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OpenTrials
Completed

NCT Number: NCT02856659

Evaluation of N6 Sound Processor in Group of Freedom Users

Study of freedom sound processor users that upgrade to N6 sound processor CP900 series. To test speech understanding in each device and usability of upgrade.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Subjects with sensorineural hearing loss
  • 12 years of age and older
  • Currently using Freedom Sound Processor
  • Recipient of a Ci22M or CI24 series implant
  • Minimum of 3 months experience with Freedom Sound Processor
  • Prior documentation of sentence recognition in noise at a +10 SNR or better
  • Native English speaker
  • Willingness to participate and comply with requirements of protocol

Exclusion criteria

  • Unable to complete test metrics
  • Unrealistic expectations regarding possible benefits
  • Additional handicaps that would prevent or restrict participation in audiological evaluations
  • ABI cochlear implant recipient

Treatment and study plan

Primary outcomes

  1. Evaluation of N6 Sound Processor in Group of Freedom Users

    Time frame: 3 months of use

    Speech recognition measures in quiet & noise via word and sentence rest and SSiQ questionnaire to compare freedom to upgrade with N6 relative to speech, spatial and quality dimensions and N6 questionnaire.

Sponsors and collaborators

Lead sponsor

Cochlear

Industry

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Aug 5, 2016
Registry last updated
Aug 5, 2016

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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