Clinical Trials in South Korea / NCT07297524
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CRESCENDO: ChildREn's muSiC ENhancement in Cochlear Implant Users
NCT07297524 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Cochlear ImplantHearing Loss
Investigational drug(s) / intervention(s)
Mobile Auditory Rehabilitation
Mobile Auditory Rehabilitation: Mobile Application for Auditory Rehabilitation
Study summary
This exploratory, single-center, single-arm study investigates the impact of a 12-week Multimodal Acoustic Therapy (MAT) intervention followed by a 12-week follow-up period on both objective and subjective auditory perception in pediatric cochlear implant users.
Eligibility
Inclusion Criteria:
* Individuals with cochlear implants
* Korean patients aged 10 to 19 years
* Capable of using a smartphone
* Scored ≤80% on MCI pre-assessment
* Voluntarily agreed to participate in this study
Exclusion Criteria:
* Has systemic medical conditions (e.g., cancer, stroke) that limit daily functioning
* Has intellectual disability, congenital malformation, or other neurological disorders affecting language or cognitive abilities
* Has diagnosed emotional disorders such as depression or anxiety
* Primarily uses sign language for daily communication
* Has undergone cochlear implant revision surgery
* Has prior experience with the investigational auditory rehabilitation application used in this study
Primary outcome measure(s)
- Melody Contour Identification (MCI) — 12 weeks
Participants complete a melody contour identification task in which they listen to brief melodic sequences and select the contour pattern (e.g., rising, falling, flat). Performance is quantified as the percentage of correctly identified contours (% correct). Higher scores indicate better melody contour perception.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Seoul National University Hospital | Seoul | Seoul |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07297524 on ClinicalTrials.gov ↗ ← All trials in South Korea