[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hearing-loss-bilateral-or-unilateral\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hearing-loss-bilateral-or-unilateral":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,46,75,96,124,152],{"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":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100565424","evaluating-how-a-tinnitus-implant-affects-tinnitus-loudness-in-adults-with-chronic-tinnitus-and-varying-levels-of-hearing-loss-100565424",false,"NCT06641999","Evaluating How a Tinnitus Implant Affects Tinnitus Loudness in Adults With Chronic Tinnitus and Varying Levels of Hearing Loss","A Prospective, Multicentric, Feasibility Investigation to Assess the Effect of the Tinnitus Implant on Tinnitus Loudness in Adults With Moderate to Severe Chronic Tinnitus Accompanied by Normal Hearing to Moderately Severe Hearing Loss.","TINIS","Inclusion criteria\n\n* 18 years or older.\n* Normal hearing to moderately severe sensorineural hearing loss defined as a pure tone average (PTA) at 500, 1000, 2000 and 4000 Hz less than 65 dB HL in both ears (separately) and best-aided phoneme recognition score more than or equal to 80% in both ears (separately).\n* Unilateral or asymmetric subjective (no pulsatile) tinnitus. In case of asymmetric tinnitus, the worst ear must be implanted.\n* Tinnitus duration of at least 6 months.\n* Severe tinnitus loudness determined by a. VAS-L score in the severe range i.e. 50-100\u002F100 b. TFI score in the severe range i.e. 52-90\u002F100\n* Tinnitus that is intractable and has not been ameliorated satisfactorily by standard of care such as CBT or hearing aid, when such interventions are potentially clinically indicated.\n* Clinically significant reduction in VAS-L score (≥ 15\u002F100 points) in response to trans-tympanic promontory stimulation\n* Willing and able to provide written informed consent.\n* Medically able to use the device and to undergo general anaesthesia for implantation taking into account their medical condition, contraindications and surgical risks.\n* Dutch language proficiency\n\nExclusion Criteria:\n\n* Pulsatile tinnitus.\n* Any anatomical or structural abnormalities of the inner ear, cochlear nerve, or brainstem that would negatively impact response to study intervention (determined in a temporal bone CT and if necessary (e.g. possibility of vestibular\u002Facoustic schwannoma) by a MRI scan of the head (of sufficient quality at the discretion of the investigator) not more than five years old at the time of enrolment\n* Medical contraindications limiting correct placement, activation, or treatment (determined by medical history; contraindications include brain or major ear surgery, brain or temporal bone tumor(s), recurrent ear infections within the last year, otosclerosis, prior major head trauma that results in sudden injury that causes damage to the brain and results in lasting cognitive impairment).\n* Any medical condition, including mental illness or substance abuse, deemed by the Investigator to likely interfere with a patient's ability to sign informed consent, cooperate and\u002For participate in the study, or interfere with the interpretation of the results (incl. pregnant or breastfeeding women or patients with unrealistic expectations).\n* Presence of clinically diagnosed depression or anxiety determined by a psychological state evaluation (if PHQ-9 \\> 9 or GAD-7 \\> 9).\n* Active (currently or within two months prior to enrolment) use of medications (taking regularly scheduled antidepressant, anxiolytic, antipsychotic or antiepileptic medications, or other neuromodulator agents) or other tinnitus treatments.\n* It is permissible to include people who use such medications at lower doses as a sleep aid or for people who intermittently use such medications for situational anxiety (e.g., Ativan before airplane travel). A change in medication during the trial should be avoided.\n* It is permissible to include people who prefer to use a hearing aid to amplify ipsilateral hearing loss. The start of using a hearing aid during the trial should be avoided.\n* Investigator site personnel directly affiliated with this study and\u002For their immediate families; immediate family is defined as a spouse, parent, child, or sibling.\n* Cochlear employees or employees of Contract Research Organizations or contractors engaged by Cochlear for the purposes of this investigation.