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RBANS-H in Older Patients Before and After Cochlear Implantation: A Protocol for a Prospective Study (RBANS-H-CI-A)

A

Antwerp University Hospital (UZA)

Status

Enrolling

Conditions

Hearing Impaired

Treatments

Device: Cochlear implant

Study type

Observational

Funder types

Other

Identifiers

NCT02794350
15/17/181

Details and patient eligibility

About

The cognitive profile of older adults with a severe to profound hearing impairment is determined by means of the Repeatable Battery for the Assessment of Neuropsychological Status, adjusted for Hearing impaired subjects (RBANS-H) before and after cochlear implantation. In this prospective, longitudinal study the participants are tested preoperatively, at six months and twelve months postoperatively and from then on yearly up to 10 years after implantation. In addition to the RBANS-H an audiological examination and an semistructured interview is conducted concerning the cochlear implant use and the self-reliance of the patient and subjective questionnaires are filled out by the subjects to assess quality of life and hearing benefit.

Enrollment

20 estimated patients

Sex

All

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • age: 55 or older
  • cochlear implant candidate (speech understanding in quiet worse than 60% at 65 decibel sound pressure level (dB SPL) in the best aided condition)

Trial design

20 participants in 1 patient group

Cohort
Treatment:
Device: Cochlear implant

Trial contacts and locations

1

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Central trial contact

Paul Van de Heyning, Prof. dr.; Annes Claes, MSc

Data sourced from clinicaltrials.gov

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