[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100625259":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":50,"collaborators":26,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":62,"minAge":26,"maxAge":26,"enrollmentInfo":63,"targetDuration":26,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":26,"overallStatus":40,"whyStopped":26,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"University of Thessaly","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"CADe assisted colonoscopy","EXPERIMENTAL","Trainees will be trained with the use of CADe",[13],"Diagnostic Test: Artificial Intelligence in colonoscopy",{"label":15,"type":16,"description":17,"interventionNames":18},"Conventional colonoscopy","SHAM_COMPARATOR","Subjects will undergo training without AI for the study period",[19],"Diagnostic Test: Conventional colonoscopy training",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DIAGNOSTIC_TEST","Artificial Intelligence in colonoscopy","Training in colonoscopy with or without CADe",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Conventional colonoscopy training","The trainees will be trained with the conventional colonoscopy for the study period",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Apostolis Papaefthymiou","CONTACT","00306973853042","appapaefthymiou@uth.gr",[38],{"facility":39,"status":40,"city":41,"state":26,"zip":26,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":26},"General University Hospital of Larissa","RECRUITING","Larissa","Greece","GR",{"type":45,"coordinates":46},"Point",[47,48],22.42112,39.62847,{"lat":48,"lon":47},{"type":51,"investigatorFullName":33,"investigatorTitle":52,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Assistant Professor","100625259","colonoscopy-training-with-or-without-artificial-intelligence-among-endoscopy-residents-100625259",false,"NCT07420309","Colonoscopy TRaining With or Without Artificial INtelligence Among Endoscopy Residents","Colonoscopy Training With or Without Artificial Intelligence Among Endoscopy Residents: a Randomized Controlled Study","c-TRAINER","Inclusion Criteria:\n\n* Trial participants: Endoscopy trainees at any time of their training, with at least one year of training ahead without previous structured exposure to CADe during their training.\n\nRecruited patient population: Adult patients undergoing diagnostic, screening, or surveillance colonoscopy will be included.\n\n1. Provision of signed and dated informed consent form understand the risks and benefits of the study\n2. Aged ≥18 years old\n3. Able to read and write in the provided language.\n4. Participants capable to provide written informed consent and comply with the trial protocol.\n\nExclusion Criteria:\n\n* Trial participants: Endoscopy trainees after their basic training, during the last year of training or with systematic exposure to CADe.\n\nRecruited patient population:\n\n1. Patients with a known contraindication for biopsy, bowel obstruction or perforation,\n2. Pregnant or lactating females\n3. Known polyposis syndromes, or who had a history of inflammatory bowel disease (IBD), CRC, or colorectal surgery.\n4. Any patient whose cecum is not reached and who were highly suspected of having polyposis syndromes, IBD, intestinal tuberculosis, or CRC.\n5. Incomplete bowel preparation (segmental Boston Bowel Preparation Score \\\u003C2, or total \\\u003C6)",true,"ALL",{"count":64,"type":65},10,"ESTIMATED","INTERVENTIONAL",[68],"NA","Type of study: Randomized controlled study\n\nInvestigated Procedure: Artificial Intelligence Software for Polyp Detection in Colonoscopy training\n\nTrial participants: Endoscopy trainees during their training with at least one year of training ahead and no previous structured exposure to CADe\n\nObjectives:\n\nPrimary: Adenoma Miss Rate (AMR) in the end of the first year of training for each group and after the crossover.\n\nSecondary: Further endoscopists-related parameters will be recorded and compared between the two arms: PDR, ADR, aADR, PMR, withdrawal time, CIR, AEs\n\nThe investigators will be asked, when possible, to follow-up the patients until they have their next colonoscopy or a diagnosis of CRC to assess for interval cancer.",[71],"Colonoscopy Training","2026-02-11",{"date":74,"type":75},"2026-02-19","ACTUAL",{"date":77,"type":65},"2026-02-01",{"date":79,"type":65},"2027-07-01",{"name":5,"class":6},1]