[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abdominal-migraine\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abdominal-migraine":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100567259","vico-trial-video-consultations-in-the-follow-up-of-children-with-functional-abdominal-pain-disorders-100567259",false,"NCT06665867","VICO-trial: Video Consultations in the Follow-up of Children With Functional Abdominal Pain Disorders","VICO","Inclusion Criteria:\n\n* Children aged 4 years to 17 years\n* Meeting the Rome IV criteria for one of the four types of Functional Abdominal Pain Disorders (FAPD's): functional dyspepsia, irritable bowel syndrome, abdominal migraine, functional abdominal pain - not otherwise specified.\n* Being able to conduct a video consultation\n\nExclusion Criteria:\n\n* If no follow-up consultation is indicated\n* If it is necessary that the follow-up consultations are face to face","ALL","4 Years","17 Years",{"count":20,"type":21},208,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this non-inferiority randomized controlled multi-center trial is to investigate the use of video consultations in the follow-up care of children aged 4 - 18 years old with functional abdominal pain disorders (FAPDs). Video consultations will be compared to face-to-face consultations. Clinical outcomes and patients' and parents' healthcare experience will be compared between both groups.\n\nPrimary outcome is adequate relief after 12 weeks: the hypothesis is that video consultations are not inferior to face-to-face consultations regarding clinical outcomes and that adequate relief will be the same for both groups.\n\nParticipants and\u002For parents will be asked to complete a diary for 1 week and a questionnaire after every consultation: at baseline, after 6 weeks and after 12 weeks.",[27,28,29,30],"Functional Abdominal Pain Disorders","Irritable Bowel Syndrome (IBS)","Functional Dyspepsia","Abdominal Migraine",[32,33,34,35],"E-health","Video consultations","Children","Functional abdominal pain disorders","RECRUITING","2024-10-29",{"date":39,"type":40},"2024-10-30","ACTUAL",{"date":42,"type":40},"2024-06-01",{"date":44,"type":21},"2025-11-30",{"name":46,"class":47},"Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)","OTHER"]