[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100548666":3},{"organization":4,"outcomesModule":7,"designInfo":21,"detailedDescription":20,"studyPopulation":20,"armGroups":27,"interventions":38,"overallOfficials":52,"centralContacts":59,"locations":65,"responsibleParty":86,"collaborators":20,"id":88,"slug":20,"hasResults":89,"nctId":90,"briefTitle":91,"officialTitle":91,"acronym":20,"eligibilityCriteria":92,"healthyVolunteers":89,"sex":93,"minAge":94,"maxAge":20,"enrollmentInfo":95,"targetDuration":20,"studyType":98,"phases":99,"briefSummary":101,"conditions":102,"keywords":20,"overallStatus":67,"whyStopped":20,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":113},{"fullName":5,"class":6},"H. Lee Moffitt Cancer Center and Research Institute","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":20},[9],{"measure":10,"description":11,"timeFrame":12},"Feasibility and acceptability of PA\u002FN and RT\u002FN programs","The number of participants who complete T1 and T0 measures.","Up to 16 weeks",[14,17],{"measure":15,"description":16,"timeFrame":12},"Examine exploratory outcomes and clinical characteristics","The number of participants who demonstrate improvements in exploratory outcome measures.",{"measure":18,"description":19,"timeFrame":12},"Compare clinical and treatment outcomes","Chi-Square testing will be used to determine if there's a significant difference in outcomes between the treatment group and a usual care comparison group.",null,{"allocation":22,"interventionModel":23,"interventionModelDescription":20,"primaryPurpose":24,"observationalModel":20,"timePerspective":20,"maskingInfo":25},"RANDOMIZED","PARALLEL","SUPPORTIVE_CARE",{"masking":26,"maskingDescription":20,"whoMasked":20},"NONE",[28,34],{"label":29,"type":30,"description":20,"interventionNames":31},"Physical activity, nutrition counseling and monitoring group (PA\u002FN)","EXPERIMENTAL",[32,33],"Behavioral: Physical Activity","Behavioral: Nutrition Counseling",{"label":35,"type":30,"description":20,"interventionNames":36},"Physical activity, tele-resistance training, nutrition counseling and monitoring group (RT\u002FN)",[32,33,37],"Behavioral: Resistance Training",[39,44,48],{"type":40,"name":41,"description":42,"armGroupLabels":43,"otherNames":20},"BEHAVIORAL","Physical Activity","Each participant will receive a Fitbit device with instruction and encouragement to self-monitor physical activity using step counts.",[29,35],{"type":40,"name":45,"description":46,"armGroupLabels":47,"otherNames":20},"Nutrition Counseling","Participants will receive nutritional counseling with a registered dietician.",[29,35],{"type":40,"name":49,"description":50,"armGroupLabels":51,"otherNames":20},"Resistance Training","Participants will engage in progressive, full-body resistance training based on American College of Sports Medicine (ACSM) guidelines.",[35],[53,57],{"name":54,"affiliation":55,"role":56},"Nathan Parker, PhD","Moffitt Cancer Center","PRINCIPAL_INVESTIGATOR",{"name":58,"affiliation":55,"role":56},"Pamela Hodul, MD",[60],{"name":61,"role":62,"phone":63,"phoneExt":20,"email":64},"Morgan Bean","CONTACT","813-745-1786","morgan.bean@moffitt.org",[66],{"facility":55,"status":67,"city":68,"state":69,"zip":70,"country":71,"countryCode":72,"cosmosGeoPoint":73,"geoPoint":78,"contacts":79},"RECRUITING","Tampa","Florida","33612","United States","US",{"type":74,"coordinates":75},"Point",[76,77],-82.45843,27.94752,{"lat":77,"lon":76},[80,81,82,83],{"name":61,"role":62,"phone":63,"phoneExt":20,"email":64},{"name":54,"role":56,"phone":20,"phoneExt":20,"email":20},{"name":58,"role":56,"phone":20,"phoneExt":20,"email":20},{"name":84,"role":85,"phone":20,"phoneExt":20,"email":20},"Sylvia Crowder, PhD","SUB_INVESTIGATOR",{"type":87,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100548666",false,"NCT06423963","Remote Exercise and Nutritional Prehabilitation for Pancreatic Cancer","Inclusion Criteria:\n\n* Age 18 years or older\n* Biopsy-proven pancreatic ductal adenocarcinoma (PDAC), borderline resectable at diagnosis\n* Eastern Cooperative Oncology Group (ECOG) performance status 0-2\n* Undergoing neoadjuvant chemotherapy with treatment plan including chemoradiation therapy and surgical resection\n* Ability to read and speak English\n\nExclusion Criteria:\n\n* Regular engagement in RT (2x\u002Fweek targeting all major muscle groups)\n* Screen failure for exercise safety based on PAR-Q\n* Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease\n* Recent fracture or acute musculoskeletal injury that precludes ability to participate in RT\n* Numeric pain rating scale greater than or equal to a 7 out of 10\n* Myopathic or rheumatologic disease that impacts physical function","ALL","18 Years",{"count":96,"type":97},26,"ESTIMATED","INTERVENTIONAL",[100],"NA","The purpose of the study is to examine the feasibility and acceptability of an exercise and nutrition \"prehabilitation\" program for patients preparing for pancreatic cancer resection (removal).",[103],"Pancreatic Cancer","2026-05-05",{"date":106,"type":107},"2026-05-06","ACTUAL",{"date":109,"type":107},"2024-02-09",{"date":111,"type":97},"2026-08",{"name":5,"class":6},1]