[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100632205":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":13,"centralContacts":21,"locations":7,"responsibleParty":27,"collaborators":7,"id":29,"slug":30,"hasResults":31,"nctId":32,"briefTitle":33,"officialTitle":34,"acronym":35,"eligibilityCriteria":36,"healthyVolunteers":37,"sex":38,"minAge":39,"maxAge":7,"enrollmentInfo":40,"targetDuration":7,"studyType":43,"phases":44,"briefSummary":46,"conditions":47,"keywords":7,"overallStatus":50,"whyStopped":7,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":7},{"fullName":5,"class":6},"Insel Gruppe AG, University Hospital Bern","OTHER",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DEVICE","Cochlear Implant","The intervention consists of temporary manipulation of the CI's settings in three separate conditions: Sound processor microphone on with spatial auditory cues provided by sound speakers, broadband noise stimulus to wireless microphone, CI off. Switching between conditions can be accomplished by manipulating the sound mixture between the two microphones (sound processor and wireless) by a standard app provided by the CI manufacturers.",[14,18],{"name":15,"affiliation":16,"role":17},"Georgios Mantokoudis, MD","Inselgruppe AG","PRINCIPAL_INVESTIGATOR",{"name":19,"affiliation":20,"role":17},"Thomas Sauter, MD","InselGruppe AG",[22],{"name":15,"role":23,"phone":24,"phoneExt":25,"email":26},"CONTACT","316323321","+41","georgios.mantokoudis@insel.ch",{"type":28,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100632205","ci-spatial-orientation-study-100632205",false,"NCT07510659","CI Spatial Orientation Study","Effect of Cochlear Implant Stimulation on Spatial Orientation in Adult Users","CISPACE","Inclusion Criteria:\n\n* \\> 18 years\n* Ability to comply with study procedures\n* Use of a CI (unilateral or bilateral) for minimum 12 months\n* Signed, written informed consent\n\nExclusion Criteria:\n\n* Vulnerable individuals\n* Cognitive impairment or altered mental status affecting participation\n* Physical conditions signficantly limiting mobility (e.g. severe gait or muscoskeletal disorders)",true,"ALL","18 Years",{"count":41,"type":42},700,"ESTIMATED","INTERVENTIONAL",[45],"NA","The goal of this clinical trial is to learn if cochlear implant activation affects spatial orientation in cochlear implant users. The main question\\[s\\] it aims to answer are\\]:\n\n* Does activation of the cochlear implant improve spatial orientation?\n* Is this improvement caused by better hearing ability through the cochlear implant?\n\nParticipants will:\n\n* Take an online survey including questions about their cochlear implants and clinical questionnaires on dizziness and spatial orientation\n* Undergo balance and spatial orientation tests under different cochlear implant conditions.",[48,49],"Cochlear Implants","Spatial Orientation","NOT_YET_RECRUITING","2026-04-01",{"date":53,"type":54},"2026-04-03","ACTUAL",{"date":56,"type":42},"2026-04",{"date":58,"type":42},"2029-12",{"name":5,"class":6}]