Cochlear Implant Comodal Treatment Evaluation

  • Research type

    Research Study

  • Full title

    Evaluation of a Comodal Treatment Approach in Cochlear Implant Recipients with a Contralateral Hearing Aid

  • IRAS ID

    246895

  • Contact name

    Dan Gnansia

  • Contact email

    dagn@oticonmedical.com

  • Sponsor organisation

    Oticon Medical

  • Duration of Study in the UK

    3 years, 0 months, 0 days

  • Research summary

    The study aims to evaluate a new treatment approach named the co-modal treatment approach where a group of cochlear implant users will be fitted and programmed with a suitable hearing aid on the opposite ear simultaneously during their cochlear implant activation. The second treatment group, named the delayed bimodal group, will include cochlear implant users who will be fitted and programmed with a suitable hearing aid on the opposite ear sequentially following 3 months of their cochlear implant activation. The delayed bimodal treatment approach is most commonly practiced and in this study, the co-modal treatment approach will be evaluated against the delayed bimodal treatment approach.

  • REC name

    London - Fulham Research Ethics Committee

  • REC reference

    19/LO/0897

  • Date of REC Opinion

    7 Jun 2019

  • REC opinion

    Favourable Opinion