[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100615261":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":38,"locations":48,"responsibleParty":68,"collaborators":71,"id":75,"slug":76,"hasResults":77,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":77,"sex":83,"minAge":84,"maxAge":42,"enrollmentInfo":85,"targetDuration":42,"studyType":88,"phases":89,"briefSummary":91,"conditions":92,"keywords":100,"overallStatus":51,"whyStopped":42,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":118},{"fullName":5,"class":6},"Colorado State University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention (Virtually Supervised Exercise Class)","EXPERIMENTAL","Live, group-based exercise classes will be delivered 2x per week on Zoom for 12-weeks along with a total of 5 behavior change discussion sessions.",[13],"Behavioral: Virtually Supervised Exercise Sessions",{"label":15,"type":16,"description":17,"interventionNames":18},"Comparator (Asynchronous Exercise Sessions)","ACTIVE_COMPARATOR","Participants will watch pre-recorded exercise and discussion videos for 12-weeks.",[19],"Behavioral: Asynchronous Group",[21,28],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Virtually Supervised Exercise Sessions","The 12-week intervention will consist of supervised exercise sessions twice per week, and PA behavior change discussion sessions twice per month (bi-weekly) throughout the study for a total of five sessions (Week 2, 4, 6, 8 and 10). Exercise and PA behavior change discussion sessions will be informed by social cognitive theory, operationalize several BCT's, and include group dynamics-based strategies to enhance group cohesion. Exercise sessions will take place twice per week, lasting approximately one hour.",[9],[27],"Live, Group-Based Zoom Class",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"Asynchronous Group","The comparator will be an \"unsupported intervention\",128 which will use the same technology and provide the same content as the intervention but subtract the human components. Participants in the control group will receive access to pre-recorded (i.e., asynchronous) videos of the exercise and discussion sessions. The exercise videos will follow the same format as those in the intervention (i.e., instructor led, circuit-style aerobic and resistance exercises). Discussion sessions will operationalize the same BCT's using PowerPoint slides. Comparator arm participants will receive instructions on how to access these videos via a unique participant login to a secure website, Canvas, the same recommendations to achieve PA guidelines, and the same home-based exercise equipment (along with instructions for use).",[15],[33],"Pre-recorded exercise videos",[35],{"name":36,"affiliation":5,"role":37},"Heather J Leach, PhD","PRINCIPAL_INVESTIGATOR",[39,44],{"name":36,"role":40,"phone":41,"phoneExt":42,"email":43},"CONTACT","(970) 491-8951",null,"heather.leach@colostate.edu",{"name":45,"role":40,"phone":42,"phoneExt":46,"email":47},"Elena M Lancioni, MPH","(970) 491-4653","elena.lancioni@colostate.edu",[49],{"facility":50,"status":51,"city":52,"state":53,"zip":54,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"Human Performance Clinical Research Lab","RECRUITING","Fort Collins","Colorado","80523","United States","US",{"type":58,"coordinates":59},"Point",[60,61],-105.08442,40.58526,{"lat":61,"lon":60},[64],{"name":65,"role":40,"phone":66,"phoneExt":42,"email":67},"Elena Lancioni","970-491-4653","patplab@colostate.edu",{"type":37,"investigatorFullName":69,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":42,"oldOrganization":42},"Heather Leach","PhD",[72],{"name":73,"class":74},"National Cancer Institute (NCI)","NIH","100615261","survivors-uniting-for-remote-guided-exercise-100615261",false,"NCT07290309","Survivors Uniting for Remote Guided Exercise","Efficacy of a Group-based Videoconference Intervention to Increase Physical Activity in Cancer Survivors","SURGE","Inclusion Criteria:\n\n* Able to speak\u002Fread English,\n* Diagnosed with any type of cancer within the last 5 years\n* Completed primary or adjuvant treatment (i.e., chemotherapy, radiation therapy, surgery) 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, immunotherapies)\n\nExclusion Criteria:\n\n* Existing participation in ≥150 minutes per week of at least moderate intensity aerobic 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 structured program or intervention intended to encourage participation in exercise or physical activity.","ALL","18 Years",{"count":86,"type":87},300,"ESTIMATED","INTERVENTIONAL",[90],"NA","The goal of this research study is to look at how live, online group exercise compares to recorded videos for helping increase physical activity levels, improve physical fitness and quality of life, and reduce loneliness among those living with and beyond cancer. The following aims have been established for this study:\n\n* Aim 1: Examine the effect of a group-based videoconference physical activity (PA) intervention on moderate to vigorous physical activity \\[MVPA\\] (i.e., aerobic and resistance exercise).\n* Aim 2: Examine the effect of the intervention on additional health-related outcomes including physical fitness (i.e., aerobic endurance, muscular strength), and quality of life at both timepoints.\n* Aim 3: Explore potential mediators and moderators of intervention effects. We will examine mediators (e.g., self-efficacy, outcome expectations, group cohesion) and moderators (e.g., age, cancer stage, neighborhood walkability) of the intervention on MVPA.\n* Exploratory Aim: Determine whether a group-based videoconference PA intervention reduces loneliness among cancer survivors.\n\nResearchers will randomize participants into one of two guided exercise groups that are 12-weeks long in duration. Participants will be asked to complete online fitness assessments and surveys as well as wear a physical activity monitor device and watch a few times throughout the study. The whole study is 9-months long in duration with a 6-month free-living period where no study activities will take place.",[93,94,95,96,97,98,99],"Cancer","Cancer (Colon Cancer, Breast Cancer, Lymphoma, Chronic Lymphoma Leukemia, Multiple Myeloma)","Physical Activity","Physical Activity Behavior","Cancer (With or Without Metastasis)","Cancer - Chronic Lymphocytic Leukemia","Cancer - Ovarian",[101,102,103,104,105,106,107,108],"Exercise oncology","Physical activity for cancer survivors","Group based exercise","Virtual exercise","physical activity","exercise","remote study","Cancer survivors","2026-03-27",{"date":111,"type":112},"2026-03-31","ACTUAL",{"date":114,"type":112},"2026-02-06",{"date":116,"type":87},"2030-03-01",{"name":5,"class":6},1]