\n* Current participation, or participation in another interventional clinical study\u002Ftrial in the past 60 days, involving an investigational drug or device (unless the other investigation was\u002Fis a Cochlear sponsored investigation and determined by the investigator or Sponsor to not impact this investigation).","ALL","18 Years",{"count":20,"type":21},16,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study will test an experimental Tinnitus Implant System that consists of a cochlear implant, sound processor and programming software. The Tinnitus implant is surgically placed under the skin just behind the ear in the mastoid bone. It has an electrode that extends from the implant into the promontory bone of the cochlea which emits electrical signals that stimulate the auditory nerve. The sound processor is worn behind the ear and powers the implant via the coil. The study will be conducted in adults with moderate to severe chronic tinnitus who have normal hearing to moderately severe hearing loss in the inner ear. The study participants will undergo a series of tests that include evaluations of tinnitus loudness and annoyance, and self-reported questionnaires on their tinnitus and general health.",[27,28,29],"Tinnitus","Hearing Loss, Bilateral or Unilateral","Normal Hearing",[31,32],"tinnitus","cochlear implant","RECRUITING","2026-06-01",{"date":36,"type":37},"2026-06-02","ACTUAL",{"date":39,"type":37},"2025-06-16",{"date":41,"type":21},"2027-07",{"name":43,"class":44},"Cochlear","INDUSTRY",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":54,"targetDuration":56,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":74},"100637479","hearing-loss-and-aid-attitudes-in-health-sciences-students-100637479","NCT07575711","Hearing Loss and Aid Attitudes in Health Sciences Students","KNOWLEDGE LEVELS, PERSPECTIVES, AND ATTITUDES OF HEALTH SCIENCES FACULTY STUDENTS TOWARD HEARING LOSS AND HEARING AID USE","Inclusion Criteria:\n\n* Students from the departments of Nursing, Midwifery, Nutrition and Dietetics, Physiotherapy and Rehabilitation, Speech and Language Therapy, Child Development, Orthotics and Prosthetics, Health Management, and Social Work\n* Voluntarily agreed to participate in the study\n* Individuals aged 18 years and older\n* No personal or family history of hearing loss,\n* No history of ear surgery,\n* Who did not use hearing aids\n\nExclusion Criteria:\n\n* Being audiology student\n* Individuals aged under 18 years\n* Who use hearing aids,\n* With a personal or family history of ear surgery or hearing loss",true,{"count":55,"type":21},600,"600 Days","OBSERVATIONAL","This study aims to examine the knowledge levels and attitudes of students enrolled in departments other than Audiology within the Faculty of Health Sciences regarding hearing loss and the use of hearing aids. This study is a descriptive. The study included students enrolled in the Faculty of Health Sciences at Ondokuz Mayıs University. Data will collect using the \"Hearing Loss and Hearing Aid Knowledge and Attitudes Questionnaire Among Faculty of Health Sciences Students,\" which consisted of 29 items. The One-Way ANOVA test was used to compare quantitative variables between groups.",[28,60],"Hearing Aid",[62],": Attitudes, Faculty of Health Sciences, hearing aid, hearing loss, knowledge level","NOT_YET_RECRUITING","2026-05-02",{"date":66,"type":37},"2026-05-08",{"date":68,"type":21},"2026-05-30",{"date":70,"type":21},"2026-06-30",{"name":72,"class":73},"Ondokuz Mayıs University","OTHER",1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":74},"100595146","effectiveness-of-speech-therapy-for-lip-reading-in-patients-with-hearing-aids-sced-study-100595146","NCT07028658","Effectiveness of Speech Therapy for Lip-reading in Patients With Hearing Aids: SCED Study","Efficacité de la rééducation Orthophonique de la Lecture Labiale Des Patients appareillés Auditifs : étude SCED","SCEDuLL","Inclusion Criteria:\n\n* Patient aged 18 or older\n* Affiliated with a social security system\n* Moderate to severe bilateral post-lingual hearing loss, fitted with hearing aids for more than 6 months\n* Wearing hearing aids for a minimum of 8 hours\u002Fday on average over the past month\n* Intelligibility in quiet \\> 80% correct responses at 60 dB (Lafon cochlear list)\n* Difficulty in noisy environments rated \\> 6 on a 0-10 EVA scale\n* French language comprehension level of at least B1 CEFR (Common European Framework of Reference for Languages)\n* Willing to participate in speech therapy rehabilitation at a rate of 2 sessions per week\n\nExclusion Criteria:\n\n* Patient who has already undergone speech therapy rehabilitation as part of their hearing loss treatment\n* Diagnosis of neurodegenerative disease or history of brain injury (traumatic brain injury, stroke, tumor, meningitis, etc.)\n* Uncorrected vision or visual impairment affecting lip reading (e.g. AMD, glaucoma, unoperated cataract, etc.)\n* Presence of severe tinnitus (score \\> 56) on the Tinnitus Handicap Inventory (THI) questionnaire\n* Significant cognitive impairment (CODEX C or D) or Montreal Cognitive Assessment (MOCA) score \\\u003C 23",{"count":84,"type":21},8,"This study aims to investigate whether lip reading rehabilitation improves viseme recognition in individuals with hearing impairments who use hearing aids.",[28],"2026-03-30",{"date":89,"type":37},"2026-04-03",{"date":91,"type":37},"2025-10-16",{"date":93,"type":21},"2026-09",{"name":95,"class":44},"Institut Pasteur",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":106,"conditions":107,"keywords":113,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":4},"100605333","sentio-systematic-evaluation-100605333","NCT07161154","Sentio Systematic Evaluation","Sentio Systematic Evaluation - SENSE","SENSE","Inclusion Criteria:\n\n* Subject who is scheduled for or have undergone Sentio implantation in clinical practice.