[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100619519":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":31,"centralContacts":35,"locations":40,"responsibleParty":53,"collaborators":12,"id":55,"slug":12,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":12,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":12,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":75,"whyStopped":12,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Yale University","OTHER",[8,13,19,22],{"label":9,"type":10,"description":11,"interventionNames":12},"Control-Usual Care","NO_INTERVENTION","Participants will receive a simple text message reminder",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Messaging Group A","EXPERIMENTAL","Participants will receive a series of outreach messages including texts with two-way messaging capabilities, mailed letter, and a reminder to their clinician. Content of the text message arm will be varied so that patients receive one of three messages (A, B or C).",[18],"Behavioral: Bundled messaging intervention",{"label":20,"type":15,"description":16,"interventionNames":21},"Messaging Group B",[18],{"label":23,"type":15,"description":16,"interventionNames":24},"Messaging Group C",[18],[26],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":12},"BEHAVIORAL","Bundled messaging intervention","A bundled intervention of text message, letter, and provider reminder. Text message content using behaviorally motivated messages will vary.",[14,20,23],[32],{"name":33,"affiliation":5,"role":34},"Ilana Richman, MD","PRINCIPAL_INVESTIGATOR",[36],{"name":33,"role":37,"phone":38,"phoneExt":12,"email":39},"CONTACT","203 737 1024","ilana.richman@yale.edu",[41],{"facility":42,"status":12,"city":43,"state":44,"zip":45,"country":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":12},"Cornell Scott Hill Health","New Haven","Connecticut","06519","United States",{"type":48,"coordinates":49},"Point",[50,51],-72.92816,41.30815,{"lat":51,"lon":50},{"type":54,"investigatorFullName":12,"investigatorTitle":12,"investigatorAffiliation":12,"oldNameTitle":12,"oldOrganization":12},"SPONSOR","100619519",false,"NCT07345676","Colorectal Cancer Screening Outreach","Optimizing Evidence-Based Interventions to Improve Colorectal Cancer Screening Adherence in Community Health Clinics","Inclusion Criteria:\n\n* Established adult medicine patient at Cornell Scott Hill health (defined as having a CSHH primary care doctor or \\>1 adult medicine visits in the last year).\n* Incomplete colorectal cancer screening test defined as an outstanding order for colonoscopy or stool-based CRC screening (e.g., fecal immunochemical test (FIT) or FIT-DNA testing), but no evidence of test completion at the time of randomization. Orders must have been placed between 90-180 days prior to randomization.\n\nOR\n\n* Abnormal stool-based test without follow-up, defined as an abnormal stool-based test result (e.g., positive FIT or FIT-DNA) with no completed diagnostic colonoscopy within 90 days of the result. Patients who meet this criterion will be included in a non randomized arm of the study.\n\nExclusion Criteria:\n\n* Because this is a pragmatic study of a behavioral intervention to improve colorectal cancer screening adherence, any participants who otherwise meet the inclusion criteria will not be excluded.","ALL","45 Years","75 Years",{"count":65,"type":66},2000,"ESTIMATED","INTERVENTIONAL",[69],"NA","This is a 4 arm pragmatic trial to test a multicomponent intervention designed to improve adherence to colorectal cancer screening.",[72],"Colo-rectal Cancer",[74],"Screening adherence","NOT_YET_RECRUITING","2026-04-28",{"date":78,"type":79},"2026-04-30","ACTUAL",{"date":81,"type":66},"2026-06",{"date":83,"type":66},"2027-07",{"name":5,"class":6},1]