[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"HASSAN 1st university\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":49},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100621465",false,"NCT07370974","Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery.","Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery : a Multicenter Randomized Controlled Trial.","Hypnoanxiety","* Inclusion Criteria:\n\n  1. Consenting patients undergoing abdominal surgery\n  2. ASA I-II physical status\n  3. Able to understand and respond to instructions\n  4. No major psychological disorders\n* Exclusion Criteria:\n\n  1. Non-consenting patients\n  2. Prior experience with hypnosis\n  3. History of mental illness\n  4. Psychoactive substance consumption\n  5. Cognitive disorders","ALL","18 Years","80 Years",{"count":20,"type":21},48,"ESTIMATED","INTERVENTIONAL",[24],"NA","This Multicenter randomized controlled trial evaluates clinical hypnosis efficacy for reducing perioperative anxiety and postoperative pain in abdominal surgery patients across 3 Moroccan centers (n=48-68). Intervention arm receives 15-20 min level 2 hypnosis session preoperatively; control receives standard psychological preparation. Primary outcome: VAS-anxiety post-intervention. Secondary: postoperative EVA-pain, analgesic consumption, length of stay.\n\nStudy Design Prospective, multicenter, parallel-group RCT (1:1 allocation, stratified by center\u002Fsex). Inclusion: consenting ASA I-II adults for abdominal surgery. Primary endpoint powered for 10mm EVA reduction (80% power, α=0.05). Registration supports PhD thesis at ISSS\u002FUniversité Hassan 1er Settat.",[27,28,29,30,31],"Hypnosis","Preoperative Anxiety","Postoperative Pain","Abdominal Surgeries","Length of Stay",[33,34,27,35],"RCT","Morocco","preoperative anxiety","RECRUITING","2026-05-30",{"date":39,"type":40},"2026-06-02","ACTUAL",{"date":42,"type":40},"2026-02-07",{"date":44,"type":21},"2026-06-03",{"name":46,"class":47},"HASSAN 1st university","OTHER",3,""]