\n* Subject who has consented to participation or are covered by consent waiver.\n\nExclusion Criteria:\n\n* Subjects enrolled in other clinical investigations leading to their Sentio implantation and subsequent follow-up deviating substantially from clinical practice",{"count":105,"type":21},100,"The study is designed as an international, multi-center, single-armed, non-interventional\u002Fobservational study including subjects who has received or are planned to receive the Sentio system as part of normal clinical practice.",[28,108,109,110,111,112,60],"Hearing Loss, Conductive","Hearing Loss, Mixed Conductive-Sensorineural","Single Sided Deafness","Hearing Loss","Hearing-Impairment",[114],"Active transcutaneous bone conduction hearing system","2025-09-03",{"date":117,"type":37},"2025-09-08",{"date":119,"type":21},"2025-09",{"date":121,"type":21},"2035-12",{"name":123,"class":44},"Oticon Medical",{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":53,"sex":17,"minAge":131,"maxAge":132,"enrollmentInfo":133,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":135,"conditions":136,"keywords":137,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":4},"100588636","how-parents-children-and-clinicians-experience-digital-health-tools-in-pediatric-audiology-100588636","NCT06943976","How Parents, Children, and Clinicians Experience Digital Health Tools in Pediatric Audiology","The Value of PROMs in Children With Hearing Loss: Patients', Parents' and Healthcare Professionals' Perspectives","Inclusion Criteria:\n\n* Children and adolescents, aged 7-18 years old, with rehabilitated unilateral or bilateral hearing loss, attending the Audiology outpatient clinic of the Erasmus MC Sophia Children's Hospital in Rotterdam, the Netherlands\n* The corresponding parents or caregivers of these pediatric patients\n* Audiologists or other health care providers who systematically use the PROMs during patient interactions at the same Audiology outpatient clinic.\n\nExclusion Criteria:\n\n* Children or adolescents who are unable to complete the questionnaire, even with support in reading and understanding the items provided by their parents or caregivers.","7 Years","90 Years",{"count":134,"type":21},80,"The goal of this observational study is to understand how children with hearing loss, their parents, and health care providers experience digital health questionnaires that are completed before audiology follow-up appointments. The study focuses on children and adolescents (aged 7-18 years old) with hearing loss, and their parents, visiting the Audiology outpatient clinic of the Erasmus MC Sophia Children's Hospital.\n\nThe main questions it aims to answer are:\n\n* How do parents, children, and clinicians experience digital questionnaires like the HEAR-QL before an audiology visit?\n* Do these digital tools help improve communication and preparation for the appointment?\n\nParticipants will:\n\n* Be invited to complete a short feedback questionnaire about their experience with digital tools\n* Share their views on how helpful or relevant the questionnaires were\n* Health care providers will also give feedback on how they use and interpret the responses in clinical care",[28],[111,138,139,140,141,142],"Quality of Life","PROMs","PREMs","Children","Digital Health Care","2025-04-17",{"date":145,"type":37},"2025-04-25",{"date":147,"type":21},"2025-05-01",{"date":149,"type":21},"2025-09-01",{"name":151,"class":73},"Erasmus Medical Center",{"id":153,"slug":154,"hasResults":11,"nctId":155,"briefTitle":156,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":53,"sex":17,"minAge":158,"maxAge":4,"enrollmentInfo":159,"targetDuration":161,"studyType":57,"phases":4,"briefSummary":162,"conditions":163,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":170,"locationsCount":74},"100578462","reliability-of-a-portable-audiometric-device-based-on-active-noise-canceling-headphones-for-clinical-hearing-assessment-100578462","NCT06811610","Reliability of a Portable Audiometric Device Based on Active Noise-Canceling Headphones for Clinical Hearing Assessment","Inclusion Criteria:\n\n* Age:≥6 years old, regardless of gender\n* Must be able to cooperate in completing pure tone audiometry\n\nExclusion Criteria:\n\n* Acute phase of otitis media or external ear canal within the secretion blockage can not be removed\n* Those suffering from mental illness or other reasons unable to cooperate with the completion of the examination Remarks: Each participant was examined by a specialist using otoscope. Those with ceruminous external auditory canal embolism or secretion blockage were cleared before audiological examination","6 Years",{"count":160,"type":21},120,"1 Month","Part One: Research Background