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A Study Using EEG to Evaluate Speech Perception Ability in Cochlear Implant Users in Noisy Environments

Central Auditory Processing Mechanisms of Speech Perception Deficits in Cochlear Implant Users in Spatialized Noise: An EEG Study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119547
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Sensorineural hearing loss (SNHL)

Interventions

Cochlear Implantation Listeners:deafness and wearing bilateral cochlear implants
Bimodal Listeners(C group):deafness and wearing a cochlear implant and a contralateral hearing aid
Normal-Hearing Participants (Group A):Behavioral testing under controlled noise conditions

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Inclusion Criteria for Normal-Hearing Participants (Group A): Normal auricle morphology, patent external auditory canal, and intact tympanic membrane. Four-frequency (500, 1000, 2000, and 4000 Hz) pure-tone average (4f-PTA) < 25 dB HL in both ears. Bilateral tympanometry shows type A curves, and ipsilateral and contralateral acoustic reflexes can be elicited. Able to cooperate with all relevant assessments and complete tests and questionnaires under guidance. Voluntarily agrees to participate and signs the informed consent form. 2.Inclusion Criteria for Bilateral Cochlear Implant Users (Group B): Patients with bilateral cochlear implants, either simultaneous or sequential implantation; the second-side cochlear implant has been activated for more than 3 months. Wears both devices regularly every day, with a total daily usage of at least 10 hours. Morphology of bilateral cochleae and auditory nerves is basically normal, without significant malformations. No clear cognitive impairment, intellectual disability, or psychiatric disorders. Able to cooperate with all relevant assessments and complete tests and questionnaires under guidance. Voluntarily agrees to participate and signs the informed consent form. 3.Inclusion Criteria for Bimodal Hearing Users (Group C): Patients with a unilateral cochlear implant, activated for more than 3 months post-implantation. Wears a hearing aid on the contralateral side, with the four-frequency average hearing threshold (500, 1000, 2000, 4000 Hz) = 50 dB HL on that side. Wears both the cochlear implant and contralateral hearing aid regularly every day, with a total daily usage of at least 10 hours. Morphology of bilateral cochleae and auditory nerves is basically normal, without significant malformations. No clear cognitive impairment, intellectual disability, or psychiatric disorders. Able to cooperate with all relevant assessments and complete tests and questionnaires under guidance. Voluntarily agrees to participate and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Active otologic diseases. 2.Severe cognitive impairment, significant intellectual disability affecting self-care, or serious psychiatric disorders. 3.History of major structural brain lesions (e.g., severe cerebrovascular disease, epilepsy, brain tumors, etc.). 4.Cervical spine disorders preventing normal head rotation. 5.Any other conditions that, in the investigator’s judgment, make the participant unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
spatial release from masking;mismatch negativity(MMN);

Secondary

MeasureTime frame
root-mean-squared error(RMSE);cortical auditory evoked potential(CAEP);

Countries

China

Contacts

Public ContactLi Jiaying

Beijing Chao-Yang Hospital, Capital Medical University

imlilyli@outlook.com+86 10 5201 0982

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026