[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"voice\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:voice":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,57,97],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":35,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":56},"100613134","developing-a-multimodal-cancer-pain-database-to-support-ai-based-automatic-pain-assessment-100613134",false,"NCT07262632","Developing a Multimodal Cancer Pain Database to Support AI-Based Automatic Pain Assessment","SENSAI: Seeing, hEaring, seNsing: Smart, Effortless and Objective Pain Assessment With Mobile AI Technology - DataBase Development","SENSAI-DBD","Inclusion Criteria:\n\n* Adult patients (≥18 years)\n* Diagnosed with cancer, active\n* Able to communicate verbally in Dutch or English\n* Able to provide written informed consent.\n* Pain group specific:\n* Experiencing pain related to cancer\n* Admitted to the hospital due to pain\n* Control group specific:\n* Not experiencing pain (NRS = 0)\n* Admitted to the hospital for chemotherapy\n\nExclusion Criteria:\n\n* Cognitive, physical, or medical limitations that prevent participation in the audiovisual recording sessions or affect facial expressions or voice (e.g. facial paralysis, tracheostomy, severe speech impairment).\n* Critical illness or end-of-life care where participation would impose an additional burden.\n* Experiencing pain not associated with cancer\n* Infectious isolation precautions that prevent safe data collection","ALL","18 Years",{"count":20,"type":21},200,"ESTIMATED","3 Weeks","OBSERVATIONAL","The goal of this observational study is to collect short video and sound recordings of people with cancer to create a secure database that can be used in future research to develop an artificial intelligence (AI) tool for pain assessment. The main aim is to build a large, high-quality collection of audiovisual data showing how people with cancer express themselves when they do and do not have pain.\n\nParticipants will include adults with cancer who are admitted to the oncology ward for pain treatment and a control group admitted for chemotherapy who have no pain. After giving consent, participants will:\n\n* Be recorded on video (from the shoulders up) for up to 60 seconds while reading a short sentence and describing their pain or daily experience.\n* Complete a short questionnaire about their mood and pain expression.\n* Allow researchers to collect some information from their medical record, such as their pain score, medications, and cancer type.\n\nThese recordings will be securely stored and used to create a database for future AI research. No medical tests, new treatments, or extra hospital visits are involved. This study will provide the foundation for developing future AI-based tools that could support doctors and patients in monitoring and managing pain more accurately and easily.",[26,27,28,29,30,31,32,33,34],"Cancer-related Pain","Pain Assessment","Artificial Intelligence (AI)","Oncology","Oncology Pain","Database","Facial Expression","Voice","Cancer",[26,36,28,29,30,31,37,38,39,40,41,42,43],"Pain assessment","Facial Action Unit","Vocalizations","Acoustic","Automatic assessment","Machine learning","Audiovisual data","Paralinguistics","RECRUITING","2026-03-10",{"date":47,"type":48},"2026-03-11","ACTUAL",{"date":50,"type":48},"2025-12-01",{"date":52,"type":21},"2027-12-31",{"name":54,"class":55},"Dr. Mark Mulder","OTHER",1,{"id":58,"slug":59,"hasResults":11,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":4,"eligibilityCriteria":63,"healthyVolunteers":64,"sex":17,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":4,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":77,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":56},"100623124","virtual-reality-as-a-tool-for-training-public-speaking-skills-in-higher-education-students-100623124","NCT07392554","Virtual Reality as a Tool for Training Public Speaking Skills in Higher Education Students","Virtual Reality as a Tool for Training Public Speaking Skills in Higher Education Students: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Higher education student\n* Speaking french fluently\n\nExclusion Criteria:\n\n* Hearing impairment\n* Voice or fluency disorder at the time of the study",true,"20 Years","30 Years",{"count":68,"type":21},80,"INTERVENTIONAL",[71],"NA","According to the scientific literature, public speaking (PS) is an important skill for students to master. However, a large proportion of students do not feel comfortable speaking in public. PS anxiety impacts oral communication (i.e., voice and fluency). These changes can affect speaker's academic and professional success, as well as his credibility. Performing a high-quality PPP with confidence is therefore rarely an innate skill, but fortunately it can be trained and improved. Therefore, training PS skills in representative settings is crucial but often challenging for PS professionals (e.g., speech therapists, vocologists, coaches).