Globally, approximately 500 million people suffer from disabling hearing loss, accounting for about 6.8% of the world's population. Hearing loss has emerged as a major global health issue. The cornerstone of hearing loss prevention and protection lies in hearing level testing. Early detection and intervention are crucial components of hearing healthcare. Currently, pure tone audiometry serves as the gold standard for hearing level testing, requiring patients to visit a hospital's standard soundproof room and complete the test under the guidance of a professional audiologist. However, existing professional audiometers are bulky, consume high power, and necessitate soundproof rooms (with background noise \\\u003C30dBA), among other drawbacks. Moreover, primary hospitals or units lack professional audiologists and soundproof rooms, making it impossible to diagnose and treat hearing loss. Therefore, a portable hearing testing device that does not require a soundproof room would be a boon for the diagnosis and treatment of hearing loss patients. Currently, Wuhan Douting Technology Co., Ltd. has produced a portable hearing testing device (E200), supporting frequencies from 125Hz to 16000Hz, covering both conventional and extended high frequencies. The frequency tolerance, total harmonic distortion, and accuracy of hearing levels fully meet the technical requirements of Grade 4 audiometers according to national standards. In addition to meeting the functional and performance requirements of general audiometers, this device offers the following technical advantages and innovations: 1. Combining active and passive noise reduction, it achieves comprehensive noise reduction of over 29dBSPL, allowing for audiometry in environments with background noise \\\u003C60dBA; 2. Supporting extended high frequencies, it can detect potential hearing damage earlier; 3. Supporting audiometry for rapid use by non-professionals, with automatic calibration, allowing non-professionals to operate by following prompts. This device is not yet on the market, and we intend to verify its reliability in assessing hearing conditions.\n\nPart Two: Research Objectives To verify the reliability of a novel portable hearing testing device in assessing hearing conditions.\n\nPart Three: Research Design Paired design\n\nPart Four: Inclusion and Exclusion Criteria\n\nInclusion Criteria:\n\nAge: ≥6 years old, no gender restriction Able to cooperate in completing pure tone audiometry\n\nExclusion Criteria:\n\nPatients with acute otitis media or unremovable secretions blocking the external auditory canal Patients with mental or psychological disorders or unable to cooperate with the examination for other reasons\n\nPart Five: Research Process This study will recruit volunteers from the outpatient and inpatient departments of Xijing Hospital. Each volunteer will undergo two audiological tests, with at least a 10-minute interval between the two tests to prevent intolerance to the hearing tests. Each audiological test will take approximately 6-8 minutes per subject.\n\nConsultation and Physical Examination:\n\nResearchers will collect general information, including name, gender, age, hearing status, and ear disease history; Conduct a physical examination of the ears; If a volunteer meets the inclusion criteria and voluntarily sign the informed consent form, researchers will determine the testing order using a random number method based on your enrollment sequence.\n\nConventional pure-tone audiometry:Patients undergo conventional pure tone audiometry using the interacoustics AC40 (Denmark) with TDH39 headphones (Telephonics; Farmingdale, NY, USA). We conducte audiometric testing in a sound-proof booth (background noise\\\u003C30dBA) and evaluate the frequency range of 125-8000 Hz. Before the audiometry, patients will be asked to identify which ear have better hearing, and the ear with better hearing was tested first. This study employ the Hughson-Westlake approach, known as the \" up-5 down-10 technique.\" The pure tone sound level was initially introduced at an estimated higher threshold and reduced by 10 dB HL after a correct response from the patient. If the patient did not respond correctly or at all, the sound level was increased by 5 dB HL. When there was a difference of 40 dB HL or more in air conduction thresholds between the ears, contralateral masking was applied to correct the cross-hearing.\n\nE200 Audiometry: Noise-canceling headphones (RAN-3500) are used for all patients during the E200 audiometry. This is conducted in a regular room (ambient noise: 42.6-58.7 dBA, measured using a standard sound level meter: AWA6292 Multi-function Sound Level Meter) adjacent to a busy hallway without a sound-proof booth to simulate an ordinary environment. The Hughson-Westlake approach and contralateral masking are applied when conducting the E200 audiometry.",[28],"2025-02-04",{"date":166,"type":37},"2025-02-06",{"date":168,"type":37},"2024-03-29",{"date":70,"type":21},{"name":171,"class":73},"Xijing Hospital"]