[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100587627":3},{"organization":4,"armGroups":7,"interventions":27,"overallOfficials":35,"centralContacts":40,"locations":51,"responsibleParty":72,"collaborators":75,"id":85,"slug":45,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":88,"acronym":30,"eligibilityCriteria":89,"healthyVolunteers":86,"sex":90,"minAge":91,"maxAge":45,"enrollmentInfo":92,"targetDuration":45,"studyType":95,"phases":96,"briefSummary":98,"conditions":99,"keywords":112,"overallStatus":54,"whyStopped":45,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":132},{"fullName":5,"class":6},"Dartmouth-Hitchcock Medical Center","OTHER",[8,14,19,23],{"label":9,"type":10,"description":11,"interventionNames":12},"CA Participant-Group 1","EXPERIMENTAL","After enrollment and completion of baseline assessments, CA Participant Group 1 will receive the HOBSCOTCH-PTE intervention consisting of 1:1 sessions delivered once per week including:\n\n* 1 pre-HOBSCOTCH Session (on webcam)\n* 1 educational session (on webcam)\n* 6 telephone sessions (option to do on webcam)\n* 1 wrap-up session (webcam or telephone)",[13],"Behavioral: HOBSCOTCH-CA",{"label":15,"type":16,"description":17,"interventionNames":18},"CA Participant-Group 2","ACTIVE_COMPARATOR","After a 3-month waiting period and having completed baseline and 3-month study assessments, CA Participant Group 2 will receive the HOBSCOTCH-CA intervention consisting of 1:1 sessions delivered once per week including:\n\n* 1 pre-HOBSCOTCH Session (on webcam)\n* 1 educational session (on webcam)\n* 6 telephone sessions (option to do on webcam)\n* 1 wrap-up session (webcam or telephone)",[13],{"label":20,"type":10,"description":21,"interventionNames":22},"CA Participant Caregiver-Group 1","After enrollment and completion of baseline assessments, CA Participant Caregiver Group 1 will receive an adapted version of HOBSCOTCH-CA alongside the CA participant by attending:\n\n* 1 pre-HOBSCOTCH Session (on webcam)\n* 1 educational session (on webcam)\n* 1 wrap-up session (webcam or telephone)",[13],{"label":24,"type":16,"description":25,"interventionNames":26},"CA Participant Caregiver-Group 2","After a 3-month waiting period and having completed baseline and 3-month study assessments, CA Participant Caregiver Group 2 will receive an adapted version of HOBSCOTCH-CA alongside the CA participant by attending:\n\n* 1 pre-HOBSCOTCH Session (on webcam)\n* 1 educational session (on webcam)\n* 1 wrap-up session (webcam or telephone)",[13],[28],{"type":29,"name":30,"description":31,"armGroupLabels":32,"otherNames":33},"BEHAVIORAL","HOBSCOTCH-CA","HOBSCOTCH is a home-based self-management program to treat cognitive symptoms and improve quality of life, while minimizing the barriers of access to care. The program is based on Problem Solving Therapy (PST) and teaches problem solving strategies and compensatory mechanisms to help manage cognitive dysfunction and enhance quality of life. HOBSCOTCH-CA is an adaptation of the HOBSCOTCH program for people who are survivors of brain cancer or a brain tumor that incorporates education about the effects from brain cancer\u002Ftumor and its treatment on cognition into the education module and gives them the option of enrolling with a Caregiver. CA Participants receive all sessions of HOBSCOTCH-CA. If they enroll with a Caregiver, the Caregiver participates in the education (introductory) session and sessions 1 and 8. The HOBSCOTCH-CA Participant may invite their Caregiver to attend all sessions.",[20,24,9,15],[34],"HOme-Based Self-management and COgnitive Training CHanges lives (HOBSCOTCH)",[36],{"name":37,"affiliation":38,"role":39},"Elaine T Kiriakopoulos, MD, MPH, MSc","Dartmouth-Health\u002FDartmouth-Hitchcock, Dartmouth College","PRINCIPAL_INVESTIGATOR",[41,47],{"name":42,"role":43,"phone":44,"phoneExt":45,"email":46},"Sarah J. Kaden, BA","CONTACT","603-650-4225",null,"sarah.j.kaden@hitchcock.org",{"name":48,"role":43,"phone":49,"phoneExt":45,"email":50},"Trina K Dawson, BA","603-650-4205","trina.k.dawson@hitchcock.org",[52],{"facility":53,"status":54,"city":55,"state":56,"zip":57,"country":58,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"Dartmouth-Health Lebanon","RECRUITING","Lebanon","New Hampshire","03756","United States",{"type":60,"coordinates":61},"Point",[62,63],-72.25176,43.64229,{"lat":63,"lon":62},[66,69,70],{"name":67,"role":43,"phone":44,"phoneExt":45,"email":68},"Kathryn Giordano","HOBSCOTCH-CA.Research@Hitchcock.org",{"name":42,"role":43,"phone":44,"phoneExt":45,"email":68},{"name":71,"role":39,"phone":45,"phoneExt":45,"email":45},"Elaine T. Kiriakopoulos, MD, MPH, MSc",{"type":39,"investigatorFullName":73,"investigatorTitle":74,"investigatorAffiliation":5,"oldNameTitle":45,"oldOrganization":45},"Elaine T. Kiriakopoulos","Elaine