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Use of Frequency Compression in Severe-profound Hearing Loss Adults

Not Applicable
Completed
Conditions
Frequency Compression
Severe-profound Hearing Impairment
Registration Number
NCT04623112
Lead Sponsor
University College, London
Brief Summary

The purpose of this study is to investigate the functional benefits of frequency compression vs no frequency compression or fitted to hearing loss in severe-profound hearing impaired adults with high frequency hearing losses. Thus, assessing whether hearing aids for this patient population can be adapted to improve speech perception.

Detailed Description

Frequency compression is a feature available on some digital hearing aids, which is aimed at increasing the audibility of high frequency sounds. It works by taking sounds above a fixed start frequency and compresses it into lower frequencies where residual hearing is better.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria
  1. Participants must be over 18 years of age- This study is looking at the use of frequency compression & its effects of speech perception in adults.
  2. No ear surgery that would make it impossible to fit a hearing aid- To ensure limited confounding variables.
  3. No history of ear surgery within the last 12 months- To ensure limited confounding variables.
  4. No history of ear infection(s) within the last 6 months- To ensure no contraindications and limited confounding variables to testing.
  5. No otoscopic abnormality making it impossible to fit a hearing aid- To ensure no contraindications to testing.
  6. Bilateral severe-profound hearing impairment with air conduction thresholds >71dBHL within the frequency range of 250Hz to 4 kHz- To analyse the effects of frequency compression on speech perception within this patient population.
  7. Post lingual deafness, with good spoken English- To ensure reliability of speech testing.
  8. Previous bilateral digital hearing aid experience (6+ months)- To ensure limited confounding variables.
  9. Written consent required.
Exclusion Criteria
  1. Participants under the age of 18 years.
  2. History of ear surgery making it impossible to fit a hearing aid.
  3. History of ear surgery within the last 12 months.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Adaptive Bamford-Kowal-Bench Test4 weeks post hearing aid fitting with adapted hearing aid feature

Aided Sentence Test

CHEAR Auditory Perception Test4 weeks post hearing aid fitting with adapted hearing aid feature

Aided Monosyllabic Speech Test

Secondary Outcome Measures
NameTimeMethod
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