Skip to content

Optimization of bimodal fitting

Optimization of bimodal fitting - OBA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00039668
Enrollment
10
Registered
2026-05-07
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Z96

Interventions

Group 1: The aim of the study is to investigate whether an optimized alignment—regarding timing, loudness, and pitch—between the hearing aid (HA) and the cochlear implant (CI) speech processor (SP) le

Sponsors

Carl von Ossietzky Universität Oldenburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Unilaterally implanted with a MED-EL C40+ or newer cochlear implant Hearing aid user on the contralateral ear (bimodal user) At least 6 months of experience with a bimodal system Fluent in German language Pure Tone Average (PTA) on the hearing aid ear of 80 dB HL or better At least 30% speech understanding on the CI No more than one deactivated CI electrode FlexSoft/Flex28 electrodes with a minimum insertion angle of 560°

Exclusion criteria

Exclusion criteria: Lack of compliance with any inclusion criteria cognitive impairments

Design outcomes

Primary

MeasureTime frame
Change in the ability of spatial sound localization, measured using a standardized localization experiment in a half-circle loudspeaker array, assessing the three different configurations (own hearing aid [HA] + own speech processor [SP], new HA + new SP, new HA + new SP optimally matched).

Secondary

MeasureTime frame
Change in speech understanding, measured using the German Matrix Test in background noise, assessing the three different configurations. Subjective evaluation of the different configurations in terms of listening comfort and sound quality using a questionnaire.

Countries

Germany

Contacts

Public ContactAndreas Radeloff

Carl von Ossietzky Universität Oldenburg

andreas.radeloff@uol.de0441 236 9698

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026