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Completed

NCT Number: NCT01184248

The Effect of Sound Stimulation on Pure-tone Hearing Threshold

The purpose of this study is to investigate if sound stimulation could improve pure-tone hearing threshold.

In the late 1990s, researchers discovered that acoustic stimuli slow progressive sensorineural hearing loss and exposure to a moderately augmented acoustic environment can delay the loss of auditory function. In addition, prolonged exposure to an augmented acoustic environment could improve age-related auditory changes. These ameliorative effects were shown in several types of mouse strains, as long as the acoustic environment was provided prior to the occurrence of severe hearing loss.

In addition to delaying progressive hearing loss, acoustic stimuli could also protect hearing ability against damage by traumatic noise. In particular, a method called forward sound conditioning (i.e., prior exposure to moderate levels of sound) has been shown to reduce noise-induced hearing impairment in a number of mammalian species, including humans.

Interestingly, recent report has suggested that low-level sound conditioning also reduces free radical-induced damage to hair cells, increases antioxidant enzyme activity, and reduces Cox-2 expression in cochlea, and can enhance cochlear sensitivity. Specifically, increased cochlear sensitivity was observed when distortion product otoacoustic emissions (DPOAEs) and compound action potentials (CAPs) were measured.

In addition to forward sound conditioning, backward sound conditioning (i.e., the use of acoustic stimuli after exposure to a traumatic noise) has been shown to protect hearing ability against acoustic trauma and to prevent the cortical map reorganization induced by traumatic noise.

Based on the results of animal studies, the investigators conducted a human study in 2007 and observed that sound stimulation could improve hearing ability. On average, the pure-tone hearing threshold decreased by 8.91 dB after sound stimulation for 2 weeks. In that study, however, the investigators observed only the hearing threshold changes by sound stimulation.

To verify the previous ameliorative effect of sound stimulation, the investigators included a control period in this study.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Earlogic Corporation

Los Angeles, California, 90005, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • You are a male or female aged between 18 and 70 years
  • You have 25~70 dB HL hearing loss at any frequency above 1.5 kHz
  • You are able to use an mp3 player
  • You are able to read English

Exclusion criteria

  • Under the medications that could cause hearing loss (such as gentamicin, aspirin, ibuprofen, or acetaminophen)
  • Chronic disease that could affect hearing (such as diabetes or high blood pressure)
  • Temporal hearing loss
  • Hearing loss more than 75 dB HL at any frequency
  • Ear infections, chronic middle ear disease or any abnormality of the ear canal or ear drum
  • Hearing aid user
  • Pregnant females

Treatment and study plan

Sound stimulation

Behavioral

Listening to sound stimuli at the lowest audible level.

Primary outcomes

  1. Changes of pure-tone hearing thresholds after sound stimulation

    Time frame: 4-6 weeks

Sponsors and collaborators

Lead sponsor

Earlogic Korea, Inc.

Industry

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2011
First posted
Aug 18, 2010
Registry last updated
Sep 8, 2011

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.

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