[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100639303":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":34,"responsibleParty":57,"collaborators":59,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":22,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":24,"enrollmentInfo":73,"targetDuration":24,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":83,"overallStatus":37,"whyStopped":24,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Hadassah Medical Organization","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Cognitive Retraining and Functional Treatment Group (CRAFT-G) intervention","EXPERIMENTAL","CRAFT-G include six remote group sessions (1.5hr each) led by an occupational therapist. The content of the meetings will be adapted from the cognitive orientation to occupational performance (CO-OP) approach accompanied with relevant psychoeducation materials. Between the sessions, participants will be guided to complete Cancer-related cognitive impairment (CRCI)-specific computerized cognitive training (CCT) 3 times per week delivered using dedicated app. In addition, psychoeducation materials will be delivered during group sessions.",[13],"Behavioral: CRAFT-G",{"label":15,"type":10,"description":16,"interventionNames":17},"Computerized cognitive training group","Participants opting for the cognitive training group will undergo computerized cognitive training (CCT), similar in content and duration to that provided in the CRAFT-G intervention group.",[18],"Other: CCT",[20,25],{"type":21,"name":22,"description":11,"armGroupLabels":23,"otherNames":24},"BEHAVIORAL","CRAFT-G",[9],null,{"type":6,"name":26,"description":16,"armGroupLabels":27,"otherNames":24},"CCT",[15],[29],{"name":30,"role":31,"phone":32,"phoneExt":24,"email":33},"Chenanit Hamami","CONTACT","+972506373099","chenanit.hamami@mail.huji.ac.il",[35],{"facility":36,"status":37,"city":38,"state":24,"zip":24,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Hadassah Medical Care","RECRUITING","Jerusalem","Israel","IL",{"type":42,"coordinates":43},"Point",[44,45],35.21633,31.76904,{"lat":45,"lon":44},[48,50,53,55],{"name":49,"role":31,"phone":32,"phoneExt":24,"email":33},"Chenanit Hamami, Mrs.",{"name":51,"role":31,"phone":24,"phoneExt":24,"email":52},"Yafit Gilboa, Prof.","yafit.gilboa@mail.huji.ac.il",{"name":30,"role":54,"phone":24,"phoneExt":24,"email":24},"SUB_INVESTIGATOR",{"name":51,"role":56,"phone":24,"phoneExt":24,"email":24},"PRINCIPAL_INVESTIGATOR",{"type":58,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR",[60,62],{"name":61,"class":6},"Israel Cancer Association",{"name":63,"class":6},"Hebrew University of Jerusalem","100639303","the-computerized-retraining-and-functional-treatment---group-intervention-100639303",false,"NCT07591857","The Computerized Retraining and Functional Treatment - Group Intervention","The Computerized Retraining and Functional Treatment: Effectiveness-implementation Hybrid Trial of Group Teleintervention Among Breast Cancer Survivors With Cognitive Impairment","Inclusion Criteria:\n\n1. women, 18 years old and older\n2. A subjective concern about declines in cognitive functioning related to a diagnosis of breast cancer and\u002For cancer related treatment\n3. Objective cognitive decline with no dementia (19\\\u003CMOCA)\n4. 6 months or more after completion of an active treatment for cancer\n5. Daily access to the internet and sufficient basic skills to operate a computer\n\nExclusion Criteria:\n\n* Unstable psychiatric or other health condition according to participants' self-report and medical file.","FEMALE","18 Years",{"count":74,"type":75},48,"ESTIMATED","INTERVENTIONAL",[78],"NA","The goal of this clinical trial is to examine the efficacy of a novel, remotely-applied group intervention, Cognitive Retraining and Functional Treatment Group (CRAFT-G), designed to improve cognitive function, mental health and functional outcome in breast cancer survivors (BCS) with Cancer-Related Cognitive Impairment (CRCI) while simultaneously collecting data on the barriers and facilitators of implementation in clinical settings. The main question it aims to answer is:\n\nWe hypothesize that participants receiving CRAFT-G will show gains in mental health, cognitive and daily function, and that the CRAFT-G benefits will endure for three months following treatment completion.\n\nParticipants assigned to the waitlist control will crossover to the CRAFT-G intervention group after 6 weeks.\n\nParticipants will ask to complete CRAFT-G intervention, which include:\n\n* Six remote group sessions (1.5hr each)\n* Between the sessions, participants will be guided to complete CRCI-specific computerized cognitive training (CCT) 3 times per week delivered using dedicated app.\n* Psychoeducation materials Assessment will take place in 3 time points: before intervention (frontal meeting for baseline assessment), post intervetion and 3 months post intervention.\n\nThe study will be conducted to explore implementation barriers and facilitators. This will be done by endline qualitative interviews with the participants' research group.",[81,82],"Cancer Related Cognitive Impairment","Breast Cancer Survivor",[84,85,86],"Tele-rehabilitation","Cognitive training","Group therapy","2026-05-11",{"date":89,"type":90},"2026-05-18","ACTUAL",{"date":92,"type":90},"2025-11-16",{"date":94,"type":75},"2028-06",{"name":5,"class":6},1]