[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621465":3},{"organization":4,"outcomesModule":7,"designInfo":26,"detailedDescription":25,"studyPopulation":25,"armGroups":33,"interventions":44,"overallOfficials":52,"centralContacts":60,"locations":70,"responsibleParty":127,"collaborators":25,"id":130,"slug":131,"hasResults":132,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":132,"sex":138,"minAge":139,"maxAge":140,"enrollmentInfo":141,"targetDuration":25,"studyType":144,"phases":145,"briefSummary":147,"conditions":148,"keywords":154,"overallStatus":110,"whyStopped":25,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":166},{"fullName":5,"class":6},"HASSAN 1st university","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":25},[9],{"measure":10,"description":11,"timeFrame":12},"Preoperative anxiety","Perioperative Anxiety (Primary Outcome) is measured using the Visual Analog Scale for Anxiety (EVA-Anxiété, 0-100 mm).\n\nPrimary Outcome Measure: preoperative anxiety level\n\nAssessment Tool: 100-mm Visual Analog Scale (VAS-Anxiety):\n\n0 mm = No anxiety (\"Je ne suis pas du tout anxieux\") 100 mm = Worst possible anxiety (\"Anxiété maximale imaginable\") Timepoints: (post-intervention, \\~10 min later). Expected hypnosis effect: ≥10 mm reduction vs. control.\n\nProtocol Specifications Patient marking: Single horizontal 100-mm line; mark position indicates intensity Scoring: Distance (mm) from \"No anxiety\" (0) to mark, precise to 1 mm","1 hour Before surgery",[14,18,22],{"measure":15,"description":16,"timeFrame":17},"Postoperative pain","Secondary Outcome Measure: Acute postoperative pain intensity at 6, and 24 hours post-surgery.\n\nAssessment Tool: 100-mm VAS-Pain Scale:\n\n0 mm = No pain (\"Aucune douleur\") 100 mm = Worst imaginable pain (\"Douleur maximale imaginable\") Timepoints: T+6h, T+24h. Expected hypnosis benefit: ≥10 mm reduction vs. control .\n\nProtocol Specifications Patient marking: Horizontal 100-mm line; precise mm measurement from 0 Analgesia standardization: Multimodal protocol identical across arms (paracetamol, NSAIDs, opioids rescue) Power: Secondary analysis leverages primary outcome sample (48-68 patients, 80% power for Δ=10 mm, σ=24 mm)\n\nClinicalTrials.gov Entry: \"Postoperative pain intensity measured by 100-mm Visual Analog Scale at rest in PACU at 1, 2, 6, and 24 hours post-surgery\"\n\nThis complements your prim","6 and 24 hours postoperatively",{"measure":19,"description":20,"timeFrame":21},"medication consumption","Secondary Outcome Measure: Anesthia drugs consumption and postoperative consumption of analgesics (morphine equivalents, paracetamol, NSAIDs, opioids) from PACU arrival to discharge.\n\nAssessment Method:\n\nTotal mg\u002Fdoses per patient, Data collection: Medication administration records (MAR), nurse logs Expected hypnosis effect: ≥20-30% reduction vs. control arm. Protocol Specifications\n\nStandardized multimodal analgesia (identical both arms):","Perioperative",{"measure":23,"description":24,"timeFrame":21},"length of stay","Secondary Outcome Measure: Time to hospital discharge (days) from surgery day (Day 0) to medical discharge order date.\n\nAssessment Method:\n\nCalendar days: Date of discharge hour date of surgery Expected hypnosis effect: ≥1 day reduction vs. control (typical LOS 3-5 days abdominal surgery).\n\nProtocol Specifications\n\nStandardized discharge criteria (identical both arms):\n\nTolerates solid diet VAS-pain ≤30 mm at rest Mobilizes independently to bathroom Afebrile, normal vital signs Data collection: medical record discharge order timestamp",null,{"allocation":27,"interventionModel":28,"interventionModelDescription":25,"primaryPurpose":29,"observationalModel":25,"timePerspective":25,"maskingInfo":30},"RANDOMIZED","PARALLEL","SUPPORTIVE_CARE",{"masking":31,"maskingDescription":32,"whoMasked":25},"NONE","This study did not use any kind of masking or blinding,",[34,40],{"label":35,"type":36,"description":37,"interventionNames":38},"Fisrt arm: patients having a session of hypnosis prior to surgery","EXPERIMENTAL","Patients randomized to the intervention arm undergo a single 15-20 minute clinical hypnosis session preoperatively for anxiety reduction, achieving level 2 hypnotic trance (somnambulism)",[39],"Other: Clincal hypnosis",{"label":41,"type":42,"description":43,"interventionNames":25},"Arm 2 : patients will be treated as usual with standard conditions","NO_INTERVENTION","Patients in this group will receive standard usual care without any hypnotic