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Reducton of fatigue with speech enhancer in LUMITY

Reducton of fatigue with speech enhancer in LUMITY - SRF-14264

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032482
Enrollment
22
Registered
2023-08-31
Start date
2023-08-14
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Moderate to severe hearing loss

Interventions

Group 1: Speech Enhancer On and OFF

Sponsors

Sonova AG
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Experienced (minimum use duration 6 months), Ability to understand instruction, Ability to describe listening experiences, Healthy outer ear

Exclusion criteria

Exclusion criteria: Clinical contraindications deformity of the ear (closed ear canal or absence of pinna), Fluctuating hearing that could influence the results.

Design outcomes

Primary

MeasureTime frame
Subjective rating of listening effort and fatigue

Secondary

MeasureTime frame
D2-R Test, Hornsby Test, CC-OLSA, Ability to multitask in the auditory and visual domains measured with multitask test

Countries

Germany

Contacts

Public ContactJan Heeren

Hörzentrum Oldenburg gGmbH

heeren@hz-ol.de+49 441 2172 245

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026