Prescription Procedures for Cochlear Hybrid Devices in Hearing Loss.

Not Applicable

• Conditions: Hearing loss; Ear - Deafness

• Registration Number: ACTRN12610000773033
• Lead Sponsor: The HEARing Cooperative Research Centre Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-09-16
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

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.

Exclusion Criteria

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified