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Study identifier: NCT06992778 Synced from ClinicalTrials.gov · July 29, 2026
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Effectiveness and Acceptability of Remote Fine-Tuning of Hearing Aids in Danish Adults

Condition: Hearing Aid · Telehealth · Hearing Aid Fitting  ·  Sponsor: Zealand University Hospital

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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: \- Are hearing aid outcomes (self-reported and objective) similar when using remote fine-tuning compared to face-to-face adjustments? Researchers will compare remote fine-tuning (using a smartphone app) to traditional face-to-face fine-tuning sessions in a clinical setting. Participants will: * Be randomized to either the remote fine-tuning group (intervention group) or the face-to-face adjustment group (control group). * Attend five scheduled consultations over a 3-month period, including baseline measurements, hearing aid fittings, and follow-up visits. Participants in the remote fine-tuning group will: \- Set up and use a hearing aid manufacturer's smartphone app to complete fine-tuning sessions from home. Participants in the face-to-face group will: \- Visit the clinic for in-person fine-tuning appointments. Data 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.

This description comes directly from the study's public registry record.

Talk to the study team

Nagehan Altinkaya, phD student  ·  +4560625058  ·  nagal@regionsjaelland.dk

Bjarki Ditlev Djurhuus

Always discuss trial participation with your own doctor first.

Locations (1)

Zealand University HospitalKøge, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06992778