[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100607284":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":29,"centralContacts":33,"locations":38,"responsibleParty":57,"collaborators":59,"id":62,"slug":63,"hasResults":64,"nctId":65,"briefTitle":66,"officialTitle":66,"acronym":24,"eligibilityCriteria":67,"healthyVolunteers":64,"sex":68,"minAge":69,"maxAge":70,"enrollmentInfo":71,"targetDuration":24,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":24,"overallStatus":41,"whyStopped":24,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Attention Control Group","EXPERIMENTAL","Participants will randomized using incorrect baseline information.",[13],"Behavioral: RISE-YA Intervention",{"label":15,"type":10,"description":11,"interventionNames":16},"InItervention Group: Remote Implementation of Supervised Exercise for Young Adult",[17],"Behavioral: Survivorship Education",[19,25],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"BEHAVIORAL","RISE-YA Intervention","Participants will receive energy conservation (EC) counseling, behavior coaching, and exercise training.",[9],null,{"type":20,"name":26,"description":27,"armGroupLabels":28,"otherNames":24},"Survivorship Education","During weeks 1-6 and 1 time a week during Weeks 7-12, participants will receive a video call which will last about 60 minutes.",[15],[30],{"name":31,"affiliation":5,"role":32},"Michael Roth, MD","PRINCIPAL_INVESTIGATOR",[34],{"name":31,"role":35,"phone":36,"phoneExt":24,"email":37},"CONTACT","(713) 792-7751","mroth1@mdanderson.org",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"The University of Texas M. D. Anderson Cancer Center","RECRUITING","Houston","Texas","77030","United States","US",{"type":48,"coordinates":49},"Point",[50,51],-95.36327,29.76328,{"lat":51,"lon":50},[54,56],{"name":31,"role":35,"phone":55,"phoneExt":24,"email":37},"713-792-7751",{"name":31,"role":32,"phone":24,"phoneExt":24,"email":24},{"type":58,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR",[60],{"name":61,"class":6},"Cancer Prevention Research Institute of Texas","100607284","cancer-related-fatigue-and-its-biological-contributors-in-adolescent-and-young-adult-brain-tumor-survivors-effects-of-a-tele-exercise-intervention-100607284",false,"NCT07186556","Cancer-related Fatigue and Its Biological Contributors in Adolescent and Young Adult Brain Tumor Survivors: Effects of a Tele-exercise Intervention","Inclusion Criteria:\n\n1. Is currently between the ages of 18-39 years\n2. Their primary brain tumor was diagnosed at age 15-39 years\n3. Is 6 months to \\\u003C5 years post curative treatment\n4. Has been treated with chemotherapy and radiation, given most patients receive both therapies.\n5. Functional Assessment of Chronic Illness therapy (FACIT)-Fatigue ≤ 43. FACIT-Fatigue will be used as a screener because this 13-item scale can be completed relatively quickly in clinic\n6. Currently engage in \\\u003C150 minutes of PA and \\\u003C 2 sessions of muscle strengthening exercise per week (assessed by Godin Leisure-Time PA Questionnaire)\n7. Must be able to speak, write, and read English\n8. No exercise contraindication as assessed by screening with the Physical Activity Readiness Questionnaire PAR-Q+. In addition, participants' care teams will be notified of their participation in the study.\n9. Must be able to provide informed consent\u002Fassent.\n\nExclusion Criteria:\n\n1. Non-English speaking\n2. Screen failure for exercise safety\n3. Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease\n4. Recent fracture or acute musculoskeletal injury that precludes ability to participate in supervised exercise training sessions\n5. History of underlying chronic disease, secondary malignances, germline genetic syndrome, or recurrent disease requiring re-irradiation of the brain\n6. Cognitive and\u002For major sensory deficits that would impede the completion of research activities and assessments as deemed by the clinical team.\n7. Self-report of pregnancy\n8. Prisoners\n9. Documented developmental disorders (e.g., Autism) or major psychotic illness (e.g., schizophrenia)","ALL","18 Years","39 Years",{"count":72,"type":73},75,"ESTIMATED","INTERVENTIONAL",[76],"NA","The goal of this research study is to learn about the effects of the RISE-YA intervention on cancer-related fatigue in young adults who are brain cancer survivors.",[79,80,81],"Cancer","Fatigue","Brain Tumor Adult","2026-03-02",{"date":84,"type":85},"2026-03-04","ACTUAL",{"date":87,"type":85},"2025-09-09",{"date":89,"type":73},"2031-12-31",{"name":5,"class":6},1]