[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100582914":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":43,"collaborators":45,"id":48,"slug":20,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":17,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":55,"maxAge":20,"enrollmentInfo":56,"targetDuration":20,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":20,"overallStatus":29,"whyStopped":20,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"University of Oklahoma","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"SUCCESS Program","EXPERIMENTAL","This includes our cancer survivorship program which entails 6 weekly group education sessions. Each session includes 25 minutes of didactic and discussion-based lecture, 25 minutes of facilitated support group, and 10 minutes of brief group-based exercise.",[13],"Behavioral: SUCCESS",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","SUCCESS","6 group-based sessions with 25 minutes of didactic content, 25 minutes of facilitated support group, and 10 minutes of group physical activity",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"Ashlea C Braun, PhD","CONTACT","15672401582","ashlea-braun@ouhsc.edu",[28],{"facility":5,"status":29,"city":30,"state":31,"zip":32,"country":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"RECRUITING","Tulsa","Oklahoma","74135","United States",{"type":35,"coordinates":36},"Point",[37,38],-95.99277,36.15398,{"lat":38,"lon":37},[41],{"name":23,"role":24,"phone":42,"phoneExt":20,"email":26},"567-240-1582",{"type":44,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR",[46],{"name":47,"class":6},"Oklahoma State University","100582914",false,"NCT06869512","Cooperative Extension and Cancer Survivorship","Cooperative Extension and Cancer Survivorship: Supportive Care Via Cooperative Extension Services (SUCCESS)","Inclusion Criteria:\n\n* Previous adult-diagnosed cancer\n* Post active cancer treatment\n* No current active treatment, hormonal therapy permitted\n* Ability to get to group sessions\n* In Oklahoma\n\nExclusion Criteria:\n\n* Current palliative or hospice care\n* Surgical or medical history that precludes participation\n* Positive screen on the Physical Activity Readiness Questionnaire+ (PAR-Q+) without a doctor's note approving study participation","ALL","18 Years",{"count":57,"type":58},80,"ESTIMATED","INTERVENTIONAL",[61],"NA","The goal of this clinical trial is to learn if a cancer survivor program, delivered via Cooperative Extension, is feasible and if it can improve health outcomes in cancer survivors who are post-active treatment.\n\nAim 1: Evaluate the feasibility and acceptability of SUCCESS. Hypothesis 1: SUCCESS will be feasible and acceptable as evidenced by delivery of the intervention among Educators (implementation), including in agreement with the curriculum in Phase 1 (fidelity) with \\>85% attendance (demand) among participants with \\>80% rating the intervention as acceptable or highly acceptable on 5-point Likert-type scale (acceptability).\n\nAim 2: Determine the preliminary efficacy of SUCCESS for improving HRQOL (primary outcome) and other psychosocial and health-related endpoints (e.g., financial toxicity) (secondary outcomes). Hypothesis 2: Compared to matched controls, adults LWBC who complete SUCCESS will have significant improvements in HRQOL per the PROMIS Global Health v1.2 at follow-up (i.e., after 6 weeks).\n\nAim 3: Examine changes in conserved transcriptional response to adversity (CTRA) gene expression in a subset of interventions participants at follow-up. Hypothesis 3: Adults LWBC who complete SUCCESS will experience significant CTRA down-regulation.\n\nThis is a single arm trial and there is no comparison group.\n\nParticipants will be asked to do survey- and Zoom-based data collection before and after completing the 6-week program.",[64],"Cancer Survivorship","2025-06-25",{"date":67,"type":68},"2025-06-26","ACTUAL",{"date":70,"type":68},"2025-02-24",{"date":72,"type":58},"2026-12-31",{"name":5,"class":6},1]