[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100573417":3},{"organization":4,"armGroups":7,"interventions":30,"overallOfficials":74,"centralContacts":78,"locations":87,"responsibleParty":107,"collaborators":42,"id":110,"slug":42,"hasResults":111,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":42,"eligibilityCriteria":115,"healthyVolunteers":116,"sex":117,"minAge":118,"maxAge":42,"enrollmentInfo":119,"targetDuration":42,"studyType":122,"phases":123,"briefSummary":125,"conditions":126,"keywords":42,"overallStatus":89,"whyStopped":42,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":137,"completionDateStruct":139,"leadSponsor":141,"locationsCount":142},{"fullName":5,"class":6},"Ohio State University Comprehensive Cancer Center","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Phase I (design)","ACTIVE_COMPARATOR","Survivor-caregiver dyads and SMEs complete semi-structured interview over 60-90 minutes and surveys over 15 minutes for intervention content, format, and feature design and development on study",[13],"Other: Survey Administration",{"label":15,"type":10,"description":16,"interventionNames":17},"Phase II (user-experience testing)","Dyads complete semi-structured interview and participate in think-aloud sessions over 60-90 minutes and complete surveys over 15 minutes to test the Healthy Buckeyes app on study.",[18,19,13],"Procedure: Discussion","Other: Interview",{"label":21,"type":22,"description":23,"interventionNames":24},"Phase III (pilot study)","EXPERIMENTAL","Dyads use the Healthy Buckeyes app to set goals, self-monitor, elicit social support, reinforcement, time management, relapse prevention, and receive exercise videos and recipes tailored to CRC survivors on study. Dyads also watch three 3 minute videos on strategies for improving healthy lifestyle behaviors weekly, wear a Fitbit and use exercise bands, and receive health coaching over 10 weeks on study. Dyads will be prompted through the app to identify specific ways they will support each other (team activity and team huddle) in meeting their goals throughout the week for 10 weeks on study.",[25,26,19,27,28,29,13],"Other: Educational Activity","Other: Internet-Based Intervention","Other: Medical Device Usage and Evaluation","Other: Questionnaire Administration","Other: Supportive Care",[31,38,43,47,50,54,58,62,70],{"type":32,"name":33,"description":34,"armGroupLabels":35,"otherNames":36},"PROCEDURE","Discussion","Participate in think-aloud sessions",[15],[37],"Discuss",{"type":6,"name":39,"description":40,"armGroupLabels":41,"otherNames":42},"Educational Activity","Receive health coaching",[21],null,{"type":6,"name":44,"description":45,"armGroupLabels":46,"otherNames":42},"Internet-Based Intervention","Use Healthy Buckeyes app",[21],{"type":6,"name":44,"description":48,"armGroupLabels":49,"otherNames":42},"Watch videos",[21],{"type":6,"name":51,"description":52,"armGroupLabels":53,"otherNames":42},"Interview","Complete semi-structured interview",[15,21],{"type":6,"name":55,"description":56,"armGroupLabels":57,"otherNames":42},"Medical Device Usage and Evaluation","Wear Fitbiit and use exercise bands",[21],{"type":6,"name":59,"description":60,"armGroupLabels":61,"otherNames":42},"Questionnaire Administration","Ancillary studies",[21],{"type":6,"name":63,"description":64,"armGroupLabels":65,"otherNames":66},"Supportive Care","Receive caregiver support",[21],[67,68,69],"Supportive Therapy","Symptom Management","Therapy, Supportive",{"type":6,"name":71,"description":72,"armGroupLabels":73,"otherNames":42},"Survey Administration","Complete surveys",[9,15,21],[75],{"name":76,"affiliation":5,"role":77},"Roberto M Benzo, PhD","PRINCIPAL_INVESTIGATOR",[79,84],{"name":80,"role":81,"phone":82,"phoneExt":42,"email":83},"The Ohio State Comprehensive Cancer Center","CONTACT","800-293-5066","OSUCCCClinicaltrials@osumc.edu",{"name":85,"role":81,"phone":42,"phoneExt":42,"email":86},"Macy Tetrick","Macy.tetrick@osumc.edu",[88],{"facility":5,"status":89,"city":90,"state":91,"zip":92,"country":93,"countryCode":94,"cosmosGeoPoint":95,"geoPoint":100,"contacts":101},"RECRUITING","Columbus","Ohio","43210","United States","US",{"type":96,"coordinates":97},"Point",[98,99],-82.99879,39.96118,{"lat":99,"lon":98},[102,106],{"name":103,"role":81,"phone":104,"phoneExt":42,"email":105},"Roberto