[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hearing-aid\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hearing-aid":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,43,69,99,126,157],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100637479","hearing-loss-and-aid-attitudes-in-health-sciences-students-100637479",false,"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,"ALL","18 Years",{"count":20,"type":21},600,"ESTIMATED","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.",[26,27],"Hearing Loss, Bilateral or Unilateral","Hearing Aid",[29],": Attitudes, Faculty of Health Sciences, hearing aid, hearing loss, knowledge level","NOT_YET_RECRUITING","2026-05-02",{"date":33,"type":34},"2026-05-08","ACTUAL",{"date":36,"type":21},"2026-05-30",{"date":38,"type":21},"2026-06-30",{"name":40,"class":41},"Ondokuz Mayıs University","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":42},"100610329","hearing-aid-benefit-in-real-world-noisy-environments-100610329","NCT07226167","Hearing Aid Benefit in Real-World Noisy Environments","Evaluating the Impact of Hearing Aid Signal Enhancement Algorithms in Real-World Contexts","Inclusion Criteria:\n\n* Over 18 years old\n* Symmetrical, bilateral, adult onset, sensorineural hearing loss\n* Experienced hearing aid users (\\> 3 months)\n\nExclusion Criteria:\n\n* Under 18 years old\n* Conductive or mixed hearing loss\n* Asymmetrical or unilateral hearing loss\n* Pre-lingual or childhood hearing loss onset\n* No hearing aid experience",{"count":51,"type":21},45,"INTERVENTIONAL",[54],"NA","Researchers are doing this study to understand why hearing aids often work well in controlled laboratory settings but don't provide the same level of benefit in everyday noisy environments. The questions they hope to answer are:\n\n* What factors contribute to hearing aid benefit in noisy environments\n* What factors limit hearing aid benefit\n* How do real-world factors interact with common hearing aid settings\n\nParticipants will complete:\n\n* Hearing and listening tests\n* Memory and attention assessment\n* Surveys on their Smartphone",[27,57,58],"Hearing Loss, Bilateral Sensorineural","Hearing Loss, Adult-Onset","RECRUITING","2026-02-20",{"date":62,"type":34},"2026-02-24",{"date":64,"type":34},"2026-02-19",{"date":66,"type":21},"2027-01",{"name":68,"class":41},"University of Wisconsin, Madison",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":52,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":98},"100612354","evaluation-of-performances-clinical-benefits-and-safety-of-the-audiocap-connected-hearing-rehabilitation-device-for-improving-audibility-in-hearing-impaired-people-in-the-context-of-ce-marking---audiocap-2-100612354","NCT07252492","Evaluation of Performances, Clinical Benefits and Safety of the 'Audiocap' Connected Hearing Rehabilitation Device for Improving Audibility in Hearing-impaired People in the Context of CE Marking - AUDIOCAP-2","Evaluation of Performances, Clinical Benefits and Safety of the 'Audiocap' Connected Hearing Rehabilitation Device for Improving Audibility in Hearing-impaired People in the Context of CE Marking","AUDIOCAP-2","Inclusion Criteria:\n\n1. Subjects presenting one or more of the following criteria: a.Subject with mild to moderate hearing loss (20dB to 50dB average at 500, 1000, 2000, and 4000 Hz) in the better ear according to WHO standards, \u002F b. Subject with a speech reception threshold (SRT) in quiet exceeding 30dB, corresponding to the minimum speech level required to achieve 50% recognition in silence (HAS eligibility criteria for hearing aid reimbursement), \u002F c. Subject with significant degradation of speech intelligibility in noise, defined as a speech-to-noise ratio (SNR) deviation greater than 3dB compared to normative reference values (HAS eligibility criteria for hearing aid reimbursement), \u002F d.Subject with high-frequency hearing loss greater than 30dB from 2000 Hz onwards, associated with a speech reception threshold exceeding 30dB in quiet and\u002For a significantly degraded speech intelligibility in noise (HAS eligibility criteria for hearing aid reimbursement).\n2. Subjects eligible for first hearing aid.\n3. Subjects over 18 years of age. French-speaking subjects.\n\n5\\. Subjects affiliated with a social security scheme. 6. Subjects who are not subject to another medical option, without external pathology and excluding implants.\n\n7\\. Subjects who have signed an informed consent. 8. Subjects available for the study.\n\nExclusion Criteria:\n\n1. Subject deprived of his\u002Fher liberty by a judicial or administrative decision\n2. Subject with severe psychiatric disorder\n3. Subject admitted to a health or social care establishment\n4. Subject not able to give consent\n5. Adults under guardianship or trusteeship.