented for participation on the study\n* CAREGIVER ELIGIBILITY CRITERIA: Able and willing to complete questionnaires in English\n\nExclusion Criteria:\n\n* PATIENT ELIGIBILITY CRITERIA: Significant cognitive or psychiatric symptoms that prevent the ability to complete the questionnaires as determined by the assessing staff in the pre-intervention evaluation\n* PATIENT ELIGIBILITY CRITERIA: Poor performance status (Karnofsky performance status \\[KPS\\] \\\u003C 60) that prevent the ability to complete the questionnaires\n* CAREGIVER ELIGIBILITY CRITERIA: Significant cognitive or psychiatric symptoms that prevent the ability to complete the questionnaires as determined by the assessing staff in the pre-intervention evaluation",true,"ALL","18 Years",{"count":90,"type":91},117,"ESTIMATED","INTERVENTIONAL",[94],"NA","This trial studies whether a customized video intervention can help to reduce anxiety in brain cancer patients undergoing radiation treatment and their caregivers. A customized neuro-imaging referenced symptom video that describes symptoms and side effects specific to the patients' tumor may result in an early and sustained reduction in anxiety and distress during and after radiation treatment, thereby improving quality of life.",[97,98,99],"Glioblastoma","WHO Grade II Glioma","WHO Grade III Glioma","2026-01-16",{"date":102,"type":103},"2026-01-20","ACTUAL",{"date":105,"type":103},"2019-06-05",{"date":107,"type":91},"2026-06-01",{"name":5,"class":6},1]