COMPLETED

Design Improvements With SONNET 3

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

Measuring user-reported satisfaction with the latest behind-the-ear (BTE) audio processor model.

Official Title

Evaluating Design Improvements With SONNET 3 in Experienced Cochlear Implant Users

Quick Facts

Study Start:2024-12-16
Study Completion:2025-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06597747

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:7 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Implanted with a MED-EL cochlear implant in at least one ear
  2. * ≥ 12 months since activation of the MED-EL audio processor
  3. * Consistently using a SONNET (EAS) or SONNET 2 (EAS) Audio Processor
  4. * Ability to complete all study procedures
  5. * Participant and parental (if applicable) commitment to comply with all study procedures for the duration of the study
  1. * Evidence that hearing loss is retrocochlear in origin
  2. * Unable to provide reliable feedback during cochlear implant programming
  3. * Skin or scalp condition precluding use of the study device
  4. * Unrealistic participant or parent (if applicable) motivation or expectations
  5. * Participants without a stable fitting map at enrollment e.g., due to changes in hearing, global health status, etc.

Contacts and Locations

Study Locations (Sites)

University of North Carolina
Chapel Hill, North Carolina, 27517
United States

Collaborators and Investigators

Sponsor: Med-El Corporation

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 Date2024-12-16
Study Completion Date2025-07-31

Study Record Updates

Study Start Date2024-12-16
Study Completion Date2025-07-31

Terms related to this study

Additional Relevant MeSH Terms

  • Hearing Loss, Sensorineural