\n\nThis project examines how oral communication skills training including simulations in virtual reality (VR) supports the acquisition of effective oral PS skills. Using acoustic analyses, outcomes from participants in the intervention group (N = 40) will be compared with those of a wait-list control group (N = 40) to determine whether significant differences emerge in filled pauses, speech rate, and vocal intonation during PS. Changes in PS self-efficacy will also be assessed. Regarding secondary outcomes, the study will evaluate changes in self-reported and physiological PS anxiety, as well as self-reported confidence as a speaker. Finally, self-perceived vocal effort during PS will be examined.",[33,74,75,76],"Speech","Virtual Reality Simulation","Healthy Adult",[78,79,33,80,81,82,83,84,85,86,87],"Public Speaking","Oral Communication","Speech Fluency","Speech Therapy","Virtual Reality","Students","Training","Glossophobia","Anxiety","Verbal Behavior","2026-01-30",{"date":90,"type":48},"2026-02-06",{"date":92,"type":21},"2026-03",{"date":94,"type":21},"2026-12",{"name":96,"class":55},"University of Liege",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":64,"sex":17,"minAge":103,"maxAge":4,"enrollmentInfo":104,"targetDuration":105,"studyType":23,"phases":4,"briefSummary":106,"conditions":107,"keywords":4,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":56},"100463821","analysis-of-musical-and-voice-skills-in-children-and-adult-cochlear-implant-users-100463821","NCT05319678","Analysis of Musical and Voice Skills in Children and Adult Cochlear Implant Users","Inclusion Criteria:\n\n* Minimum age of 6 years.\n* Patients aged 6-17 years must have been implanted before the age of 3 years (to ensure adequate CI performance).\n* Minimum 12 months experience with the device\n* Indications: unilateral (one CI), bilateral (two CIs), bimodal (one CI in one ear and a hearing aid in the other)\n* At least 80% of electrodes active at the time of assessment.\n* Fluency in Spanish\n* Signed and dated informed consent prior to starting any study procedure.\n\nExclusion Criteria:\n\n* Not meet inclusion criteria.\n* Prelingual or perilingual adults.\n* Disability in addition to hearing impairment (e.g., mental disability).","6 Years",{"count":68,"type":21},"12 Months","Aims: To evaluate the perception and enjoyment of music in cochlear implant (CI) users using specific questionnaires, and comparing their results with a control group of subjects with normal hearing (NH). To analyze the musical abilities of implantees using the musical tool Meludia, and compare the results with the control group. To perfom a voice analysis in implanted patients, compare it with their NH peers, and check if an association with musical perception is observed.\n\nDesign: Cross-sectional study, both the CI recipients and NH control subjects were assessed once.\n\nSetting and subjects: Pre-or perilingual patients aged 6 to 17 years old, and postlingual adults who underwent cochlear implantation from 2000 to January 2023 at La Paz University Hospital. Control group is set up with their NH peers.\n\nStudy Variables: Socio-demographic and clinical (current age, age at implantation, sex, educational level) variables will be collected, as well as hearing loss (aetiology, duration of deafness), and surgical (type of implant, complete or partial insertion of the electrodes, date of surgery) data. Data from CI fitting (number of active electrodes, type of audio processor) and hearing outcomes with the CI will also be reviewed.\n\nOutcome variables: Specific musical skills questionnaires for adults: Munich Music Questionnaire (MuMu) and Music Related Quality of Life Questionnaire (MuRQoL), which will be validated. Musical questionnaire developed specifically for subjects between 6-17 years old. Musical tool (Meludia) to assess musical perception. Praat software for voice analysis. Analysis of the impact of the different audiological, sociodemographic and clinical variables on hearing outcomes, and on musical perception after cochlear implantation, and comparison with the NH control group.",[108,109,33],"Cochlear Implant","Music","2025-08-06",{"date":112,"type":48},"2025-08-12",{"date":114,"type":48},"2022-02-10",{"date":116,"type":21},"2025-12-31",{"name":118,"class":55},"Fundacion para la Investigacion Biomedica del Hospital Universitario la Paz"]