T. Kiriakopoulos, MD, MPH, MSc Assistant Professor of Neurology, Geisel School of Medicine at Dartmouth Director, HOBSCOTCH Institute for Cognitive Health & Well-Being Dartmouth Hitchcock Epilepsy Center",[76,79,81,83],{"name":77,"class":78},"Congressionally Directed Medical Research Programs","FED",{"name":80,"class":6},"Mayo Clinic",{"name":82,"class":6},"University of North Carolina",{"name":84,"class":6},"Dartmouth College","100587627",false,"NCT06930846","HOBSCOTCH-CA (HOme-Based Self-management and COgnitive Training CHanges Lives in Brain CAncer)","CA Participants will be referred to the study by their providers (Oncologist) who will be made aware of the study and inclusion\u002Fexclusion criteria. Inclusion Criteria 2. - 5. and Exclusion Criteria 1. - 3. will be confirmed by referring providers. Participants who learn about the study here and elsewhere will be instructed on how to confirm their eligibility with their provider.\n\nInclusion Criteria for CA Participant:\n\n1. 18 + years\n2. Service members, Veterans and civilians with a diagnosis of brain cancer (excluding glioblastoma)\n3. Diagnosis of primary brain tumor with expected survival of 2 years or greater (e.g., low-grade glioma, oligodendroglioma, IDH mutant astrocytoma, meningioma) defined as the presence of a primary lesion on neuroimaging (CT or MRI), confirmed by histopathological examination (Note: some patients being treated for meningioma may be treated with radiotherapy without need for initial histopathologic confirmation)\n4. Patients undergoing surgical and\u002For radiation therapy will have completed their treatment at least 3 months prior to being enrolled in trial (Note: patients receiving chemotherapy or other systemic therapy will be included)\n5. Stable on all CNS acting medications for one month prior to enrollment\n6. Subjective cognitive complaints\n7. Literate and proficient in English\n8. Internet access for the pre-session and Session 1 of the HOBSCOTCH-CA program; telephone access for sessions 2-8\n\nExclusion Criteria for CA Participant:\n\n1. Presence of a neurodegenerative disease (e.g., Alzheimer's disease, Parkinson's disease)\n2. Acute psychiatric disorder or substance abuse\n3. Patients with glioblastoma (GBM)\n\nInclusion Criteria for CA Participant Caregiver:\n\n1. Age 18 +\n2. Caregiver to a patient with a confirmed diagnosis of brain cancer\u002Ftumor survivor\n3. CA Subject has given permission for their caregiver to participate\n4. Literate and proficient in English\n5. Internet access (for Pre-HOBSCOTCH and Session 1)\n6. Telephone access (for Session 8)\n\nExclusion Criteria for CA Participant Caregiver:\n\n1. Significant visual impairment precluding reading or writing\n2. No reliable telephone or internet access","ALL","18 Years",{"count":93,"type":94},125,"ESTIMATED","INTERVENTIONAL",[97],"NA","The purpose of this study is to assess the ability of the home-based intervention, HOBSCOTCH-CA, to improve the quality of life and cognitive function in Service Members, Veterans and civilians who are survivors of brain cancer or a brain tumor (CA participants). This study will also assess the ability of the HOBSCOTCH-CA program to improve quality of life in caregivers of patients with brain cancer\u002Ftumor and to reduce caregiver burden. Enrolling with a Caregiver is optional for CA participants.\n\nInvestigators will compare two groups of CA participants and their Caregiver (enrolling with a Caregiver is optional): one who receives HOBSCOCTCH-CA immediately (Group 1) and another group that will receive HOBSCOTCH-CA (Group 2) after a 3-month waiting period. Participants will be in the study for about 6 months total.\n\nHOBSCOTCH-CA involves 45 to 60 minute one on one virtual sessions with a certified Cognitive Coach including a \"pre\" program session and 8 weekly sessions thereafter. Participants will learn about problem solving therapy and mindfulness or relaxation training. CA participants are asked to do short homework assignments and keep a brief daily diary on a smart phone app. All participants complete study questionnaires or surveys at enrollment, 3 months later and at 6 months (at the end of the study).",[100,101,102,103,104,105,106,107,108,109,110,111],"Brain Cancer","Brain Tumor","Brain Neoplasms","Primary Brain Tumor","Low-grade Glioma","Oligodendroglioma","Meningioma","Low Grade Astrocytoma","Cognitive Dysfunction","Memory Impairment","Memory Disorders","Memory Dysfunction",[113,114,115,116,117,118,119,120,121,122],"Brain cancer survivor","Brain tumor survivor","Cognition","Self-management","Cognitive training","Memory disorders","Cognitive remediation","Caregiver","Caregiver burden","Mindfulness","2025-11-18",{"date":125,"type":126},"2025-11-21","ACTUAL",{"date":128,"type":126},"2025-11-03",{"date":130,"type":94},"2028-12",{"name":5,"class":6},1]