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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05619575
Other study ID # CLTD5836
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 20, 2022
Est. completion date January 10, 2024

Study information

Verified date January 2024
Source Cochlear
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acceptance and performance of the CP1170 sound processor in experienced adult cochlear implant recipients compared with the CP1150 sound processor and their current sound processor.


Description:

This investigation is planned to investigate the performance and clinical benefits of features that are new to the CP 1170 Sound Processor. This study will build on the evidence previously collected on OTE (off the ear) sound processors and ForwardFocus, with particular focus on the acceptance and satisfaction of the automation of ForwardFocus in the CP1170 Sound Processor and associated components in general.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date January 10, 2024
Est. primary completion date January 10, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Aged 18 years or older 2. Post lingually deafened 3. Implanted with the CI600 Series (CI612, CI632, CI622, CI624), CI500 Series (CI512, CI532, CI522); Freedom Series (CI24RE(CA), CI24RE(ST), CI422) or N24 Series (CIC3). 4. At least 6 months experience with a cochlear hearing implant 5. At least 3 months experience with any Nucleus sound processor and SCAN program 6. Able to score 30% or more at +15 SNR with CI alone on a sentence in babble test 7. Willingness to participate in and to comply with all requirements of the protocol 8. Fluent speaker in English as determined by the investigator 9. Willing and able to provide written informed consent. Exclusion Criteria: 1. Additional disabilities that would prevent participation in evaluations 2. Unrealistic expectations on the part of the subject, regarding the possible benefits, risks and limitations that are inherent to the procedures 3. Unable or unwilling to comply with the requirements of the clinical investigation as determined by the Investigator 4. Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling 5. Cochlear employees or employees of Contract Research Organisations or contractors engaged by Cochlear for the purposes of this investigation, as determined by the Investigator. 6. Current participation, or participation in another interventional clinical study/trial in the past 30 days, involving an investigational drug or device (unless the other investigation was/is a Cochlear sponsored investigation and determined by the investigator or Sponsor to not impact this investigation).

Study Design


Related Conditions & MeSH terms


Intervention

Device:
CP1170 sound processor
The CP 1170 sound processor will be used to determine the hearing performance with the new implementation of ForwardFocus in SCAN 2 (SCAN 2 FF), as assessed by speech perception in noise.
CP1150 Sound processor
Active comparator off the ear sound processor.

Locations

Country Name City State
Australia Cochlear Macquarie Macquarie Sydney

Sponsors (2)

Lead Sponsor Collaborator
Cochlear Avania

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Speech perception testing - Speech in Noise using CP1170 sound processor using FF (forwardfocus) Paired difference in dB SRT between the CP1170 SCAN 2 FF (Automated ForwardFocus ON) and CP1170 SCAN 2 (ForwardFocus OFF) (65 dB SPL (sound pressure level) S0Nrearhalf 4Talker Babble). One day (in booth testing)
Secondary Speech perception testing - Speech in Noise using CP1170 sound processor using FF (forwardfocus) Paired difference in dB SRT between the CP1170 SCAN 2 FF (ForwardFocus ON) and CP1170 SCAN 2 (ForwardFocus OFF), (65 dB SPL S0N3 Babble). One day (in booth testing)
Secondary Speech perception in quiet with CP1170 and CP1150 Sound Processors Paired difference in percentage CNC (consonant-nucleus-consonant) Words correct in quiet (50 dB) between the CP1170 sound processor and CP1150 sound processor (commercial version) One day (in booth testing)
Secondary Subjective acceptance and satisfaction between the CP1170 sound processor and the subject's own processor. Ratings based on the CP1170 Questionnaire after a minimum 2-weeks actual-use of the CP1170 sound processor in the home environment and the subject's own processor.
The CP1170 Questionnaire has a 5-point Likert scale for each rating in the questionnaire for at home usage ( with the values ranging from) : 1 = least favourable option to 3 = Neutral to 5 = most favourable option.
2 weeks
Secondary Subjective hearing performance between the CP1170 sound processor and the subject's own processor Paired difference in Global SSQ12 scores after experience with the CP1170 sound processor and own processor.
The SSQ-12 is comprised of 12 items using the response format on a scale from 0 to 10, were 0 equals no ability and 10 equals perfect ability. These are divided into three sub-scales and the questions 1-5 are from the speech sub-scale, 6-8 from the spatial, and 9-12 from the qualities sub-scale. The three sub-scales are the average of the questions within. A 'not applicable' option is given for each item.
The change from baseline is then calculated and the theoretical score could vary between -10 to +10. The higher the score the better benefit and positive score indicates improved hearing, a negative value an impaired hearing.
One day
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