\n6. Subjects with disabling tinnitus that are not suitable for adaptation (THI\\>56).\n7. Subjects eligible for a cochlear implant.\n8. Subjects not able to participate in the study according to the investigator.\n9. Subjects with acute and chronic suppurative otitis media, congenital ear atresia, or any type of ear discharge.\n10. Subjects with congenital atresia of external ear or deformity of any part of the ear canal.\n11. Subjects with deafness that is unstable and with a degree of hearing loss often fluctuating.\n12. Subjects with persistent headaches, dizziness, earaches, or other symptoms that are not suitable for adaptation.\n13. Subjects with sudden onset of hearing loss within the past 3 months, rapid progressive deafness, unilateral hearing loss or other acute ear disease.\n14. Subjects with effusion (secretions\u002F discharge) in the ear and\u002For frequent purulence (pus).\n15. Subjects with central deafness (central nervous system) or non-organic deafness.\n16. Subjects with acute otitis extrema and tympanitis.\n17. Subjects who are allergic to materials of the device.",{"count":78,"type":21},100,[54],"The goal of this clinical trial is the evaluation of performances, clinical benefits and safety of the 'Audiocap' connected hearing rehabilitation device for improving audibility in hearing-impaired people.\n\nThe main question it aims to answer is to demonstrate, after one month's use of the Audiocap connected hearing aid, that the audiological gain for the patient is better than with a placebo hearing aid.\n\nPlacebo hearing aid is a Audiocap connected hearing aid with a 'NONE' setting (flat frequency response for the patient (equivalent to not wearing hearing aid).\n\nParticipants will be first-time hearing aid users, eligible for hearing aid fitting, and adults according to French legislation (18 years and older).",[58,27],[83,84,85,86,87],"Aides auditives","Prothèses auditives","Perte auditive","Appareillage audition","Adulte audition","2025-11-24",{"date":90,"type":34},"2025-11-26",{"date":92,"type":34},"2025-09-10",{"date":94,"type":21},"2027-09",{"name":96,"class":97},"Archean Technologies","INDUSTRY",4,{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":105,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":107,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":108,"conditions":109,"keywords":115,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"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":78,"type":21},"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.",[26,110,111,112,113,114,27],"Hearing Loss, Conductive","Hearing Loss, Mixed Conductive-Sensorineural","Single Sided Deafness","Hearing Loss","Hearing-Impairment",[116],"Active transcutaneous bone conduction hearing system","2025-09-03",{"date":119,"type":34},"2025-09-08",{"date":121,"type":21},"2025-09",{"date":123,"type":21},"2035-12",{"name":125,"class":97},"Oticon Medical",{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":131,"acronym":132,"eligibilityCriteria":133,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":134,"targetDuration":4,"studyType":52,"phases":136,"briefSummary":137,"conditions":138,"keywords":142,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":42},"100592388","effectiveness-and-acceptability-of-remote-fine-tuning-of-hearing-aids-in-danish-adults-100592388","NCT06992778","Effectiveness and Acceptability of Remote Fine-Tuning of Hearing Aids in Danish Adults","Exploring the Effectiveness and Acceptability of Remote Fine-Tuning of Hearing Aids in Danish Adults: A Non-blinded, Non-inferiority Randomized Controlled Trial With an Embedded Qualitative Study","EARFit","Inclusion Criteria:\n\n* Adult patients with hearing loss who desire HA treatment (+18 of age).\n* Danish language skills both written and oral.\n* Acquisition of digital proficiency in terms of being familiar with operating a smartphone, including navigating menus, opening and closing apps, and interacting with the touchscreen with capabilities for audio and video calls.\n* Access to a smartphone that are compatible with manufacturers' system requirements.\n* Access to a stable network connection on the mobile device, with either Wi-Fi or mobile data.\n\nExclusion Criteria:\n\n* Patients with tinnitus requiring treatment or scoring more than 58 in the 'Tinnitus Handicap Inventory' (THI) grading system.\n* Patients with Ménière disease, due to its complications and symptoms as dizziness, balance problems and fluctuating hearing loss, that can affect the HA treatment.\n* Patients who will receive in-the-ear (ITE) hearing aids, due to potential limitations in connectivity for remote fine-tuning.\n* Patients which are recommended\u002Foffered unilateral HA treatment.",{"count":135,"type":21},120,[54],"The aim of this clinical trial is to evaluate the effectiveness and user satisfaction of remote fine-tuning of hearing aids compared to traditional face-to-face adjustments. The main questions aims to answer:\n\n\\- Are hearing aid outcomes (self-reported and objective) similar when using remote fine-tuning compared to face-to-face adjustments?\n\nResearchers will compare remote fine-tuning (using a smartphone app) to traditional face-to-face fine-tuning sessions in a clinical setting.\n\nParticipants will:\n\n* Be randomized to either the remote fine-tuning group (intervention group) or the face-to-face adjustment group (control group).\n* Attend five scheduled consultations over a 3-month period, including baseline measurements, hearing aid fittings, and follow-up visits.\n\nParticipants in the remote fine-tuning group will:\n\n\\- Set up and use a hearing aid manufacturer's smartphone app to complete fine-tuning sessions from home.\n\nParticipants in the face-to-face group will:\n\n\\- Visit the clinic for in-person fine-tuning appointments.\n\nData will be collected through questionnaires (e.g., SSQ-12, IOI-HA, and COSI) and objective measures such as the Speech Intelligibility Index (SII) and speech comprehension in noise (DS-FF). Additional qualitative data will be gathered from interviews with participants in the remote fine-tuning group.",[27,139,140,141],"Telehealth","Hearing Aid Fitting","Effectiveness",[143,144,145,146,147],"Remote fine-tuning","Teleaudiology","Randomized controlled trial (RCT)","Hearing aids","Denmark","2025-08-13",{"date":150,"type":34},"2025-08-14",{"date":152,"type":34},"2025-05-27",{"date":154,"type":21},"2026-03-30",{"name":156,"class":41},"Zealand University Hospital",{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":16,"sex":17,"minAge":163,"maxAge":164,"enrollmentInfo":165,"targetDuration":4,"studyType":52,"phases":167,"briefSummary":168,"conditions":169,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":42},"100492584","a-prospective-cohort-study-on-change-of-cognitive-function-in-aged-related-hearing-loss-with-hearing-aids-100492584","NCT05694039","A Prospective Cohort Study On Change of Cognitive Function In Aged-related Hearing Loss With Hearing Aids","Inclusion Criteria:\n\nAge\\>60yrs，≤85yrs（MCI prevalence was 6.7% for ages 60-64, 8.4% for 65-69, 10.1% for 70-74, 14.8% for 75-79,and25.2% for80-84）; Sensorineural Hearing loss with pure-tone thresholds 25-70 dB HL at octave frequencies between 250 and 4000 Hz, 4 frequency PTA of ≥ 30 dB HL, and the PTA ≤ 90 dB HL; Diagnosed as Presbycusis; Score of 23 or below on Mini-Mental Status Exam (MMSE); Score of 22 or below on Montreal Cognitive Assessment (MoCA);\n\nExclusion Criteria:\n\nHearing loss exceeding the limits that can be successfully aided with hearing aids (i.e., profound hearing loss); Significant history of otologic or neurologic disorders; Hearing loss remediated with a cochlear implant (cannot wear hearing aids); Any clinically significant unstable or progressive medical condition; Any condition which, in the opinion of the investigator, places the participant at unacceptable risk if he or she were to participate in the study.","60 Years","85 Years",{"count":166,"type":21},388,[54],"Background:\n\nDeafness is one of the nine potentially modifiable risk factors for dementia simulated by the Lancet dementia Prevention, intervention and Care Committee in 2017. Some studies have found that the risk factors of dementia in deafness system, with the increase of the degree of deafness, the risk of cognitive decline increases, while after long-term wear of hearing aids, the deterioration of immediate and delayed memory is less, and the possibility of cognitive decline slows down. Therefore, it is necessary for us to improve the auditory ability of patients with deafness through auditory intervention, so as to slow down its effect on dementia and reduce the incidence of dementia. At present, auditory intervention methods include hearing aid wearing and cochlear implant.\n\nHowever, there are few studies on cognitive function of presbycusis patients in China, and there is no research on how many years of auditory intervention can effectively slow down the incidence of dementia in presbycusis patients with MCI. Therefore, we intend to conduct a prospective cohort study on the changes of cognitive function of presbycusis under hearing aid intervention.",[170,171,27,172],"Age-related Hearing Loss","Hearing Loss, Sensorineural","Cognitive Function Abnormal","2023-01-20",{"date":175,"type":34},"2023-01-23",{"date":177,"type":34},"2022-03-09",{"date":179,"type":21},"2028-03-09",{"name":181,"class":41},"Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University"]