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OpenTrials
Completed

NCT Number: NCT04623112

Use of Frequency Compression in Severe-profound Hearing Loss Adults

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.
  • No ear surgery that would make it impossible to fit a hearing aid- To ensure limited confounding variables.
  • No history of ear surgery within the last 12 months- To ensure limited confounding variables.
  • No history of ear infection(s) within the last 6 months- To ensure no contraindications and limited confounding variables to testing.
  • No otoscopic abnormality making it impossible to fit a hearing aid- To ensure no contraindications to testing.
  • 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.
  • Post lingual deafness, with good spoken English- To ensure reliability of speech testing.
  • Previous bilateral digital hearing aid experience (6+ months)- To ensure limited confounding variables.
  • Written consent required.

Exclusion criteria

  • Participants under the age of 18 years.
  • History of ear surgery making it impossible to fit a hearing aid.
  • History of ear surgery within the last 12 months.

Treatment and study plan

Hearing aid feature: Frequency Compression

Device

FC Deactivated/Activated & set to default/Activated & set to hearing loss

Other names: Non-linear Frequency Compression

Primary outcomes

  1. CHEAR Auditory Perception Test

    Time frame: 4 weeks post hearing aid fitting with adapted hearing aid feature

    Aided Monosyllabic Speech Test

  2. Adaptive Bamford-Kowal-Bench Test

    Time frame: 4 weeks post hearing aid fitting with adapted hearing aid feature

    Aided Sentence Test

Sponsors and collaborators

Lead sponsor

University College, London

Other

Registry information

Official study title

Do Severe-profound Hearing Impaired Adults Perform Better in Speech Perception With Frequency Compression Switched on or Off or Fitted to Hearing Loss

Acronym: FC

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Nov 10, 2020
Registry last updated
Nov 10, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.