Prescription Procedures for Cochlear Hybrid Devices to optimise the acoustic-to electric output requirements for adults who use a Hybrid device.

The HEARing Cooperative Research Centre Limited0 sites16 target enrollmentSeptember 16, 2010

Overview

No summary available.

Registry

who.int

Start Date

September 16, 2010

End Date

TBD

Last Updated

6 years ago

Study Type

Interventional

Sex

All

Sponsor

The HEARing Cooperative Research Centre Limited

•1\. Will be eighteen years of age or older at the time of evaluation.
•2\. Will be users of a Cochlear Hybrid System with a minimum of 12 months experience prior to enrolment.
•3\. The audiometric criteria for residual hearing in the implanted ear will be within the range of normal to profound.
•4\. A willingness to wear all device conditions (New hearing aids and Hybrid sound processor) on a daily basis for the duration of the study.
•5\. A willingness to participate in and to comply with all requirements of the protocol including a willingness to complete all tests and questionnaires.

•1\. Children under the age of 18 years of age.
•2\. People whose primary language is other than English (LOTEs).
•3\. Additional needs or disability that would prevent participation in evaluations.
•4\. Unrealistic expectations on the part of the participant, regarding the possible benefits and limitations of the study.