intervention, only with routine psychological preparation.",[45],{"type":6,"name":46,"description":47,"armGroupLabels":48,"otherNames":49},"Clincal hypnosis","Patients randomized to the intervention arm receive a single 15-20 minute individual clinical hypnosis session 30-60 minutes preoperatively. The standardized protocol includes:\n\n* Induction phase (3-5 min): Eye fixation, progressive relaxation breathing\n* Deepening phase (5 min): Level 2 somnambulistic trance achievement\n* Therapeutic suggestions (7-10 min): Anxiety reduction imagery, surgical calm visualization\n* Emergence phase (2-3 min): Safe awakening to alert consciousness\n\nDelivered by certified hypnotherapist using validated script for preoperative anxiety in abdominal surgery patients.\" Key Elements Required Timing: Preop holding area, 30-60 min before incision Provider: Trained clinician (specify certification) Dose: Single 15-20 min session Target: Level 2 hypnosis (somnambulism) Outcome link: EVA anxiety scale pre\u002Fpost This matches your 3-center RCT design (\\~16 patients\u002Fcenter, stratified randomization) and distinguishes from control arm (standard psychological preparation",[35],[50,51],"Hypnosis, hypnotism","Hypnosis session",[53,57],{"name":54,"affiliation":55,"role":56},"NAOUFAL HIMMOUCHE HIMMOUCHE, Professor","Laboratory of health sciences and technlmogies, Higher Institute of Health sciences, Hassan Fisrt University, Settat Morocco","STUDY_DIRECTOR",{"name":58,"affiliation":59,"role":56},"YASSINE HAFIANI, Professor","Pedagogical Unit of Anesthesia and Intensive Care, Rabat Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco",[61,66],{"name":62,"role":63,"phone":64,"phoneExt":25,"email":65},"YOUSSEF EL-ALLAM EL-ALLAM, Phd student","CONTACT","+212653977028","youssef.el-allam.doc@uhp.ac.ma",{"name":67,"role":63,"phone":68,"phoneExt":25,"email":69},"NAOUFAL HIMMOUCHE Pr Himmouche, Professor","+212619544601","naoufal.himmouche@uhp.ac.ma",[71,85,108],{"facility":72,"status":73,"city":74,"state":75,"zip":76,"country":77,"countryCode":78,"cosmosGeoPoint":79,"geoPoint":84,"contacts":25},"Kenitra, Rabat Sale Kenitra region, Morocco","COMPLETED","Kenitra","Province","14000","Morocco","MA",{"type":80,"coordinates":81},"Point",[82,83],-6.5802,34.26101,{"lat":83,"lon":82},{"facility":86,"status":87,"city":88,"state":75,"zip":89,"country":77,"countryCode":78,"cosmosGeoPoint":90,"geoPoint":94,"contacts":95},"Settat, Casablanca settat region , Morocco","NOT_YET_RECRUITING","Settat","26000",{"type":80,"coordinates":91},[92,93],-7.61662,33.00103,{"lat":93,"lon":92},[96,100,103,105],{"name":97,"role":63,"phone":98,"phoneExt":25,"email":99},"YOUSSEF Mr EL-ALLAM, PhD student","+212653997028","youssef.el-allam.doc@gmail.com",{"name":101,"role":63,"phone":102,"phoneExt":25,"email":69},"Noufal Himmouche Pr HIMMOUCHE, Professor","+21219544601",{"name":62,"role":104,"phone":25,"phoneExt":25,"email":25},"PRINCIPAL_INVESTIGATOR",{"name":106,"role":107,"phone":25,"phoneExt":25,"email":25},"AYOUB LILOU Mr LILOU, Masters degree","SUB_INVESTIGATOR",{"facility":109,"status":110,"city":111,"state":75,"zip":112,"country":77,"countryCode":78,"cosmosGeoPoint":113,"geoPoint":117,"contacts":118},"Youssoufia, Marrakech-Safi Morocco","RECRUITING","Youssoufia","46300",{"type":80,"coordinates":114},[115,116],-8.52941,32.24634,{"lat":116,"lon":115},[119,120,124,125],{"name":97,"role":63,"phone":98,"phoneExt":25,"email":99},{"name":121,"role":63,"phone":122,"phoneExt":25,"email":123},"ABDELAAZIZ BOUSBEGH Mr BOUSBEGH, Head Nurse Anesthetist","+212630175700","abdelaazizbousbegh@gmail.com",{"name":62,"role":104,"phone":25,"phoneExt":25,"email":25},{"name":126,"role":107,"phone":25,"phoneExt":25,"email":25},"Aasmae Benhssayne Mme BENHSSAYNE, anesthestist nurse",{"type":104,"investigatorFullName":128,"investigatorTitle":129,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"YOUSSEF EL-ALLAM","Principal investigator","100621465","effect-of-clinical-hypnosis-in-preoperative-anxiety-among-patients-undergoing-an-abdominal-surgery-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":142,"type":143},48,"ESTIMATED","INTERVENTIONAL",[146],"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.",[149,150,151,152,153],"Hypnosis","Preoperative Anxiety","Postoperative Pain","Abdominal Surgeries","Length of Stay",[155,77,149,156],"RCT","preoperative anxiety","2026-05-30",{"date":159,"type":160},"2026-06-02","ACTUAL",{"date":162,"type":160},"2026-02-07",{"date":164,"type":143},"2026-06-03",{"name":5,"class":6},3]