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Evaluation of Frequency Lowering Technique

P

Phonak

Status

Completed

Conditions

Hearing Loss

Treatments

Device: hearing aid NaidaUP
Device: hearing aid NaidaSP

Study type

Interventional

Funder types

Industry

Identifiers

NCT02303210
012FrL2612901

Details and patient eligibility

About

The purpose of this study is to examine two frequency lowering techniques in case of audibility, recognition, distinction, discriminability and sound quality.

Full description

This is a controlled, single blinded and randomised comparative study which is conducted monocentric at Hoerzentrum Oldenburg, Germany. The focus is to test two frequency lowering techniques with an amount of 30 moderate to severe, symmetrically sensorineural hearing impaired adult subjects. The subjects, all of them native German speakers, individually conduct a number of laboratory standard tests and home trials (questionnaires) during 6 months including seven appointments of 2 hours.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • female and male adults (>18 years old)
  • mild to severe Hearing Loss
  • symmetric Hearing Loss
  • german native speakers

Exclusion criteria

  • persons who are not able to attend multiple appointments
  • persons who are not able to handle a hearing aid
  • persons with a mental handicap
  • persons with limited access to multiple hearing situations
  • persons with psychological disease
  • no acclimatization to hearing aids

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

hearing aid NaidaUP
Other group
Description:
Within subject design: compare frequency lowering one with frequency lowering two.
Treatment:
Device: hearing aid NaidaUP
hearing aid NaidaSP
Other group
Description:
Within subject design: compare frequency lowering one with frequency lowering two.
Treatment:
Device: hearing aid NaidaSP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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