Skip to content

Study on Auditory Remodeling Mechanism in Hearing Loss Population Based on EEG-MEG-fMRI

Study on Auditory Remodeling Mechanism in Hearing Loss Population Based on EEG-MEG-fMRI

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600130667
Enrollment
Unknown
Registered
2026-08-23
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Asymmetric Hearing Loss, AHL

Interventions

Asymmetric Hearing Loss Group:None
Single-sided Deaf Group:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 60 years old; 2. The score of the Montreal Cognitive Assessment Scale, after adjusting for years of education, is >= 26 points, and the individual can independently or under the guidance of the researcher complete the research process; 3. Has the ability to understand Mandarin; 4. Voluntarily participates in this study and signs the written informed consent approved by the ethics committee. A. Normal Hearing Group: 1. Self-reported normal hearing, without hearing-related complaints; 2. Pure tone audiometry of both ears (0.5, 1, 2, 4 kHz) with average air conduction pure tone threshold (Pure Tone Average, PTA) = 70 dB HL, while the PTA on the unaffected side at these frequencies is = 15 dB HL; 2. Apart from hearing, other physiological and intellectual developments are basically normal, and there are no known language, cognitive, or motor impairments or previous brain injuries.

Exclusion criteria

Exclusion criteria: 1. Have active external otitis, otitis media, acute attack of Meniere's disease, diagnosed acoustic neuroma or other definite structural lesions of the central auditory pathway; 2. Have a history of epilepsy, uncontrolled severe vertigo, stroke, Parkinson's disease, severe anxiety disorder or depression, etc., neurological or mental psychological diseases; 3. Have contraindications for magnetic resonance examination, such as implanted non-compatible cardiac pacemakers, cochlear implants, nerve stimulators, ferromagnetic implanted devices like metal aneurysm clips in the body, or those with severe claustrophobia and unable to cooperate with long-term lying still scans; 4. Pregnant women, lactating women or those planning to get pregnant; 5. Participate simultaneously in other interventional clinical trials that may affect audiological or cognitive function assessment; 6. Have poor compliance and cannot cooperate with electrophysiological tests, functional magnetic resonance imaging examinations and later follow-up; 7. The investigator judges that there are any other situations that may affect the safety of the study, data quality or the rights and interests of the subjects.

Design outcomes

Primary

MeasureTime frame
Lateralization Index of Target Speech Neural Tracking;

Secondary

MeasureTime frame
Association Between Neural Indices and Clinical Auditory or Cognitive Measures;Attended–Ignored Speech Neural Tracking Difference;Behavioral Comprehension Accuracy During Speech Listening;

Countries

China

Contacts

Public ContactZhang Ke

Peking University Third Hospital

zhangkebysy@163.com+86 10 82266502

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026