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Optimization of remote assessment in cochlear implant recipients.

Optimization of remote assessment in cochlear implant recipients. - ORACI1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON56547
Enrollment
44
Registered
2024-01-31
Start date
2024-05-01
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deafness

Interventions

NA. In this study we use cochleair implants and matching sound processors. These devices are used in this research, but are not part of the research question itself.&nbsp

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
16 Years to 99 Years

Inclusion criteria

Inclusion criteria: CI-users: • Postlingually deafened adults (>16 years). • Legally capable • Excellent spoken and written Dutch, at the level of a *native*. • Implanted with a cochlear implant of Advanced Bionics at least on one side. • Using the AB Naida M90 sound processor. • At least 3 weeks experience with their Cl (subjects in rehabilitation). • At least 12 months experience with their Cl (experienced subjects). • Speech scores in quiet of at least 50%. Normal hearing: • >16 years • Legally capable. • Excellent spoken and written Dutch, at the level of a *native*. • Hearing threshold averaging

Exclusion criteria

Exclusion criteria: • Disorders other than a hearing impairment that could affect the study results. • Not able to complete 2 hours of testing.

Design outcomes

Primary

MeasureTime frame
Outcomes on audiological tests: NVA phoneme scores, DIN test, and Matrix test.

Secondary

MeasureTime frame
The secondary study parameters are comparisons between scoring mechanisms (clinician vs. self-scoring) of the tests mentioned above. We will also compare outcomes on the different tests both within-subjects and between subjects. Additionally, secondary study parameters are subject characteristics possibly influencing performance and discrimination abilities. Demographic data will be gathered to accurately describe the study sample, such as type of implant, experience with implant, duration of deafness etc.

Countries

Netherlands

Contacts

Public ContactC.A.A. Windmeijer

Leids Universitair Medisch Centrum

c.a.a.windmeijer@lumc.nl0715264600

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026