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Audiological benefits and subjective satisfaction with adhesive bone-conduction device in conductive hearing loss patients

Audiological benefits and subjective satisfaction with adhesive bone-conduction device in conductive hearing loss patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019012
Enrollment
Unknown
Registered
2018-10-08
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

conductive hearing loss

Interventions

Case series:An adhesive form of bone-conduction hearing device, 8 weeks of use during waking hours

Sponsors

The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Unilateral or bilateral conductive hearing loss, as defined by the affected ear(s) having bone-conduction thresholds of no worse than 25 dB(HL) at 0.5 – 4 kHz and air-bone gaps of at least 10 dB at three of the tested frequencies; 2. Absence of skin or scalp conditions that may preclude attachment of the adhesive adapter, or interfere with audio processor usage; 3. Aged 6 years and above and can comply with evaluation procedures; 4. Cantonese as the primary language; 5. Willingness to attend extra audiological sessions for evaluating device benefits; 6. Willingness to fill out journal regarding device usage and questionnaires regarding user satisfaction; 7. Willingness and being able to provide daily care to a loaned device; 8. Gives consent to taking part in the study.

Exclusion criteria

Exclusion criteria: 1. Does not meet one or more of the inclusion criteria listed above; 2. Any type of hearing loss other than conductive; 3. Health, physical, or cognitive conditions that would interfere with the completion of, participation in, or provision of valid responses during the required audiological evaluations, or interfere with adherence to study procedures.

Design outcomes

Primary

MeasureTime frame
Change in sound-field audiometric threshold;Change in sentence reception threshold in noise;Self-rated hearing qualities associated with device use;

Secondary

MeasureTime frame
User experience with the adhesive bone-conduction device;

Countries

China

Contacts

Public ContactMichael Tong

Department of Otorhinolaryngology, Head and Neck Surgery, The Chinese University of Hong Kong

mtong@ent.cuhk.edu.hk+852 3505 1277

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026