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Clinical Trials/NCT02794623
NCT02794623
Completed
N/A

Evaluation of Tinnitus Suppression for Cochlear Implant Recipients

The Hearing Cooperative Research Centre1 site in 1 country12 target enrollmentOctober 18, 2014
ConditionsTinnitus

Overview

Phase
N/A
Intervention
Not specified
Conditions
Tinnitus
Sponsor
The Hearing Cooperative Research Centre
Enrollment
12
Locations
1
Primary Endpoint
Tinnitus Severity Questionnaire
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Tinnitus is the perception of sound in the absence of an external sound. Prevalence in the general population is 10 to 15%, with tinnitus severely impacting quality of life in 1-2 percent of the population. Tinnitus therapy is based on counselling, cognitive and behavioural therapies in combination with sound therapies which mostly rely on masking.

For cochlear implant candidates, the ability to use hearing aids and maskers is limited by the degree of their hearing loss. Reports of tinnitus prevalence in this group range from 67 to 100% with a mean of 80%.

In cochlear implant (CI) recipients, tinnitus suppression primarily occurs during active use of the cochlear implant system. In some CI recipients residual inhibition of tinnitus occurs when the implant is switched off. While the benefits of CI implantation on tinnitus are well documented, there is a group of recipients where tinnitus remains a concern in the implanted ear post-operatively.

The primary aim of this study is to investigate the benefits of using tinnitus masking via a CI sound processor that optimises tinnitus suppression with minimal annoyance to the user. Furthermore a questionnaire will be employed to capture the prevalence, degree and nature of tinnitus in recipients.

Registry
clinicaltrials.gov
Start Date
October 18, 2014
End Date
June 8, 2018
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
The Hearing Cooperative Research Centre
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Freedom or CI500 series implant
  • At least 3 months experience with the cochlear implant
  • Native speaker in the language used to assess speech perception performance
  • Willingness to participate in and to comply with all requirements of the protocol
  • Self-reported tinnitus in the implanted ear
  • Reside local to investigational site

Exclusion Criteria

  • Signs of retrocochlear or central origin to hearing impairment as confirmed by medical examination and test including MRI
  • Additional handicaps that would prevent participations in evaluations
  • Unrealistic expectations on the part of the subject, regarding the possible benefits, risks and limitations that are inherent to the study

Outcomes

Primary Outcomes

Tinnitus Severity Questionnaire

Time Frame: Testing over 6 months

Tinnitus severity questionnaire using Visual Analog Scale

Word recognition scores in quiet

Time Frame: Testing over 6 months

Monosyllabic word scores in quiet

Speech recognition scores in noise

Time Frame: Testing over 6 months

Sentence recognition scores in noise

Secondary Outcomes

  • Degree of handicap as a result of tinnitus(Testing over 6 months)

Study Sites (1)

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