[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"orl-cancer\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:orl-cancer":63},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":13,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":24,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100555843",false,"NCT06517355","Acceptability and Benefits of an Onco-sexology Program for Laryngectomy Patients and Their Partners","ABSENS","Inclusion Criteria:\n\nFor patients:\n\n1. Patient to be treated for ORL cancer by total (pharyngo)laryngectomy\n2. Patient WHO 0-1-2\n3. Age greater than or equal to 18 years\n4. Patient who has not objected to participation in the study.\n\nFor partners (if applicable) :\n\n1. Age greater than or equal to 18 years\n2. Subject who has not objected to participation in the study.\n\nExclusion Criteria:\n\nFor patients:\n\n1. Patient with another co-existing malignant disease at the time of inclusion.\n2. Any psychological, familial, geographical or sociological condition that does not allow for compliance with the medical follow-up and\u002For procedures foreseen in the study protocol.\n3. Patients deprived of their liberty or under legal protection (guardianship and tutorship, safeguard of justice).\n\nFor partners (if applicable):\n\n1\\. Patients deprived of their liberty or under legal protection (guardianship and tutorship, safeguard of justice).","ALL","18 Years",{"count":18,"type":19},45,"ESTIMATED","OBSERVATIONAL","Single-centre prospective pilot study designed to demonstrate the acceptability of onco-sexology management for laryngectomy patients and their partners in order to improve their perception of their intimate life. This is a non-interventional study (category 3 Loi Jardé), which will not result in any change in patient management. All procedures will be carried out in accordance with standard practice.\n\nPatients will be followed for 14 months.",[23],"ORL Cancer",[25,26,27],"ORL cancer","Onco-sexology care","Laryngectomy","RECRUITING","2026-06-12",{"date":31,"type":32},"2026-06-16","ACTUAL",{"date":34,"type":32},"2024-07-30",{"date":36,"type":19},"2028-03",{"name":38,"class":39},"Institut Claudius Regaud","OTHER",1,{"id":42,"slug":4,"hasResults":10,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":53,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":40},"100434656","NCT04940000","Evaluation of the Interest of a Video-assisted Remote Speech Therapy Consultation in Patients With ORL Cancer (TELE ORTHOPHONIE)","Inclusion Criteria:\n\n1. Age ≥ 18 years at study entry.\n2. Patient with carcinological pathology of the VADS, relevant to surgery and\u002For radiotherapy and\u002For chemotherapy.\n3. Patient managed at the IUCT-O and by a private speech therapist (near the patient's home).\n4. Patient affiliated to a Social Security system in France.\n5. Patient having signed informed consent prior to inclusion in the study and prior to any specific study procedure.\n\nExclusion Criteria:\n\n1. Pregnant or lactating women.\n2. Any psychological, familial, geographical or sociological condition that does not allow for compliance with the medical follow-up and\u002For procedures foreseen in the study protocol.\n3. Patients deprived of their liberty or under legal protection (guardianship and tutorship, safeguard of justice).",{"count":47,"type":19},105,"INTERVENTIONAL",[50],"NA","Interventional, prospective, single-centre study aimed to evaluate the impact of a video-assisted remote speech therapy consultation in relation to the complexity and specificity of the care of patients with ORL cancer. Three indications will be studied: phonation problems, swallowing problems and other problems.\n\nThe study will be conducted on a population of patients with T3, T4 ORL cancer requiring speech therapy.\n\nEach patient included will have a video-assisted speech therapy consultation with a private speech therapist and an expert speech therapist. At the end of this video consultation, the patient and the private speech therapist will be asked to complete a satisfaction questionnaire.\n\nAt the follow-up visit following the video-assisted consultation, the patient will have completed participation in the study.",[23],[54],"Video-Assisted Speech Therapy","2025-07-28",{"date":57,"type":32},"2025-07-31",{"date":59,"type":32},"2021-09-02",{"date":61,"type":19},"2028-09",{"name":38,"class":39},""]