Quality of Life With Bone Conduction Hearing Device (NCT03864731) | Clinical Trial Compass
CompletedNot Applicable
Quality of Life With Bone Conduction Hearing Device
Austria24 participantsStarted 2019-02-25
Plain-language summary
The aim of this study is to compare the audiological and quality of life performance patients have with an ADHEAR (adhesive bone conduction device) compared to no hearing device.
Who can participate
Age range13 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Unilateral and/or bilateral conductive hearing loss (CHL)
* Conductive hearing loss \>10 decibel on average
* Subjective benefit from the device
* Subjects aged 13 years or older
* Capable of the German language
* Willingness and ability to perform all tests required for the study
* Signed, and dated informed consent before the start of any study specific procedure
Exclusion Criteria:
* Pregnancy or breastfeeding
* Patient uses a hearing aid or plans to acquire a hearing aid
* Patient is intolerant of the materials as described by Manufacturer
* Patient presents with a skin or scalp condition that may preclude the attachment of the adhesive adapter.
* Patient cannot perform the audiological tests or is unable to fill out the questionnaires.
* Patient presents with retrocochlear, or central auditory disorder.
* any physical, psychological, or emotional disorder that would interfere with the ability to perform on test and rehabilitation procedures