M. Benzo, PhD","614-293-3675","Roberto.Benzo@osumc.edu",{"name":103,"role":77,"phone":42,"phoneExt":42,"email":42},{"type":77,"investigatorFullName":108,"investigatorTitle":109,"investigatorAffiliation":5,"oldNameTitle":42,"oldOrganization":42},"Roberto Benzo","Principal Investigator","100573417",false,"NCT06746012","Designing a Dyad-Based mHealth Intervention to Improve Adherence to Lifestyle Recommendations in Colorectal Cancer Survivors and Their Family Caregivers","Designing a Dyad-Based mHealth Intervention to Improve Adherence to Lifestyle Recommendations in Colorectal Cancer Survivors and Their Family Caregivers: Human-Centered Study","Inclusion Criteria:\n\n* PATIENTS INCLUSION:\n* Adults (18 years of age or older)\n* Diagnosis of stage I-III colon or rectal cancer\n* Undergone curative-intent complete surgical resection (patients who have received non-operative management for rectal cancer may be eligible)\n* Completed treatment (i.e., neo-adjuvant, adjuvant cytotoxic chemotherapy, radiation, or surgical resection) at least six months prior\n* Own a smartphone with internet access and can receive text messages\n* Able to speak, read, and understand English\n* Self-report ability to independently engage in physical activity determined by the Physical Activity Readiness questionnaire (PAR-Q), and if indicated obtain physician clearance\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 determined via medical chart review\n* Presence of a family caregiver (i.e., informal or formal caregiver) willing support the patient and participate in the study\n* Able to provide informed consent\n* FAMILY CAREGIVER INCLUSION:\n* Any adult that resides in the same household as the patient\n* Willing to participate in all aspects of the intervention and in the assessments required for those in the wait-list control condition if applicable\n* Meets the patient inclusion criteria number 1, 5, 6, and 10\n* SMES INCLUSION:\n* Medical, radiation, and surgical oncologists; advanced practice providers, registered nurses; dietitians; exercise physiologists; physical therapists, patient navigators and champions\u002Fadvocates, and social workers with at least 12 months of experience working with CRC survivors\n\nExclusion Criteria:\n\n* PATIENTS EXCLUSION:\n* People with potential contraindications to exercise based on the PAR-Q, for those we are unable to obtain physician clearance\n* Planned major surgery during the study period\n* Scheduled to receive any form of cancer therapy during study participation\n* Concurrent, actively treated other cancer (except non-melanoma skin cancer, in situ cervical cancer or localized prostate cancer treated with surveillance only)\n* Self-reported history of severe cardiovascular, respiratory, musculoskeletal disease, or joints problems that preclude moderate physical activity (PA)\n* Self-reported history of psychiatric disorders that preclude participation in the study intervention or prevent the patient from giving informed consent\n* Concurrent participation in another weight loss, PA, or dietary intervention clinical trial\n* Currently pregnant or trying to become pregnant during the study period\n* living outside the United States (US) during the study period\n* Currently a prisoner\n* FAMILY CAREGIVER EXCLUSION:\n* The same as the patient exclusion criteria",true,"ALL","18 Years",{"count":120,"type":121},70,"ESTIMATED","INTERVENTIONAL",[124],"NA","This clinical trial develops and tests a mobile health (mHealth) intervention to improve adherence to lifestyle recommendations in colorectal cancer (CRC) survivors and their family caregivers. The current challenge for cancer survivorship is identifying novel approaches to help adhere to the lifestyle recommendations that have been shown to improve symptom burden, health outcomes, and health-related quality of life (HRQoL). The development of a digital health intervention specifically for CRC survivors and family caregivers may improve adherence to the American Cancer Society Nutrition and Physical Activity Guideline for Cancer Survivors and improve family health.",[127,128,129,130,131,132],"Stage I Colon Cancer AJCC v8","Stage I Rectal Cancer AJCC v8","Stage II Colon Cancer AJCC v8","Stage II Rectal Cancer AJCC v8","Stage III Colon Cancer AJCC v8","Stage III Rectal Cancer AJCC v8","2026-04-05",{"date":135,"type":136},"2026-04-09","ACTUAL",{"date":138,"type":136},"2024-05-03",{"date":140,"type":121},"2026-12-31",{"name":5,"class":6},1]