[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"exercise-oncology\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:exercise-oncology":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100637924","first-sask-study-protocol-a-remote-exercise-oncology-intervention-100637924",false,"NCT07617220","FIRST-Sask Study Protocol: A Remote Exercise Oncology Intervention","FIRST-Sask Study Protocol: A Randomized Controlled Trial of a Remote Exercise Oncology Intervention","FIRST-Sask","Inclusion Criteria:\n\n* confirmed diagnosis of any type of cancer (except non-melanoma skin cancer);\n* having received cancer treatment within the past 12 months;\n* self-identifying as rural resident; or residing in areas outside of the city of Saskatoon or Regina;\n* age ≥65;\n* ability to communicate in English;\n* ability to provide informed consent;\n* physically suitable to participate by research personnel based on PAR-Q and physical performance screening.\n\nExclusion Criteria:\n\n* persistent light-headedness during physical activity of or syncopal episodes within the past month;\n* other comorbidities or musculoskeletal complications that preclude participation in the exercise programs as deemed by the exercise interventionist;\n* unstable bone metastases.","ALL","65 Years",{"count":20,"type":21},37,"ESTIMATED","INTERVENTIONAL",[24],"NA","Older adults undergoing cancer treatment experience substantial treatment-related burden and reduced quality of life (QoL). Exercise is an effective supportive care intervention, but access is limited in rural and geographically dispersed settings. Evidence on flexible delivery models that accommodate patient preferences and real-world constraints remains scarce.\n\nThis study seeks to evaluate the feasibility and acceptability of a hybrid exercise program for older adults with cancer in rural settings and to obtain preliminary efficacy estimates to inform a larger trial. This randomized controlled trial tests a 12-week, multimodal exercise intervention co-designed with patient partners. The program uses a hybrid delivery model with options (in-person, remote, or combined formats) based on preference, geography, season, and alignment with routine travel (e.g. clinic visits). Older adults (≥65) with breast, lung, prostate, colorectal, or hematologic cancers are recruited using a multipronged strategy. Assessments at baseline and 12 weeks include cardiovascular endurance, upper and lower limb strength, balance, and QoL. Feasibility and acceptability will be examined via recruitment, retention, adherence, exit surveys and interviews. Exercise prescription will follow FITT principles. Adherence, dose modifications, and fidelity will be monitored using standardized procedures. Analyses will follow an intention-to-treat approach, with between-group and over-time effects estimated using generalized linear and mixed-effects models. This study will inform the development of a scalable exercise rehabilitation model to improve equitable access to supportive care in rural settings.",[27],"Exercise Oncology","NOT_YET_RECRUITING","2026-05-28",{"date":31,"type":32},"2026-06-01","ACTUAL",{"date":34,"type":21},"2026-05",{"date":36,"type":21},"2027-07-30",{"name":38,"class":39},"University of Saskatchewan","OTHER",{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":48,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":22,"phases":51,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100543695","sustaining-physical-activity-after-cancer-exercise-sessions-100543695","NCT06359210","Sustaining Physical Activity After Cancer Exercise Sessions","An Adaptive Physical Activity Maintenance Intervention","SPAACES","Inclusion Criteria:\n\n* ≥18 years old,\n* Able to speak\u002Fread English,\n* Diagnosed with any type of cancer,\n* Completed primary or adjuvant treatment (i.e., chemotherapy, radiation therapy, surgery) within the previous five years, with no planned treatment within the next nine months. This does not include long-term or chronic therapies such as anti-hormone or targeted therapies (e.g., aromatase inhibitor, androgen deprivation therapy),\n* Participant is registered\u002Fenrolled to participate in one of three community-based exercise programs.\n\nExclusion Criteria:\n\n* Existing participation in ≥90 minutes per week of at least moderate intensity aerobic exercise AND two or more days per week of resistance exercise or known contraindications for exercise.\n* Known contraindications for non-medically supervised moderate or greater intensity exercise (e.g., uncontrolled hypertension, inability to walk without an assistive device)\n* Current or planned participation in another exercise oncology program (not one of the three community partner exercise programs), or previous participation in another or one of the three community partner exercise programs in the past 12-months.","18 Years",{"count":50,"type":21},105,[24],"The goal of this clinical trial is to develop and test an adaptive physical activity (PA) maintenance intervention for cancer survivors, after participating in a community-based exercise oncology program. The main questions it aims to answer are:\n\n* Aim 1: Examine the feasibility and acceptability of the intervention among cancer survivors and community partners. The researchers will utilize quantitative surveys, focus groups, and semi-structured interviews to collect information about feasibility, implementation, adaptation, and sustainability.\n* Aim 2: Examine the effects of the intervention among cancer survivors. The researchers will compare the proportion of participants achieving the exercise guidelines for cancer survivors six-months following completion of the initial exercise program.\n\nParticipants will participate in a community-based exercise oncology program and then return to three months of free living. Based on the PA measured at the three-month follow-up, participants will be categorized as a \"Responder\" or \"Incomplete Responder\", and then randomized to the PA maintenance intervention. Researchers will compare those that are classified as Responders (meeting exercise guidelines for cancer survivors) and Incomplete Responders (not meeting guidelines for cancer survivors) to see what level of intervention is needed to influence sustainable behavior change in this population.",[27,54,55],"Physical Activity Behavior","Behavior Change Interventions",[57,58,59,60,61,62,63],"exercise oncology","physical activity","behavior change","adaptive intervention","cancer survivors","physical activity maintenance","community partnerships","RECRUITING","2026-03-17",{"date":67,"type":32},"2026-03-19",{"date":69,"type":32},"2024-03-04",{"date":71,"type":21},"2026-12-31",{"name":73,"class":39},"Colorado State University",3]