RECRUITING

Perceptual Consequences of Cochlear Implant Electrode-neuron Interfaces

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Despite the success of cochlear implants, devices surgically placed in the inner ears of patients with severe hearing loss, there remains substantial variability in the overall speech perception outcomes for the children and adults who receive them. The main goals of this project are: i) to improve our understanding of how cochlear implants affect the developing auditory system, ii) apply that knowledge to test new methods for programming children and adults, and iii) to study how long it takes listeners to adapt to new cochlear implant programs over the short- and long-term. The results will improve our understanding of how the deafened auditory system develops with cochlear implant stimulation and advance clinical practice to improve hearing outcomes in cochlear implant listeners.

Official Title

Development and Assessment of Listener-tailored Programming for Cochlear Implant Listeners

Quick Facts

Study Start:2022-09-16
Study Completion:2027-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05867173

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:6 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult at least 18 years old
  2. * Native speakers of American English
  3. * Wears a cochlear implant manufactured by Advanced Bionics (Clarion Hi-Focus I or newer), Cochlear, or MED-EL
  4. * Children at least 6 months old
  5. * Native speakers of American English
  6. * Wears a cochlear implant manufactured by Advanced Bionics (Clarion Hi-Focus I or newer), Cochlear, or MED-EL
  7. * For both children and adults with a cochlear implant, some study criteria might pertain to a subset of subjects, such as a specific age at which the subjects developed a hearing loss, or was implanted.
  1. * Inability to provide informed consent
  2. * Does not meet the inclusion criteria for a specific study protocol, such as age of onset of hearing loss, age of cochlear implantation, duration of deafness, number of active electrodes in the cochlear implant device
  3. * Unable to carry out the study protocol or tasks required in the study
  4. * Inability to provide informed consent
  5. * Hearing loss, or significant history of hearing related issues
  6. * Unable to carry out the study protocol or tasks required in the study

Contacts and Locations

Study Contact

Julie Arenberg
CONTACT
617-807-7904
julie_arenberg@meei.harvard.edu

Principal Investigator

Julie Arenberg
PRINCIPAL_INVESTIGATOR
Massachusetts Eye and Ear

Study Locations (Sites)

Mass Eye and Ear
Boston, Massachusetts, 02114
United States
Boston Children's Hospital
Waltham, Massachusetts, 02453
United States

Collaborators and Investigators

Sponsor: Massachusetts Eye and Ear Infirmary

  • Julie Arenberg, PRINCIPAL_INVESTIGATOR, Massachusetts Eye and Ear

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-09-16
Study Completion Date2027-03-31

Study Record Updates

Study Start Date2022-09-16
Study Completion Date2027-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • Deafness